Careers at Merck KGaA, Darmstadt, Germany

ERP Senior Project Manager (Burlington, Massachusetts, US, 01803)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

As a Sr. ERP Project Manager, you will lead ERP projects from conception to implementation or be part of a larger Program to do so. You will work closely with business units and IT teams to ensure that ERP solutions align with company goals and integrate seamlessly with our existing systems. Your leadership will help our Life Science Business enhance its operational efficiencies and support our ongoing digital transformation. Part of your responsibilities are:

Project Planning and Management: Define project scope, goals, and deliverables that support business objectives in collaboration with senior management and stakeholders. Develop full-scale project plans and associated communications documents.
Project Leadership: Lead and mentor project team members and contractors and influence them to take positive action and accountability for their assigned work.
Stakeholder Management: Manage stakeholder communication and ensure ongoing engagement. Act as a mediator between stakeholders and team members.
Budget and Resource Allocation: Develop and deliver budget proposals and recommend subsequent budget changes. Estimate the resources and participants needed to achieve project goals.
Risk Management: Identify and manage project dependencies and critical path. Plan for and mitigate risks that can affect the project timeline and deliverables.
Quality Assurance: Ensure project deliverables meet quality standards and requirements. Implement project standards across projects to ensure consistency and efficiency.
ERP Expertise: Stay updated on SAP capabilities and trends. Ensure SAP solutions are leveraged to maximize ROI for the company.

Who You Are

Minimum Qualifications:

Bachelors Degree in Project Management, Business Administration or related field
At least 8 years of experience in an information systems environment
At least 5 years of IT project delivery experience in Life Science industry, leading high-profile projects across one or more functional domains
Experience navigating and successfully implementing and deploying ERP (SAP) systems. Drive project delivery schedule and support process, ensuring compliance to project standards and timely program delivery

Preferred Qualifications:

Masters Degree in Project Management, Business Administration or related field
Experience in ERP project methodologies. Ability to provide input to functional specifications and make recommendations to system optimization, support, and guidance.
Experience with SAP S4/HANA
Experience in requirements gathering, prioritization, collaborating across multiple business teams.
Excellent interpersonal, written, and verbal communication skills. Demonstrated ability to effectively communicate with a variety of audiences including various levels of management, vendors, business teams with varied levels of skill/experience. Ability to clearly communicate technical subject matter to a non-technical audience. Strong people skills in a diverse cultural environment.
Demonstrated ability to prioritize and execute tasks in a demanding environment and make sound decisions in urgent situations. Must possess strong analytical, problem-solving, and prioritization skills.
Must have experience and knowledge of change management principles and methodologies and can formulate innovative programs to generate excitement and engagement.
Financial acumen along with a sound understanding of data flows and one or more functional areas (e.g., Manufacturing, Supply Chain, Finance, Sales/Trade, Human Resources).
A highly collaborative work style which includes working effectively across all organizational levels
Proven ability to influence cross-functional teams without formal authority, especially among development teams.
Ability to manage multiple, concurrent projects and be responsive to users and IT staff in a timely manner.
Demonstrated ability to establish strong partnerships across business and technology areas

Location

This position is required to be site based in either our Burlington, MA or St. Louis, MO office. We do offer a hybrid flexible work arrangement.

Pay Range: $116,300-$159,400

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Manager, Inhouse Consulting (Burlington, Massachusetts, US, 01803)

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This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your role:

We love consulting! Do you? As the company's internal consultancy, we tackle strategic projects across Healthcare, Life Science, Electronics, and Enabling Functions. Our diverse team of around 75 colleagues brings expertise from top-tier external consultancies, major industry players, and top academic institutions. With offices in Darmstadt (HQ), the Greater Boston Area (USA), and Singapore, we deliver high-impact projects to the company's most critical business challenges.

Working directly with senior management, we lead local, regional, and global initiatives that drive organizational success. Beyond providing consulting services, we serve as a talent incubator for our company, with a considerable number of colleagues transitioning into key leadership or expert roles throughout the organization every year. Combining both, business consulting and people development, we contribute to the company's success and accelerate your career!

You will work as part of project teams, providing business consulting for strategy development, commercial excellence, and operations, before transitioning to the next exciting career step within our company after approximately 2-4 years. As a colleague and trusted partner, you support projects from design to implementation, inspiring change throughout the organization. You own projects end-to-end, handling interactions with internal clients and guiding project teams in flat team structures. As Data & AI are key drivers of innovation and performance at our company, you proactively identify and apply Data & AI opportunities in your projects.

Our approach differs from external consulting. We offer:

Empowerment: You own your projects from proposal development to steering committee presentations, and project closure. Project assignments are matched with your individual development goals and reflect your level of seniority. You will be able to directly experience the impact your work has on our business and patients worldwide.
Career development: Your leadership in challenging consulting projects will give you high visibility across our business sectors, allowing you to cultivate a deep internal network and ultimately positioning you for a successful transition into your next chapter within our company. While advancing your own professional growth, you simultaneously invest in mentoring and developing junior colleagues.
Flexibility of work: You will experience our high-impact culture with less business travel and more flexible work arrangements than in external consulting. Moreover, we run a hybrid workplace approach with a healthy mix of remote work and office presence.

Who you are:

Minimum Qualifications

Master’s degree in natural sciences, engineering, or business
Work experience of 2-5 years in management consulting
Proficiency in English

Preferred Qualifications

An advanced degree (PhD or MBA) is a plus
Industry-related experience in pharma, biotech, diagnostics, bioprocessing, biology, medical devices or similar

Strong track record of leading projects across multiple functional areas with exposure to different hierarchical levels. More extensive leadership experience is a plus
Practical experience in applying Data & AI to solve business challenges, and the passion to continue developing skills in this field
Excellent communication and presentation skills, creativity, analytical strength, and strategic thinking
Proactive, self-motivated work approach with a passion for working in teams

Location: Burlington, MA, USA; Hybrid 3x week onsite

Travel: <15%; International and Domestic

Pay range for this position: $123,500.00 - $185,300.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Distributor Account Manager, Tissue Diagnostics (Field Based) (Burlington, Massachusetts, US, 01803)

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This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

In this pivotal role, you will serve as a trusted expert and strategic partner within the clinical diagnostics market, driving revenue growth and expanding distributor relationships across an assigned territory. Your deep knowledge of in vitro diagnostics (IVD) and the clinical pathology landscape will be central to shaping how customers adopt and benefit from our diagnostic solutions.

You will design and execute territory business plans, develop targeted campaigns and promotions, and deliver technical training to distributor partners and end customers. By leveraging your expertise in technical sales and partner management, you will ensure sustainable, long-term account growth. You will be expected to travel up to 50% within your assigned territory, with occasional travel across the US and internationally for training and business meetings.

This position is remote, with a location preference for candidates in any U.S. location.

You will be expected to travel up to 50% within your assigned territory, with occasional travel across the US and internationally for training and business meetings.

Who You Are

Minimum Qualifications:

Bachelor's degree in Life Sciences or a Business discipline, OR an Associate's degree combined with a Clinical Laboratory Certification
5 or more years of experience in Sales, Marketing, or a customer-facing role within healthcare diagnostics, OR 5 or more years of experience working within healthcare diagnostics or IVD regulated diagnostic products
Demonstrated experience developing and delivering technical presentations to diverse audiences

Preferred Qualifications:

Experience in immunohistochemistry or a strong working knowledge of the clinical pathology market
Proven track record of meeting or exceeding sales targets in a territory-based role
Experience managing distributor relationships and navigating complex, multi-level account structures
Ability to work independently and collaboratively within a global, matrixed organization, inspiring teamwork to achieve shared goals
Proficiency with sales tools and technology, including CRM platforms such as Salesforce, Microsoft Office, and sales analysis software
Strong organizational, communication, time management, and interpersonal skills with a detail-oriented approach
Sound judgment and problem-solving ability in handling distribution, product, and customer challenges

US Base Pay Range: $115,000 – $181,200

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Export Operations Manager (CR)

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Your Role

At the heart of our global Life Science business, this role puts you in charge of a critical operation: leading the Americas Export Customer Service team that connects our science and technology portfolio with customers in markets where we operate without a local legal entity.
You will own the end-to-end order-to-invoice process across the Americas region, ensuring every customer interaction, from quotation through shipment to final invoice, is handled with precision, compliance, and care.
You will lead, coach, and develop a dedicated team, setting clear priorities and building a culture of accountability and continuous improvement. You will act as the escalation point for complex cross-border issues, drive performance through KPI monitoring, and partner closely with Sales, Supply Chain, Logistics, Regulatory, and Trade Compliance stakeholders. Ensuring full adherence to export controls, sanctions, embargo restrictions, and country-specific documentation requirements will be central to your mandate. You will also identify and lead process improvement and digitalization initiatives that raise the bar for how export customer service is delivered across the region.

Who You Are

You bring at least 5 years of experience in Export Operations, or a related customer-facing environment, combined with demonstrated people management and leadership experience.
You have a strong command of end-to-end order management and Lead-to-Invoice processes, with hands-on experience in international logistics, export documentation, and complex cross-border shipments.
You have a solid understanding of export regulations and trade compliance, including sanctions, embargo restrictions, export licenses, import permits, and country-specific shipping documentation.
You are a confident people leader who coaches, motivates, and develops teams, drives performance management, and fosters a customer-focused, accountable team culture.
You are skilled at managing escalations, balancing competing priorities, and making sound, risk-aware decisions under pressure.
You bring strong stakeholder management skills and the ability to influence and collaborate effectively across functions and organizational levels.
You are comfortable working with ERP systems such as Oracle or SAP, CRM platforms, and reporting tools, and you thrive in complex, international, and evolving environments.
You communicate fluently in English, both in writing and verbally; proficiency in additional languages is an advantage.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior AWS Cloud Architect (Mollet del Valles, Barcelona, ES, 08100)

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United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role

Ready to shape the future of digital, data and information technology in healthcare manufacturing and supply chain? As Senior AWS Cloud Architect, you will design and implement scalable, secure and AI ready cloud architectures that turn business needs into reliable data, analytics, automation, machine learning and generative AI solutions. You will act as a trusted architectural partner for business and technology stakeholders, create reusable blueprints and engineering patterns, and guide internal and external teams from concept through delivery. Working across a global matrix, you will oversee platform architecture, strengthen automation and observability, support production solutions, and promote responsible adoption of cloud and AI capabilities.

You will translate complex requirements into pragmatic solution designs, implementation guidance and standards aligned with security, enterprise architecture and responsible AI principles. You will evaluate AWS services, build proof of concepts, define model integration and operationalization patterns, and provide third level support for manufacturing and supply chain applications. By mentoring colleagues and sharing knowledge, you will help teams deliver high quality solutions with the right balance of scalability, resilience, performance, reusability and cost efficiency.

Who You Are

A master's degree in computer science, engineering, data science or a comparable discipline, or equivalent professional experience.
Five to eight years of hands on experience in AWS cloud architecture and engineering, including at least three years working with data warehousing, data lake and cloud native analytics concepts.
Practical experience with AWS artificial intelligence and machine learning services, including Amazon SageMaker, Amazon Bedrock, AWS Lambda, API Gateway, Glue, Step Functions, Athena, Redshift and EMR, or comparable enterprise platforms.
Experience designing AI ready architectures with secure data access, model integration, prompt and API orchestration, retrieval augmented generation patterns, observability and responsible AI guardrails.
Strong expertise in APIs, application deployment, integration patterns, continuous integration and continuous deployment using Azure DevOps and Git, plus infrastructure as code using CloudFormation or comparable tooling.
At least three years of experience with container architectures, Docker and Kubernetes on AWS, together with strong knowledge of services such as S3, Redshift, RDS, Glue, Step Functions, Lambda and EMR.
Strong Python, SQL and PySpark skills, with experience building scalable applications, data processing pipelines, monitoring, alerting, health checks and production grade solutions.
Strong communication and stakeholder engagement skills, experience in agile delivery, mentoring and cross team collaboration, plus professional fluency in English. AWS certifications are highly desirable.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Site Head Cherokee, St Louis (St. Louis, Missouri, US, 63118-3306)

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Your Role:

The St. Louis, MO, Cherokee CDMO site is a center of excellence for antibody drug conjugates (ADCs), bioconjugates, and small molecule production. We are currently completing a $76M investment to optimize existing production capacity and enhance process and analytical labs to support the rapidly expanding ADC market.

The Site Head of the St. Louis, MO, Cherokee site is responsible for the strategic planning, directing, and controlling of development, manufacturing and quality operations. You are responsible for development and implementation of programs to permanently improve safety and quality systems and processes and ensure GMP compliant and cost-efficient manufacturing through effective utilization of resources, equipment, facilities, and materials. In addition, this individual assures production/supply chain schedules are met to fulfill forecasted market demand.

The Cherokee Site Head is critical in the realization of our CDMO business, Advanced Solutions Life Science ambition and Integrated Supply Chain Operation (ISCO) strategic goals to become the market leading CDMO player in the industry with a best-in-class supply chain.

Key accountabilities in this role include:

Ensure safe and compliant operation, making Safety and Quality the top priorities for your site.
Ensure the successful and profitable operation of the facilities, including the General Manufacturing Practices manufacture and the in-spec and on-time release of products.
Provide leadership to the site, supervising the site leadership team including process and analytical development, manufacturing, engineering, quality, and supply chain; total staff ~400.
Make final decisions on critical operations matters and ensure best in class services are delivered to customers.
Partner and collaborate with customers, business development, project management, and various Group Functions such as Innovation, Supply Chain, EHS, Quality, HR, Finance.
Ramp-up production capacity in the facility with the approved expansion project, ensuring Commercial Readiness across all functions.
Support and drive development of robust manufacturing processes for drug product from clinical to commercial.
Ensure appropriate staffing of people resources and capabilities and drive production schedule, optimizing utilization of resources and assets.
Develop the budget and manage areas of responsibility within approved budget and contracted scope of work.
Make recommendations concerning long-range capacity planning, as well as upgrading of capital investments into existing site which is in line with strategic planning.
Develop relevant KPIs for CDMO Excellence in collaboration with other CDMO sites and drive performance accordingly.
Ensure highly effective and efficient training.
Drive digitalization, automation and advancement of manufacturing and quality technologies in collaboration with company-wide initiatives.
Support commercial team with customers’ request for proposals, business presentations, etc.
Strengthen site in their customer engagement and focus on value creation for the customer needs.
Ensures service targets and customer’s on-time delivery in full expectations are met.
Be the accountable host for regulatory and customer audits and site visits.
Identify and mitigate risks in operations including manufacturing, engineering, facilities management and quality that could adversely impact project outcomes and timely delivery of critical treatment to patients.
The St. Louis, Cherokee site is dedicated to CDMO business, with close partnership with the Bioconjugation & Small Molecules Modality leadership to ensure strategic business needs are included and voiced in both the manufacturing strategy and operational targets for the site.

Who you are:

Minimum Qualifications:

Bachelor’s degree in relevant technical discipline (Chemical Engineering, Immunology, Biochemistry, or related scientific discipline).
A minimum of 10-15 years' experience in Manufacturing/Operations/Quality in the Biotech/Life Science CDMO Industry.
A minimum of 5 years at a senior level leading an organization of significant size in a life science, GMP/FDA regulated industry such as pharmaceutical and biopharmaceutical.
Experience with regulated products or services.
Strong cross-functional communication abilities across both Operations and Business communities, as well as customers.

Excellent management and communication skills at C-level as well as at operators’ level.
Excellent working knowledge of US and EU GMP regulations, and direct experience in communicating with regulatory authorities.
Leadership skills in managing change, influencing others outside areas of direct responsibility, attracting/developing talent.
Strong situational leadership - ability to couple high performance standards and can-do attitude with strong coaching and empowerment approach.
Ability and proven track record to build and grow high performing teams.
Interested and experienced in driving digitalization effort.
Strong problem-solving skills based on analytical strengths, active listening, and a diversity mindset .
Experience with troubleshooting and technology transfers.
Strong business acumen and experience with financial management.

Preferred Qualifications:

Masters, PhD and/or MBA preferred.
Experience with common continuous improvement tools (e.g. six sigma).
Ideally participated in the design, construction and commissioning of expanding manufacturing facilities.
Ability to travel domestically and internationally, up to 10%.

Pay Range for this position: $208,000 - $340,900

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Digital Products Quality Engineering Lead (St. Louis, Missouri, US, 63103-1433)

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Your Role:

Digital Products Quality Engineering Lead is responsible for the strategic guidance and direction of quality assurance and quality control of digital products developed / maintained following Agile framework. You will lead a team of software quality engineers to ensure the digital products meet the quality standards that will enable the end customers to meet their quality and regulatory/validation needs. You will work with cross-functional global teams in various disciplines, promote built-in quality, shift-left practices, continuous verification and enable the software quality engineers to meet the quality objectives of digital products. You are responsible for end-to-end quality assurance and quality control activities for digital products, applying 4 eye principles, managing escalations, solving problems promptly, and fostering a collaborative, high-performance culture.

You are familiar with relevant industry standards and guidance, including GAMP 5 supplier-focused principles and applicable Software related ISO standards, and understand the quality expectations of customers in regulated life-science environments

Can be located in Burlington or St. Louis

Who You Are:

You bring 10+ years of combined experience as manager/supervisor level managing; software development / engineering, digital transformation, software quality assurance / control, software quality management, proficiency in life science / pharma regulations/ industry standards / related ISO standards.
You have a strong command in software product life cycle, change management, agile ways of product development, DevOps, Lean, Plan-Do-Check-Act, software test automation, risk-based quality management systems, building and developing the team competency/management, cloud-based platforms, implementation experience of CSA-Computer Software Assurance is a plus.
You have a proven track record in, shaping digital product’s quality engineering, converting challenges into actions to enable faster Go-to-Market Transformation, software operational controls (change, incident, audit support, questionnaire, supplier quality, periodic review, deviations), Continuous Integration and Continuous Delivery software development, communicate with clarity, able to influence software engineering team’s quality mindset.

You bring hands on experience in, establishing software development processes and its continuous improvement, workflows, template, defining / monitoring key quality indicators, mentoring quality assurance/control team members, design reviews/verification, review of software engineering artifacts (specifications, code/objects, test scripts, executions evidence), product engineering traceability, defect management and corrective/preventive management.

You are experienced in ensuring digital product quality meets customer expectations, quality promises, compliance with required/applicable science regulations, industry standards/ benchmark guidance, including GAMP 5 supplier focused principles, related ISO standards, digital product development/lifecycle artifact’s inspection readiness, facilitating quality/product audits / inspections, life regulated industry is a plus.

Bachelor’s or higher degree in Computer Science, Engineering disciplines, Information/ Operational Technology, Digital and Data management or Information Science / Management, Bio-Medical Science, or other Life Science disciplines. Willingness to travel globally based on the need of project and business.

Minimum Qualifications:

Bachelor’s or higher degree in Computer Science, Engineering disciplines, Information/ Operational Technology, Digital and Data management or Information Science / Management, Bio-Medical Science, or other Life Science disciplines.
10+ years of combined experience in software development / engineering, digital transformation, software quality assurance / control, software quality management, proficiency in life science / pharma regulations/ industry standards / related ISO standards.

Preferred Qualifications:

Good written and verbal skills.
Excellent computer skills, i.e., Project Planning, Word, Excel, PowerPoint, SharePoint.
Experience with GMPs, GCPs, GLPs, GAMP and Part 11 compliance
Global travel based on the need of project and business.

Pay Range for this position: $111,400-$196,000

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Modality Leader APeC (Singapore, Singapore, SG, 609927)

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Job Title: Senior Modality Leader APeC

As a member of the Customer Application team, the Senior Modality Leader, APeC will provide strategic and technical leadership in novel and strategic modalities. The role will work closely with commercial partners, customers, and cross-functional teams to develop integrated solutions, identify growth opportunities, strengthen market positioning, and support business development across the APeC, excluding China region.

This role can be based in either Singapore, India or Korea.

Your Role:

Regional strategy and commercial collaboration

Partner with Commercial and Customer Application teams to develop and execute regional initiatives for integrated solutions focused on strategic modalities.
Support Regional Strategy Execution, Strategy, Field Marketing, and Commercial teams in planning, coordinating, and delivering regional Plans of Action.
Apply knowledge of customers, industry trends, market drivers, and competitive dynamics to identify opportunities for market-share growth and business expansion.
Collaborate with Sales to identify, qualify, and pursue new commercial opportunities, particularly pre-sales projects involving strategic modalities.
Develop and implement regional objectives for strategic modalities, including the assessment of business dynamics associated with strategic customers and projects.
Prepare and validate the information required to prioritize customer projects and commercial opportunities.

Customer engagement and consultancy

Represent the company’s expertise in novel modalities through face-to-face and virtual customer engagements.
Provide high-level technical and commercial consultancy on novel modalities and their applications.
Identify customer needs, assess business potential, and apply technical expertise to support the effective use of technologies within the relevant regulatory environment.
Build trusted relationships with industry decision-makers and opinion leaders to strengthen the company’s market presence and share of mind in strategic modalities.
Use customer feedback and market experience to help internal teams understand emerging trends, regulatory considerations, customer pain points, and evolving market needs.

Marketing, market intelligence, and portfolio development

Support brand awareness and the marketing of the company’s products and solutions for pharmaceutical and biotechnology customers across the assigned territory.
Support the successful launch of new products and contribute to initiatives that reinforce product positioning and selling strategies.
Maintain strong technical knowledge across the company’s full Process Solutions Strategic Modalities portfolio.
Monitor competitor activity, changing customer requirements, and emerging market trends, and communicate relevant insights to leadership, business, and strategy teams.
Share customer and commercial feedback, best practices, and identified capability gaps with relevant stakeholders to support business and portfolio development.
Track changes in local market dynamics and translate these insights into actionable business strategies in collaboration with Customer Application and business stakeholders.
Contribute market and customer insights that may influence future product and solution development.

Knowledge sharing and capability building

Participate in and contribute to capability-building activities, including seminar series and other Technology Team programs.
Share relevant customer, market, regulatory, and technology insights with internal teams to strengthen organizational knowledge and support consistent customer engagement.

Who You Are:

Education and Experience

Bachelor’s degree or equivalent qualification in Life Sciences, Biotechnology, Chemical Engineering, or a related discipline.
A Masters in Business Administration PhD, or equivalent combination of education and relevant industry experience is preferred.
At least 10 years of experience in either a professional expert or managerial role.
Strong scientific experience, ideally including hands-on work with strategic modalities such as mRNA, pDNA, vaccines, plasma, peptides, or GLP-1-based products.
Strong understanding of the Process Solutions business

Ability to manage complex and dynamic projects with a variety of key stakeholders.

Personal attributes

Customer-focused and commercially aware.
Digitally agile and comfortable using data and technology to support decision-making.
Proactive, action-oriented, and accountable.
Curious, inquisitive, and skilled at asking insightful questions.
Assertive, influential, and confident when engaging with senior stakeholders.
Able to connect perspectives across functions and maintain an integrated, enterprise-wide mindset.

Technical and functional expertise

Knowledge of the biopharmaceutical market, biopharmaceutical manufacturing processes, and Advanced Therapy Medicinal Products, with particular expertise in novel modalities.
Understanding of customer strategy and commercial business development.
Knowledge of sales and go-to-market strategy.

Strong reporting, data analysis, and business insight capabilities.
Fluency in English and, where applicable, the relevant local language.

Behaviors and capabilities

Prioritizes and organizes work effectively in a fast-paced environment.
Thinks and acts strategically while adapting with agility to changing customer and business needs.
Communicates clearly and effectively, both verbally and in writing, including through presentations and stakeholder interactions.
Builds and maintains strategic working relationships across functions and organizational levels.
Uses strong influencing skills to shape decisions and engage senior stakeholders.
Demonstrates strong project management and execution skills in complex, multi-stakeholder environments.
Can assess customer manufacturing processes, identify areas of opportunity, and connect customer needs to the company’s products, services, and solutions.
Maintains a curious, growth-oriented mindset and actively seeks to learn about new applications, technologies, and therapeutic areas.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Specialist Group Technical Operations Controlling (Darmstadt, Hessen, DE, 64293)

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Your role:

You will be integral part of our Group Controlling team driving all topics related to production cost controlling in close collaboration with the business sectors. On one hand we drive forecasting and actual reporting of production costs and net working capital. On the other hand, we provide a platform for the cost reporting and performance measurements for all production sites. We give guidance to ensure correct cost accounting, driving projects to increase transparency and identifying potential financial improvements.

Your role will include two main topics. First, Gross Profit Reporting (Review, Forecast, and Strategy): Create financial reports and business analyses, act as a developed expert with sound professional knowledge and bring in your perspective in the decision-making process. Second, Net Working Capital: Further develop our Controlling tools to measure the performance of working capital management and the related cash conversion in close collaboration with the business sectors.

Who you are:

You have an analytical mindset including high interest in translating data analysis into clear business recommendations.
You have a talent to explain complex topics with simple words and you are confident in interacting with senior leadership.
You like creating new ideas and driving finance projects across departments.
You have experience in production controlling or related functions.
You have an IT affinity to support the digitalization.
You have a degree in business administration, economics or engineering
You are skilled and proficient with related systems (Powerpoint, Excel, TM1, BO analyzer)
You are fluent in English

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Werkstudent (m/w/d) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Sind Sie bereit, neue Wege zu gehen, Herausforderungen zu meistern und Neues zu entdecken? Wir wissen, dass Sie große Pläne haben – und die haben wir auch! Unsere Kolleg:innen auf der ganzen Welt lieben es, mit Wissenschaft und Technologie innovativ zu sein und das Leben der Menschen durch unsere Lösungen zu bereichern. Gemeinsam haben wir Großes im Sinn und engagieren uns mit Leidenschaft für Menschen, Kund:innen, Patient:innen und die Erde, auf der wir leben. Deshalb sind wir stets auf der Suche nach neugierigen Köpfen, die sich vorstellen können, mit uns Großartiges zu erreichen.

Ihre Aufgaben:

Für unser Distributionszentrum suchen wir Ihnen als Verstärkung. Wir versenden täglich tausende Produkte in dutzende Länder. Werde Teil eines diversen und engagierten Teams, das tagtäglich vielfältige Aufgaben übernimmt. IHre Aufgaben sind unter anderem die termingerechte, vollständige und korrekte Bearbeitung von Kundenaufträgen. Dazu gehören zum Beispiel das Zusammenstellen und Transportieren von Paketen und Paletten (hauptsächlich Chemikalien verpackt in unterschiedlichen Flaschen und Behältern). Die Aufgaben eignen sich gut, um erste Einblicke in die Abläufe eines Distributionszentrums zu bekommen.

Ihre Qualifikationen:

Interesse an modernen und innovativen Logistik- und Distributionsprozessen – auch für Gefahrgut
Gültige Zuverlässigkeitsüberprüfung nach § 7 Abs. 1 Luftsicherheitsgesetz (LuftSiG) - diese kann von uns beantragt werden (Voraussetzungen müssen erfüllt sein)
Eingeschriebener Student (m/w/d) an einer Universität
Hohe Teamfähigkeit und Offenheit für neue Aufgaben und Herausforderungen
Erfahrung in Dokumentation und Datenverarbeitung (z.B. Scanner)
Sehr gute Deutschkenntnisse in Wort und Schrift (C1)
Flexibilität und Bereitschaft tagsüber in Gleitzeit zu arbeiten
Sie sind körperlich in der Lage, bei einem Technikausfall bis zu 25kg zu heben und auf akustische Warnsignale zu reagieren

Was wir bieten:

Umfassende Einarbeitung und Schulungen
Flexible Arbeitszeiten, die sich mit deinem Studium vereinbaren lassen
Starkes Team mit vielfältigen Hintergründen, Perspektiven, Berufs- und Lebenserfahrungen

Was können Sie bei uns erwarten? Wir sind neugierige Köpfe, die ein breites Spektrum an Hintergründen, Perspektiven und Lebenserfahrungen mitbringen. Wir sind überzeugt, dass diese Vielfalt außergewöhnliche Leistung und Innovation fördert und unsere Fähigkeit stärkt, in Wissenschaft und Technologie an der Spitze zu stehen. Wir setzen uns dafür ein, dass alle Menschen die Möglichkeit haben, sich in ihrem eigenen Tempo zu entwickeln und zu wachsen. Unterstützen Sie uns dabei, eine Kultur der Integration und Zugehörigkeit zu schaffen, die Millionen von Menschen erreicht und jeden ermutigt, sich für den Fortschritt der Menschheit einzusetzen.

Bewerben Sie sich jetzt und werden Sie Teil eines Teams, das Neues entdeckt und die Menschheit voranbringt.

Global Business Process Expert - R2R - Site2Service Accounting (f/m/d) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

The “Global Business Process Expert for Site Service accounting” (gBPE S2S) plays a critical part in managing and optimizing the end-to-end process in accounting for Site2Service charging (cross-charging of services related to Merck sites in Germany, e.g. fire department, plant maintenance services, rental fees), commonly known as "Site Service Charging". Site Service Charging contains the fully automated end-to-end process from charging request input by service provider, validation of incoming data, creation of Sales Order, Billing and posting of incoming invoice at receiver in Merck Group. Site Service charging covers mainly Merck Intercompany charges, but as well Intracompany charges and 3rd party customer invoices. The gBPE S2S drives global structural process improvements, standardization, and automation in close collaboration with the Innovation and Analytics team, business units, service delivery teams, and support functions. The gBPE S2S establishes core capabilities within GES to support enterprise strategy and transformation initiatives.

Key Responsibilities:

End-to-end accountability for process optimization, reconciliation activities, transformation initiatives, and strategic business-critical programs (e.g., ERP).
Continuous assessment and enhancement of the end-to-end Site Service Charging process with focus on automation, standardization, and efficiency improvements.
Implementation and support of resource planning initiatives.
Definition, design, architecture, and implementation of a global end-to-end process model to optimize operations across all organizational units (within and outside GES).
Promotion of process simplification, standardization/modularization, and automation in close alignment with operational units, business units, and support functions.
Management and assurance of appropriate processes for business and support functions.
Identification and implementation of internal and external best practices.
Ownership of tools, applications, systems, policies, and process design in close collaboration with relevant stakeholders.
Definition and execution of process governance in collaboration with the BPM team, including: Change control processes, Compliance assurance, Documentation and maintenance, Definition of control and risk points and audit tracking
Close collaboration with the Data team to ensure data governance.
Accountability for strategic initiatives such as ERP implementation, automation programs, and peripheral solutions (e.g., BTP Apps, workflows).
Leadership of process improvement initiatives leveraging modern technologies and best practices to drive efficiency gains.
Definition, management, and maintenance of KPIs to measure operational performance and process standardization.
Promotion of automation and continuous enhancement of relevant reporting tools.
Internal and external KPI benchmarking.
Definition and management of SLAs for Site Service Charges delivered by operational units in global alignment with relevant stakeholders.
Enhancement of quality, user experience, and effectiveness across the end-to-end process.
Own the scope extension and penetration both vertically and horizontally to deliver further services covers to the business and enabling functions.
Build critical competencies within the value-stream team to identify, prioritize, develop solutions, and drive improvement measures.
Alignment with operational leaders in the R2R area to develop learning pathways for subject matter experts (SMEs).
Establishment of learning and knowledge-sharing platforms by sub-process to promote best practices and knowledge exchange.
Fostering a virtual process network to enhance quality and productivity.
Close collaboration with delivery teams and their leaders in hubs and/or service centers.
Interface function (dotted-line reporting) between functional leaders in the R2R Subledger area and BPO R2R-SL.

Who you are:

Master’s degree or Bachelor’s degree from an accredited university in accounting & finance or equivalent; relevant certification highly desirable (MBA, MSc, CPA, CMA)
Proven experience (ideal 5+ years) in a senior accounting expert role in a big multinational organization and/or Shared Services / Global Business Service organizations with strong insight in general accounting and R2R processes with dedicated focus on SAP supported Intercompany and 3rd party Service Charging.
Sound understanding of accounting standards and financial reporting (IFRS, local GAAP, etc.)
Experience in business process design, ideally with SAP S/4HANA
Experience with process automation and technologies in the R2R environment (e.g., ERP customization, RPA)
Proven experience in managing multi-year transformation and improvement programs (standardization, automation, policy adjustments)
Strong analytical and problem-solving skills
Innovation Mindset: Proactive identification of technology-enabled solutions to close process gaps and drive operational excellence
Analytical Strength: Strong analytical and problem-solving capabilities with continuous orientation toward improvement
Results-Oriented & Team Player: Goal-focused, reliable team contributor with excellent interpersonal skills, flexible communication style, and ability to thrive in complex matrix organizations
Communication Excellence: Effective collaboration with cross-functional teams, audit functions, and external partners
Decision Making: be able to take decisions on business process based on cross-functional legal and business requirements
Hands-On Curiosity & Critical Thinking: Openness to identifying opportunities, capability to drive solutions through obstacles, combined with creative and reflective thinking
Project Leadership: Proven track record leading process improvement projects across multiple organisational units (standardization, automation, policy changes)

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of Platform Architecture (all genders) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

Your Role

You will shape the technical foundation that makes enterprise-grade digital platforms and data products trusted, scalable, and ready for customers. In this pivotal role, you will own the end-to-end platform architecture across a portfolio of cloud-native products and deployment models — translating ambiguous business and customer needs into clear technical strategy, reusable capabilities, and executable roadmaps. You will define architectural principles covering security, scalability, resilience, and maintainability, and design data and AI platforms that span ingestion, transformation, storage, analytics, lineage, access control, and secure multi-tenancy. You will lead decisions on deployment strategies — including multi-cloud, hybrid, and customer-managed models — balancing data residency, cost, portability, and compliance. Applying security-by-design and defense-in-depth, you will ensure platforms are certifiable and audit-ready, translating frameworks such as ISO/IEC 27001, SOC 2, NIST, GDPR, and GxP into concrete architectural controls. You will stay close to implementation — reviewing designs, prototypes, and critical code paths, establishing practices for infrastructure-as-code, continuous delivery, observability, and production operations, and helping teams move confidently from prototype to production. Beyond the technical work, you will lead, develop, and grow the platform architecture team: hiring, onboarding, coaching, managing performance, planning succession, and raising the technical bar across all levels. You will communicate architectural decisions, trade-offs, and constraints clearly to engineers, product leaders, customers, partners, auditors, and senior stakeholders — making complexity accessible without losing precision.

Who You Are

You bring significant experience designing and delivering enterprise-scale software, cloud, data, or AI platforms and customer-facing digital products, with a proven ability to translate complex customer problems into architectures and executable roadmaps.
You have deep, hands-on expertise in cloud-native architecture on at least one major provider (AWS, Microsoft Azure, or Google Cloud Platform) — including containers and Kubernetes, serverless, networking, identity and access management, and observability — alongside practical working knowledge of at least one additional provider.
You have substantial experience owning secure architecture decisions in production environments, with working knowledge of relevant frameworks such as ISO/IEC 27001, SOC 2, NIST, GDPR, and, where applicable, HIPAA or GxP/GAMP 5, including designing platforms that are certifiable and audit-ready.
You have experience designing secure multi-tenant platforms and data architectures covering ingestion, transformation, storage, analytics, lineage, access controls, tenant-aware governance, and data quality, across multi-cloud, hybrid-cloud, or customer-managed deployment models.
You have several years of direct experience managing and developing technical teams — including hiring, onboarding, performance management, coaching, career development, succession planning, and resource planning — and the credibility to challenge and mentor senior and principal engineers while remaining accountable for technical quality and delivery outcomes.
You hold a degree in Computer Science, Software Engineering, Data Science, Mathematics, Physics, or a related discipline, or bring equivalent practical experience, combined with typically 10 or more years in software engineering, cloud architecture, data-platform engineering, or related technical disciplines, including at least 7 years delivering production-grade, enterprise-scale platforms.
You are proficient enough in modern programming languages such as Python, TypeScript, Java, or Go to review designs and critical code paths and guide implementation teams, and you have experience building commercial software products, SaaS platforms, or customer-managed deployments.
You communicate fluently in English and can explain architectural decisions, limitations, costs, and trade-offs clearly to engineers, product leaders, customers, partners, auditors, and executives.

Location: Location-independent, hybrid flexibility.

Role evaluation:

Role department:

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

(Senior) Internal Auditor Operational Audits (Darmstadt, Hessen, DE, 64293)

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Your role:

We're seeking highly motivated individuals to join our dynamic, diverse, and very engaged internal audit team! We offer a high-profile internal audit function, with good visibility on all management levels and a track record for developing employees into senior roles in the organization. In this role, you will have dual responsibilities that include classic operational audit activities as well as leveraging our audit analytics initiatives.

For the operational audits, you lead, coordinate, and participate in the organization and execution of internal audits of different types (subsidiary, processes, or project reviews as well as special audits) within our company globally. Responsibilities include scoping, fieldwork, coordination, communication with senior management and action planning, as well as supervise and review the work of other Internal Audit team members. You perform data analytics during fieldwork in your respective audit area, prepare meaningful, standardized audit reports documenting audit procedures and results and present audit results to senior management including recommendations.

To further leverage data analytics in our audit landscape, you will strongly contribute to changes of audit techniques and methodology through data analytics and create value using data, digital tools, platforms, technologies, services, and processes. This role includes significantly contributing to internal control topics and continuous improvement on a group level through data analytics as well as to the audit analytics strategic roadmap.

Who you are:

University degree in Business, Finance, or equivalent and audit-specific qualifications (for e.g., CPA, CIA, or CFE certification) required. Relevant professional experience (minimum seven years in audit) in an internationally operating company or in a Big 4 accounting firm is required.
Multiple years of experience in leading complex audits in accordance with the Institute of Internal Auditors (IIA) Standards. Industry experience in the Pharma, Biotech, Life Science or Electronics sector is preferred.
Strong audit experience in the areas of Finance, Order-to-Cash, Source-to-Pay, Business Governance, Healthcare Compliance (Marketing & Medical activities), etc. as well as ability to independently scope and conduct audits of complex global processes is required.
Experience in managing strategic internal projects related to continuous improvement of internal audit quality and execution.
Extensive experience in using data analytics through projects or assignments and familiarity with handling ERP system data and data analytics tools (for e.g., Microsoft Power BI, Tableau, Qlik, etc.).
Ability to be agile, open-minded and to manage audits and stakeholders of different cultures (good intercultural and communication skills), to work in a matrix organization together with a desire to develop your leadership skills; good project management and organizational skills with the ability to handle multiple responsibilities at the same time.
Business-level fluency in English; additional language skills are an advantage.
Willingness to travel globally (approx. 20% travel time).

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Corporate Counsel Legal Expert / all genders / Part-fulltime (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

Your role:

As Corporate Counsel, you will advise internal clients on digital transformation initiatives, emerging technologies, and technology-related legal regulations, including the AI Act, Data Act, Cyber Resilience Act, and other digital regulations. You will support the development and implementation of governance frameworks, policies, and processes relating to artificial intelligence, data, software, IT security, and digital innovation across the organization. Furthermore, you will advise on a broad range of legal issues relating to AI, data, intellectual property, open-source software, digital business models and emerging technologies.

You will draft, review, and negotiate complex technology and commercial agreements, including software licensing, SaaS, cloud services, digital solutions, IT projects and outsourcing arrangements. As a trusted advisor, you will support strategic digital initiatives and technology-drive business models, helping the organization identify opportunities while managing legal and compliance risks.

As a member of LE-XPERTS Enabling Functions (LE-X) in the Group Legal & Compliance (LE), you will be involved in several LE-X and LE initiatives to enhance cross-collaboration and your individual development. You will collaborate closely with colleagues across Legal, including Compliance and Data Privacy as well as Cybersecurity, Procurement, IT, Digital Office and business functions to deliver pragmatic and integrated solutions that enable innovation and sustainable business growth.

You will manage internal stakeholders as well as external partners and service providers, taking into account specific corporate governance aspects. This will require professional alignment with a broad range of internal and external stakeholders including senior management. Furthermore, you will act as a bridge between the business, the relevant Enabling Functions and our internal Legal and Compliance teams.

Who you are:

Legal degree with a minimum of 5 years of experience working as a lawyer, preferably in an international law firm or in the legal department of a multinational company.
Experience in technology law, IT law, artificial intelligence, digital regulation, cybersecurity, software licensing, and commercial contracting.
Fluent in German and in English, both written and spoken.
Comfortable working and interacting with all levels of management, including senior management.
Combine sound legal judgment with a pragmatic, solution-oriented mindset and can balance legal risks with business objectives.
Open, energetic, empathic, proactive and a team player.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Regional Sales Head / all genders / Part-fulltime (Darmstadt, Hessen, DE, 64293)

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Everything we do in Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers.

Your role:

As Regional Sales Head Europe & USA, you will shape the commercial success of the region and help accelerate growth in the semiconductor industry. You will define and execute a clear regional go-to-market and sales strategy that wins new business and increases revenue. You will build, scale, and lead a high-performing sales organization by hiring, mentoring, and coaching regional account managers. With your leadership, the team will pursue ambitious targets while developing strong, lasting customer relationships. You will cultivate strategic partnerships with global key accounts and identify opportunities to drive further growth. You will manage complex sales cycles and oversee contract management from negotiation through execution. By tracking sales metrics and forecasting performance, you will turn data into decisive commercial action. You will report regional results and insights to executive leadership with clarity and confidence. Working closely with Marketing, Product Management, Customer Application, and Customer Fulfilment teams, you will align priorities and shared KPIs to deliver an excellent customer experience.

Who you are

You have at least five years of sales experience in the semiconductor industry, ideally in a field such as lithography.
You have at least two years of experience leading and managing a sales team.
You have a strong track record of achieving revenue targets and winning new business.
You are experienced in managing complex, long-cycle sales processes and strategic customer relationships.
You bring strong leadership, coaching, negotiation, and presentation skills.
You are confident using sales data, metrics, and forecasts to guide decisions and communicate performance.
You collaborate effectively across Marketing, Product Management, Customer Application, and Customer Fulfilment teams.
You are fluent in written and spoken English and German.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Field Service Engineer (all genders) Frankfurt/Darmstadt Region (Darmstadt, Hessen, DE, 64293)

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Your Role

As a Field Service Engineer (all genders) you will be affiliated with our Darmstadt office while providing field service support to customer sites across Germany and, when required, throughout Europe. In this role, you will install, maintain, troubleshoot, and repair production material systems used in semiconductor manufacturing. These systems enable the production of chips found in technologies such as smartphones, LEDs, and flat-screen TVs. You will ensure the reliable operation of gas and chemical distribution systems, blending equipment, critical monitoring, and life-safety systems while delivering excellent customer service. In this role, you will perform preventive maintenance, equipment inspections, technical troubleshooting, and accurate service documentation, while providing practical solutions for equipment operation and configuration. This position requires up to 85% travel and a strong commitment to quality, safety, and operational excellence.

Who you are

Associate’s or Bachelor’s degree in Mechanical Engineering, Electrical Engineering, or another technical discipline
2+ years of experience in the semiconductor, chemical or other manufacturing setting is an advantage
Strong analytical and troubleshooting skills with the ability to interpret technical documentation
Experience in performing preventive maintenance, equipment troubleshooting, and documenting service activities
Committed to quality, safety, and following established procedures and escalation processes
Strong communication and customer service skills with the ability to work independently and remotely; Excellent written and verbal communication skills in English; basic German language skills are required
Physically able to perform the essential duties of the role, including lifting equipment, climbing ladders, working in confined spaces, and wearing and using required personal protective equipment (PPE)
ISO 9000/9001 awareness or knowledge of semiconductor manufacturing processes is an advantage; A valid passport and driver’s license with a clean driving record (past 36 months) are required

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Werkstudent (m/w/d) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Ihre Rolle:
Im Automatiklager, in der Distribution Darmstadt, suchen wir einen Werkstudenten (m/w/d) für sechs Monate. Zu Ihren täglichen Aufgaben zählen die Abwicklung von Kundenaufträgen sowie das Kommissionieren, Verpacken und Versenden der Ware.

Zu Ihren Hauptaufgaben gehören:

Fahren von Flurförderzeugen aller Art (Staplerschein kann vor Ort erworben werden)
Kommissionieren und Etikettieren von Kundenaufträgen
Zusammenstellung von Kundenaufträgen nach Systemvorgaben
Quantitatives und Qualitatives Kontrollieren von Waren und Gütern
Eigenverantwortliches Beladen aller Verkehrsträger und Lademittel

Ihre Qualifikationen:

Gültige Zuverlässigkeitsüberprüfung nach §7 Abs.1 Luftsicherheitsgesetz (LuftSiG) (wird innerbetrieblich beantragt)
Hohe Kunden- und Zielorientierung sowie Teamfähigkeit
Ausgeprägte Belastbarkeit, Flexibilität und Eigeninitiative
Fließend (C1) Deutsch in Wort und Schrift

Bewerben Sie sich jetzt und werden Sie Teil eines Teams, das Neues entdeckt und die Menschheit voranbringt.

Pharmaziepraktikant (m/w/d) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Gemeinsam für Patienten wollen wir in unserem Unternehmensbereich Healthcare dazu beitragen, Leben zu schaffen, zu verbessern und zu verlängern – das ist unser Daseinszweck. Wir entwickeln Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit. Unsere Teams auf 6 Kontinenten arbeiten mit Leidenschaft und unablässiger Neugier zusammen, um Patientinnen und Patienten in jeder Lebensphase zu unterstützen. Verstärken Sie unser Healthcare-Team und werden Sie Teil einer vielfältigen, integrativen und flexiblen Arbeitskultur und profitieren Sie von hervorragenden Möglichkeiten zur persönlichen Entwicklung sowie internationalen Karrierechancen.

Ihre Rolle & Aufgaben

Während Ihres sechsmonatigen Praktikums ab Mai 2027 arbeiten Sie in der Abteilung Global Analytical Development. Die analytische Entwicklung ist über den gesamten Zeitraum der Entwicklung von neuen Arzneimitteln die zentrale Funktion für alle analytischen Fragestellungen und Prüfungen von Wirkstoffen und Arzneimitteln sowie deren Zwischenstufen. Bei uns wird Sie ein Einsatz in einem der folgenden Aufgabenbereiche erwarten:

Unterstützung analytischer Fragestellungen (z.B. mittels HPLC) im Projektlabor
Entwicklung von analytischen Methoden zur Charakterisierung von Wirkstoffkandidaten
Entwicklung/Anwendung von in vitro Dissolution Assays zur Abschätzung der Wirkstofffreisetzung im Menschen und/oder zum Zwecke der Qualitätskontrolle
Evaluation innovativer Analyseverfahren oder Entwicklung von analytischen Methoden für innovative Wirkstoffklassen

Wir bieten Ihnen ein halbjähriges Pharmaziepraktikum gemäß § 4 Abs. 2 Approbationsordnung an sowie die Möglichkeit, erste Erfahrung in einem pharmazeutischen Unternehmen zu sammeln.

Wer Sie sind

Pharmazeut (m/w/d) mit erfolgreich abgeschlossenem 2. Staatsexamen
Kommunikationsstärke in Deutsch und Englisch
Spaß an der Arbeit im Team
Exakte und zuverlässige Arbeitsweise
Fit im Umgang mit MS Office

Bitte geben Sie in Ihrer Bewerbung an, für welchen der möglichen Aufgabenbereiche Sie eine Präferenz zeigen.

Your Role & Tasks

During your six-month internship starting in May 2027, you will work in the Global Analytical Development department. Analytical development is the central function for all analytical questions and tests of active substances and medicinal products as well as their intermediate stages throughout the entire period of development of new drugs. You will be expected to work with us in one of the following areas:

Support of analytical questions (e.g. by HPLC) in the project laboratory
Development of analytical methods for the characterization of drug candidates
Development/application of in vitro dissolution assays for the estimation of drug release in humans and/or for quality control purposes
Evaluation of innovative analytical methods or development of analytical methods for innovative drug classes

We offer you a six-month pharmaceutical internship in accordance with § 4 para. 2 of the licensing regulations as well as the opportunity to gain initial experience in a pharmaceutical company.

Who you are

Pharmacist (m/f/d) with successfully completed 2nd State Examination
Strong communication skills in German and English
Enjoy working as a team
Beeing accurate and reliable
Fit in MS Office

In your application, please indicate which of the possible tasks you have a preference for.

Bewerben Sie sich jetzt und werden Sie Teil eines Teams, das Neues entdeckt und die Menschheit voranbringt.

Sr Expert-Dangerous Goods SAP NEO (Milwaukee, Wisconsin, US, 53209-3650)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Global Life Sciences initiative to consolidate business operations into a single SAP NEO ERP requires senior subject matter expertise in each functional area. In this role, you will serve as the Dangerous Goods (DG) Substream expert, responsible for designing business rules for the identification, storage, packaging, and distribution of materials regulated for transport. You will act as both a senior SME and the primary coordinator among the Global Dangerous Goods team, Global Packaging Compliance, and the Transportation Compliance and Operations Integration Program Manager to ensure regulatory and business requirements are incorporated into the global ERP design. As the DG substream expert, you will work on SAP NEO project streams impacted by DG requirements (e.g., Distribution, Transport Management), necessitating a mature end-to-end understanding of operations. You will coordinate the technical and operational inputs from various SMEs and substreams, translate them for developers, develop and validate critical DG scenarios, and document results in alignment with project timelines.

Can sit in Milwuakee or St. Louis

Who You Are

Minimum Qualifications:

Bachelors or Masters degree in chemistry or other life science focus
Know-how of regulations concerning dangerous goods transport, storage, and GHS

Preferred Qualifications:

Professional accreditation in dangerous goods preferred
Can translate regulatory language into technical instructions
Extensive experience with SAP required; in-house understanding of legacy systems strongly preferred
Outstanding technical writing skills
Confident in enforcing regulatory compliance in large group settings
Well-rounded understanding of global warehousing, distribution, transportation logistics
Effective communication skills across technically variable audiences
Strong problem solving skills
Systems testing experience preferred (SAP)
Solution oriented mindset
Willing to travel for department meetings, workshops, training, and audits as needed
Willingness to work cooperatively within a global team
Team spirit, outstanding initiative, reliable

Pay Range for this position: $101,000-$169,700

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Gerente de Ventas - Endocrinología (Naucalpan de Juarez, Estado de Mexico, MX, 53370)

Aplica tu Magia con nosotros

¿Estás listo para explorar, romper barreras y descubrir mucho más? Sabemos que tienes grandes planes. Nosotros, también, innovar con la ciencia y la tecnología para enriquecer la vida de las personas con las soluciones en Healthcare, Life Science y Electronics apasiona a nuestros colegas en el mundo entero. Juntos, soñamos en grande y compartimos el entusiasmo por cuidar a una gran diversidad de personas, clientes, pacientes y al planeta. Por eso, siempre buscamos mentes curiosas que imaginen lo nunca visto con nosotros.

Unidos como uno solo para los pacientes: nuestra meta en Healthcare es ayudar a crear, mejorar y prolongar vidas. Creamos tratamientos, dispositivos inteligentes y tecnologías innovadoras en campos terapéuticos como la oncología, la neurología y la fertilidad. Nuestros equipos colaboran en 6 continentes con pasión y una curiosidad incesante con el objetivo de ayudar a los pacientes en cada etapa de su vida. Unirte a nuestro equipo de Healthcare significa formar parte de una cultura de trabajo diversa, inclusiva y flexible, que ofrece fantásticas oportunidades para el desarrollo personal y profesional en todo el planeta.

Tu Rol

Liderar un equipo comercial en el área de Endocrinología es una oportunidad para generar un impacto real en la salud de los pacientes y en el crecimiento sostenible del negocio. En este rol, serás responsable de inspirar, desarrollar y guiar a tu equipo hacia resultados sobresalientes, asegurando la ejecución efectiva de la estrategia comercial en el mercado mexicano.

Gestionarás relaciones estratégicas con distribuidores, mayoristas y clientes clave, liderando negociaciones comerciales que impulsen el crecimiento del canal. Monitorearás indicadores de desempeño —incluyendo productividad, cobertura, frecuencia y ejecución en campo— y transformarás datos en decisiones de negocio concretas. Trabajarás de manera transversal con equipos de Marketing, Medical y Supply Chain para garantizar una ejecución integral de la estrategia, asegurando la disponibilidad del producto mediante una gestión eficiente de inventarios y planeación de la demanda.

Quién Eres

Cuentas con licenciatura en Administración, Marketing, Ciencias de la Salud o áreas afines, o experiencia equivalente demostrable.
Tienes mínimo 5 años de experiencia en la industria farmacéutica y al menos 2 años liderando equipos comerciales con resultados comprobados.
Tienes experiencia sólida en manejo de distribuidores, mayoristas y canales indirectos, incluyendo negociación comercial y desarrollo de planes de negocio.
Dominas la gestión de inventarios, planeación de la demanda, y el análisis de indicadores de sell-in y sell-out para optimizar el desempeño del canal.
Tienes alta capacidad analítica y orientación a resultados: conviertes datos en decisiones de negocio con agilidad y precisión.
Demuestras liderazgo inspirador, capacidad para desarrollar talento y construir relaciones de largo plazo con diferentes grupos de interés internos y externos.

Lo que ofrecemos: Somos mentes curiosas que provienen de una amplia gama de antecedentes, perspectivas y experiencias de vida. Creemos que esta variedad impulsa la excelencia y la innovación, fortaleciendo nuestra capacidad para liderar en ciencia y tecnología. Estamos comprometidos a crear acceso y oportunidades para que todos se desarrollen y crezcan a su propio ritmo. Únete a nosotros para construir una cultura de inclusión y pertenencia que impacte a millones y empodere a todos para defender el progreso humano.

¡Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!

Head - Territory Sales (North & West Region), Discovery Solutions, Life Science, India (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Role Summary

The Head - Territory Sales for the North & West region will drive revenue growth, market expansion, and customer success for Discovery Solutions in India. This role oversees the North and West regional sales leadership, aligns with the Head of Discovery Solutions, India, and executes the regional sales strategy to meet and exceed annual targets. The role requires deep domain knowledge, strategic cross-functional collaboration, and a strong track record in high-growth B2B sales within life sciences, research, or related sectors.

Key Responsibilities

Strategic Revenue Leadership

Develop and own the North & West regional sales strategy aligned to the overall India country plan.
Translate strategic goals into actionable sales plans, forecasts, and budgets; monitor progress and adjust plans as needed.
Establish aggressive yet achievable revenue targets, and lead the regional teams to achieve and surpass them.

Team Leadership & Development

Lead, mentor, and manage the North Sales Head and West Sales Head; foster a high-performance culture.
Drive talent acquisition, onboarding, coaching, succession planning, and performance reviews.
Facilitate cross-region collaboration to share best practices, market insights, and customer success stories.

Market & Customer Intelligence

Oversee market segmentation, opportunity identification, and account planning for major strategic customers.
Build deep understanding of customer needs, competitive landscape, and regulatory considerations affecting Discovery Solutions.
Represent the customer voice in strategic planning and product/solution improvements.

Go-to-Market Execution

Drive multi-channel sales initiatives (direct field sales, channel partnerships, digital campaigns) to maximize reach and efficiency.
Ensure rigorous opportunity management, qualification, and pipeline hygiene; implement standardized sales processes.
Champion solution selling for Discovery Solutions offerings (e.g., discovery platforms, data analytics, consultative services).

Partnerships & Stakeholder Management

Collaborate with Marketing, Product, Customer Success, and Support to ensure a cohesive go-to-market approach.
Build and nurture executive-level relationships with key customers and strategic accounts in the North and West regions.
Coordinate with regional leadership to align demand generation and field activities.

Financial & Operational Excellence

Manage regional P&L, ensure cost-effective operations, and optimize resources to maximize ROI.
Monitor and report on key performance indicators (KPIs) and sales metrics; provide accurate forecasts to leadership.
Ensure compliance with internal controls, governance, and regulatory requirements.

Customer Success & Retention

Ensure high levels of customer satisfaction, renewals, and expansion within existing accounts.
Collaborate with Customer Success to minimize churn and maximize lifetime value.

Brand and Compliance

Promote Discovery Solutions’ value proposition ethically and responsibly.
Ensure adherence to company policies, safety standards, and regulatory guidelines

Qualifications

Education

MBA or equivalent degree in Business, Life Sciences, or a related field.

Experience

12+ years of progressively responsible sales leadership experience in B2B solutions, preferably within life sciences, R&D, biotech, or related sectors.
Demonstrated success in managing large, multi-region territories and leading senior sales leaders.
Proven track record of achieving revenue growth, managing complex deals, and building strategic customer partnerships.

Industry Knowledge (preferred)

Familiarity with discovery platforms, laboratory informatics, data analytics, or similar scientific software/services.
Understanding of laboratory workflows, research environments, and procurement processes in academia, pharma, and biotech.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Analyst - SAP Product Compliance (Bangalore, Karnataka, IN, 560100)

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Your Role:

• A great opportunity has opened within the Life Science IT Supply Chain Planning, Regulatory & Distribution team.

• As part of the Regulatory team, you will work closely with the product compliance business community to drive and simplify process design.

• Deliver solutions in SAP Product Compliance and Global Label Management.

Who You Are:

Minimum Requirements:

• Graduate degree (or equivalent) in computer science, engineering, or chemistry. 3-7 years of experience in a relevant field.

• Strong experience in the configuration of SAP Product Compliance (EH&S).

• Knowledge of chemical regulations.

• Understanding of chemical labelling requirements.

• Familiarity with dangerous goods transportation regulations.

Preferred Requirements:

• Configuring SAP Product Compliance (EH&S) to meet regulatory requirements.

• Experience with Loftware labelling solutions is a plus.

• Proficiency in JavaScript is a plus.

• Strong analytical and problem-solving skills.

• Excellent communication and collaboration abilities.

• Ensuring compliance with chemical regulations and labelling requirements.

• Managing knowledge of dangerous goods transportation.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Technical Lead, Full-Stack Engineering (Bangalore, Karnataka, IN, 560100)

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We are seeking a skilled Full Stack technical lead with mandatory proven experience in Next.js,React, and REST APIs to join our Data & AI team. The role requires hands-on, enterprise-grade experience with Next.js, React, and REST APIs, plus deep understanding of design patterns. The candidate should also bring experience in at least one backend language (C#, Java, or Scala) and strong SQL to support backend development. Knowledge of Snowflake, AWS And Azur DevOps is a plus, enabling end-to-end delivery on enterprise cloud platforms.

Desired Skills and Attributes:

• Strong communication, collaboration, and problem-solving abilities

• Ability to work in a cross-functional, multinational environment

• Eagerness to learn and adapt to changing technologies and business needs

Your Role:

• Proficient in Next.js, React, TypeScript, REST API design, and front-end testing strategies

• Backend proficiency in one of: C#, Java, or Scala; solid SQL skills (Snowflake or comparable) and experience in Python

• Collaborate with product managers, UX designers, and backend engineers to design robust, user-centric solutions

• Write clean, testable code and establish front-end testing strategies (Jest, React Testing Library)

• Design, implement, and optimize CI/CD pipelines in Azure DevOps.

• Containerize services (Docker or equivalent) with observability (CloudWatch, logs,metrics)

• Work with Snowflake SQL for data access patterns, reporting, and analytics collaborations

• Ensure security best practices, accessibility, responsive design, and performance optimization

• Participate in code reviews, knowledge sharing, and documentation

Qualifications:

• Mandatory: Production experience with Next.js and React, including front-end testing (Jest, React Testing Library or equivalent) and a solid understanding of web security, authentication, and authorization

• Mandatory: Proficiency with TypeScript, Python and modern front-end patterns

• Mandatory: Experience with at least one programming language (C#, Java, or Scala)

• Mandatory: SQL experience with Snowflake or equivalent data platforms

• Mandatory: Azure DevOps (CI/CD)

• Experience building on or integrating with AWS (ideally Enterprise AWS); familiarity with Snowflake and DevOps practices is advantageous.

• Nice-to-have: Infrastructure as Code (IaC), Terraform, knowledge of containers,Lambda

• Bachelor’s degree in Computer Science, Engineering, or a related field, or equivalent practical experience

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of ERP O2C Order Management (Bangalore, Karnataka, IN, 560100)

This role typically involves leading a team, managing projects, and ensuring smooth operation of all Global SAP ERP systems and their related processes. In the Sales topics you are responsible for providing state-of-the-art solutions and services for our customers. This includes assessing the implementations and following established processes to meet customer demands. You need to manager internal and external stakeholders alike and secure all processes are being followed for their deliverables.

Lead weekly or bi-monthly team meetings and guide team members in delivering towards KPIs. Ensuring project milestones are met, deliverables are completed on time, and risk management is effective. Act as a single point of contact of procurement operations area; Provides input for Optimization calls. Needs to be involved in identifying and implementing process improvements within the SD and SSC modules. Maintain key metrics for quality, efficiency and productivity for application support. Implement improvement projects to drive quality, productivity and efficiency. Continuous Improvement: own detailed trend analysis and reports regarding application

In this role we require an excellent knowledge of SAP Sales and the adjacent modules combined with a good understanding of associated O2C (Order to Cash) business processes integrated with ERP systems. Thus he/she should be in a position to consult business partners to find suitable and sustainable solutions to meet customer demands.

Responsibilities

Ensure customer satisfaction through proper solution design delivery and applications life cycle management while maintaining necessary internal (process, security) and external (GxP, GDPR, license) compliance.

Manage operational support projects and change initiatives through the project life cycle, ensuring delivery to required time, cost & quality.

Provide technical support and troubleshooting for data issues and incidents.

Support SAP Deployments, Acquisitions and Divestitures, Continuous Improvements projects

Job Functions:

Managing, Owning and Driving team in securing deliver of customer demands on time.
Good exposure on RFCs and ecommerce integration.
Strong exposure to integration technologies including EDI, IDOC, ALE, RFC, PI and Web-Services
Demonstrate capability to manage the team to use best practices for supporting SAP ERP Configurations in Order management for the business.
Proven ability to understand the Business Processes of the organization and the core application environments.
Ability to handle multiple tasks and adapt to changing priorities

Problem Management

Lead master plan and priorities toward ticket elimination and automation.
Proactively suggest possible solutions and propose an action plan for improvement to Senior Management.
Lead the resolution of critical or complex incidents including related crisis management when appropriate.

Change and Release Management

Establish documentation of current and target application architecture (incl. CMDB).
Establish and implement the Life Cycle Management plan for applications in scope.
Secure Change Management processes in line with relevant SOPs.
Drive team to follow existing release management processes within the organization.

Project Delivery

Guide team to lead technical design of applications/solutions in portfolio
Provide technical services and functional advice on the implementation of business applications
Provide functional/technical support to project teams

Who you are:

Education/Professional Experience

Bachelor/Master’s degree or equivalent in Computer Sciences and/or Business Administration
Experience in managing large SAP SD teams.
12+ years’ experience in software or applications services
6 years’ experience within an international environment
Must have experience of all life cycles of implementing an SAP SD Solution

Languages

English mandatory (written and spoken)
An additional language (German, Spanish or Portuguese) is an asset

Skills and Competencies

Strong interpersonal and organizational skills
Strong written and oral communication skills
Good problem-solving skills
Ability to make difficult decisions and act autonomously
Integration skills regarding the use of functionality within SAP SD
Knowledge in EDI and IDocs
Knowledge in Output determination
Good knowledge in the surrounding modules (LE, MM-PUR, MM-IM, FI, CO, GTS)
Basic knowledge in ABAP – development, exits, debugging, etc.
Basic knowledge in Archiving

Analyst - Biomonitoring PMOps (Bangalore, Karnataka, IN, 560100)

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Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Your Role:

SME supports Product Managers, Marketing Managers and Project Managers in execution of tasks related to Product Life Cycle Management/New Product Introduction by collaborating with Cross-functional teams using various systems for Biomonitoring Business.
Act as a primary interface with Operational Organizations [Manufacturing, Purchasing, Tech Service, QA, etc]
Supports Product Life Cycle Management / New Product Introduction activities through SAP & Web Data Maintenance using various tools
Review NPDI completeness, Master data completeness and correctness
Support master data management including data review, data cleansing, data enrichments and data consistency checks.
Review web data compilation and data cleansing. Trouble shoot WEB PDP data
Support all relevant steps of product life cycle management and Portfolio review activities.
Upload product documents (technical bulletins/product information sheet review, certificate of analysis, certificate of origin) on web whenever required.
Create product listing on the website.
Meeting the SLA and TAT as per the agreed guidelines with the STAKEHOLDERS.
Accountable for meeting and maintaining defined standards for quality and productivity.
Ensure that internal and external customers’ requirements are met on timely basis.
Demonstrate good process knowledge within the process on all the activities.
Assist Team Lead with ISO and other additional activities to support.
Initiate process improvement projects/ideas.

Who You are:

Postgraduate in Life Sciences (Biochemistry/Biotechnology/Microbiology) from a reputed University.

Experience: 1-3 Years in Scientific Industry

Scientific Knowledge – In depth Proficiency and functional command expected over Life science subject.
Understanding of roles and responsibilities of Business Operations.
In depth Proficiency with internet and e-mail.
Very good skills in Office 365 tools (Excel, Teams, Outlook, SharePoint) and ability to set up complex database queries.
Navigate different t-codes in SAP PRD, PRE & MDGM.
Extract Data report - ERP (SAP) User Knowledge.
Capable of Initiating the Change records/Controlled Document Management - Trackwise/Mango.
Basic knowledge on Palantir.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Expert Quality Control (Bangalore, Karnataka, IN, 560100)

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Job Title: Expert Quality Control

Your Role

As an Expert in Quality Control within our Life Science division in Bangalore, you will play a vital role in ensuring the integrity and accuracy of analytical processes that directly support product quality and compliance. In this position, you will execute timely sampling and analysis in line with defined turnaround times, maintain first-time-right standards, and contribute to data trending and continuous improvement initiatives. You will operate and maintain analytical equipment, prepare standards and stock solutions, and document all results and observations in accordance with department guidelines. You will actively participate in shift monitoring, communicate technical findings to supervisors and colleagues, and contribute to Root Cause Analysis teams to investigate quality deviations. Your commitment to quality management systems and your drive to implement process improvements will be central to your success in this role.

Who You Are

You hold a degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline, or bring equivalent practical experience in a Quality Control laboratory environment.
You have hands-on experience in analytical techniques, sample analysis, and laboratory operations within a regulated manufacturing or Life Science setting.
You demonstrate a solid understanding of Quality Management Systems and are experienced in following and writing standard operating procedures.
You bring a continuous improvement mindset, with experience participating in Root Cause Analysis, investigations, or Kaizen initiatives.
You are detail-oriented and disciplined in maintaining accurate records, logbooks, and documentation in line with Good Laboratory Practice.
You communicate technical results clearly and effectively to supervisors, peers, and internal stakeholders.
You are comfortable working in a shift-based environment and can manage multiple analytical priorities while maintaining compliance with KPIs.
Proven experience in designing, optimizing, and validating robust analytical methods to ensure accuracy and compliance.
Strong hands‑on expertise with advanced instrumentation including HPLC, ICP‑OES, ICP‑MS, and GC for reliable routine testing.
Skilled in fundamental methods such as titrations, UV spectroscopy, and IR spectroscopy, ensuring comprehensive characterization capabilities.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

ORACLE APEX Service Delivery Manager (Bangalore, Karnataka, IN, 560100)

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Job Description:

We are seeking an experienced Oracle APEX Service Delivery Manager who is not only an expert developer but also possesses strong project management and business analysis skills. The ideal candidate will have a minimum of 12 to 15 years of experience in Oracle APEX development, project delivery, and leading teams. This role demands a highly skilled professional who can estimate project durations, assign tasks to team members, willing to create FRS documentations and serve as the primary point of contact for business stakeholders.

Key Responsibilities:

Service Delivery Management:

- - - Oversee the delivery of Oracle APEX projects, ensuring alignment with business goals and objectives.
    - Estimate project timelines and resource requirements, assigning tasks effectively to team members to meet deadlines.
    - Act as the primary point of contact (POC) for business stakeholders throughout the project lifecycle.
    - Implement automation cases as part of service improvement using AI to enhance operational efficiency and effectiveness.
    - Perform thorough assessment of business requirements and provide informed recommendations to the project team on whether to implement the solution using Oracle APEX or Snowflake, ensuring the chosen technology best aligns with business needs and technical feasibility.

2.Development Leadership:

- - Lead the design, development, and deployment of Oracle APEX applications in line with business requirements.
  - Write Functional Requirements Specifications (FRS) and User Requirements Specifications (URS) to guide development and ensure stakeholder alignment.
  - Support business and developers in drafting comprehensive FRS and URS documentation.

3.Technical Skills and Capabilities:

- - Proficiency in Oracle APEX, PL/SQL, Oracle SQL, and RESTful Web Services integration.
  - Experience with reporting tools and frameworks, such as Jasper Reports and integration with platforms like Snowflake and GoAnywhere.
  - Strong understanding of application migration processes, particularly from Oracle Forms to Oracle APEX.
  - Familiarity with Agile methodologies, JIRA, and version control systems like GIT and SVN.
  - Knowledge of Jenkins for continuous integration and deployment practices.
  - Capability to conduct thorough code reviews, testing, and ensure compliance with quality standards.

4. Solution Architecture:

- - Collaborate with technical teams to design scalable and efficient solutions for new projects.
  - Ensure that architectural designs meet business needs and adhere to best practices in application development.

5.Technical Mentorship:

- - Provide technical leadership to both internal and external teams, fostering a collaborative and innovative environment.
  - Mentor junior developers, offering guidance on best practices in Oracle APEX development and project management.

6.Stakeholder Communication:

- - Communicate effectively with technical and non-technical stakeholders to gather requirements, provide project updates, and facilitate decision-making.
  - Ensure that all project documentation is maintained and updated regularly.

Qualifications:

- - Minimum 12 to 15 years of experience in Oracle APEX development and service delivery management.
  - Strong knowledge of Oracle APEX, PL/SQL, Oracle SQL, and JavaScript.
  - Proven experience in writing FRS and URS documents.
  - Extensive experience in integrating applications with REST APIs and third-party platforms.
  - Hands-on experience in project management and agile methodologies.
  - Proven experience in developing Oracle APEX applications integrated with AI technologies to enhance application capabilities, automate business processes, and increase overall team productivity.
  - Excellent communication skills with the ability to engage with business stakeholders at all levels.
  - Experience leading diverse teams and managing multiple projects concurrently.
  - Strong analytical skills and problem-solving capabilities.
  - Oracle APEX certified is preferred.

Note : The candidate should be willing to work in hybrid model (2-3 days working from office) and in UK shift 1.30 PM to 10.30 PM IST.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

IT Configuration Specialist - Medidata CTMS\SSU & eTMF (Bangalore, Karnataka, IN, 560100)

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Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Who you are:

Configure, customize, and maintain Medidata CTMS, SSU, and eTMF systems to support clinical trial planning, execution, and oversight.
Partner with cross-functional stakeholders to gather business requirements and implement system enhancements or workflow improvements.
Ensure data quality, system integrity, and compliance with industry standards such as FDA, ICH, and GCP.
Provide end-user training, guidance, and support to facilitate effective system usage and adherence to best practices.
Troubleshoot and resolve system issues by coordinating with internal IT teams and external vendors as needed.
Develop, maintain, and update documentation, including configuration specifications, process flows, and user guides.
Stay current with system upgrades, Medidata platform releases, and industry trends to recommend process or technology improvements.
Outage Management
Support and manage planned and unplanned outages, including communication, troubleshooting, and service restoration.
Release and Change Management
Manage all aspects of release and change activities, including planning, documentation updates, deployment, and postimplementation review.
L3 Incident Management and Troubleshooting
Provide Level3 support for complex incidents, perform advanced troubleshooting, and timely resolution.
Interface Team Coordination
Collaborate with interface/integration teams to provide required technical details, troubleshooting assistance, and impact analysis.
Problem Management
Conduct problem investigations, identify root causes, recommend corrective actions, and support prevention of recurring issues.
Audit Support
Provide required evidence, documentation, and support during internal and external audits.
Qualification Documentation Updates
Update and maintain operational phase qualification documents, including TS, TRA, CS, FRS, Admin Guides, and related artifacts.
Review of Data Integrity, Backup, and Disaster Recovery (DR)
Perform periodic reviews of data integrity controls, backup processes, and DR readiness for compliance and operational continuity.
Act as the final escalation point for high-impact or recurring issues from L1/L2 support teams.
Perform deep root cause analysis (RCA) and implement permanent fixes or preventive controls.
Support approved configuration changes and minor enhancements in line with change management processes.
Manage and resolve incidents, problems, and change requests within defined SLAs.
Coordinate with internal IT teams, vendors, and platform providers for issue resolution and defect remediation.
Support production deployments across DEV, TEST, and PROD environments following validated procedures.
Perform impact assessments for platform releases, patches, and hotfixes affecting live studies.
Ensure all changes and configurations comply with FDA, ICH, GCP, and GxP requirements.
Support validation activities, audit readiness, inspection support, and periodic access reviews.
Ensure data integrity, audit trail compliance, and adherence to security and blinding controls.
Create and maintain technical documentation, configuration notes, SOPs, work instructions, and knowledge base articles.
Provide technical guidance and mentoring to L1/L2 support teams.
Contribute to continuous improvement initiatives to enhance system stability and support efficiency.

Your Role :

Bachelor’s degree in Life Sciences, Computer Science, Information Technology, or a related discipline.
3 to 8 years of experience in configuration and administration of Medidata CTMS, SSU, and eTMF systems.
Strong understanding of clinical trial operations and applicable regulatory frameworks (FDA, ICH, GCP).
Proficiency in system configuration, data management, and issue resolution.
Excellent analytical, problem-solving, and communication skills.
Ability to work effectively in a dynamic, cross-functional environment, managing multiple priorities simultaneously.
Experience with additional clinical trial management or electronic data capture (EDC) systems.
Knowledge of database concepts, analytics, and reporting tools.

Apply now and become a part of our diverse team!

Solution Architect, SAP Supply Chain Planning DMC (Bangalore, Karnataka, IN, 560100)

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Job Title: Solution Architect - SAP Supply Chain Planning & Digital Manufacturing

The Solution Architect - SAP Supply Chain Planning & Digital Manufacturing is responsible for designing, implementing, and continuously improving SAP-enabled digital manufacturing solutions. The role covers SAP Digital Manufacturing Cloud (DMC), SAP Manufacturing Integration and Intelligence (MII), SAP Manufacturing Execution (ME), and related SAP PP, EWM, QM, MM-IM, and PM capabilities.

Working closely with Manufacturing, Operations, and Plant IT, the role delivers reliable, scalable, and maintainable solutions that provide real-time operational visibility, enable intelligent production planning, and connect shop-floor activities with enterprise processes. The position plays a key role in improving productivity, quality, traceability, and regulatory compliance.

Your Role:

Lead end-to-end SAP digital manufacturing initiatives from discovery through design, build, test, deployment, and continuous improvement.

Architect and implement solutions across SAP Digital Manufacturing Cloud, SAP MII, SAP ME, SAP PP/EWM/QM/MM-IM/PM, and SAP ECC/S4HANA/EWM integration points.

Collaborate with production, quality, maintenance, and logistics teams to map business processes to SAP capabilities (e.g., production planning, order execution, batch management, quality inspection, asset management, stock transfer).

Design and configure real-time shop-floor dashboards, KPIs, alerts, and analytics to enable data-driven decision making.

Integrate SAP digital manufacturing solutions with MES, ERP, IoT platforms, and third-party systems (e.g., PLCs, historians, SCADA, and OT data sources).

Lead data modelling efforts for master data, bill of materials, routings, work centres, and production orders to support manufacturing operations.

Define and execute testing strategies (functional, integration, regression) and support user acceptance testing.

Establish governance for change management, version control, security, access controls, and data quality within SAP solutions.

Provide technical leadership and mentoring to project teams, business analysts, and end-users.

Prepare and manage project plans, budgets, risk registers, and status communications to stakeholders.

Develop and maintain operational documentation, runbooks, SOPs, and training materials for end users.

Stay current with SAP product roadmaps, industry best practices, and regulatory requirements (e.g., GMP, ISO) impacting manufacturing operations.

Who You are:

Required Qualifications

Bachelor’s degree in information technology, Computer Science, Industrial Engineering, or a related discipline; equivalent professional experience may be considered.
At least 5+ years of experience implementing or sustaining SAP-based manufacturing solutions.
Hands-on experience with SAP Digital Manufacturing Cloud (DMC) and/or SAP Manufacturing Integration and Intelligence (MII); knowledge of SAP ME and SAP PP/EWM/QM/MM-IM/PM is highly desirable.
Strong integration experience between SAP ECC, S/4 Hana, EWM using SAP Clound connector with SAP DM and MES/OT systems, including API design, middleware, and data mapping.
Solid understanding of manufacturing processes (discrete, batch, process) and shop-floor realities.
Experience with real-time analytics, dashboards, and KPI design for manufacturing operations.
Familiarity with data governance, security, and compliance in manufacturing IT environments.

Preferred Qualifications

SAP certifications relevant to digital manufacturing (e.g., SAP MII, SAP ME, SAP PP/PM, SAP Digital Manufacturing Cloud).

Experience with SAP S/4HANA integration patterns and SAP Cloud Platform.

Knowledge of OT/IT convergence, IIoT, OPC/UA, MQTT, and data historian architectures.

Programming or scripting skills (e.g., SQL, ABAP, JavaScript) to support custom developments or data extraction.

Experience in GMP/AML/ISO-compliant manufacturing settings.
Experience leading change management, user adoption, training, and enablement activities.

Certification or formal training in IoT, manufacturing analytics, data science, or a related discipline.

Skills and Competencies

Strong analytical and conceptual thinking, with a data-driven approach to problem-solving.
Excellent troubleshooting and root-cause analysis skills.
Strong stakeholder-management, facilitation, and communication abilities.
Ability to collaborate effectively across business, IT, engineering, and operations teams in a global environment.
Highly organised, detail-oriented, and committed to clear, accurate documentation.
Proactive approach to identifying risks, dependencies, and opportunities for improvement.
Ability to manage competing priorities and multiple initiatives while maintaining delivery focus.
Adaptability and willingness to continuously learn as SAP capabilities and manufacturing technologies evolve.

Work Environment and Other Requirements

Willingness to travel domestically and internationally as required; typical travel is approximately 10–20%, depending on project needs.
Ability to work periodically on-site at manufacturing facilities.
Ability to operate effectively in a global, cross-functional environment and support initiatives across multiple locations and time zones.

Opportunity and Impact the SAP Digital Manufacturing Professional enable smarter, more connected manufacturing with improved throughput, quality, traceability, and regulatory compliance. This role is pivotal in transforming operational data into actionable insights and sustaining a competitive advantage through digital manufacturing excellence.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Technician (Bangalore, Karnataka, IN, 560100)

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Your Role

• Job Title: Maintenance Technician (Chemical Industry)

• Department: Maintenance / Operations

• Reports To: Maintenance Supervisor / Engineering Supervisor

• Key Responsibilities:

- Perform preventive, predictive, and corrective maintenance on mechanical and electrical equipment (pumps, valves, motors, gearboxes, instrumentation, electrical panels, PLC interfaces where applicable) per SOPs.
- Diagnose and troubleshoot equipment faults; execute timely repairs and coordinate with spare parts procurement as needed.
- Carry out alignments, lubrication, part replacements, and commissioning of modified or new equipment.
- Monitor equipment performance, record data in logbooks and CMMS, and participate in RCA/CAPA processes.
- Support energy efficiency and reliability initiatives; contribute to TPM and maintenance optimization efforts.
- Ensure a clean, safe work environment and adhere to 6S/5S practices.
- Maintain compliance with safety, environmental, and quality standards (ISO 9001/14001/45001, local regulations).
- Prepare and maintain shift handovers, work orders, and incident reports; participate in investigations as required.
- Assist with start-up, commissioning, and qualification activities for new or modified equipment.

Who You Are

• You are a Diploma holder in Mechanical or Electrical Engineering (or equivalent) with 5+ years’ experience in maintenance within a chemical/processing plant.

• You have hands-on experience maintaining mechanical and electrical equipment in a medium-to-large plant.

• You can read mechanical drawings, P&IDs, wiring diagrams, and have familiarity with control systems basics (SCADA/DCS/PLC).

• You understand preventive maintenance concepts, CMMS usage, and basic reliability principles.

• You have strong problem-solving, diagnostic, and troubleshooting skills.

• You communicate effectively, work well in teams, and can operate across shifts.

• You are proactive in safety and continuous improvement initiatives.

Basic Qualifications

• Diploma in Mechanical or Electrical Engineering (or equivalent).

• 5+ years’ experience in a chemical/processing environment.

• Proficiency with SOPs, logbooks, and basic data recording.

• Familiarity with safety systems and regulatory requirements.

Preferred Qualifications

• TPM/RCI/RCA experience; RCA-based problem-solving skills.

• Certification in maintenance/industrial safety (e.g., electrical safety, mechanical upkeep).

• Experience with CMMS, predictive maintenance, energy/waste optimization initiatives.

• Exposure to automation, data logging, and basic analytics tools.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

CMC & GM Sales Representative (Santiago de Chile, RM.de Santiago, CL, 7520282)

Tu Rol
- Conocer y manejar correctamente cada uno de los perfiles farmacológicos de nuestros productos así como sus características, ventajas y beneficios.
- Mantener actualizada su cartera de Médicos, favoreciendo la inclusión en ella de aquellos médicos con alto potencial prescriptivo, procurando los cambios necesarios para su optimización.
- Enviar a través del instrumento electrónico bajo su responsabilidad su “Plan de Visitas” en tiempo y forma, con todos los datos de los médicos, farmacias y/o instituciones completos, conforme las pautas establecidas.
- Establecer un adecuado nivel de empatía con nuestros clientes, estando a entera disposición para resolver sus inquietudes y necesidades dentro de los preceptos establecidos por la Gerencia de la División Farma e instrucciones de su jefe inmediato.
- Administrar las Muestras Médicas y todo Material Promocional bajo su responsabilidad de acuerdo al Plan Promocional del ciclo en curso.
- Participar en campañas y/o eventos especiales ya sea de orden promocional, capacitación o social según sea requerida su presencia.
- Estar alerta acerca de las actividades de la competencia e informar permanente y oportunamente a los Gerentes de Producto y sus Supervisores.
- Cumplir con los objetivos de calidad y medio ambiente establecidos en el Sistema de Gestión Integrado de la empresa.
- Ser la imagen institucional de la Empresa frente al cuerpo médico, y las instituciones de servicios de salud.

Tu Perfil
- Profesionales titulados/as o estudiantes avanzados/as de carreras afines al área de la salud, como Biología, Obstetricia, Farmacia u otras disciplinas relacionadas.
- Al menos 3 años de experiencia en visita médica, ventas en el área de la salud o posiciones similares, idealmente en la industria farmacéutica.
- Conocimientos avanzados en el área científico-biológica y capacidad para comprender y comunicar información técnica relacionada con productos farmacéuticos.
- Formación o capacitación en ventas, idealmente en venta consultiva o promoción médica.
- Manejo de Microsoft Office y conocimientos en plataformas CRM, preferentemente Veeva CRM.
- Conocimientos sobre legislación aplicable a la industria farmacéutica, normas ISO y aspectos ambientales relacionados con sus actividades.
- No se requiere manejo de inglés.
- Capacidad para planificar y organizar autónomamente su jornada, jerarquizando tareas y procesos según su nivel de importancia y urgencia.
- Perfil analítico, autónomo y organizado, capaz de identificar necesidades, anticiparse a posibles dificultades y proponer soluciones.
- Orientación a resultados, foco en el cliente, iniciativa, responsabilidad y compromiso con los objetivos de la organización.
- Adecuadas habilidades interpersonales, empatía y comunicación efectiva para relacionarse con médicos, profesionales de la salud, instituciones, sociedades médicas y puntos de venta.
- Capacidad para trabajar colaborativamente con distintas áreas internas y representar profesionalmente la imagen de la empresa.
-. Orientación a la mejora continua, disposición al aprendizaje y apertura para recibir retroalimentación y elevar sus estándares de desempeño.
- Disponibilidad para trabajar jornada completa, sin horario fijo y bajo modalidad de artículo 22.
- Disponibilidad para trasladarse y desarrollar sus funciones en las regiones de Atacama, Coquimbo y Metropolitana.
- Licencia de conducir clase B vigente.

¡Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!

Senior Accounting Business Partner (Wroclaw, Dolnoslaskie, PL, 53-616)

Work Your Magic with us!

Your role:

You'll own financial reporting for a portfolio of legal entities, ensuring it's accurate, compliant and audit-ready under both IFRS and local GAAP standards. Working as the key accounting contact for entity CFOs, you'll provide clear visibility on reporting status, flag risks early, and drive resolution across teams. You'll coordinate with centralized accounting, Tax, Treasury and Group Functions to balance standardized global processes with local requirements. This is a role where your expertise shapes reporting quality, your challenge keeps standards high, and your collaboration unlocks solutions across the organization.

Who you are:

You have at least 5 years of professional accounting, finance or audit experience, including time in an expert-level position.
You hold or are working toward professional credentials like CPA or ACCA.
You know local accounting laws, tax regulations and international standards like IFRS or GAAP inside out.
You review financial information with confidence, spot risks quickly and communicate accounting matters clearly to stakeholders at all levels.
You're self-driven, take ownership of your work and deliver accurate, timely and compliant results without being asked twice.
You work well across functions, facilitate problem-solving and build trust with multiple stakeholders.
You exercise sound judgment, challenge constructively when needed and stay committed to continuous improvement and strong controls.

YOUR MAIN BENEFITS:

Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card
Work-Life balance: Enjoy additional paid days off, flexible working hours.
Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.

Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Specialist - SAP MDG (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Your Role :

Seeking an experienced Senior Specialist with 5+ years experience to lead the end-to-end delivery of complex Data Migration in MDG Material, Vendor and analytics solutions
This role is responsible for overseeing the strategy, planning, and execution data migration, ensuring high-quality deliverables, data integrity, and alignment with overall business objectives.
The ideal candidate should have a proven track record of managing cross-functional teams and senior stakeholders, leveraging their deep technical expertise and delivery to drive successful outcomes and innovation.

Who you are:

- Strong data-migration background with hands-on experience in data migration using SAP BODS with IDOCs, BAPIs LSMW and BDC. Must have worked on S4 Hana Data Migration projects.

- At least 5-9 years’ experience working with ERP migration using BODS. Domain expertise for SAP Module - Material,Vendor,Customer. Experience in Data Quality module of Data Services. Proven experience in a leadership role, managing and mentoring cross-functional teams. Manage all aspects of data migration, including data profiling, extraction, cleansing, transformation (ETL/ELT), loading, validation, and reconciliation, ensuring accuracy and minimal business disruption

- Collaborate with cross-functional teams and business stakeholders, including domain leads, business process architects, support team to design and improve end-to-end processes for operations. Focus on cross-team and cross-project delivery, making sure multiple projects, products, and services are delivered in sync, aligned with business outcomes, and free of blockers

- Bridge gaps between product, technology, support, and business leadership, making the role broader and more outcome-driven

- Manage parallel workstreams, juggle stakeholders, balance business & tech priorities, sustain team performance. Lead Daily Scrum calls, align cross-functional teams, resolve blockers, adapt playbooks. Lead process improvement initiatives by identifying areas for enhancement, conducting data analysis, and developing actionable recommendations as per the business standards

- Performs Quality reviews of the design in our tools. Provide established level of service and support of Qlik/BODS to ensure minimal business disruption. Using Qlik, BODS and MDG, design and develop dashboards and other solutions involving data.. Committed to the scrum methodology, agile principles, best practices and should also remain flexible

- Sound knowledge of SAP Information Steward Components like Data Insight and Cleansing. Package Builder to create data quality rules and dictionaries to standardize the data.

Excellent communication, presentation, and negotiation skills, with the ability to effectively communicate complex technical information to senior leadership and non-technical stakeholders.
Strong analytical, problem-solving, and critical thinking abilities.Proactively identify, assess, and mitigate risks and issues related to project delivery, data quality

- Strong understanding of SAP Data Services with knowledge of relevant components including Designer, Job Server, Engine, Repository, Access Server, Administrator. Ability to design and implement SAP DS solutions and to create technical specifications

Apply now and become a part of our diverse team!

Senior Associate (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

1.Follow the MPR and able to perform batch by using PLC/SCADA operated system
2.Recording information, such as ingredients, weights, and temperature, and input into the database while execution batch without deviating the compliance
3.Troubleshooting issues with production equipment and processes.
4.Observe a follow the all safety and quality regulations.
5.Reporting accidents, safety violations, or other concerns.
6.Assisting in planning and improving processes and product quality.
7.Working with other team members to complete the production process.
8.Meeting physical requirements of the position, including walking, standing, or sitting for extended periods, lifting heavy objects, climbing, crouching, operating tools, and wearing safety gear.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

Business Excellence - Asia Commercial (Sanpada New Mumbai, Maharashtra, IN, 400705)

Work Your Magic with us!

Your Role

Shape and execute commercial strategies to improve regional performance across Asia.
Strengthening forecast accuracy, market intelligence, and brand presence across sub-regions.
Lead cross-regional initiatives to streamline operations and improve commercial effectiveness.
Collaborate with sales teams to deliver targeted training, workshops, and capability-building initiatives.
Conduct business analysis across Asia by consolidating market, customer, sales, and financial data to identify performance drivers, opportunities, and risks.

Who You Are

You bring 5 or more years of experience in business excellence, commercial operations, or process improvement, ideally within a commoditized or life science market.
You hold a degree in Business Administration, Marketing, Finance, or a related field, or equivalent professional experience; a postgraduate qualification is an advantage.
You are confident working with analytics platforms and business information systems, and you are proficient in advanced Microsoft Excel for data modeling and dashboard development.
You have a proven track record of leading cross-functional teams and managing budgets, with the ability to translate complex data into clear, actionable insights for diverse stakeholders.
You demonstrate strong problem-solving skills and a self-driven approach to proposing innovative solutions, including experience with structured improvement methodologies.
You communicate with clarity and confidence in English, and you thrive in a collaborative, cross-cultural environment where you can influence without direct authority.
You understand how artificial intelligence tools work, including their practical applications, limitations, and ethical implications, and you can apply this knowledge to make informed, responsible decisions in a commercial context.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Quality Control Engineer (12개월 계약직, 포승 근무, 셔틀버스 제공, 신입/경력) (Pyeongtaek, Gyeonggi, KR, 459-827)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

커리어 여정을 계속해서 탐험하고, 발견하고, 도전할 준비가 되셨나요? 커리어에 대한 열정으로 가득한 여러분처럼, 머크도 거대한 포부로 가득하답니다! 머크의 전 세계에 있는 구성원들은 과학 기술의 혁신으로 헬스케어, 생명과학, 그리고 전자소재 부문에서 사람들의 삶을 풍요롭게 만들고 있습니다. 머크의 구성원들은 한마음이 되어 고객, 환자, 인류, 더 나아가 지구의 지속 가능함을 위해 힘쓰고 있습니다. 그것이 바로 머크가 호기심 가득한 인재를 원하는 이유랍니다, 호기심은 모든 것을 상상할 수 있게 만드는 원동력이니까요.

일렉트로닉스 소재 분야에서 저희가 행하는 행동은 모두 회사를 지원하는 회사가 되고 디지털 삶을 촉진하려는 저희의 목적을 달성하는 데 도움이 될 것입니다. 저희는 전자 산업, 자동차 및 화장품 산업 분야에 하이테크 소재, 서비스 및 특수 화학물질을 공급하는 믿을 수 있는 공급업체가 되려고 최선을 다하고 있습니다. 저희는 고객을 획득하려는 열렬한 열정을 지니고 호기심이 극도로 많으며 신속하게 행동하는 개인으로 구성된, 전 세계적으로 협력하는 조직을 육성하고 있습니다. 간단히 말해, 저희는 저희 고객을 위해 더 많은 것을 가능하도록 하기 위해 과학의 지평을 넓히고 있습니다.

Your Role:

Perform the analysis of quality parameters, preparation of samples, report analysis data and interpretation results to proper reporting line. Responsibility for measurement system. Deviation case handling.
Working in QC lab according to ISO 9001 & 14001 process and EHS guideline in Korea.
Carrying out analysis work in QC with data reporting for daily operation & external/internal customer’s request
Preparation and reporting analysis data and interpretation results
Proper maintenance and troubleshooting of measurement system
Optimizing existing method and support developing new method
Deviation handling: issue proper report and support for RCA

Who You Are:

Bachelor’s degree of Chemistry, Chemical Engineering or equivalent
신입 가능. 1-3 years’ experience in the related area
Good communication skills in both written and spoken English
Knowledge on basic statistics is preferred
Knowledge on basic chemistry is preferred
Experienced skills for documentation with MS-office is preferred
Collaborative: Team Work & Results-driven: Take Responsibility

<유의사항>

•여러분이 찾고 계시는 채용 포지션이 없으신가요? 그렇다면 인재풀(클릭))에 여러분의 이력서를 등록해주세요! 향후 인력 수요가 있을 경우 최우선으로 안내드리겠습니다.

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•당사는 입사지원자에게 이전, 재직중인 회사의 영업비밀 또는 기밀정보를 당사 채용 및 업무 수행과정에서 사용, 활용하거나 유출하지 않도록 요구하며, 관련 서약서를 통해 이를 확인하고 있습니다.

•만약 재직 회사의 영업비밀 침해 등 후보자님의 책임 있는 사유로 회사(머크)에 대한 법적 문제가 발생할 가능성이 있는 경우, 회사는 설사 채용된 이후라도 채용을 취소할 수 있습니다

•The company reserves the right to withdraw the offer if it discovers subsequently that a candidate has given false information in application or has provided false or fraudulent documentation in support of his/her application.

• We require candidates not to use, exploit, or leak the trade secrets or confidential information of their previous or current employers during our hiring and work processes, and we confirm this through relevant declarations.

• If there is a possibility of legal issues arising against the company (머크) due to a candidate's responsible actions, such as the infringement of trade secrets of their current employer, the company may cancel the hiring even after the candidate has been employed.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

우리가 제공하는 것: 우리는 다양한 배경, 관점, 그리고 삶의 경험을 가진 호기심 많은 인재들입니다. 이러한 다양성이 탁월함과 혁신을 이끌어내며, 과학과 기술 분야에서 우리의 리더십을 강화한다고 믿습니다. 우리는 모든 이가 자신의 속도에 맞춰 발전하고 성장할 수 있는 기회와 접근성을 제공하는 데 집중하고 있습니다. 우리와 함께 포용과 소속의 문화를 구축하여 수백만 명에게 긍정적인 영향을 미치고, 모두가 인류의 발전을 이끌 수 있도록 합시다!

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

QC Supervisor (Ansan-Si, Gyeonggi-do, KR, 15420)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

The QC Supervisor will lead the Quality Control team responsible for Incoming Inspection and Leak Testing of equipment, panels, controllers, enclosures, UHP/HP components, and related parts. This role ensures that inspection activities comply with approved specifications, quality control plans, safety requirements, and applicable procedures. The QC Supervisor will also oversee inspection prioritization, quality issue escalation, supplier quality coordination, inspection records, and continuous improvement activities to support customer delivery, product reliability, and compliance.

Your role

Lead and supervise Incoming Inspection and Leak Testing activities, including inspection and quality decisions for controllers, enclosures, panels, UHP/HP parts, and other components.
Oversee visual, dimensional, functional, HI-POT, insulation resistance, surface roughness, helium leak, pressure, regulator functional, Inboard, Outboard, and Internal Leak Testing.
Review inspection results, inspection reports, quality records, and SAP quality data.
Lead nonconformance management, root-cause analysis, corrective actions, and preventive measures.
Coordinate quality issues with suppliers and cross-functional teams, including Production, Engineering, Purchasing, and Supply Chain.
Ensure the calibration status of inspection and testing equipment and maintain safe operating conditions.
Train and develop team members, standardize work processes, and drive continuous improvement.
Support internal, customer, supplier, and regulatory audits.

Who you are

Associate degree or higher in Engineering, Quality, or a related technical field.
At least 5 years of experience in Quality Control, Quality Assurance, or manufacturing quality.
At least 2 years of experience leading or supervising a quality team.
Ability to interpret and apply engineering drawings, purchase specifications, inspection criteria, and tolerances.
Experience with Incoming Inspection of mechanical or electrical components or industrial equipment.
Experience with nonconformance management, quality notifications, corrective actions, and supplier quality issues.
Experience using SAP QM or an equivalent quality management system.
Strong safety awareness when working with high voltage, high-pressure gas, and industrial testing equipment.

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Associate Architect - IT Solution Design (Madrid, Madrid, ES, 28006)

Work Your Magic with us!

Your Role

At the intersection of technology and business impact, you will shape how IT solutions are designed, governed, and delivered across a global science and technology company. In this pivotal role, you will translate complex business requirements into scalable, secure, and end-to-end IT solution designs spanning Application, Infrastructure, and ERP domains. You will serve as the technical bridge between business stakeholders and technology teams, ensuring that every solution aligns with enterprise architecture standards, regulatory requirements, and delivers measurable business value. Collaborating with cross-functional teams and third-party partners, you will govern design quality, mentor engineers, and drive continuous improvement — making a tangible difference to how technology enables the organization to move forward.

Who You Are

You bring 8 or more years of experience in IT solution design, with hands-on exposure across multiple technology domains including Application, Infrastructure, and ERP.
You hold a degree in Information Technology, Computer Science, Engineering, or a related field, or bring equivalent professional experience.
You have strong knowledge of IT infrastructure and cloud solutions, and are familiar with architecture and design frameworks.
You are familiar with industry standards and regulations for IT/OT integration, including Industry 4.0 frameworks.
You apply systems thinking to translate business needs into actionable, practical IT designs, with strong analytical and problem-solving skills.
You communicate complex technical concepts clearly to non-technical stakeholders and collaborate effectively across cross-functional teams and third-party partners.
Knowledge of application technology and ERP systems is an advantage.
You demonstrate AI literacy: an understanding of how artificial intelligence technologies work, their practical applications and limitations, and the ethical considerations around bias, fairness, privacy, and governance — enabling you to critically assess AI tools and make informed, responsible decisions in your role.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Field Service Engineer (Metrology & Inspection) 新竹preferred (Zhubei City, Hsinchu County, TW, 302)

與我們攜手施展你的超能力！

準備好接受挑戰，探索更多可能性嗎? 我們跟你一樣希望精益求精，持續突破! 我們全球的夥伴熱衷於科技創新，透過我們醫藥保健、生命科學和電子科技業務的解決方案豐富人們的生活。讓我們一起環抱著熱情和夢想關懷我們的員工、客戶、病患和這個世界。這就是我們不斷尋找具備好奇心的新血加入的原因，與我們一起大膽想像各種可能。

我們在電子科技領域裡所做的一切，都是為了能成為眾多企業身後推動數位化生活的推手。我們致力於成為值得信賴的供應商，為電子、汽車和化妝品行業提供高科技材料、服務和特種化學品。我們培養了一個全球協作的組織，每位員工都擁有取勝的熱情、秉持客戶至上的態度、充滿好奇心且行事果決。我們齊心努力突破科學的極限，為客戶創造更多的可能性。

Your Role

1. Responsible for providing quality repair and preventive maintenance service of company equipment at customer sites. May install or relocate customer equipment and perform associated start-up and check-out procedures under supervision.
2. Perform on-site preventive maintenance. Order and replace defective units, components or parts as appropriate.
3. Troubleshoot equipment problems and conduct diagnostic procedures to isolate problems and take steps to minimize downtime or system interruptions and eliminate equipment malfunctions.
4. Determine corrective actions required and escalate for assistance and prompt resolution with the support of technically more experienced staff for assistance and guidance when assessing severity of malfunctions and determining corrective actions required.
5. On the job Training (OJT) to assist with installing and start up and/or relocating equipment at customer’s site.
6. Remain up to date on equipment/tools through appropriate training, manuals, factory periodicals and other relevant materials.
7. Execute project action items under direct supervision.
8. Perform other related duties as assigned by senior FSE / supervisor.

Leadership
May Provide on-site instruction to sub-contractors and customers.

Customer Relation
1. Professionally represent the company to the customer. Be committed to customer satisfaction and develop good customer relations by maintaining standards of conduct acceptable to both Lam and customers.
2. Shadow more experienced engineer at customer site.

Who You Are:

- 3+ years of related working experience such as Equipment Engineer (設備工程師)
- Understanding of Semi-con industry/factory
- Work as a team but is self-motivated and can work independently
- Willing to travel and support other sites
- Can understand English and is willing to speak

我們來自不同背景、視角與生活經歷，因對世界的好奇心而聚集在一起。我們深信，多元能夠催生卓越與創新，並持續強化我們在科學與技術領域的領導地位。我們致力於為每一個人創造機會，讓大家能依自己的節奏發展與成長。加入我們，一同打造一個充滿包容與歸屬感的文化，影響數百萬人的生活，攜手推動人類的進步！

立即申請，成為這個致力於激發探索精神、提升人類未來的團隊一員！

Head of Sales - East (Rockville, Maryland, US, 20850-3301)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

Your Role

Candidate must live East of the Mississippi

The Head of Sales - East is a field based commercial role leading a team of Business Development Managers, each responsible for a sales territory, and reports to the Head of Commercial for North America. The sales region spans over multiple states, selling BioReliance Biosafety Testing Services. BioReliance is the world's largest provider of pharma and biopharma GMP manufacturing and biologics safety testing.

Responsible for driving region-wide business performance with a strong emphasis on coaching, forecasting accuracy, customer relationship management, proactiveness, and cross-functional collaboration. Demonstrates proactive leadership and strategic account stewardship to grow revenue.

Reach or exceed quarterly and yearly sales targets
Monitor and improve the region’s sales performance, identify gaps, and implement actionable plans with clear milestones and owner accountability.
Lead, mentor, and develop the sales team through regular, structured coaching; establish and communicate best practices for forecasting, deal execution, and customer relationship management.
Ensure accurate and timely forecasting; maintain a robust, properly staged pipeline; implement rigorous review cadences with leadership and account teams.
Develop a comprehensive sales plan within the region focusing on growth activities and based on a target account list for each territory within the region
Provide feedback and recommendations on the workforce and support required for the success of the plan
Track pricing and price increase success within the region to protect business profitability
Develop relationship with key decision-makers at target accounts within the region as well as foster the networking activities of the Account Managers at these customers
Support Business Development Managers (BDM) during specific situations where an escalation process is needed to either solve a significant issue or protect/win a significant piece of business
Provide clear focus and prioritization to the regional BDM team
Represent the team in key meetings and calls to ensure visibility and impact.
Evaluate individual performance at mid-year and year-end and allocate compensation accordingly
Work collaboratively with business partners (customer service, technical service, field marketing, technology management, demand planning, etc.)
Maintain reliable accessibility during business hours to support the team, respond to issues, and remove obstacles to order progress.
Travel requirement within sales territory is approximately 50%, with minimal international travel.

Who you are:

Minimum Qualifications:

Bachelor's Degree in Biology, Biochemistry, or related Life Science
8-10+ years of commercial sales experience in the biotech industry including the use of CRM software, forecasting tools and other sales-related programs
Experience leading teams - coaching, developing, and motivating a high-performing sales team
Knowledge of Contract Testing Services (CTS) within the pharmaceutical and biotech drug production segment, or related experience
Strong quantitative skills; proficient in pipeline management, opportunity assessment, and data-driven decision making.
Data-driven; uses metrics to coach and drive decisions.
Proactive problem-solver; identifies risks early and assigns ownership.

Preferred Qualifications:

Advanced Degree (MBA, MS, PhD)

Pay Range for this position: $140,100 - $220,700. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Business Process Expert R2R General Accounting & Reporting (all genders) (Weiterstadt, Hessen, DE, 64331)

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Your Role

Are you an experienced accounting professional with a strong background in General Ledger processes and process automation? Join our team as a Business Process Expert (all genders) and contribute your expertise to improving financial processes, driving automation, and ensuring effective governance across the organization. In this role, you will perform regular Business Process Expert tasks, including control design and governance, KPI review, automation and governance, develop and maintain global work instructions and procedures, as well as conduct training for subject matter experts. You will improve financial processes within General Ledger and ensure processes comply with International Financial Reporting Standards (IFRS). You will collaborate with auditors during internal and external audits, define and set automation rules, assist the technical team during configuration and implementation stages, work closely with cross-functional teams to ensure smooth integration and manage changes across the organization, and support the BPO and Team Lead with ad-hoc requests and project tasks.

This position is limited to 2 years.

Who you are

You have 5+ years of experience in accounting or finance roles and hold a degree in Accounting, Finance, Business Administration, or a related field. Professional certifications such as CPA or ICA are highly desirable.
You possess strong process improvement skills and hands-on experience with process automation for Record-to-Report (R2R), General Ledger Accounting Process, including tools and methodologies, and have extensive knowledge of ERP systems, particularly SAP S/4 HANA or SAP ECC.
You understand core accounting processes, including Financial Accounting (FI), Controlling (CO), Asset Accounting (AA), General Ledger (GL), Accounts Receivable (AR), and Accounts Payable (AP).
You have participated in large-scale transformation projects and can design and document comprehensive accounting processes with a focus on compliance and efficiency.
You excel in dynamic environments, demonstrating adaptability and a positive attitude.
You are proficient in Microsoft Office and have experience with data visualization and reporting tools; Experience with Redwood (RunmyFinance) or Blackline Finance Automation is an advantage.
Excellent verbal and written communication skills in English are essential.
PMO exposure or experience supporting project governance, reporting, and process improvement; familiarity with PMO tools and methodologies is a plus.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Quality Associate Scientist (Round Rock, Texas, US, 78665)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Quality Associate Scientist (Analytical) is responsible for performing analytical testing of finished products, raw materials, custom analytical projects, and in-process samples. In this role you will assist in solving problems and optimizing processes and methods, also participate in Out of Specification (OOS) investigations. All work is to be performed accurately, and in compliance with MilliporeSigma, Round Rock Quality and Safety policies.

Conduct work in a professional manner.
Undertake a narrow range of analytical analyses in support Of MilliporeSigma catalog, custom and new products.
Assist in technical problem solving, implementation of new processes and initiatives.
Complete laboratory maintenance and housekeeping activities in accordance with safety and quality policies and procedures.
Complete laboratory equipment calibrations, verifications, and maintenance activities on schedule with documentation.
Train on and demonstrate understanding of a narrow range of analytical techniques.
Demonstrate understanding of departmental goals, MilliporeSigma processes, safety policies and quality systems.
Work in accordance with documentation, quality and process policies and procedures.

Who You Are

Minimum Qualifications:

Bachelor’s Degree in Chemistry, Biology or other Life Science discipline.
1+ years of experience with FTIR, ROI, KF, MP, BP, GCHS, HPLC, GC/HS, IC, ICPMS or Titration testing.

Preferred Qualifications:

Master’s Degree Chemistry, Biology or other Life Science discipline.
1+Years of experience with ISO 9001, 17025 or 17034 standards.
The associate Scientist has knowledge of and may have experience. in analytical methods and interpretation of analytical results.
Effective verbal and technical writing skills. Ability to write procedures, reports, OOS reports, technical presentation, etc.
Fundamental understanding of MilliporeSigma products, their applications and requirements.
Understanding of MilliporeSigma quality system for ISO regulatory requirements.

Pay Range for this position: $25.00 - $39.00

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Account Manager_BioProcess_Delhi Region (New Delhi, Delhi, IN, 110049)

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Your Role:

Pharmaceutical and biotech manufacturing is at the heart of some of the most complex and consequential science in the world.You will be at the forefront of that work, serving as a trusted partner to key accounts across the full spectrum of drug development and production. In this pivotal role, you will own the end-to-end sales cycle for a defined portfolio, driving revenue growth by deeply understanding customer processes across biologics, small molecules, injectables, ophthalmics, novel drug delivery systems, and beyond. You will develop and execute both short and long-term key account strategies, identify and convert growth opportunities across R&D and manufacturing functions, and build lasting relationships with stakeholders at every level of the customer organisation. You will communicate compelling value propositions, introduce customers to innovative technologies, and resolve challenges with speed and precision. Working closely with internal support teams, you will maintain a robust opportunity pipeline, contribute market intelligence on the competitive landscape, and ensure that every customer interaction reflects the highest standard of scientific and commercial expertise. This is a role for someone who combines deep technical knowledge with the commercial acumen and relationship skills to shape the success of the business across a dynamic and growing region.

Who You Are:

With 3-7 Years of Exeprience,and Degree in life sciences, pharmacy, biotechnology, chemistry, or a related discipline, or equivalent professional experience in a scientific or technical sales environment
Proven track record in technical or scientific sales, with experience managing key accounts in the pharmaceutical, biotech, or life science industry
Strong understanding of pharmaceutical manufacturing processes, including biologics (vaccines, monoclonal antibodies), small molecule dosage forms (liquid, solid, injectables, ophthalmics), and novel drug delivery systems
Demonstrated ability to develop and execute account strategies, manage complex sales cycles, and consistently achieve or exceed revenue targets
Skilled in identifying customer pain points and translating them into tailored solutions from a broad product and technology portfolio
Experienced in negotiating commercial agreements, developing quotes, and managing stakeholder alignment across multiple customer departments

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

中央市场准入经理 (Beijing, Beijing, CN, 100016)

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Your role:

Relationship building and engagement with NHSA（affiliated institutes），related industry organizations and association to build strategic partnership on the agenda of “life-cycle price management”.
Closely monitor、analyze and advocate on National VBP, RPS and price administration policy in order to anticipate forthcoming changes and the consequence to support business growth.
Partnering with highly matrixed cross-functional teams in China and global, to generate company's policy position and provide professional guidance to VBP and price protection objectives.
Establish and maintain the policy platforms for goals achievement, include effectiveness management and implementation of VBP and price administration policy.
Problem solving, risk mitigation and issue management.
Support VBP and Price policy project internal communication.

Who you are:

Education: Master's degree or above, major in public health, medical or related areas is preferred.
Languages: Excellent English both in oral and in writing
Experience: At least 5 years working experience on market access related position or consultant background in pharmaceutical industry, Good slides and data analysis skill.

Location: Beijing

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Rare Disease Specialist (Prague 4, Praha, CZ, 14000)

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Pro segment inovativní léčby vzácných onemocnění v onkologii hledáme nového kolegu či kolegyni na pozici Rare Disease Specialist, kterého/kterou bude bavit aktivní práce v terénu s pokrytím pracovišť po celé ČR. Mezi Vaše hlavní zodpovědnosti bude patřit:

Budovat dlouhodobé partnerské vztahy s KOL a dalšími klíčovými stakeholdery ve svém regionu (Česká republika) a rozumět tomu, kde pacienti na své cestě narážejí na překážky.
Nadchnout se pro naše poslání: zlepšovat cestu pacientů se vzácnými nádorovými onemocněními od diagnózy až po léčbu.
Zodpovídat za plnění všech obchodních cílů, včetně uvedení portfolia nových inovativních produktů na trh v oblasti vzácných nádorů.
Zpracovávat key account plány, na základě získaných poznatků z terénu, analýzy trhu a potřeb KOLs a pacientů.
Mít jasný plán i prostor pro iniciativu, sdílet poznatky z terénu i o trhu a být oporou kolegům ve strategickém plánování projektů.
Dobře znát svůj region a spolu s kolegy připravovat a realizovat plány v souladu s produktovou strategií.
Organizovat odborná setkání se zdravotnickými pracovníky a být pro ně důvěryhodným partnerem
Průběžně se vzdělávat a prohlubovat znalosti v terapeutické oblasti s cílem edukovat zdravotnické odborníky o svěřených léčivých přípravcích.

Kdo jste:

Vysokoškolské vzdělání, výhodou vzdělání v oboru medicíny, farmacie, biochemie, biologie nebo příbuzném vědeckém směru.
Schopnost vést rovnocennou, odbornou diskuzi s lékaři a KOLs.
Osobní nadšení, lidskost a touha pomáhat pacientům se vzácným a těžko diagnostikovatelným onemocněním.
Porozumění systému zdravotnictví, úhradovým mechanismům (§ 16) a schopnost odhalit překážky v cestě pacienta.
Schopnost se dobře adaptovat na dynamické prostředí launchovací fáze, kde se věci mění a vyvíjejí. Otevřenost zpětné vazbě, akceptace změn s lehkostí a odhodlání dosáhnout týmových cílů.
Plynulá čeština i angličtina – slovem i písmem.
Řidičský průkaz sk. B je samozřejmostí.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Business Operation Specialist (Bangkok, Klongtoey, TH, 10110)

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What You Do

Support SEA & TW commercial operations by coordinating and preparing quarterly business reports (Q1–Q4), enabling leadership visibility on regional performance and strategic priorities.
Assist SEA & TW commercial planning and Business Review processes by coordinating country submissions, ensuring completeness and quality of data, and facilitating timely clarification and alignment.
Drive execution and closure of Business Review actions through proactive follow-up with country teams, ensuring accountability and timely completion of business priorities.
Enable cross-country collaboration and commercial alignment across SEA & TW through regional initiatives, capability-building activities, and business forums to strengthen organizational connectivity and knowledge sharing.
Support local and regional engagement initiatives, partnering with country teams to coordinate internal events and strengthen employee engagement and organizational culture.
Lead internal communication deployment across SEA & TW via corporate communication channels, ensuring timely and effective dissemination of organizational updates, leadership messages, and employee announcements.
Analyze Employee Engagement Survey (EES) outcomes and partner with country stakeholders to monitor action plans, driving engagement improvement and organizational effectiveness.
Support pricing and performance excellence initiatives by analyzing PVE outcomes, monitoring country progress, identifying improvement opportunities, and coordinating engagement with pricing champions across SEA & TW.
Maintain regional organizational governance and workforce visibility by tracking organizational changes, validating country submissions, and ensuring alignment between workforce records and organizational structures.
Manage and maintain SEA & TW employee database integrity across enterprise systems, ensuring accurate and updated employee information to support operational efficiency and organizational reporting.
Oversee SEA & TW communication and distribution lists to ensure accurate stakeholder connectivity and effective internal communication across countries and functions.
Maintain temporary workforce and records to ensure accurate workforce tracking, operational continuity, and reliable data management where formal HR records may be limited.
Coordinate SEA & TW leadership meeting governance through preparation of meeting minutes, tracking action items, and ensuring timely follow-up to support execution discipline and leadership alignment.
Support strategic supply and localization initiatives, including supplier scouting and long-term regional projects to mitigate regulatory risk and strengthen business continuity, particularly in Indonesia.
Serve as coordination focal point for the Commercial Head of SEA & TW by managing scheduling priorities, facilitating urgent meeting arrangements, and supporting leadership responsiveness and decision-making.

Who You Are

Bachelor's degree in Sciences and a Master’s degree in Business Administration is a plus.
3 to 5 years of experience in business operations, commercial support, or a related function, ideally within a science, technology, or multinational environment.
Strong command of data management and reporting, with the ability to consolidate information from multiple sources, identify trends, and present findings clearly to stakeholders.
Proficient in MS Office, particularly PowerPoint.
Demonstrate strong organizational and coordination skills, with the ability to manage multiple priorities, track action items, and ensure timely follow-up across cross-functional and cross-country teams.
Strong stakeholder management skills.
English proficiency, both written and spoken, able to draft clear internal communications, meeting minutes, and leadership updates for diverse audiences.
Positive attitude and willingness to learn.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Digital Expert / IT Intern (Bangkok, Klongtoey, TH, 10110)

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What You Do

Leverage your expertise in digital technologies, data and innovation to design, develop, test, implement and optimize digital solutions that improve process performance and user experience. Collaborate with teams around the network, drive the adoption of best practices and digital tools, while supporting the community members with technical expertise and guidance.

Collaborate with business teams and process owners to understand and document digital solution requirements
Design and document digital solutions based on business needs
Evaluate and select appropriate technologies and platforms with special focus on interfaces that enable end-to-end solutions
Oversee developers for solution development, testing and implementation
Develop, test and maintain digital solutions when required
Generate frameworks and guidelines to share best practices within warehouse.
Provide technical support to help team develop digital solutions
Learn about new digital technologies and develop prototypes to assess technology value and applicability

Who You Are

Bachelor’s Degree: Information System
Certificates: Machine Learning Expert, UiPath Automation Explorer, Google Data Analytics Professional
TOEIC Score: 785 – 945 (B2 - Upper-Intermediate)

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Apprenti - Opérateur.trice sur machine automatisées CFC (m/d/f) (Aubonne, Vaud, CH, 1170)

Exprimez votre talent avec nous !

Vous voulez explorer, franchir des obstacles, faire des découvertes ? Nous savons que vos projets sont ambitieux. Les nôtres aussi ! Dans le monde entier, nos collègues ont la passion de l’innovation scientifique et technologique qui enrichit les vies humaines grâce à nos solutions dans les domaines Healthcare, Life Science et Electronics. Ensemble, nous voyons grand et avons à cœur de prendre soin de notre large diversité de collaborateurs, clients, patients et de la planète. C’est pourquoi nous sommes toujours à la recherche d’esprits curieux qui souhaitent imaginer l’impossible avec nous.

Tous unis pour les patients : l’objectif de la branche Santé est de contribuer à créer, améliorer et prolonger des vies. Nous développons des médicaments, des dispositifs intelligents et des technologies innovantes dans les domaines thérapeutiques tels que l’oncologie, la neurologie et la fertilité. Nos équipes travaillent sur les 6 continents avec passion et curiosité dans le but d’aider les patients à tous les stades de leur vie. Rejoindre notre équipe Santé signifie participer à une culture professionnelle diversifiée, ouverte et flexible offrant de belles opportunités pour le développement personnel et l’évolution de carrière à travers la planète.

Date de début: 01.08.2027
Durée: 3 ans
Localisation: Aubonne, Suisse
Position: Apprentissage / CFC

Ton rôle :Tu seras responsable de travailler sur les lignes de production et de piloter une ou plusieurs machines. Tu devras régulièrement surveiller le bon fonctionnement des machines et des produits tout au long du processus de production. De plus, tu assureras les maintenances des équipements et interviendras en cas de panne.

Ton profil :

Curieux·se et motivé·e : tu aimes apprendre et acquérir de nouvelles compétences.
Esprit d’équipe : Tu as la capacité à collaborer efficacement et à contribuer à un environnement dynamique.
Gestion du stress : Tu sais garder ton calme et rester concentré·e dans des situations qui peuvent être stressantes.
Esprit logique : Tu as de solides compétences en mathématiques et apprécies résoudre les problèmes de manière créative.
Langues : Maîtrise du français indispensable, l’anglais et/ou l’allemand sont un atout

Ce que nous offrons : nous sommes des esprits curieux, issus d’horizons variés et de perspectives et d'expériences de vie diverses. Nous croyons que cette diversité stimule l'excellence et l'innovation, renforçant ainsi notre capacité de leader dans les domaines de la science et de la technologie. Nous nous engageons pour que toutes et tous aient accès à des opportunités de développement et pour que chacun avance à son propre rythme. Rejoignez-nous pour construire une culture d'inclusion et d'appartenance qui impacte des millions de personnes et permet à chacun d’accompagner le progrès humain !

Postulez dès maintenant et devenez membre de notre équipe dont la vision est de stimuler les découvertes pour élever l'humanité !

Manager, In-house Consulting Asia Pacific (Singapore, Singapore, SG, 118222)

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Who are we?
Inhouse Consulting (IC) is an internal management consulting group function working exclusively for all functions and sectors. IC projects span topics like strategy & execution, processes & efficiency, integration, innovation & business development, R&D, organizational development, and PMO across the company. Our team consists of 80 colleagues that work globally. The IC Head Office is at the HQ in Darmstadt, Germany, with the Americas office in the Boston area, USA, and the Asia-Pacific (APAC) office in Singapore. This position offers a smooth transition from an external consultancy environment to an industry. IC work leverages your consultancy skillset and maintains the merits of consultancy like the variety of strategic projects, international travel, and high-level visibility. In addition, IC offers complete autonomy and freedom to drive your projects and develop your career.

Your role:

Based in Singapore, you will provide management consulting services for our internal customers, with a major focus on APAC. With your know-how, energy, structured problem solving and leadership skills, and your experience in the digital transformation you will drive cross-functional projects to develop concepts, and sustainable solutions as well as to optimize internal processes and organizational governance. You will consult all management levels within the company including the Executive Board and ensure the achievement of all project objectives.
This role will prepare you for a leading position at the company or one of its subsidiaries in the future by working closely with the business units and functions. Additionally, you will have several responsibilities within Inhouse Consulting like the mentoring and coaching of our associates and junior consultants.

Who you are?

You have completed an advanced degree (master’s degree, PhD or MBA) in a relevant field (Engineering, Sciences, Biotechnology, Chemistry, Biology, Physics, and/or Business Administration) with outstanding success
You have at least five years of working experience with international exposure within a leading management consultancy, ideally with exposure to the pharmaceutical, life science, chemical, and/or electronics industry
You have extensive experience in leading national and international cross-functional projects, with exposure to the Asia Pacific region as well as global initiatives
You have experience engaging with commercial and strategy functions
You have very strong problem solving, analytical skills, excellent communication and presentation skills
You have broad experience with aligning stakeholders, managing conflict and communicating information to ensure that the management has transparency on the underlying issues and potential solutions
You enjoy a large measure of independence and display an entrepreneurial mindset in a growing team
You have a self-assured and confident personality with a client-centric attitude
Excellent written and verbal communication skills in English. Chinese is a plus
Ambition to pursue an international career
Ability to travel up to 20% internationally is required

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Delivery Key User (Bonifacio Global City, Metro Manila, PH, 1630)

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Job Description:

As Delivery Key User you will play both critical and vital role in Procurement Organization  providing in deep knowledge and processes expertise in Accounts Payable, Operational Purchasing and Vendor Master Data Maintenance in a multiple ERP Systems. Enabling issue resolution assistance, training and support resource for questions and guidance, process improvement in identifying opportunities for efficiency, and close collaboration with cross functional teams such as procurement, Finance, and IT

Your Role:

First Level Ariba and ERPs Support through Service Now: Answer how-to questions related to specific ERPs; Maintain release strategies; Explain system functionalities in depth.

Incident Management: Start and follow up incident management process. Training: Train new purchasing agents and onboard new Key Users; Perform regular end user trainings via Teams in English; Maintain and update Training Material, act as the content owner for Procure4You articles.

Lead change request (CR) management, including creating and updating requirements as needed.

Perform Multiple Test Cases for major release updates, test solutions for incidents plus Change Requests for Process improvement/ change projects.

Process improvement and system enhancements: seeking for efficiency potential in system usage and functionalities.

Involve in Multiple Project Transformation, Migration and Deployment Projects.

Enable post-go-live end-user support activities to facilitate system adoption and proficiency.

Process standardization: you will support the standardization of the P2P processes across systems and propose streamlining solutions with focus in Accounts Payable.

Fostering knowledge management in virtual Key User meetings. Furthermore, you will bring benefit to the organization by providing insights of performance and efficiency measurements as well as deep dive reports.

Who you are:

Minimum of 5 years of complex/ international Procure To Pay process with expertise in "end to end Accounts Payable process"

Strong Purchase – to - Pay process knowledge or willingness to obtain it in case of different functional background.

Strong determination, self-motivation and goal setting to pro-actively drive Catalog implementations.

Knowledge in Vendor Master Data Maintenance is a plus

Advanced knowledge of ERP systems such as SAP, Oracle, Opentext, etc.

Knowledgeable in reading Test Scripts and Process Mapping.

Must know how to execute Multiple Testing in HPALM Systems

Knowledge in Data Management, Data Mining and Data Migration techniques and practices

Excellent critical and problem-solving skills Strong communication and interpersonal skills

High attention to detail and a commitment to accuracy

Experience with process improvement methodologies such as Lean or Six Sigma is advantageous for identifying opportunities to enhance efficiency.

Ability to work under pressure and meet tight deadlines.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Finance Functional Performance Management Lead (Bonifacio Global City, Metro Manila, PH, 1630)

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Your Role:

The holder of this position is accountable for designing and driving a transparent Finance performance management approach across the organization. The role connects Finance strategy, operational performance, business-sector priorities and senior stakeholder decision-making. It translates performance data into clear insights, actions and governance routines that improve Finance effectiveness and value delivered to the business.

Finance performance management

Design, implement and continuously improve the Finance Performance Management framework, including the KPI architecture, definitions, targets, reporting cadence and governance routines.
Translate Finance strategy and transformation priorities into measurable performance objectives for Finance services, processes and enabling activities.
Coordinate the collection, validation and interpretation of Finance performance data, ensuring that reporting is consistent, meaningful and focused on business outcomes.
Support Finance organizations in analyzing performance results, identifying root causes and defining appropriate corrective or improvement actions.
Distinguish topics requiring structural changes or full-scale improvement projects from topics that can be managed through daily management, standard problem solving or 3C-like action tracking.
Review performance measures with Finance leadership and relevant process or service owners to ensure that the right topics are measured and remain relevant for clients.
Conduct external benchmarking, where relevant, to support ambitious but realistic Finance targets and identify opportunities for process and service improvement.
Join and, where required, co-lead performance review sessions with Finance stakeholders, business partners, business sectors and other Enabling Functions.
Use sector knowledge to interpret performance differences, assess the relevance of Finance KPIs and tailor analyses and recommendations to the needs of individual business sectors.
Build trusted relationships with sector leadership teams, Finance business partners, Finance service owners and relevant Enabling Functions.

Who You Are:

Bachelor degree in relevant discipline (e.g. Finance, Business Administration, IT, etc.)
Master degree is a plus
At least 5 years of experience in Finance, performance management, business partnering, transformation, process excellence or a corporate/consulting environment with varying scopes and responsibilities.
Several years of experience working in diverse international teams and demonstrating success in roles involving multiple departments and senior stakeholders.
Proven success in major projects or initiatives that delivered measurable process, service or performance improvements.
Experience in a global, shared-services, GBS or complex corporate environment.
Experience working with stakeholders from different business sectors, functions, countries, regions and global teams.
Experience preparing management information, performance reviews, executive presentations or business review materials.
Experience with Finance processes, performance metrics, data interpretation and action tracking.
Strong Finance and performance management expertise, including KPI design, target setting, trend analysis and performance governance.
Demonstrated understanding of different business-sector operating models and the ability to translate sector priorities into Finance performance insights.
Excellent stakeholder management and business partnering skills, including the ability to work effectively with senior leaders.
Strong analytical and problem-solving skills, with the ability to turn complex data into clear messages and practical actions.
Demonstrated familiarity with and active use of Lean methodologies/tools and ways of working to identify improvement opportunities and drive sustainable performance improvements.
Excellent communication, facilitation, change management and influencing skills.
Result-oriented, structured and collaborative way of working; able to challenge constructively and take ownership.
Strong intercultural and virtual-team collaboration skills.
Very good understanding of Finance processes and their impact on business performance; familiarity with related HR, Procurement and IT processes is beneficial.
Fluent in English.
AI literacy: understanding of how artificial intelligence technologies work, their practical applications and decision-making implications, and the ethical considerations involved, including bias, fairness, privacy and accountability.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Warehouse Operator (Daejeon, Daejeon, KR, 34002)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

📌직무명: Warehouse Operator
📌계약형태: 계약직 (2년 계약직, 12개월 계약 후 재계약)
📌근무지: 대전광역시 유성구 국제과학18로 85 (기숙사 X)
📌근무형태: 주간 근무 (생산 계획에 따라 교대 근무 형태로 변경될 수 있음)
📌담당 업무
• 입고 및 출고 관련 업무 (PDA, SAP)
• 제품 피킹 및 제품 포장
• 제품 상차 및 하차
• 제품 검수
• 재고 조사
• 패킹용 자재 및 소모품 관리
• 입고 검수/ 출고 박스 수량 확인
• 6S 관리
• 장비 관리 및 청소
• 화학 제품 또는 의약품 취급
• 장비 관리 및 운영 (포크리프트, 팔레트 체인저, 진공 리프트, 랩핑기 등)
• 창고, 생산, 품질관리(QC) 및 기타 부서 소모품 관리

📌자격요건
• 전문대학교 졸업 이상의 학력
• 신입 지원 가능
• 1년 이상의 물류 관련 경력 우대

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Chemical Sales Consultant (3년 이상, Chemistry/Technical Sales, 서울 근무) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your Role:

Serve as the primary commercial and technical lead for our Stable Isotope portfolio in the Asia-Pacific (APeC) region, specializing in Carbon-13 (C13) and Deuterium (D2) labeled compounds.
Proactively drive revenue growth by identifying and capturing new opportunities across semiconductor, pharmaceutical, nutraceutical, and advanced materials sectors.
Deepen strategic relationships with existing production-scale customers to strengthen business partnerships.
Act as the regional subject matter expert on stable isotope chemistry, translating complex technical specifications into compelling value propositions for diverse customers such as semiconductor process engineers, analytical chemists, formulation scientists, and regulatory affairs teams.
Leverage deep product knowledge alongside an acute understanding of APeC’s semiconductor supply chain—including leading-edge fabs in South Korea and Japan—as a key advantage.
Design and deliver high-impact technical presentations showcasing our stable isotope manufacturing capabilities, quality certifications, and traceability standards.
Collaborate closely with Product Management, Applications, Supply Chain, and Quality teams to assist customers with qualification, custom synthesis requests, and long-term supply assurance programs.
Maintain disciplined pipeline management using Salesforce (SFDC), including opportunity tracking, accurate forecasting, and data-driven account planning to support commercial success.
Gather proactive market intelligence and engage closely with regional commercial teams to identify emerging application areas and competitive gaps, reinforcing our position as the preferred global supplier of isotope-labeled materials in APeC.

Who You Are:

Bachelor’s degree in Chemistry, Chemical Engineering, Materials Science, or related technical discipline, with 3+ years in technical sales, applications support, or business development involving isotopically labeled compounds or specialty chemicals.
Strong technical knowledge of Carbon-13 (C13) and Deuterium (D2) stable isotopes, including synthesis pathways, analytical methods, and applications.
Deep understanding of the APeC semiconductor market, including process chemistry, key fab customers, and supply chain dynamics in South Korea and Japan.
Proven ability to deliver technical presentations to senior scientific and engineering audiences, effectively communicating product value.
Experience supporting customer qualification and custom specifications in regulated or high-purity production environments.
Excellent English communication skills; proficiency in Mandarin, Japanese, or Korean is a strong plus.
Willingness and ability to travel up to 40–50% within the APeC region.
Preferred advanced degree (Master’s or PhD) in Isotope Chemistry, Organic Chemistry, or related fields, with hands-on experience using NMR, MS, or similar analytical techniques.
Familiarity with semiconductor process applications for isotope-labeled precursors, GMP/ISO quality standards, cross-functional collaboration, pharma and nutraceutical stable isotope applications, supply assurance, and having a strong professional network in the APeC semiconductor or advanced materials sectors.

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Internship - Software Engineering (m/f/d) (Eysins, Vaud, CH, 1262)

Work Your Magic with us!

Start date: as soon as possible

Duration: 3-6 months

Location: Eysins

Role Level: Internship

As a Software Engineering Intern, you will have the unique opportunity to work on cutting-edge digital health solutions that are transforming patient care and enhancing health outcomes. This is your chance to apply your skills in a dynamic environment while contributing to projects that make a real difference in people's lives.

Your role:

Collaborate with our teams to design, develop, and implement proof of concepts for digital health solutions.
Participate in the full proof-of-concepts development lifecycle, including requirements gathering, coding, testing, and deployment.
Contribute to the development of innovative features that enhance the functionality of digital health products.

Your profile:

Have strong programming skills, demonstrated in one or more project.
Have excellent problem-solving abilities, an agile mindset, and a passion for technology.
Have experience with version control.

Would be nice if you also have:

Knowledge of mobile app development and cross-platform frameworks.
Knowledge of web development frameworks and technologies.
Familiarity with microservices architecture and its principles.
Understanding of containerization technologies and use for microservices deployment.
Experience with CI/CD tools and practices.

What we offer:

A collaborative and inclusive work environment that values innovation and creativity where your ideas can spark impactful changes that shape the future of digital health.
Gain real-world experience from a world leading company and a highly experienced team.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Working Student Data & Automation Analyst Intern (BI & Power Platform) (Lima, Lima, PE, 15023)

Work Your Magic with us!

Tu Rol

Brindar soporte en el desarrollo y mantenimiento de procesos ETL, dashboards en Power BI y bases de datos para facilitar la toma de decisiones.
Apoyar en la extracción, transformación, carga, limpieza y validación de información proveniente de diversas fuentes.
Participar en la actualización y optimización de reportes, consultas, tablas, vistas y modelos de datos.
Documentar procesos, atender incidencias y contribuir a la automatización y mejora continua de las soluciones de Business Intelligence.

¿Quien eres?

Estudiante de la carrera de Ciencia de Datos, Ciencias de la Computación, informatica, Sistemas, ingenierias, administracion o un campo afín.
Con conocimientos de Power BI, Power Query, DAX, SQL y Excel. Power Apps, Power Automate (intermedio avanzado)
Experiencia en ETL y dashboards.
Dominio de inglés (hablado y escrito comprobable); (intermedio - avanzado)

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Warehouse Operator 1 (Allentown, Pennsylvania, US, 18106-9289)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Warehouse Operator 1 at MilliporeSigma’s Allentown, PA site will support the shipment of customer orders following procedures and guidelines for selecting, checking, packing and unpacking inbound and outbound shipments. Responsibilities include the following:

Check chemicals, catalog number, lot number, special request information, unit size, and weights against order documentation found in packing instructions

Accurately pull and stage materials from storage locations, ensuring order accuracy and stockroom organization

Package materials and apply all required labeling in strict accordance with established procedures and hazardous materials regulations

Stage finished boxes to be metered and shipped and distribute completed orders to the appropriate area of the facility

Use proper equipment for appropriate order (size of order, weight, etc.,)

Unload inbound trucks and unpack shipments, distributing materials to designated storage locations

Store and organize unpacked items and packing material in appropriate areas of warehouse and perform shelf maintenance in stock areas

Pick up trash and debris in work station and stock areas

Hours: Monday–Friday. Core shift hours are typically 8:00 AM – 5:30 PM, with flexibility in start and end times (up to a one-hour variance). Eligible for overtime. Occasional weekend hours may be necessary

Physical Attributes:

Stand, walk and move between areas for the duration of shift

Who You Are

Minimum Qualifications:

High School Diploma or GED

Preferred Qualifications:

1+ year of experience in a warehouse or manufacturing setting

Experience with pallet jack operation, selecting carts, packing equipment (tape machines and various cutting instruments)

Experience with PC and printer operation

Pay Range for this position - $16.00 - $25.00/Hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of Financial Planning & Analysis Operations (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

As a Head of Financial Planning & Analysis, you will be reporting to the Country Hub leader as well as to Global Functional Solutions leader of FP&A handling

Your Role:

Stakeholder Relationship Management:
Strategic:
- Present service scope/offerings, demonstrate capabilities & competencies to internal stakeholders.
- Prepare & present business cases on role transitions, mitigate risks, and ensure seamless Go-Live in delivery hubs.
Tactical:
- Engage regularly with internal stakeholders to understand expectations and derive action plans.
- Communicate action plans to the team and ensure "Obsessed with stakeholders" behavior.
Operational:
- Manage L2 escalations and executive escalations, resolving issues within a reasonable timeframe.
- Roll out NPS surveys, gather feedback, devise improvement plans, and execute through managers.
People Management:
Strategic:
- Visualize the north star for the FP&A delivery team aligned with overall FP&A global vision.
- Design a robust, sustainable organization chart to serve the journey towards the north star.
Tactical & Operational:
- Recruit, orient, train, and scale up FP&A team managers and leaders.
- Lead by example to engage, influence, and inspire the FP&A team.
- Foster a learning culture, lead training requirements, and represent the function in Hub Leadership meetings.
- Contribute to the employee lifecycle through career planning, growth assignments, and upskilling.
Process Management:
Knowledge Management:
- Design, monitor, and review mechanisms for knowledge retention through process documentation and cross-training.
Process Transformation:
- Initiate and facilitate improvement initiatives, set targets, and deliver actionable business insights.
- Ensure sustainable process health and improve maturity and penetration.
- Advocate for a LEAN work culture, conduct kaizen events, and define new "To Be" processes.
- Achieve productivity targets through process efficiency and optimization of efforts.
- Plan and operate within sanctioned budgets.
- Influence cross-functional teams and serve as a consultant on finance topics.

Who You Are:

Qualifications:
Professionally qualified CPA/CMA with 15+ years of experience in finance, including at least 8 years in FP&A/Controlling.
Experience managing a team of 50+ members for at least 5 years.

Required Skillsets:
Fluent in English.
Financial analytics and modeling experience preferred.
Prior work experience in complex matrix organizations in MNCs.
Global stakeholder management experience across US, Europe, and APAC.

Behavioral Attributes:
Result-oriented: Focus on delivering value and raising the bar.
Seasoned player: Able to handle pressure, multitask, and maintain emotional balance under conflict.
Transformation mindset: Challenge the basics and adopt an outward-in focus.
Versatile mindset: Flexible for lateral moves across the leadership team in the future.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Team Lead, General Ledger (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

As the General Ledger Team Lead, you will be a pivotal leader within our Manila Shared Service Center. You will be responsible for overseeing and guiding a team of 10-15 General Ledger Accountants, ensuring the accurate and timely completion of all GL operations for assigned entities. Your expertise will be crucial in maintaining financial integrity, driving process improvements, and fostering a collaborative environment.

Your Role:

Team Leadership and Management:

Lead, mentor, and develop a team of 10-15 General Ledger Accountants.
Assign tasks, monitor performance, and provide regular feedback and coaching.
Foster a positive and collaborative team environment.

General Ledger Operations Oversight:

Oversee the daily GL operations, including month-end close (MEC) activities, ensuring accuracy and compliance with established guidelines and policies.
Ensure the preparation and delivery of accurate financial data and reports to internal customers.
Monitor and manage accounting processes, general ledger postings, payroll and benefits (where applicable), master data maintenance, and account reconciliations.
Review and approve complex journal entries and reconciliations.

Financial Reporting and Analysis:

Oversee the preparation of reports required by local finance and Group Accounting.
Conduct financial analysis and support pre-audit tasks.
Ensure compliance with IFRS, GAAP, and tax regulations.
Escalation Management and Advanced Processing:
Handle escalations and resolve complex GL issues.
Perform advanced processing for sensitive GL activities.
Provide support for user testing on ERP/GL-related tasks.

Process Improvement and Operational Excellence:

Drive continuous improvement initiatives to enhance GL processes.
Contribute to process excellence initiatives and operational performance reporting.
Identify and implement best practices to optimize efficiency and accuracy.
Stakeholder Collaboration:
Collaborate effectively with local entity finance to resolve issues and ensure smooth operations.
Communicate effectively with global teams.

Who You Are:

Bachelor’s degree in Finance, Accounting, or a related field required.
Master’s Degree in Finance/Accounting or CPA accreditation preferred.
Minimum of 5-8 years of progressive experience in General Ledger Accounting Operations, with demonstrated leadership experience.
Profound knowledge of accounting principles (IFRS, GAAP, Tax).
Experience working in a Shared Services Center environment preferred.
Strong proficiency with SAP or other ERP systems required.
Excellent English communication skills, both written and verbal.
Willing to work on-site in BGC, Taguig.
Amenable to work on a mid-shift/night-shift schedule (Regular Schedule: 3 PM-12 AM, month-end: 9 PM – 6 AM).
Proven ability to manage and lead a team.
Strong analytical and problem-solving skills.
Excellent organizational and time-management skills.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Delivery Key User (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

Job Description:
As Delivery Key User you will play both critical and vital role in Procurement Organization providing in deep knowledge and processes expertise in Accounts Payable, Operational Purchasing and Vendor Master Data Maintenance in a multiple ERP Systems. Enabling issue resolution assistance, training and support resource for questions and guidance, process improvement in identifying opportunities for efficiency, and close collaboration with cross-functional teams such as procurement, Finance, and IT

Your Role:

First Level Ariba and ERPs Support through Procure4You: Answer how-to questions related to specific ERPs; Maintain release strategies; Explain system functionalities in depth.
Incident Management: Start and follow up incident management process.
Training: Train new purchasing agents and onboard new Key Users; Perform regular end user trainings via Teams in English; Maintain and update Training Material, act as the content owner for Procure4You articles
Lead change request (CR) management, including creating and updating requirements as needed.
Perform Multiple Test Cases for major release updates, test solutions for incidents plus Change Requests for Process improvement/ change projects
Process improvement and system enhancements: seeking for efficiency potential in system usage and functionalities.
Involve in Multiple Project Transformation, Migration and Deployment Projects
Enable post-go-live end-user support activities to facilitate system adoption and proficiency.
Process standardization: you will support the standardization of the P2P processes across systems and propose streamlining solutions.
Fostering knowledge management in virtual Key User meetings. Furthermore, you will bring benefit to the organization by providing insights of performance and efficiency measurements as well as deep dive reports.

Who you are:

3+ years of complex/ international purchasing or accounts payable experience
Strong Purchase – to - Pay process knowledge or willingness to obtain it in case of different functional background.
Strong determination, self-motivation and goal setting to pro-actively drive Catalog implementations.
Knowledgeable in Vendor Master Data Maintenance (Back-End)
Advanced knowledge of ERP systems such as SAP, Oracle, Opentext, etc.
Knowlegeable in reading Test Scripts and Process Mapping
Must know how to execute Multiple Testing in HPALM Systems
Knowledge in Data Management, Data Mining and Data Migration techniques and practices
Excellent critical and problem-solving skills
Strong communication and interpersonal skills
High attention to detail and a commitment to accuracy
Experience with process improvement methodologies such as Lean or Six Sigma is advantageous for identifying opportunities to enhance efficiency.
Ability to work under pressure and meet tight deadlines.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

I2P Specialist (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

Overview A dynamic, detail-oriented professional to join a shared services environment in the Accounts Payable (AP) function. The role covers end-to-end AP processing, reporting, issue resolution, process improvement, and supporting internal/external audits. This is a generic posting suitable for confidential use and not traceable to any specific organization.

Responsibilities

Execute day-to-day AP end-to-end activities: invoice posting, payment processing, issue resolution, reporting, and reconciliations in line with SLA targets.
Validate and investigate AP transactions for compliance with internal policies, financial reporting standards, and management requirements.
Produce and deliver AP reports and reconciliations in a timely manner.
Respond to internal/external inquiries; escalate issues as needed.
Monitor supplier accounts to ensure timely and accurate payments.
Lead and participate in process improvement initiatives to enhance efficiency and accuracy.
Perform GRIR, vendor accounts, and other AP account reconciliations as needed.
Support month-end closing activities and related reporting.
Assist with internal and external audits and audit requests.
Contribute to ad hoc or special projects as directed.

Qualifications

Education: Bachelor’s/College degree in Finance, Accounting, or related field.
Experience: Minimum 4 years of end-to-end Accounts Payable experience (invoice posting, payments, issue resolution, reporting, reconciliation).
Accounting Knowledge: Strong understanding of accounting concepts and financial reporting; experience with GRIR and vendor account reconciliations; ability to analyze and identify irregularities.
ERP Experience: Proficient with SAP or other ERP systems (e.g., Oracle, Ariba).
Language: Fluency in English (verbal and written).
Communication: Excellent written and verbal communication; collaborative and able to work with internal and external stakeholders.
Skills: Quick learner, flexible, responsible, result-oriented; able to work under pressure; resourceful, proactive, and independent.
Work Environment: Experience in a shared services center or multi-cultural environment is desirable.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Intercompany Accounting Specialist (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

Your Role:

Intercompany accounting department is responsible for transactions between our group of companies.

In our global team you would be responsible for: creation of cross charges to group entities and posting on the Accounts receivable side, posting of received cross charges on the Accounts Payable side, verification of invoices with regards to accounting standards, tax regulations, and group guidelines, reconciliation and reporting of different types of accounts, performing of monthly closing activities, reconciling of differences in the Balance Sheet and P&L between group companies, maintaining of master data, contribution to process developments and projects.
In case of any accounting blockings, differences or deviations from the processes, it will be welcome that you proactively and efficiently look for solutions.
There will be mainly communication with international stakeholders in English.

Who You Are:

In-depth knowledge and hands-on experience in end-to-end Intercompany Accounting processes.
Good knowledge and experience with SAP FI would be a plus
Experience in doing reconciliation (e.g. bank processing, accounts)
Experience within a Shared Services Center preferred
Fluent English language skills required
Strong ability to work in an international team and intercultural sensitivity.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Counsel, Fertility & HIV (Boston, Massachusetts, US, 02210)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Senior Counsel, Fertility & HIV will provide comprehensive legal support to a Therapeutic Area, including Commercial, Medical and Patient Support functions. Specifically, this role will be part of the legal team supporting Fertility and HIV, one of EMD Serono’s key Therapeutic Areas, and will report to the Senior Vice President and General Counsel and work closely with the Associate General Counsel and Head of US Legal, Fertility & HIV.

The role requires a deep understanding of healthcare laws and regulations applicable to pharmaceutical commercialization, including the Anti-Kickback Statute, False Claims Act, FDA promotional regulations, OIG guidance, and laws governing patient support and affordability programs. The ideal candidate will be a proactive, collaborative legal partner who enables business goals while ensuring compliance with ethical standards.

Key Responsibilities:

Primary Legal Counsel: Serve as lead attorney for a key brand of the Fertility & HIV Therapeutic area, including: review of marketing (promotional) materials; advice regarding Marketing and Sales Operations; review of scientific (non-promotional) materials; advice regarding Medical Affairs and Medical Operations; advice regarding Patient Support operations, manage outside counsel as specialized advice is required for Therapeutic Area projects; work collaboratively with paralegals.
Compliance & Regulatory Oversight: Ensure all activities comply with FDA, OIG, CMS, and state requirements, as well as company policies and industry codes (e.g., PhRMA Code).
Contracting & Negotiations: Draft, review, and negotiate agreements as need to support the Therapeutic Area.
Training & Education: Deliver legal training on relevant healthcare laws and company compliance requirements.
Cross-Functional Collaboration: Partner closely with Commercial, Compliance, Medical Affairs, and Regulatory teams to align business practices with legal standards. Collaborate with US and Global colleagues in order to ensure business strategies and objectives comply with applicable laws, regulations and policies.
Risk Management: Proactively identify, counsel, and communicate potential legal issues to mitigate risk. Manage risks through counseling, training and practical application of relevant legal and regulatory requirements, Company policies and procedures to Therapeutic Area operations.

Who You Are

Minimum Qualifications:

Juris Doctor (JD) degree from an accredited U.S. law school.
Active bar membership in good standing in at least one U.S. jurisdiction.
Minimum 10 years of legal experience in a firm and/or in-house.
Strong ability to interpret and apply laws, regulations, and guidance in a practical, business-oriented manner.
Excellent communication, drafting, and negotiation skills.
Proven ability to work collaboratively across multiple functions in dynamic and fast-paced environment.

Preferred Qualifications:

Prior in-house experience at a pharmaceutical or biotechnology company.
Demonstrated expertise in healthcare fraud and abuse laws, FDA regulatory matters, and patient support program compliance.
Experience supporting commercial business units, including contracting, supporting the development of commercial strategies.
Experience participating in or advising MLR/Promotional Review Committees.
Background in compliance counseling or interaction with government agencies (OIG, DOJ, FDA).
Strategic thinker with strong business acumen.

Excellent judgment and risk-based decision-making.
Collaborative, practical, and solutions oriented.
Ability to manage multiple priorities and stakeholders effectively.
Committed to ethics, compliance, and patient-centered values.

Location: Onsite – Boston, minimum 3 days per week. Must be US based.

Travel: <15%; International and Domestic

Pay range for this position: $200,400.00 - $300,600.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Director, Global Labeling - Regulatory Affairs (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

About SpringWorks Therapeutics:

SpringWorks Therapeutics, a healthcare company of Merck KGaA, Darmstadt, Germany, is a commercial-stage biopharmaceutical company dedicated to improving the lives of patients with rare tumors.

We developed and are commercializing the first and only FDA and EC approved medicine for adults with desmoid tumors and the first and only FDA and EC approved medicine for both adults and children with neurofibromatosis type 1 associated plexiform neurofibromas (NF1-PN).

At SpringWorks, we are committed to finding answers people with rare tumors need. We thrive in an atmosphere of passion and tenacity, fueled by the excitement of the possibilities science may unlock and driven to work with urgency because of the importance of our work. We value authenticity because diverse backgrounds, cultures, styles and abilities can only help us find the answers that people with rare tumors are looking for.

Your Role:

The Director of Global Labeling (Director of GL) provides strategic regulatory labeling expertise and operational leadership to cross functional teams, ensuring the successful development of company core data sheets (CCDS), regional labeling (US Prescribing Information [USPI] and EU Summary of Product Characteristics [SmPC]) and target product labels, in line with target product profiles and overall program goals. In some instances, the Director of GL may also take on the role of Team Lead for a therapeutic area (TA), overseeing Labeling Project Leads (LPLs) working on products within that TA and fostering strong collaborations with TA leadership. Additionally, the Director of GL assists the Head of Labeling and Advertising and Promotion in preparing for and facilitating interactions with the Labeling Decision Board (LDB), and also driving forward global labeling initiatives.

Location Classification – Hybrid:

This role will be required to work onsite 3 days a week (Tuesday - Thursday) or more depending on business needs. #LI-Hybrid

Key Accountabilities:

Lead the development, review, approval, and implementation process for CCDSs, USPIs, EU SmPCs and labeling documents with cross-functional labeling teams. Prepare for senior management (LDB) review and approval.
Ensure all labeling is scientifically accurate and meets the needs of healthcare professionals and patients.
Provide tactical guidance to labeling teams regarding the labeling process, and regulatory requirements including application to product labeling content.
Disseminate labeling for implementation in the US/EU and support country regulatory affairs in implementation changes locally.
Support products in development by providing input into investigational brochures, development safety update reports and integrated evidence planning. In some cases, develop regulatory labeling strategy and content for products in development (i.e., target product label) with subject matter experts.
Maintain expertise regarding key labeling requirements worldwide and stay updated with FDA/EMA labeling guidelines and regulations.
Participate in labeling negotiations with agencies resulting in product approvals or labeling updates.
In collaboration with department head, develop and periodically review labeling policies and standards. Provide guidance, and in some cases, drive process improvement initiatives.
Support audits and CAPA resolutions.
Represent labeling on cross-functional leadership programs and advisory boards.

Minimum Qualifications:

Bachelor’s degree in science or health-related discipline
8+ years of relevant pharmaceutical industry experience with 5+ years of relevant Regulatory Affairs Labeling experience
Deep knowledge and application of labeling requirements in the US/EU
Experience managing labeling personnel and/or teams

Preferred Qualifications:

Advanced degree (PhD, MD, MS, PharmD, MBA)
Advanced proficiency with MS Office (Word, Excel, PowerPoint, Project), SharePoint and regulatory systems (e.g., EDMS)
Meticulous in reviewing regulatory documents for accuracy, consistency, and compliance
Excellent written and oral communication skills
Knowledge and application of labeling requirements in global countries including Japan and China
Knowledge of global drug‐development and life‐cycle management regulations

SpringWorks Leadership Principles:

Change Steward - Recognize that change is essential; set goals that align to the Company’s strategy and create positive momentum for change; adapt business practices as necessary to adjust to ever changing requirements
Excellence Driver - Drive high performance and ownership through an open dialog; recognize performance, empower teams and create accountability for results
Growth Coach - Set clear expectations, provide frequent feedback, coaching, and encourage continuous learning; leverage individual strengths to help SpringWorkers unleash their potential and grow in their jobs and careers
Community Builder - Establish connections with others to build strong teams that trust each other and are great at collaborating to achieve goals; create a diverse, inclusive, and psychologically safe environment

Compensation & Benefits:

The expected salary range for this position is $182,100 - 273,100. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Medical Director, Global Clinical Development Oncology (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role
As a Senior Medical Director in Global Clinical Development Oncology, you will provide strategic, clinical, and scientific leadership for development programs in oncology. Your focus will be experience with drug development for solid tumors and ideally with experience in targeted therapies and antibody-drug conjugates (ADCs).

Key Accountabilities:

Lead and shape clinical development strategy across the development continuum, from Phase 1 through Phase III, including registration-enabling activities, regulatory submissions, dossier contributions, and Health Authority interactions.
Provide senior medical leadership on study design, execution, data interpretation, and key development decisions to support the advancement of oncology programs.
Guide indication strategy, patient selection, dose optimization, and overall development pathways
Integrate clinical, translational, and biomarker data into program decision-making
Oversee review and interpretation of safety and efficacy data to support development decisions
Drive and review key clinical and regulatory documents, including development plans, protocols, investigator brochures, clinical study reports, briefing books, submission documents, and dossiers
Lead or shape registration-enabling activities and regulatory submission strategy
Lead or represent Clinical Development in interactions with Health Authorities and internal governance bodies, as appropriate.
Serve as a senior leader within cross-functional and global teams, partnering closely with Program Leadership and Management, Translational Medicine, Clinical Operations, Biostatistics, Regulatory Affairs, Clinical Pharmacology, Safety, and Medical Writing.
Influence strategic direction, represent Clinical Development in key forums, and help ensure high-quality and timely delivery of development objectives in an office-based global environment.
Partner effectively with cross-functional stakeholders across including Program Leadership and Management, Clinical Operations, Safety, Regulatory Affairs, Biostatistics, Clinical Pharmacology, Translational Medicine, and Medical Writing
Provide strategic leadership within global matrix teams to ensure alignment, execution, and delivery against timelines

Provide leadership and oversight to team members within Clinical development, as needed
Contribute to business process improvement and organizational development initiatives, as appropriate.

Who You Are
Minimum Requirements:

MD with expertise in clinical drug development
Strong expertise in Oncology
Minimum 5 years of industry experience in clinical R&D within pharma/biotech
Experience leading or supporting clinical studies across Phase 1 through Phase III
Experience contributing to clinical development strategy, registration-enabling activities, and regulatory submissions
Familiarity with clinical dossiers, regulatory documentation, and interactions with Health Authorities
Demonstrated ability to interpret and apply clinical, translational, and biomarker data to development decisions
Experience leading cross-functional, matrixed, and international teams
Familiarity with ICH-GCP, FDA and/or EMA expectations, and clinical trial regulations
Excellent written and verbal communication skills in English
Ability to work effectively in an office-based environment and across global time zones

Preferred Requirements:

Experience in targeted therapies, ADCs, immuno-oncology, and/or hematology/hematologic oncology
Experience across early and late clinical development
Experience with registration strategy and major regulatory submissions
Experience engaging with Health Authorities and internal governance forums
Experience with precision medicine, and/or biomarker-driven development
Experience mentoring, guiding, or managing medical team members
Strong strategic thinking, project leadership, and decision-making skills.

Key Competencies

Strong clinical and scientific judgment in oncology
Strategic thinking and development leadership
Ability to translate complex clinical and scientific data into development strategy
Effective leadership in cross-functional and global matrix teams; team player mentality
Clear and persuasive communication
Ownership, accountability, and execution focus
Comfort working in a fast-paced, global organization

Location: Billerica, MA, USA; Onsite (Hybrid)

Travel: <20%; International and Domestic

Pay range for this position: $251,000.00 - $409,300.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Medical Director, Immunology (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Responsibilities include but are not limited to:

Provide medical leadership across rheumatology/immunology clinical development programs, ensuring scientific rigor and patient-centric development.
Lead clinical development planning and contribute to target product profile, indication strategy, and evidence generation plans.
Drive protocol development and medical oversight through execution (population, endpoints, dosing rationale, safety monitoring, biomarkers as applicable).
Lead governance preparation and decision-making, documenting recommendations, rationale, key risks, and mitigation/contingency plans.
Partner cross-functionally (Clinical Operations, Safety, Biostats, Regulatory, Quality, Medical Affairs, Business Franchise) to ensure integrated strategy and high-quality delivery.
Support regulatory submissions and interactions (briefing packages, responses, meeting participation) as medical lead.
Interpret clinical data and communicate results via CSRs, publications, congress materials, and internal updates.
Engage external experts (investigators/KOLs) compliantly to inform scientific strategy and study design.
Provide matrix leadership and mentoring; may manage direct reports depending on organizational needs.
Matrix leadership across global cross-functional teams.
Talent development: mentoring and coaching Clinical Scientists/medical staff; direct reports may be included based on organization needs.
This role will be based for a minimum of 3 days a week onsite in Bilerica, MA.

Who You Are:

Minimum Qualifications:

Medical Degree (MD) or international equivalent
Board Certification in Rheumatology and/or Clinical Immunology and/or advanced degree (MD/PhD)

Preferred Qualifications:

Significant clinical experience in Rheumatology and/or Clinical Immunology (typically 5–7+ years), including prior hands-on patient care
5+ years medical leadership in pharmaceutical/biotech clinical development, including regulatory submissions and interactions (FDA/EMA/others)
Experience designing clinical development plans and leading global clinical trial execution in a matrix environment
Strong track record of delivering milestones under tight timelines
Deep knowledge of drug development and clinical trial methodology in immune-mediated inflammatory diseases/rheumatology
Strong understanding of GCP, ICH, FDA/EMA requirements
Sound clinical judgment and ability to make decisions with incomplete/ambiguous data; clearly communicates rationale and trade-offs
Excellent cross-functional leadership, stakeholder management, and influence without authority
Strong medical writing and document review skills (protocols, IBs, CSRs, briefing books)
Excellent communication and presentation skills for governance and external forums
Willingness to travel as needed (domestic/international)
Ability to work at a computer for extended periods (reading/writing/reviewing documents, virtual meetings).
Ability to communicate effectively verbally and in writing.
Ability to travel as required (including navigating airports/hotels/sites).
Ability to attend in-person and virtual meetings, including occasional early/late meetings across time zones.

Pay Range for this position: $229,800 - $381,700

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Medical Director, Global Clinical Development Oncology (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

As a Medical Director in Global Clinical Development Oncology, you will provide clinical and scientific leadership for development programs in oncology, ideally with experience in targeted therapies, antibody-drug conjugates (ADCs), and/or immuno-oncology. Next to experience with drug development for solid tumors, experience with hematology/hematologic oncology is viewed favorably.

In this role, you will independently drive day-to-day clinical development activities while contributing to high-quality execution of the overall clinical strategy in a global matrix environment.

Key Accountabilities:

Lead assigned clinical studies and contribute to broader program strategy across the development continuum, from Phase 1 through Phase III, including support for registration-enabling activities, regulatory submissions, and Health Authority interactions.
Integrate clinical, translational, biomarker, and emerging data to support indication strategy, patient selection, dose strategy, and key development decisions.
Operate as a core member of cross-functional teams and the Global Project Team, partnering closely with Program Leadership and Management, Translational Medicine, Biostatistics, Clinical Pharmacology, Regulatory Affairs, Clinical Operations, Safety, and Medical Writing.
Support study design, dose strategy, patient selection, and indication prioritization
Integrate clinical, translational, and biomarker data into development decisions
Provide medical monitoring and clinical oversight for assigned studies
Review and interpret safety and efficacy data to support study decisions
Author and contribute to key clinical and regulatory documents, including protocols, investigator brochures, clinical study reports, briefing books, submission documents, and dossiers
Contribute to registration-enabling activities and regulatory submissions
Support interactions with Health Authorities and internal governance bodies
Drive execution of deliverables across global teams and timelines
Contribute to a high-performing, collaborative matrix environment.

Who You Are

Minimum Qualifications:

MD with expertise in clinical drug development
Required expertise in Oncology
Minimum 3 years of industry experience in clinical R&D within pharma/biotech
Experience supporting or leading clinical studies across Phase 1 through Phase III
Experience contributing to clinical development strategy, regulatory submissions, and registration-enabling activities
Familiarity with clinical dossiers, regulatory documentation, and Health Authority interactions
Demonstrated ability to integrate translational and biomarker data into clinical development decisions
Experience working in cross-functional, matrixed, and international teams
Familiarity with ICH-GCP, FDA and/or EMA expectations, and clinical trial regulations
Strong written and verbal communication skills in English
Ability to work independently, manage multiple priorities, and collaborate across time zones in an office-based environment.

Preferred Qualifications:

Experience in targeted therapies, ADCs, immuno-oncology, and/or hematology/hematologic oncology
Experience across early and late clinical development
Experience contributing to study designs that support potential registration pathways
Experience with precision medicine, and/or biomarker-driven development
Strong project leadership skills with a track record of driving timelines and decision points
Board certification in Medical Oncology/Hematology or relevant subspecialty.

Key Competencies

Strong clinical judgment in oncology
Scientific and analytical rigor
Ability to translate complex clinical, translational, and biomarker findings into development strategy
Effective cross-functional collaboration; team player mentality
Clear and concise communication
Ownership, accountability, and execution focus
Comfort working in a fast-paced, global matrix organization

Location: Billerica, MA, USA; Onsite (Hybrid)

Travel: <20%; International and Domestic

Pay range for this position: $200,800.00 - $301,300.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of Platform Architecture (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

We are looking for a senior, hands-on platform architect to own the technical foundation for commercial, enterprise-grade data products and digital platforms. Together with your team, you will translate complex customer and business needs into secure, resilient and maintainable architectures, while staying close enough to implementation to remain credible with principal and staff engineers. You will define reusable capabilities that help teams move from prototype to customer-ready product without compromising product ownership or customer value.

Can sit in Burlington or Billerica

Your responsibilities:

Own the platform architecture

Define and communicate the target architecture for commercial, cloud-native data platforms and digital products across a portfolio of products and deployment models, translating ambiguous customer and business needs into technical strategy, platform capabilities and delivery roadmaps.
Establish architectural principles, standards and decision frameworks covering reuse, security, scalability and supportability.
Design data and AI platforms across heterogeneous sources, including ingestion, transformation, storage, analytics, provenance, lineage, quality, access control and secure multi-tenancy.
Design appropriate SaaS, multi-cloud, hybrid and customer-managed deployment strategies, balancing security, data residency, resilience, cost and portability.
Design APIs, integration patterns, identity and authentication services, event-driven and distributed components.
Make build-versus-buy-versus-partner decisions across platforms such as Palantir Foundry, cloud services, managed SaaS and open source.

Architect for security and compliance

Apply security-by-design and defense-in-depth, including threat modeling, identity, least privilege, encryption, secure software delivery and vulnerability management.
Design platforms that are certifiable and audit-ready, partnering with security, privacy, quality, legal and audit functions on controls, evidence and customer assessments.
Translate relevant security, privacy and regulated-industry frameworks, such as ISO 27001, SOC 2, NIST, GDPR and GxP, into concrete architectural controls.
Shape secure multi-party data ecosystems that preserve data ownership, provenance, permissions, isolation and control over data use.

Stay technically close to implementation

Review designs, prototypes and critical code paths to surface architectural and operational risk early.
Establish practices for infrastructure-as-code, CI/CD, testing, release management, observability and production debugging.
Help teams industrialize prototypes and MVPs and resolve difficult problems across application, infrastructure, data and security boundaries, choosing technologies according to the problem rather than habit.

Lead and communicate

Provide technical direction and mentorship across levels, including senior and principal engineers, and raise the technical bar without becoming a bottleneck.
Support hiring, team design and capability development in partnership with engineering leadership.
Explain architectural decisions, limitations, costs and trade-offs clearly to engineers, product leaders, customers, partners, auditors and executives.

Who You Are

Minimum Qualifications:

Platform architecture depth: significant experience designing and building sophisticated software, cloud, data or AI platforms and customer-facing digital products at enterprise scale, with the ability to translate customer problems into architectures and executable roadmaps.
Multi-tenant and deployment architecture: experience designing secure multi-tenant platforms and multi-cloud, hybrid-cloud or customer-managed deployment models.
Security and compliance: substantial hands-on experience owning secure architecture decisions in production, with working knowledge of relevant frameworks such as ISO/IEC 27001, SOC 2, NIST, GDPR and, where relevant, HIPAA or GxP/GAMP 5.

Preferred Qualifications:

Building platforms that connect sensitive data, including healthcare or clinical data, across organizational, business or legal boundaries.
Palantir Foundry or comparable enterprise data platforms, including data products, ontology, governance and lineage.
Experience building commercial software products, partner ecosystems, customer-managed deployments or cyber-physical and digital-twin solutions.
Cloud-native architecture: demonstrated depth on at least one major provider, including containers, serverless, networking, IAM and observability.
Data-platform architecture: experience with ingestion, transformation, storage, analytics, lineage, access controls, tenant-aware governance and data quality.
Technical leadership: credibility to challenge senior engineers, communicate across technical and commercial audiences, and lead collaboratively as a player-coach.

Pay Range for this position: $195,800-$293,800

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of Customer Application Process Solutions China (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Your Role:

Lead and develop the CA China team across all PS franchises; ensure clear goals, active IDPs, and a ONE PS collaborative mindset.
Partner with PS China Sales and Global CA leadership to co-develop and execute the China CA strategy, aligned to commercial targets.
Drive pre-sales engagements — Competitive Conversions, New Product Introductions, Product Adoption, and Application-Based Solutions — with focus on complex, multi-franchise opportunities.
Leverage knowledge of China's biopharma landscape (domestic innovators, CDMOs, global pharma subsidiaries) to identify and prioritize strategic growth opportunities.
Ensure the team maintains technical excellence across PS modalities (mAbs, ADCs, mRNA, Cell & Gene Therapy, small molecules); champion application consultancy to link customer needs to PS solutions.
Monitor China market trends and NMPA regulatory developments; feed intelligence back to Global CA and Business Units.
Serve as the primary CA interface between PS China and Global/Regional CA teams; collaborate with MSAT, TSS, Field Marketing, RSE, and Marcomm for integrated commercial execution.

Who You Are:

Master's degree in Life Sciences, Biotechnology, Chemical Engineering, or a related field. Additional education or certification in Business, Management, or Marketing is preferred.

>12 years of relevant experience in the life science / biopharma industry, with significant China market exposure.
>5 years of people management experience leading commercial or technical teams.
Strong knowledge of the China biopharma landscape, including domestic pharma/biotech, CDMOs, and the NMPA regulatory environment.
Proven commercial experience across the full sales cycle in the Biopharmaceutical industry.
Experience with biological production across modalities: mAbs, ADCs, vaccines, mRNA, Cell and/or Gene Therapy.
Track record of managing complex, multi-stakeholder projects in a matrixed, international organization.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

(高级)产品经理 (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Job Title: (Senior) Product Manager

Location: Shanghai/Beijing, China

Your role:

Product management: Support the Rare Tumor Market Lead, plan and manage the indication lifecycle to ensure sustained competitiveness and market leadership in China; participate in local strategy development and execution plans, and liaise with HQ to coordinate resources and push local implementation.
Strategy development: Contribute to the development of brand and market-entry strategies, including target audience, positioning, differentiators, pricing/coverage strategies, channels, and promotional direction, and drive local execution of these strategies.
Market analysis and insights: Conduct market research and analysis, collect and organize competitive intelligence, monitor market performance data, regularly produce analysis reports, generate insights, and provide data support for brand strategy development.
Activity Execution: Lead cross-functional collaboration to execute marketing promotions, focusing on initiatives aligned with the indication strategy; ensure the execution process is measurable, traceable, and optimizable across stages; deliver marketing activities on time and with high quality.
Promotion material production and sales training: Create promotional materials and training content, ensuring alignment with clinical, sales, and regulatory compliance requirements and effective communication.

Who you are：

Education background: Bachelor’s degree or above; majors in Marketing, Medicine, Pharmacy, or related fields preferred.
Work experience: 3+ years of marketing experience in an MNC; priority given to candidates with rare disease, oncology, or specialized medicine experience.
Language proficiency: Proficient in English for daily work.
Cross-functional collaboration: Excellent cross-functional communication and collaboration skills, with the ability to reach consensus and implement unified action plans.Data-driven mindset:
Strong sensitivity to market data, with strategic thinking, solid data analysis and tools proficiency, and proven insight generation capabilities.
Project & time management: Strong project management and time management skills, capable of driving progress and delivering results in complex environments.
Personal attributes: Proactive, responsible, and collaborative with a strong team spirit.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

市场传播经理 (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Job Description: Marcom Manager China

Job Title: Marcom Manager China
Department: Market Strategy
Reports to: Head of Market Strategy China
Location: Shanghai, China

Job Summary:
We are seeking a dynamic and strategic Marcom Manager to develop and execute integrated marketing and communication programs that elevate the Susonity brand across China. This role will be instrumental in increasing brand awareness, driving industry engagement, facilitating cross-brand collaboration, and supporting the overall business strategy through targeted campaigns and high-impact event presence.

Key Responsibilities:

· Develop and implement brand communication strategies to enhance Susonity's visibility and reputation in key sectors such as coatings, automotive, and cosmetics
· Plan, manage, and execute participation in major trade shows, exhibitions, and industry events across China
· Create and manage cross-industry marketing initiatives to broaden brand reach and engagement beyond core sectors
· Foster collaboration with group brands (CQV and Chesir) to develop joint marketing campaigns and maximize cross-brand synergies
· Collaborate closely with the Head of Strategy to ensure alignment between brand messaging and business objectives
· Produce high-quality marketing content and materials for both online and offline channels
· Measure and report on campaign performance to optimize future marketing efforts

Qualifications:

· Bachelor's degree in Marketing, Communications, Business, or a related field
· 5+ years of experience in marketing communications, preferably in B2B or multi-industry environments
· Proven track record in managing trade shows, events, and multi-channel marketing campaigns
· Experience in cross-brand collaboration and partnership marketing is highly desirable
· Strong project management skills and ability to work effectively in a cross-functional team
· Excellent written and verbal communication skills in English and Mandarin
· Creative thinker with strong analytical and execution capabilities

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Gerente de Acesso (Mercado Público) - Nordeste ou Brasília (Barueri - SP, Sao Paulo, BR, 06455-035)

Faça sua mágica acontecer conosco

Você está pronto para explorar, quebrar barreiras e fazer novas descobertas? Sabemos que você tem grandes planos — e nós também! Mundialmente, nós adoramos inovar em ciência e tecnologia para agregar valor à vida das pessoas com nossas soluções de Healthcare, Life Science e Electronics. Juntos, sonhamos alto e somos obstinados por cuidar da nossa rica mistura de pessoas, clientes, pacientes e do planeta. Por isso, estamos sempre em busca de mentes curiosas que se veem imaginando o inimaginável conosco.

Unidos As One for Patients: nosso propósito na área de Cuidados com a Saúde é ajudar a criar, melhorar e prolongar vidas. Nós desenvolvemos medicamentos, dispositivos inteligentes e tecnologias inovadoras em áreas terapêuticas como Oncologia, Neurologia e Fertilidade. Nossas equipes trabalham juntas nos seis continentes com muita paixão e curiosidade para auxiliar os pacientes em todas as etapas da vida. Unir-se à nossa equipe de Cuidados com a Saúde significa fazer parte de uma cultura de trabalho diversificada, inclusiva e flexível, com grandes oportunidades de desenvolvimento pessoal e evolução profissional por todo o mundo.

Sua Função

Você terá um papel estratégico e de alto impacto na expansão do acesso de pacientes a terapias inovadoras no sistema de saúde público brasileiro. Nesta função, você liderará a implementação de planos de ação junto a gestores públicos de saúde, com o objetivo de minimizar barreiras de acesso ao mercado para produtos estratégicos. Utilizando ferramentas de economia da saúde, medicina baseada em evidências e diretrizes de avaliação de tecnologias em saúde, você demonstrará o valor dos produtos a pagadores e influenciará positivamente decisões de reembolso, alinhando-se aos imperativos estratégicos da área. Você gerenciará relacionamentos com gestores-chave de saúde e suas redes de influência, atuando em parceria com as equipes de vendas, marketing, médica e inteligência estratégica para integrar diferentes áreas e otimizar os resultados das ações de acesso. Além disso, você coordenará ações de padronização de produtos em instituições de interesse estratégico, conduzindo discussões e apresentações de dossiês técnico-científicos junto aos comitês responsáveis pelas avaliações nos diferentes segmentos da saúde pública.

Quem Você É

Experiência sólida em acesso ao mercado, economia da saúde ou áreas correlatas no setor farmacêutico;
Conhecimento aprofundado em avaliação de tecnologias em saúde (ATS), medicina baseada em evidências e ferramentas de economia da saúde, incluindo modelos de custo-efetividade.
Capacidade comprovada de construir e gerenciar relacionamentos com gestores públicos de saúde, formuladores de políticas e redes de influência no âmbito do SUS.
Habilidade para elaborar e apresentar dossiês técnico-científicos a comitês e instituições de saúde pública, com clareza e embasamento científico.
Perfil colaborativo e orientado a resultados, com experiência em atuação transversal com equipes de vendas, marketing, médica e inteligência estratégica.
Capacidade analítica para interpretar dados científicos e de mercado, transformando evidências em argumentos de valor junto a pagadores e tomadores de decisão.
Graduação em áreas da saúde, ciências biológicas, farmacêuticas, econômicas ou equivalente; pós-graduação em economia da saúde, saúde pública, epidemiologia ou área correlata será considerada um diferencial.

O(a) profissional poderá estar localizado(a) no Nordeste ou em Brasília.

O que oferecemos: Somos mentes curiosas que vêm de uma ampla gama de origens, perspectivas e experiências de vida. Acreditamos que essa variedade impulsiona a excelência e a inovação, fortalecendo nossa capacidade de liderar em ciência e tecnologia. Estamos comprometidos em criar acesso e oportunidades para todos se desenvolverem e crescerem no seu próprio ritmo. Junte-se a nós para construir uma cultura de inclusão e pertencimento que impacta milhões e capacita todos a defender o progresso humano!

Candidate-se agora e torne-se parte de uma equipe dedicada a Despertar a Descoberta e Elevar a Humanidade!

Senior Expert Technical Accounting Solutions & Compliance (all genders) (Wroclaw, Dolnoslaskie, PL, 53-616)

Work Your Magic with us!

Your Role: We are looking for a Senior Expert Technical Accounting Solutions & Compliance (TASC) (all genders) to join our Global Enterprise Solutions team. In this role, you ensure the integrity, accuracy, and compliance of financial reporting across the organization. You bring strong technical accounting expertise combined with hands-on operational experience, advising on IFRS standards and policies while understanding how reporting processes work in practice. You lead compliance monitoring, audit management, process reviews, and continuous improvement and automation initiatives. You also support IFRS and policy change implementation, strengthen internal controls, and provide technical expertise for cross-functional projects and process transformations across global teams.

Who you are:

8+ years of experience in accounting, financial reporting, compliance, or audit
Deep expertise in IFRS and financial reporting principles
Hands-on experience in operational financial reporting within a global environment
Proven track record in audit coordination and managing corrective actions
Experience in process improvement, automation, or IFRS implementation projects
Strong analytical, communication, and stakeholder management skills
Professional certification (CPA, ACA, ACCA or equivalent) is a strong advantage
Degree in Accounting, Finance, Business Administration, or a related field

YOUR MAIN BENEFITS:

Health and well-being: As part of your benefits, get access to private medical care, life insurance, and sports card, and receive a prepaid lunch card.
Work-Life balance: Enjoy additional paid days off and flexible hours.
Learning and Development: Take advantage of co-financing language courses, training, and certifications as well as other development opportunities.
Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

General Ledger Specialist (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

Your Role:

As Management Accounting Specialist (Sr. Accountant), you support in the areas of cost accounting and profitability analysis for one or more entities assigned and support local finance and controlling units in both areas. You support in managing maintenance and posting processes in cost accounting to provide an accurate and timely picture of the overhead cost situation as basis for controlling analysis and business decisions. You will also act as a mentor to junior accountants and a catalyst for continuous process improvement.

Key Responsibilities:

Cost Accounting, Profitability Analysis & Reporting Excellence

Own and perform assigned management accounting activities across monthly, quarterly and annual close, ensuring accurate and timely completion in line with agreed closing calendar.
Prepare, review and explain management accounting reports, cost-center reports and profitability analyses for local finance, controlling, ABP, CFO organizations and other internal customers.
Ensure reconciliations, supporting schedules and reporting outputs are complete, consistent and ready for review.
Execute and review cost accounting processes, including allocations, assessments, distributions
Perform cycle profitability accounting activities, transaction flows and posting on reporting positions.
Support the consistent application of global management accounting standards and guidelines across supported entities.

Audit, Compliance & Risk Management

Serve as the primary liaison for internal and external auditors; prepare comprehensive audit schedules, pre-audit analyses, and resolve complex audit queries.
Ensure all processes strictly adhere to internal controls (SOX/ICFR), Group accounting policies, and local statutory regulations.

Process Optimization & Technology Driving

Identify and implement opportunities for standardization, simplification, automation and workflow improvement to reduce manual effort and improve service quality.
Support system changes, User Acceptance Testing (UAT), migrations and other initiatives as a Management Accounting subject-matter expert.
Track relevant operational metrics and contribute ideas that improve close performance, data quality and stakeholder experience.

Stakeholder Management & Escalation Resolution

Act as a first point of escalation for complex management accounting questions, system issues and process exceptions within the assigned scope.
Foster strong, consultative partnerships with cross-functional teams (ABP, General Ledger, Product Costing and Controlling) to ensure end-to-end process alignment.

Leadership & Capability Building

Provide guidance, mentorship, and technical support to junior MA accountants, fostering a culture of continuous learning. Develop and maintain up-to-date Standard Operating Procedures (SOPs) and training documentation.

Who You Are:

Bachelor’s degree holder in finance, accounting or any related field required
At least 3 or more years of experience in accounting/finance with direct related experience with full-cycle cost accounting and profitability analysis
Experience within a Shared Services Center preferred
Experience with Cost Accounting and Profitability Accounting
Experience with SAP CO-OM and CO-PA or and reporting tools
Fluent English language skills required
Willing to be based in BGC, Taguig
Amenable to work on a mid-shift / night shift schedule (varying shifts every MEC and NONMEC)
With automation experience (VBA, other automation tools)

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

QA Senior Manager_ Biopharma (Tokyo, Tokyo, JP, 106-0041)

メルクと一緒に、あなたの力を発揮しよう！

冒険、限界への挑戦、そして発見に焦がれるあなたへ。あなたの大志を、メルクで羽ばたかせましょう！科学とテクノロジーを駆使したイノベーションに情熱を注ぐメルクのスタッフは世界中で活躍中です。ヘルスケア、生命科学、エレクトロニクスの分野で、メルクのソリューションは人々の暮らしをますます豊かなものにしています。あなたとメルクの力を合わせて、大きな夢を抱きましょう。メルクは、人、顧客、患者、そしてこの地球という惑星が共存する豊かな世界の構築に情熱を注いでいます。このためメルクでは、好奇心にあふれた人材を募集中です。メルクと一緒に、想像を超えた世界を開拓しませんか？

患者さんのためにひとつになって団結し、生命の誕生、QOLの向上、命をつなぐサポートをすることか、ヘルスケアにおける私たちの目的です。私たちは、腫瘍学、神経学、不妊治療などの疾患領域において、医薬品、インテリジェント装置、革新的技術を開発します。私たちのチームは、人生のすべてのステージで患者さんを助けるために、情熱と執拗な好奇心を持って6大陸全体で協力して働いています。ヘルスケアチームに入ることは、多様的で包含的、そして柔軟な職場文化の一部となることです。世界中で個人的な能力開発とキャリアアップの素晴らしいチャンスが待ち受けています。

Your Role

In this pivotal role, you will shape and oversee the local quality strategy for Japan, protecting patients and supporting reliable access to medicinal products. You will lead quality and compliance activities across good manufacturing practice, good distribution practice and good quality practice, translating global direction and the Pharmaceutical and Medical Device Act into practical standards and a robust quality management system. You will guide complex operational issues, including changes, deviations, complaints, recalls and corrective actions, while coordinating inspection readiness with manufacturing sites and health authorities. By advising local management, leading quality councils and management reviews, and connecting local, global and external stakeholders, you will strengthen performance, risk management and continuous improvement across the area.

Who You Are

Degree or equivalent background in pharmacy, chemistry, life sciences, pharmacology, medicine or a related field.
At least 3 years of experience in the pharmaceutical or related industry, with exposure to quality assurance, manufacturing, distribution, warehouse operations or related activities.
Practical experience with good manufacturing practice, good distribution practice and good quality practice in Japan, together with experience in quality assurance systems.
Working knowledge of Japan’s regulatory framework, including the Pharmaceutical and Medical Device Act, and experience supporting health authority inspections.
Experience managing quality processes such as change controls, deviations, technical complaints, product recalls or withdrawals, quality risk management and corrective and preventive actions.
Ability to analyze complex operational issues, prioritize work and make sound decisions with substantial professional responsibility.
Strong collaboration, negotiation and influencing skills to work effectively with local, global and external stakeholders.
Willingness to travel nationally and internationally; basic project management experience and familiarity with standard office applications are beneficial.

私たちが提供するもの：私たちは、さまざまな背景、視点、人生経験を持つ好奇心旺盛な人々で構成されるグループです。この多様性が卓越性と革新を促進し、科学と技術のリーダーシップを強化すると信じています。私たちは、すべての人が自分のペースで成長し発展するためのアクセスと機会を創出することにコミットしています。何百万もの人々に影響を与え、誰もが人類の進歩を支持できるようにする包括性と帰属感のある文化を築くために私たちに参加してください！

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

Chemical Operator 1 - Overnight (Jaffrey, New Hampshire, US, 03452)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

We are seeking a detail-oriented and safety-focused individual to join our team in a hands-on manufacturing environment. This role is centered on operating, monitoring, and troubleshooting production equipment while supporting efficient manufacturing operations in a fast-paced industrial setting. Responsibilities include setting up and adjusting automated and mechanical equipment, safely moving raw materials throughout the production process, and ensuring equipment is operating at peak performance. This position involves setting up mechanical equipment, handling web and chemical materials.

The ideal candidate will have experience working in a manufacturing or production environment and be comfortable operating automated equipment, including programmable logic controllers (PLCs). Additional responsibilities include performing in-process quality checks, monitoring production performance, identifying opportunities for process improvements, and maintaining compliance with all safety, quality, and operational procedures. This position also requires maintaining an organized work area and collaborating with the production team to maximize equipment uptime, product quality, and overall manufacturing efficiency.

Physical Attributes

Lift up to 50 lbs.
Stand/bend/twist for an 8-hour shift

This is a C shift position 9:30PM-6:30AM

Who You Are

Minimum Qualifications

High school diploma or GED
2+ years of manufacturing operator experience
Knowledge of EH&S, ISO, cGMP, and other manufacturing regulatory requirements

Preferred Qualifications

Strong understanding and application of basic math skills
Familiarity with Microsoft Excel and Word
Computer hardware/software experience
Experience handling chemicals
Adaptability and willingness to learn multiple operations and tasks
Excellent verbal and written communicate skills
Work well independently while also being a positive contributor to a strong, cohesive team

Pay Range for this position: $23.00-$36.00 per hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Cloud Solutions Architect (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your Role:

Ready to shape the future? As Senior Cloud Solutions Architect, you will be actively designing, implementing, and operating cloud-native backend systems and data services on AWS, contributing directly to our Data & AI platform and R&D product roadmap. You write production code, build pipelines, own deployments, and take end-to-end accountability for the solutions you deliver. If you thrive building things that matter, in a team that values quality, ownership, and continuous improvement, this role is for you.

Your key responsibilities:

Implement new features and maintain platform functionalities using AWS services (Lambda, Step Functions, Glue, Athena, API Gateway, and more); own deployments end to end.
Design and implement data processing pipelines, data archive processes, and RESTful/microservice integrations; apply serverless and event-driven patterns.
Write clean, well-tested, documented Python code; apply OOP and design patterns; participate actively in code reviews.
Build and maintain CI/CD pipelines in Azure DevOps; apply IaC principles using Terraform, CloudFormation, or CDK.
Embed AWS security best practices and our security standards into every solution; ensure observability through monitoring and health checks.

In return, we offer direct impact on life-changing R&D, a high-autonomy engineering culture with experienced peers, flexible working models, and the purpose-driven environment of a global science and technology company.

Who You Are:

Mindset & Ways of Working

Strong sense of ownership and accountability – you build it, you run it.
Curious and eager to learn; comfortable adapting to evolving technologies and requirements.
Collaborative team player in a cross-functional, international environment.

Experience & Qualifiscations

University degree in Computer Science, Engineering, or equivalent.
8+ years of relevant experience building secure, scalable, resilient cloud-native backend systems at enterprise scale.
Deep proficiency in Python (incl. boto3) and SQL; background in an additional OOP language (Scala, Java, or C#) is a plus.
Solid AWS expertise: Lambda, Step Functions, Glue, Athena, API Gateway, IAM, S3; serverless and event-driven design patterns.
CI/CD experience with Azure DevOps and Git; IaC with Terraform, CloudFormation, or CDK.
Security awareness: AWS security best practices including IAM policies, encryption, and MFA.
Nice to have: containerization (Docker, Kubernetes, Fargate), Snowflake, Apache Iceberg, NoSQL DBs.
Business-fluent English (written and spoken)

Operator Chemische Produktion (all genders) (Schaffhausen, Schaffhausen, CH, 8200)

Entfalte das Besondere mit uns!

An unserem Standort in Schaffhausen entwickeln und produzieren wir pharmazeutische Wirk- und Hilfsstoffe, die entweder direkt als Medikament zum Patienten gehen oder in klinischen Studien für künftige Therapiemethoden eingesetzt werden.

Eine Vielzahl verschiedener Prozesse sowie stetig neue Produkte stellt unser Produktionsteam dabei auf neuesten Technologien und Spezialequipment her.

Sie haben eine natürliche Neugier für chemische Prozesse im Produktionsumfeld und wollen eine entscheidende Rolle dabei einnehmen das Leben unzähliger Menschen zu verbessern? Dann freuen wir uns Sie kennenzulernen.

Ihre Aufgaben:

Auf unseren Produktionsanlagen im Massstab bis maximal 630L stellen Sie im Team pharmazeutische Wirkstoffe und Zwischenprodukte unter Einhaltung von cGMP-Richtlinien her. Dafür erlernen Sie eine extreme Bandbreite an unterschiedlichsten Prozessen und Technologien. Sie bedienen und überwachen die (Pilot)anlagen, protokollieren die Abläufe GMP-konform und sind für die fachgerechte Reinigung der Geräte verantwortlich. Als Profi vor Ort erkennen, interpretieren und beheben Sie Anlagenstörungen sowie Prozessabweichungen. Sie werden in die Prozessentwicklungen mit einbezogen und koordinieren parallele Tätigkeiten, auch abteilungsübergreifend.

Das bringen Sie mit:

Eine abgeschlossene Ausbildung als Chemikant bzw. Chemie- und Pharmatechnologe, Dipl. Chemietechnologe oder alternativ Chemielaborant mit Erfahrung im Aufgabengebiet.
Hohes Sicherheitsbewusstsein.
Kenntnisse in chemischer Verfahrenstechnik.
Sie besitzen gute GMP- sowie Deutschkenntnisse und sind idealerweise vertraut mit Anlagensteuerungen, explizit WinCC Professional von Vorteil.
Sie besitzen eine rasche Auffassungsgabe, sind dynamisch und flexibel.
Sie sind ein zuverlässige(r) Teamplayer/in und haben Freude an praktischer Arbeit.

Bewerben Sie sich jetzt und werden Sie Teil eines Teams, das Neues entdeckt und die Menschheit voranbringt.

Account Manager - Discovery Solution (Ho Chi Minh City, Ho Chi Minh, VN, 70000)

Work Your Magic with us!

Report to: Head of Sales Vietnam

Location: Ho Chi Minh City, Vietnam

Your Roles:

In this role, you will be at the heart of advancing scientific discovery, driving revenue growth and building lasting partnerships with life science researchers, laboratories, and distributors across your territory in Vietnam.
You will own the full sales cycle for a portfolio of discovery solutions, from prospecting and opportunity development through to closing and account expansion.
By combining deep scientific knowledge with commercial acumen, you will translate customer needs into tailored solutions, grow market share, and deliver measurable impact for both your customers and the business.
You will collaborate closely with internal stakeholders to develop and execute account plans, maintain a robust opportunity pipeline, and leverage digital tools to sharpen your sales effectiveness.
Your insights into the competitive landscape will directly inform go to market decisions, making you a key contributor to the commercial success of the Discovery Solutions business in the region.

Who Are You:

Bachelor's or Master's degree in Life Sciences, Chemistry, Biotechnology, or a related field.
At least 4 to 7 years of direct business to business sales experience in the life sciences industry.
Strong communication skills in English
Proven ability to manage sales & marketing activities in an assigned territory and meet sales targets.
Strong knowledge of competitor analysis, product positioning, pricing strategies, and related tactical skills.
Experience applying leading Sales Excellence processes (e.g., Solution Selling, Key Account Agreements, Channel Sales, pricing).
Proficient with classic sales tools and processes (e.g., Salesforce.com) and ability to follow daily sales processes; timely updates on market, customers, and activities.
Excellent communication, interpersonal, and relationship-building skills; customer-centric with integrity, trust, and respect.
Demonstrated ability to implement and execute plans; action-oriented with a drive for results and perseverance; professional and positive demeanor.
Strategic thinker with the ability to anticipate future trends and make critical decisions for the business.
Able to work in a complex, multi-cultural selling environment and manage diverse stakeholders.
Ability to identify and develop new customers, participate in product promotions, and maintain accurate customer data.
Awareness of competitor activity and local industry events; capable of forecasting customer potential for sales planning.
Focus on compliance and code of conduct while achieving targets.
Territory knowledge and a proven track record in direct B2B sales.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Recepcionista (Montevideo, Montevideo, UY, 91605)

Tus responsabilidades

Es responsable de la operación de la central telefónica, atendiendo llamadas y distribuyéndolas a las extensiones correspondientes. Recibe a visitas y proveedores, asegurando el correcto ingreso de sus datos en la herramienta definida por la compañía, y poniéndolos en contacto con los sectores correspondientes. Se encarga del control de stock de papelería, cafetería e higiene institucional, y de realizar los pedidos mensuales de reposición, asegurando siempre un stock mínimo de insumos. Apoya a Coordinador de Gerencia en actividades de Comunicación Interna a través de diversos canales así como también en la organización de eventos internos de la organización y actividades de RSE.

Quien eres

Estudios técnicos en Administración, Secretariado Ejecutivo, Atención al Público o similares.

Mínimo 2 años de experiencia en cargos similares.

Inglés fluido oral y escrito, es excluyente.

Manejo completo de MS Office, es excluyente.

¡Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!
En el marco de la Ley 19.691 el llamado comprende a candidatos que estén inscriptos en el Registro Nacional de Personas con Discapacidad que funciona en el Ministerio de Desarrollo Social.

Executive Assistant to Head of Hyper Automation & Process Excellence (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Job Description

Job Title: Executive Assistant & Communications Coordinator

Position Summary

The Executive Assistant & Communications Coordinator provides dedicated support to senior leaders through a combination of executive administration, communication management, stakeholder coordination, and event support. The role is responsible for ensuring smooth leadership operations, enabling effective communication across the organization, and supporting the planning and execution of leadership meetings, visits, town halls, and engagement activities.

Your Role:-

Executive Assistant Support

Manage executive calendars, appointments, and meeting schedules.
Coordinate travel arrangements, visitor management, and other administrative activities.
Prepare presentations, reports, briefing materials, and meeting documentation.
Organize and maintain records, correspondence, and confidential information.
Support leaders in managing priorities and ensuring timely follow-up.

Leadership Meeting Management

Coordinate leadership team meetings and governance forums.
Prepare and distribute agendas, pre-read materials, and meeting minutes.
Track action items, decisions, and follow-ups, ensuring closure within agreed timelines.
Liaise with stakeholders to gather updates and prepare status reports for leadership reviews.

Internal Communications

Draft and coordinate leadership communications, organizational updates, announcements, and employee messages.
Support the development and dissemination of communication materials for key business initiatives.
Ensure consistency of messaging and adherence to organizational communication standards.
Coordinate communication plans for leadership visits, town halls, and employee engagement activities.

Event & Engagement Coordination

Support the planning and execution of leadership visits, town halls, team meetings, workshops, and employee engagement events.
Prepare event agendas, speaker notes, communication plans, and briefing packs.
Coordinate logistics, stakeholder communication, and event schedules to ensure seamless execution.
Partner with internal teams to drive employee engagement and leadership visibility initiatives.

Stakeholder Coordination

Act as a key point of contact between leadership and internal/external stakeholders.
Facilitate effective communication and collaboration across teams and functions.
Support special projects and initiatives as assigned by leadership.

Who you are

Bachelor's degree in Business Administration or a related field.
Relevant experience in Executive Assistant, Communications, Administration, or Business Support roles.
Excellent written and verbal communication skills. Strong organizational and coordination abilities with attention to detail.
Ability to manage multiple priorities and work effectively in a fast-paced environment.
High level of professionalism, discretion, and stakeholder management skills.

Key Competencies

Executive Administration
Internal Communications
Content Drafting & Messaging
Event & Engagement Coordination
Stakeholder Management
Planning & Organization
Follow-up & Execution Excellence
Confidentiality & Professional Judgment

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

China Clinical Research Scientist (Beijing, Beijing, CN, 100016)

Work Your Magic with us!

Your role:
As a subject matter expert, the China Clinical Research Scientist (CRS) partners with the Clinical Lead to provide scientific, clinical, strategic, and operational input to an early or late-stage clinical development program. The CRS contributes to data interpretation, study designs, regulatory and study documents, and publication efforts as well as providing scientific input into pipeline programs. Medical Monitoring and Medical Data Review activities are conducted in close collaboration with the Clinical Lead, including oversight of any Medical Monitoring activities performed by contracted vendors. The China CRS mainly focus on R&D China programs and assigned global programs per need.
The CRS interacts with a multi-disciplinary, global/local team ensuring that scientific, clinical and other topics are appropriately considered with respect to highly complex data findings and escalated to clinical Lead.

Within the frame of the clinical development of new medicines, the CRS is responsible for：

Managing assigned activities within clinical study in support of the clinical Lead;
Providing clinical/scientific input and gathering necessary information from other areas to clinical development plans;
Involved in Medical Monitoring and Medical Data Review in close collaboration with the Clinical Lead;
Assisting closely with Contract Research Organizations and other vendors on medical monitoring activities, supporting to the operational excellence of project execution in partnership with Global Development Operations;
Working on the design of clinical trial concepts, study protocols, assessment schedules, patient information material as well as clinical study reports in support of the Clinical Lead;
Preparing the relevant sections of the common technical document dossier while supporting clinical trial-related submission activities and marketing authorization submissions;
Assisting in the design and organization of the content for relevant Advisory Board Meetings or KTL consultation;
Drafting sections for clinical trial protocols, including most recent literature citations.

Who you are:
The CRS is an individual contributor with high analytical skills, strategic thinking, and a growth mindset.

With direct oversight and guidance, able to work on assigned tasks or projects with scientific rigor and utilizing up-to-date information technology
Expert knowledge of scientific principles and concepts
Knowledge of regulatory requirements, including ICH-GCP strongly preferred
Aptitude to interpret and to integrate complex data, including, clinical safety and efficacy data, pharmacokinetics, biomarker and next generation sequencing data
Good medical or clinical knowledge and experience in clinical development/operations with the capacity to monitor laboratory data and other clinical trial data
Capability to perform literature searches and to utilize library services, digest the information, and synthesize the key take-away points
Good communication and presentation skills
Normally receives general instruction on routine work and more detailed instruction on new assignments
Educational and/or work experience in the respective therapeutic area is desirable
Proficient level of organizational and project management skills
Able to oversee Medical Data Reviewers with the support of Medical Lead. Adeptness to work in a matrix environment of cultural diversity and in a global setting.
Master degree of clinical medicine is preferred. M.D. will be an advantage.
Fluent English is a must.
Experience in product and clinical development (minimum of 1 year, with at least 3 years in a comparable setting in the pharmaceutical industry or biopharma/healthcare setting) preferred.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Customer Service Specialist with German (all genders) (Wroclaw, Dolnoslaskie, PL, 53-616)

Work Your Magic with us!

Work model: 5 days per week from office in Wroclaw for onboarding and initial collaboration, after which a hybrid model will be followed

YOUR ROLE:

In your role as a Customer Service Specialist, you will be the primary point of contact for our customers, ensuring every interaction is smooth and professional. You’ll take charge of the entire order cycle — from initial entry to monitoring shipments — using tools like Oracle and SAP to keep things on track. When issues or service complaints arise, you’ll use your problem-solving skills to find effective solutions quickly.

Working closely with our Commercial, Finance and Distribution teams, you’ll ensure every interaction is seamless. This is a fantastic opportunity to grow your career while mastering diverse skills sets in a dynamic, collaborative international environment. This role is based in our local office with standard contact center hours from 8:00 am to 5:30 pm CET.

WHO YOU ARE

Excellent command of German and good command of English are required.
Minimum of 2–3 years of experience in a fast-paced customer service environment.
Proven ability to learn and adapt quickly to multiple ERP and CRM systems (experience with SAP, Oracle, or Salesforce is a plus).
Skilled at managing order processing and resolving service complaints.
Strong communication skills with a focus on delivering high-quality customer experience.
Ability to prioritize tasks effectively in a collaborative, international team.
Proactive mindset with a commitment to continuous improvement and knowledge sharing.

YOUR MAIN BENEFITS:

Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card
Work-Life balance: Enjoy additional paid days off, flexible working hours.
Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.

Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Global Head, Medical Writing (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

Your Role:

As the Global Head of Medical Writing, you will shape and lead a high-performing, global function that sits at the heart of clinical development and regulatory success. In this pivotal senior leadership role, you will build, develop, and manage a team of over 100 medical writing professionals, driving the delivery of timely, high-quality clinical documentation across a complex and fast-moving global portfolio. You will set the strategic direction for medical writing standards, processes, and tools, ensuring the organization remains at the forefront of regulatory science and documentation excellence. Working in close partnership with clinical, regulatory, and vendor management stakeholders, you will translate organizational priorities into operational plans that consistently deliver results at scale. This is a rare opportunity to leave a lasting impact on how a global medical writing function operates, innovates, and elevates the quality of science that ultimately serves patients worldwide.

Location: 3x/week hybrid schedule in Billerica, MA.

Key Accountabilities:

Responsible for building, leading, and managing the Global Medical Writing Team (5-10 direct reports, Total staff >100)
Identify project staffing requirements, develop and maintain staffing plans to meet project demand
Ensure the delivery of timely and high-quality MW deliverables according to global project plans
Work closely with vendor management to ensure implementation of operating model and delivery to contracts
Oversee the preparation of strategies documents prepared by Medical Writing Leads, Identify gaps in skills and drive continuous improvement
Develop clinical documentation processes that ensure consistency and control
Oversee and ensure standards for clinical documents are developed, used and maintained.
Ensure the company follows state of the art standards / regulations / tools in medical writing activities
Oversee, coach and supervise vendors to ensure milestones meet timelines and deliverables are of high quality

Who You Are:

Minimum Qualifications:

Advanced degree in a scientific or writing discipline (Master’s or PhD).
At least 12 years of relevant Medical Writing experience in the pharmaceutical/biotech industry.
A minimum of 5 years established track record managing large medical writing teams within global, matrixed organizations.
Ability to travel as needed.

Preferred Qualifications:

Demonstrated skill and engagement in state of the art medical writing tools.
Established track record driving the adoption of modern tools to facilitate efficient and effective medical writing.

Pay Range for this position: $234,800 – 352,200
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Global Inventory Strategy and Optimization Lead (Chandler, Arizona, US, 85226)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Location: The Global Inventory Strategy & Optimization Lead is a hybrid position located in Allentown, PA or Chandler, AZ with 15% travel required to meet business needs.

Your Role:

The Global Inventory Strategy & Optimization Lead serves as the central point of coordination for global inventory management & governance including material risk across regions. Working closely with regional planning and procurement teams, this role consolidates regional inventory positions, supply constraints, inventory exposures, and mitigation strategies into a single source of truth that supports executive decision-making.

In a global Make-to-Order (MTO) environment, this role establishes inventory policies, leads optimization and allocation governance, and provides the analytics and reporting needed to proactively surface risks, opportunities, and trade-offs while instilling inventory discipline across the organization.

The ideal candidate is a highly analytical planning professional who combines expertise in inventory management, materials planning, supply risk management, and business analytics with exceptional communication skills. They are comfortable working with large datasets, defining inventory strategies, and influencing leaders across operations, finance, and regional planning teams without direct authority.

Key Responsibilities:

Global Inventory Strategy & Governance

Lead the global inventory strategy by establishing inventory policies, safety stock methodologies, planning parameters, and governance processes that balance customer service, working capital, and supply continuity.
Coordinate with regional inventory planning teams to ensure consistent application of inventory strategies, challenge inventory assumptions, and identify opportunities to optimize inventory across the network.
Develop global inventory segmentation, safety stock, replenishment, coverage, and inventory positioning strategies that support business objectives while minimizing excess inventory and reducing supply risk.
Partner with operations, finance, and planning teams to align inventory investment and inventory objectives across the enterprise.

Inventory Analytics & Business Insights

Serve as the planning organization's inventory analytics expert by developing and maintaining executive dashboards, KPI scorecards, and reporting tools that provide visibility into inventory performance, material availability, allocation status, inventory exposure, and supply risk.
Analyze inventory performance, material shortages, excess and obsolete inventory, service impacts, and inventory trends to identify risks, quantify business impacts, evaluate scenarios, and support leadership with data-driven recommendations.
Continuously improve inventory reporting capabilities, inventory metrics, and planning analytics to enhance decision quality and inventory effectiveness.

Regional Inventory Integration & Governance

Drive global inventory alignment by consolidating regional inventory positions, validating planning assumptions, identifying cross-regional inventory opportunities, and supporting cross-functional decision-making while promoting standardized inventory management practices across the organization.
Maintain standardized inventory policies, planning parameters, governance processes, inventory definitions, planning calendars, and data quality standards.
Act as the global steward of inventory governance to ensure a disciplined, repeatable inventory management process across all regions.

Material Risk & Allocation Management

Lead the global management of material constraints, inventory exposure, allocation decisions, and long-term supply risks, particularly for strategic and long lead-time components.
Chair and coordinate the Allocation Board by facilitating stakeholder alignment, evaluating competing business priorities, and driving decisions consistent with established allocation policies and prioritization frameworks.
Identify customer, operational, financial, and inventory risks resulting from material shortages and supply constraints, while ensuring visibility of mitigation and recovery plans across the enterprise.
Coordinate network inventory balancing strategies to prevent simultaneous shortages and excess inventory across regions and manufacturing locations.

Executive Reporting

Develop executive-ready inventory reviews that communicate inventory performance, inventory projections, supply risk exposure, shortage outlooks, allocation decisions, excess inventory trends, recovery plans, KPI performance, scenario analyses, and key recommendations.
Ensure leadership receives timely, accurate, and actionable information to support strategic and operational decision-making.
Own the global inventory control tower, establishing the single source of truth for inventory position, inventory exposure, allocation status, material availability, and supply risk visibility across the enterprise.

Who You Are

Minimum Qualifications:

Bachelor’s degree in Supply Chain, Industrial Engineering, Business, or related field.
5+ years of supply chain planning experience in a manufacturing environment.
Experience supporting multi-site MTO (Make-to-Order) manufacturing and intercompany supply networks.
Hands-on experience with SAP planning solutions, MRP, APO SNP & PPDS.

Preferred Qualifications:

APICS CPIM or CSCP certification.
Experience working with complex BOM (bill of materials) and supporting manufacturing operations.
Advanced analytical organizational and communication problem solving skills.
Deep understanding of material planning, inventory management, MRP, safety stock methodologies, inventory optimization, and supply chain processes.
Working knowledge of SAP including material management and SAP purchasing processes.
Proven ability to work effectively with cross-functional teams (global manufacturing, procurement, and supply chain organizations) and influence stakeholders and drive accountability.

Pay Range for this position: $120,000 - $150,000

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Director R&D Sustainability and Medical Governance Operations (Billerica MA) (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Director, R&D and Medical Governance Operations holds a dual mandate: supporting the Head CMO Governance & Operations in the full spectrum of CMO-GO business operations activities, and serving as the orchestrator and oversight lead for R&D Sustainability initiatives across the R&D organization. The role ensures the smooth execution of governance processes, operational workflows, data systems management, vendor coordination, and training delivery, while simultaneously driving the planning, coordination, and reporting of R&D’s sustainability project portfolio in alignment with the company’s broader ESG and corporate sustainability commitments.

Impact:

Enables the Head CMO Governance & Operations to focus on strategic priorities by owning and executing the operational backbone of CMO-GO.
Acts as the central orchestrator of R&D Sustainability projects, ensuring cross-functional alignment, milestone delivery, and transparent reporting to R&D and corporate leadership.
Strengthens the organization’s compliance posture through rigorous maintenance of governance documentation, data systems, audit readiness, and training completion.
Embeds sustainability thinking into R&D operations by translating corporate ESG commitments into concrete, measurable R&D-level initiatives and workplans.

Complexity:

Operates simultaneously across two demanding remits — governance operations and sustainability orchestration — each requiring deep cross-functional engagement and independent judgment.
Manages competing operational priorities across governance initiatives, sustainability projects, vendor engagements, and stakeholder reporting cycles.
Navigates an evolving external sustainability regulatory landscape (e.g., EU CSRD, GHG reporting) and translates requirements into R&D-specific actions.

Accountability / Independence:

Accountable for the timely and accurate delivery of business operations tasks delegated by the HeadCMO Governance & Operations.
Fully accountable for the orchestration, oversight, and reporting of the R&D Sustainability project portfolio, working independently with minimal guidance.
Exercises judgment in prioritizing workload across both remits and proactively managing stakeholder expectations across functions and geographies.

Who You Are

Minimum Qualifications:

Degree in Medicine or Life Sciences required; an advanced scientific degree (Master’s, PhD, or MD) is preferred.
Additional qualification in business administration, project management, or a related discipline is an advantage. Substantial professional experience (typically 8–12 years) in clinical R&D, Medical Affairs, or a comparable function, ideally within an international matrix organization.
Demonstrated experience in business operations, process management, and governance in a pharmaceutical or biotech environment.
Proven track record in orchestrating complex, multi-workstream programmes or project portfolios, including governance design and stakeholder management.
Experience in or strong working knowledge of corporate sustainability / ESG programme management; familiarity with frameworks such as GHG Protocol, CSRD, SBTi, or equivalent is a distinct advantage.
Knowledge of clinical studies, Early Access Programs, Patient Support Programs, and relevant therapeutic areas.
Experience in vendor management, including contracting, performance oversight, and budget tracking.
Familiarity with audit management processes and experience supporting audit preparation and follow-up activities.
Expert knowledge of ICH-GCP and applicable international regulations, laws, and guidelines for clinical studies, Patient Support Programs, and Early Access.
Experience in developing and delivering training programs to diverse internal and affiliate audiences.

Preferred Qualifications:

Strong programme and project management skills: able to design governance structures, manage interdependencies, and drive delivery across complex, multi-stakeholder portfolios.
Sustainability literacy: understanding of ESG reporting obligations, carbon accounting principles, and the integration of sustainability into R&D operations.
Excellent organizational, prioritization, and time management skills; able to manage multiple concurrent workstreams effectively across two distinct remits.
Strong written and verbal communication skills; able to prepare clear reports, presentations, and governance documents for senior and executive audiences.
Proven ability to build effective working relationships and influence without direct authority in a complex global matrix environment.
High attention to detail and commitment to data quality, documentation standards, and compliance.
Strong digital and database literacy; proficiency with project management tools, data management platforms, and ESG reporting systems.
Fluent in English; additional languages are an advantage.
Willingness to travel domestically and internationally up to 10% as required.

Location: Billerica MA

Pay Range for this position: $174,600 – 262,000

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Project Manager (영어 필수, 유관 경력 5년 이상, 대전 근무) (Daejeon, Daejeon, KR, 34002)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Join our team and take a leading role in driving the success of our Cell Culture Media, Process Liquids & Buffers portfolio one of the fastest-growing areas within our Life Science / Process Solutions business.

As Project Manager, you will be at the center of gravity for a dynamic and expanding portfolio, playing a pivotal role in shaping how we deliver complex, integrated custom solutions to our customers. This is your chance to make a real impact from the first customer conversation all the way through to successful project and product delivery.

Your role:

Drive the successful management and execution of new customer-facing projects, with a focus on custom Cell Culture Media and Process Liquids & Buffers
Collaborate closely with customers, commercial colleagues and operational partners to define clear project requirements
Deliver compelling project proposals covering product requirements, pricing, and estimated delivery timelines
Lead cross-functional internal teams to bring customer solutions to life on time, on budget, and to the highest quality standards

Stay ahead of day-to-day portfolio needs by identifying and closing process gaps and mitigating risks early
Work hand-in-hand with a strong network of internal stakeholders to ensure seamless execution and continuous improvement

Act as the primary point of contact for product line inquiries, critical quality issues, and supply disruptions ensuring swift, effective resolutions
Drive proactive, transparent communication in direct customer interactions, empowering key sales stakeholders with the insights they need to succeed

Who you are:

Bachelor’s degree in science, Engineering, or Business. Master’s degree or MBA preferred.
5+ years of professional experience in the Life Science and/or pharmaceutical industry.
Fluent in English
Strong background in Marketing and Project Management experience involving successful management of projects, resources, timelines, budgets and coordinating between functional teams
Project Management certification (PMP, Prince2, etc.)
Understanding of bio pharmaceutical applications and customer processes.

Strong ownership and problem-solving mentality, "Can-do attitude," enjoying solving complex problems and simplifying processes.
Strong communication and persuasive skills.

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Site Director - Megasys (Leixlip, Dublin, IE, W23 CX73)

Work Your Magic with us!

The Role:

MEGASYS® specializes in managing gases, chemicals, and slurries, providing essential on-site support in semiconductor manufacturing environments.

As the MEGASYS® Site Director, you will lead and direct the on-site MEGASYS® operation team, ensuring effective management and operational excellence. This role involves close collaboration with customers to guarantee that their service needs are met and adequately supported, fostering a safe and efficient operational environment that prioritizes customer satisfaction.

In this position, you will have the opportunity to collaborate with other sites, participate in off-site meetings, and engage in occasional travel for training and strategic initiatives. Your leadership will be crucial in driving the success of our operations and enhancing customer relationships.

Key Responsibilities:

Establishes and cascades teams goals and objectives for overall site operations.
Creating an inspiring team environment with an open communication culture.
Acts as primary interface between customer and EMD Electronics for all site wide business issues.
Manages all on-site services escalations with customer.
Collaborates with Customer on operational improvements.
Shares all Safety and quality data with customer driving operational improvements.
Delegating tasks and set deadlines for your internal team.
Accountable for appropriate staffing levels, training, and support of site activities.
Prioritizes resources and site initiatives that align with organizational and customer goals.
Supports MEGASYS® and customer base during excursions, post event root cause analysis, etc.
Responsible for the development of the site operation and leadership team.
Develops and monitors key performance indicators across the site.
Negotiate any changes to the TCGM operating agreement, including operational changes, modifications to scope of work, and fees for service.

The MEGASYS® Site Director, role is an on-site position located in Leixip with 10% travel required to meet business needs.

Who You Are:

Minimum Qualifications:

Bachelor’s degree in chemistry, engineering, or a related technical field, with 7+ years of experience in chemical operations or manufacturing, demonstrating progressive responsibility; or 10 years of relevant experience may substitute for a degree.
Experience in managing a small to medium sized team direct or in-directly or 5 people or more.

Preferred Qualifications:

Strong preference for semiconductor industry experience.
Background in customer management as a service provider.
Proven track record in issue resolution and customer prioritization.
Ability to lead teams in meeting safety, health, and environmental standards.
Knowledge of OSHA regulations and ISO quality systems required.
Excellent verbal, written, and interpersonal skills with the ability to motivate and influence others.
Strong presentation skills, able to communicate clearly to customers and executives.
Proficient in business software, particularly Microsoft Office; capable of learning company-specific systems (SAP, Oracle, etc.) and experienced with labor models and ERP systems.
Experience in implementing solutions for cost reduction and continuous improvement.
Willingness to travel, including overnight and potential international trips, with approximately 10% travel expected.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Regulatory Affairs Expert (all genders) Biocides (EU & GB) (Darmstadt, Hessen, DE, 64293)

Design a more beautiful world with us

Join the team behind the shimmer in cosmetics, the gleam in concept cars and the science that sparks innovation. At SUSONITY, we don’t just create materials – we bring beauty and performance to life. And we’re just getting started. As a global team of thinkers, makers and innovators, we’re united by a simple belief: that surfaces can do more than look good – they can perform brilliantly. Join us and help build the next generation of beauty, durability and design.

The role

An exciting opportunity is available within our Product Compliance Department. As Senior Regulatory Affairs Expert for Biocides (EU & GB), you will coordinate and execute regulatory activities for our insect repellent business, with a primary focus on the EU Biocidal Products Regulation (BPR, Regulation (EU No 528/2012) and GB BPR. You will also contribute to registration projects across global markets.

Working closely with colleagues in Product Management, Sales and Product Development, you will help ensure that our portfolio meets regulatory requirements and remain fit for market. Following onboarding, you will act as a key regulatory contact for authorities, industry associations and customers. You will become part of a global team responsible for product compliance, sustainability and quality oversight across our portfolio.

Your responsibilities

Coordinate and execute regulatory activities for the PT19 insect repellent business under the EU and GB BPR at active substance and biocidal product level, including authorisations, renewals, changes and other post-authorisation activities.
Monitor and assess regulatory developments and their potential impact on our portfolio.
Contribute to and coordinate regulatory registration projects across international markets.
Act as a key regulatory contact for competent authorities, industry associations and customers.
Work closely with global colleagues and cross-functional partners in Product Management, Sales and Product Development.
Support the global team in ensuring product compliance, sustainability and quality oversight across SUSONITY’s portfolio.

Your profile

Master’s degree or Ph.D. in natural sciences, preferably with a background in toxicology.
At least 7 years of professional experience in regulatory affairs under the EU BPR and practical knowledge working under the GB BPR. Professional experience with EU/GB BPR legislation and regulatory requirements, including regulatory procedures at active substance and biocidal product level.
Experience with human health risk assessments and the interpretation of toxicological data in a regulatory context.
Practical experience with dossier preparation in IUCLID and dossier submission in R4BP 3.
Experience with SAP ERP software and document management systems is preferred.
Strong customer orientation, self-motivation and a genuine interest in networking.
Very good analytical and process-oriented thinking, combined with a structured, solution-oriented approach.
Strong interpersonal, verbal and written communication skills, as well as proactive problem-solving and troubleshooting abilities.
Ability to manage and deliver work in a matrix organisation and to collaborate effectively in a global, cross-functional environment.
Effective negotiation and presentation skills.
Fluency in English, both written and spoken, and proficiency in at least one additional major European language.

What we offer

At SUSONITY, you’ll have the opportunity to make a global impact — shaping the commercial foundation of a fast-evolving organization. We offer a culture that values empowerment, collaboration, and innovation, giving you the freedom to lead initiatives that drive real business success.

We support our colleagues in their development and promote an open and inclusive culture. We believe it's our duty to meet our fundamental responsibilities in topics like human rights, labor conditions and anti-corruption practices. We are committed to creating access and opportunities for all to develop and grow at your own pace. People are responsible for the success of our organization, so people play an important role in all we do and how we achieve it.

Apply now and join the bright minds behind brilliant surfaces.

Pharma Technology Technician (Mollet del Valles, Barcelona, ES, 08100)

Tu rol:

Diseñarás y mejorarás nuevos procesos de fabricación y limpieza, incluyendo la gestión del ciclo de vida de los procesos, aplicando los principios de seguridad, calidad y eficiencia.
Liderarás y coordinarás el equipo de trabajo, prepararás la documentación necesaria para llevar a cabo las validaciones y realizarás el seguimiento de la fabricación cuando proceda.
Serás la persona de referencia para los procesos y productos bajo tu responsabilidad, identificando oportunidades de mejora en los procesos y las limpiezas, así como definiendo las opciones más adecuadas de acuerdo con los principios de seguridad, calidad y eficiencia.
Serás responsable de llevar a cabo las revalidaciones de los procesos y la verificación continuada de los procesos y las limpiezas bajo tu responsabilidad, dentro del ciclo de vida del producto.
Participarás en la homologación de nuevas empresas proveedoras y en los cambios de proveedor.
Definirás los tiempos de validez entre las distintas fases de los productos intermedios de fabricación.
Definirás la estrategia de control de los procesos.
Darás soporte en la gestión de las incidencias relacionadas con los procesos productivos que puedan surgir durante la fabricación rutinaria de los lotes.
Evaluarás los cambios impulsados tanto desde tu área como desde otras áreas de la organización.
Darás soporte en la gestión de desviaciones e investigaciones con impacto en la calidad del producto o del proceso productivo, así como en la definición y el seguimiento de las acciones correctivas y preventivas asociadas.

Desarrollarás estas tareas en colaboración con otras áreas y funciones, y formarás parte de equipos de proyecto para implementar nuevos procesos o instalaciones.

Tu perfil

Formación universitaria en Ciencias de la Salud o Ingeniería.
Experiencia mínima de tres años como profesional de Tecnología Farmacéutica o en una posición similar.
Conocimientos de las normas GMP.
Conocimientos avanzados de estadística.
Conocimientos básicos de gestión de proyectos.
Conocimientos avanzados de herramientas ofimáticas, como Word, Excel y PowerPoint.
Conocimientos básicos de herramientas informáticas para la gestión de proyectos, como Microsoft Project o similares.
Nivel fluido de inglés oral y escrito, equivalente al First Certificate.

Site: Mollet del Vallés

Contrato indefinido

¡Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!

Apprentissage MPC 3+1 - Documentation & Training (m/f/d) (Corsier-sur-Vevey, Vaud, CH, 1804)

Exprimez votre talent avec nous !

Date d'entrée en fonction : 1er août 2027
Durée : 1 an
Lieu : Corsier-sur-Vevey, Suisse

Au sein de l’équipe Quality Systems, ton rôle sera:

Supporter les activités de routine liée à la documentation
Supporter les activités de routine liée à la formation
Apporter de l'améioration continu au coeur de projet afind 'augmenter la performance de nos systèmes
Travailler au sein d’une équipe pluridisciplinaire gérant plus de 14 systèmes qualités différents mais aussi avec des collaborateurs répartis dans tous les départements
Découvrir ce qu’est une entreprise internationale spécialisée dans la fabrication de biomédicament et ainsi découvrir les différentes spécialités, corps de métier et activités autour de nos processus de fabrication

Ton profil :

Tu es actuellement à l'école de commerce dans le modèle MPC 3+1 et cherches un stage pour ta dernière année
Autonome et orienté.e solutions
Proactif.ve, bon esprit d'équipe
Bonnes compétences en communication
Français courant

Postulez dès maintenant et devenez membre de notre équipe dont la vision est de stimuler les découvertes pour élever l'humanité !

Market Access Manager (all genders) (Brussels, Vlaams-Brabant, BE, 1040)

Work Your Magic with us!

Your role

As MAP & GAP Manager, you will help shape reliable market access, pricing and reimbursement outcomes across Belgium and Luxembourg. You will coordinate accurate, timely reimbursement and pricing submissions, ensuring that documentation, approvals and authority interactions are handled with care. You will monitor legislative and competitor developments and translate relevant changes into clear implications for the business. You will also own the end-to-end tender pipeline, from early opportunity identification and milestone planning through governance, submission and post-tender review. Working closely with Business Units, Finance, Supply Network Organization, Regulatory Affairs, Medical, Quality, Compliance and regional teams, you will turn complex inputs into decision-ready actions. You will prepare tender business cases with a clear view of pricing, profitability, supply, contractual and risk considerations. You will maintain transparent records, audit trails and trackers so that every critical decision and commitment can be followed through. In addition, you will support governmental affairs and policy activities through focused analysis, stakeholder intelligence and well-prepared engagement. Your structured, proactive approach will help protect patient access, compliance and business quality while continuously improving local processes.

Who you are

You have at least 3-5 years of experience in a pharmaceutical environment, market access, pricing, reimbursement, tender management or a closely related function.
You hold a Bachelor’s or Master’s degree, ideally in life sciences, economics, health economics, business, pharmacy or a related discipline.
You have experience with pricing and reimbursement submissions and with implementing administrative or cross-functional processes.
You bring working knowledge of the Belgian and Luxembourg pricing, reimbursement and tender environments, or the ability to build this knowledge quickly and accurately.
You are professionally fluent in English, Dutch & French are nice to haves
You understand the financial and profitability parameters relevant to tender and market access decisions.
You work confidently with Microsoft Word, Excel, structured databases and tracking systems, and can create concise status updates, timelines and decision-ready summaries.
You are accurate, accountable and process-minded, with strong planning, prioritisation, communication and follow-through, sound ethical judgement and a commitment to compliance, confidentiality and quality.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Director Real World Evidence Scientist (Oncology) (all genders) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

This position can be filled either in Switzerland (Eysins) or Germany (Darmstadt) in a hybrid format.

Your role

Real-world evidence is reshaping how medicines are developed, approved, and valued — and in this role, you will be at the forefront of that transformation. As a Director Real-World Evidence Scientist in Oncology, you will own and drive the end-to-end RWE strategy for one or more complex, high-priority oncology programs, operating as a recognized scientific authority across the organization and beyond.

You will define and lead the integration of RWE into clinical development and regulatory strategies, working directly with global program teams and cross-functional partners across clinical, regulatory, market access, and commercial functions. You will design, initiate, and oversee non-interventional studies — from protocol development through to study reporting — and ensure the selection of fit-for-purpose real-world data sources that address critical research questions. Your scientific judgment will directly inform decision-making at the most senior levels of the organization.

Beyond program delivery, you will represent the organization in interactions with health authorities, contribute to peer-reviewed publications, and present at international conferences — actively shaping the external scientific landscape. You will also champion methodological innovation, drive process improvements, and serve as a scientific mentor to colleagues within the function, contributing to a culture of rigor, collaboration, and continuous learning.

Who you are

You hold a Master’s degree or PhD in Epidemiology, Public Health, Health Economics and Outcomes Research, Biostatistics, or a related discipline, and bring 8 or more years of RWE experience gained in a pharmaceutical, biotechnology, or contract research organization setting.
You have deep expertise in studies based on secondary data use — including claims data, electronic medical records, and registries — across multiple healthcare environments (Europe, US, and/or Asia), as well as experience in primary data collection.
You are proficient in working with federated data networks and familiar with data standards such as OMOP CDM or FHIR, and bring strong methodological skills spanning epidemiology, pharmacology, and pharmacovigilance.
You have a proven track record of leading RWE strategy at a global program level, navigating complex, matrixed organizations and collaborating effectively across clinical development, regulatory affairs, and market access functions.
You bring experience in regulatory and/or payer submissions and interactions, and a thorough understanding of the evolving regulatory environment for RWE.
You communicate with clarity and confidence — translating complex scientific content for diverse audiences, including senior leadership and external stakeholders — and you are fluent in English.
Ideally, you also bring experience with AI/ML applications in RWE (including NLP), patient-reported outcomes (PRO), health technology assessment, and a track record of thought leadership through publications, conference presentations, or advisory roles.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

高级工艺开发科学家-上游 (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Position Responsibilities

• Expert in bioprocessing/biomanufacturing/process development focus on upstream process, include cell line development, CCM screening and optimization, cell culture process development and optimization, PD scale bioreactor operation, etc.

• Work closely with customers, providing technical support，hands-on guidance and on-site trial support for upstream process products，especially for CCM, to address key current and future needs within the industry through sound science and engineering.

• Design and perform hands on upstream process development (mainly CCM screening and optimization) following self-developed protocols that are aligned with best practices.

• Process and analyze trial data to demonstrate technical expertise through scientific thought process and recommendation.

• Engage and deliver thought leadership activities which includes conference and seminar presentation, customer trainings, webinars.

• Lead scale down study and process scale up to support troubleshooting and investigation.

• Deliver high quality communication to ensure an outstanding customer experience (written reports, telecons, face to face meetings).

• Develop and establish trusted relationship and partnership with customers through direct customer engagement and technical support.

• Collaborate effectively with internal teams to effectively address customer needs.

• Proactively identify and capture upstream process opportunities using sales effectiveness tools.

Education / Work Experience

• B.S or M.S. in Bioengineering, Biotechnology, or a related Engineering or science discipline;

• 5+ years’ experience in biopharmaceutical upstream process technical roles in manufacturing, pilot, and/or lab scale environments with direct, hands-on exercise for upstream process step, as cell line development, CCM development, screening and optimization in shake flask and bench top scale bioreactor (Preferred), cell culture process development and optimization, operation of bioreactors and other upstream process-related equipment.

• Sound knowledge of science and engineering fundamentals coupled with a hands-on, practical sensibility of engineering design.

• Technical mastery of one or more Bioprocess applications (process requirements, best practices, and industry standards) ideally for CCM.

• Strong experience in the application of scaling & implementation requirements for biopharmaceutical upstream process.

• Extensive experience in clear & concise communication to diverse audiences in both written and oral formats.

• Commercially astute, you understand market needs and trends.

• Open minded and customer-focused.

• Effective team player, know how to work with different teams in a multicultural matrix environment.

• Essential skills: customer centricity, strategic thinking and integrated mindset, teamwork awareness, excellent English communication skills.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of EHS (UK operations) (Irvine, North Ayrshire, GB, KA12 8NB)

Work Your Magic with us!

The Role

You will develop and execute the EHS strategy for the UK operations, aligning priorities with business goals and ensuring that environmental, health and safety standards are consistently applied across our sites.

You will:

Lead and support the UK EHS community, working closely with site leaders and EHS managers across multiple locations.
Develop/Execute EHS strategy at Irvine site, with direct leadership over the local EHS team .
Set strategic objectives, performance measures and governance frameworks for EHS, including the oversight of the EHS function budget.
Establish effective approaches to identify, assess and reduce risk, using data, trend analysis and root-cause insights to drive prevention.
Ensure compliance with relevant environmental, health and safety legislation, sustainability requirements, waste-management obligations and organisational standards.
Lead emergency preparedness and response planning for critical events, including chemical spills, fires and other serious incidents.
Promote strong process safety management and the effective integration of EHS requirements into operational activities.
Oversee the development and reporting of EHS KPIs, using performance data to identify opportunities for improvement.
Ensure safety protocols, training and expectations are embedded across employees, contractors, vendors and other external partners.
Champion innovation and continuous improvement, including the evaluation and adoption of new technologies and leading practices.
Coach and develop EHS talent, helping to build capability, succession strength and empowered, autonomous teams.

This is a visible leadership role with the opportunity to influence how EHS is managed across the UK operations and to make a lasting contribution to our safety, health, environmental and sustainability performance.

Who you are

You bring strong EHS leadership experience and the ability to translate strategy, regulation and data into practical improvements across operational environments. You are comfortable leading through influence, collaborating across functions and engaging people at every level of the organisation.

You have:

Experience leading an EHS team and programmes in a manufacturing, life science or similarly regulated environment.
A strong understanding of environmental, health and safety legislation and standards, including requirements relating to sustainability, waste management and environmental compliance.
Knowledge of process safety management, operational technology standards and relevant building or site requirements.
Proven experience with risk assessment, hazard identification, risk reduction and proactive incident prevention.
The ability to use EHS data, trends and root-cause analysis to inform decisions and improve performance.
Experience developing emergency response plans and managing or supporting responses to serious incidents.
Experience establishing EHS KPIs, governance and reporting processes.
A track record of embedding training, safety protocols and compliance requirements across employees and external partners.
Strong communication, influencing and problem-solving skills, with the confidence to work with site management and operational teams.
A commitment to coaching, mentoring and developing EHS talent.
A proactive, pragmatic and improvement-focused approach, with the curiosity to explore new technologies and better ways of working.

You will be recognised as a role model for safety and sustainability: someone who builds trust, challenges constructively and enables teams to take ownership of EHS performance.

Join us and help shape a safer, more sustainable future across our UK operations.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Global Marketing Director - Gomekli/Ezmekly (Boston, Massachusetts, US, 02210)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

Bringing a new therapy to patients with Rare Tumors requires more than scientific excellence — it demands bold, globally coordinated brand leadership. As Global Marketing Director – NF1-PN, you will be at the heart of shaping and executing the global brand strategy for a Rare Tumor brand, driving its successful launch and long-term lifecycle performance across international markets. Working in close partnership with the Global Brand Lead and with the Global Marketing Director (Pediatric Focus), jointly owning the overall global brand strategy, positioning, and messaging framework, while taking the lead on translating that strategy for the adult NF1-PN patient population. Together with a broad cross-functional team, you will translate complex scientific and clinical insights into compelling, credible brand narratives that resonate with healthcare professionals and stakeholders worldwide. Your work will directly influence how this therapy is positioned, communicated, and adopted across markets — making a tangible difference for patients and the teams that serve them

In this pivotal role, you will:

Partner closely with the Global Brand Lead to develop and evolve the global brand strategy, including brand positioning, messaging frameworks, digital engagement platforms, and campaign architecture.
Translate global brand strategy into actionable toolkits — such as messaging guides, launch playbooks, and best practice libraries — to enable effective regional and local execution
Ensure effective two-way knowledge transfer between global and local teams, disseminating global strategy while integrating local insights and on-the-ground perspectives.
Lead and oversee global congress strategy and execution, and provide strategic guidance to regional and local congress planning.
Develop a deep scientific understanding of the disease area, mechanism of action, clinical data, and competitive landscape to shape compelling and credible brand narratives.
Provide strategic input and leadership within the Global Brand Team and broader cross-functional governance structures.
Collaborate with cross-functional partners including Medical Affairs, Market Access, HEOR, Commercial Operations, and Regulatory Affairs to ensure aligned and compliant execution.
Proactively identify strategic opportunities, design initiatives to address them, and drive excellence in implementation.
Manage agencies, vendors, and project budgets to deliver high-quality, timely outputs.

Who You Are

Required

Bachelor’s degree or equivalent; an advanced degree such as an MBA or a postgraduate qualification in life sciences, business, or a related field is strongly preferred.
10 or more years of commercial experience in the pharmaceutical or biotechnology industry, including at least 5 years of global or local oncology marketing experience; experience in rare disease is a strong advantage.

Preferred

You have a proven track record in product launch and in-line brand management; prior experience in a sales or field-facing role is an advantage.
You demonstrate a deep scientific curiosity and the ability to translate complex clinical and medical data into clear, compelling brand narratives for diverse audiences.
You have a strong record of influencing senior stakeholders and cross-functional teams, both with and without direct authority, in a global and matrixed environment.
You are a skilled communicator and collaborator, able to build trust and alignment across functions, geographies, and organizational levels.
You are highly organized, results-oriented, and able to manage multiple priorities with a strong sense of urgency in a remote or hybrid work environment.
You are willing and able to travel occasionally, including overnight stays, as required by business needs.
English fluent, additional languages are a plus

Pay Range for this position: $186,500-279,700

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior VAT Expert (all genders) (Wroclaw, Dolnoslaskie, PL, 53-616)

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This role can be done hybrid: 2 days from the office in Wrocław.

Your Role
In your role as a Senior VAT Expert, you will drive indirect tax compliance and advisory activities across the European Union. You will prepare, submit, and review periodic VAT returns alongside required reporting like EC Sales Lists and Intrastat. Working closely with our global service center, you will provide strategic VAT advice, identify necessary system changes, and deliver internal training. You will lead or support key ERP and financial transformation projects to maximize outcomes. This position offers fantastic opportunities for professional growth as you champion operational standards within an international, collaborative environment.

Who you are:

At least 5–10 years of experience in finance with a strong focus on indirect taxation within a global corporate environment or an international professional service provider.
Academic degree in Business Administration, Finance, or a related field; a certified tax advisor qualification is highly desirable.
Profound knowledge of EU indirect tax compliance, VAT accounting principles, and the ability to manage end-to-end VAT registration services.
Strong hands-on experience with SAP (R3 and S/4 HANA) for checking individual transactions, reporting, and automated tax determination processes.
Proven track record leading or supporting complex ERP deployments, financial transformations, or system optimization projects.
Experience working within a Shared Service organization, featuring solid skills in establishing service standards and driving process governance.
Advanced Excel capabilities matched with top-tier analytical, conceptual, and problem-solving skills.
Excellent English communication and presentation skills, combined with a collaborative, proactive "can-do" attitude

YOUR MAIN BENEFITS:

Health and well-being: Get access to private medical care, life insurance, and sports card, receive a prepaid lunch card
Work-Life balance: Enjoy additional paid days off, flexible working hours, and a hybrid working model.
Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Data Transformation Project Manager_ Life Science (Tokyo, Tokyo, JP, 106-0041)

Your Role:

As our Data Transformation Project Manager based in Japan, you will lead the technology modernization of our Life Science Quality and Regulatory operations in Japan — designing scalable system architectures, establishing engineering best practices, and laying the groundwork for future-ready digital infrastructure. You will collaborate closely with local and global teams, acting as the technical anchor for this program.

What you will do:

Design and implement scalable, maintainable IT system architectures suited to the regulatory and quality requirements of our Japan Life Science operations.
Define and enforce engineering standards across software development practices, ensuring solutions are reproducible, secure, and built to last.
Drive code quality through automated testing, structured code reviews, and disciplined Git workflows.
Communicate technical concepts clearly to both engineering teams and non-technical business stakeholders, including Quality and Regulatory functions.
Contribute to the company's broader AI capabilities where applicable, supporting the design of agentic or LLM-based systems as the program matures.

Who You Are:

Experienced software engineer and system architect with a proven track record in complex, production-grade environments.
Hands-on with core AWS services and proficiency in Infrastructure as Code (Terraform, AWS CDK, or CloudFormation).
Solid grasp of CI/CD, containerization (Docker / Kubernetes), automated testing, and observability.
Security-conscious, with knowledge of authentication, authorization, and secure system design.
Strong communicator, able to align cross-functional teams and bridge technical and business perspectives.
Culturally adaptable, ideally with experience working in or with Japan-based organizations. Proficiency in Japanese is a plus.
Familiarity with agentic system design or LLM-based architecture (e.g. LangChain, RAG pipelines, vector databases) is an asset, though not a primary requirement for this role.

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

Product Engineer (Shanghai, Shanghai, CN, 200131)

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SPECIFIC JOB DESCRIPTION

Position Summary

This position is accountable for DS&S Engineering scope in China. DS&S is the business that offers Specialty Gas Delivery Equipment/Specialty Chemical Delivery Equipment/Turnkey Installation of Gas/Chemical systems and Poly Flow products. Individual is expected to have technical design capability in order to be able to develop products for end customers.

In order to better capture the opportunities of LDS (Liquid Delivery System), the creation of a dedicated LDS Product Line has been decided. Within this product line, Product Engineer will have to develop, manage and maintain in term of technology, integration, reliability, and competitiveness.
With the fast pace of innovations in semiconductors, you must be able to interact with staff in all functions to meet customer requirement, enhance tool performance and improve quality.
We expect that you’ll collaborate, share and work as a team that partners closely with all stakeholders.

Key Accountabilities

Lead the development of new product in compliance with DS&S technology and safety standards:

Define the product strategy for the product development as per the market requirement.

In collaboration with Strategy Product Manager to ensure out portfolio remains innovative managing the opening and closing of the products.

Coordinate with Engineering Team to ensure the delivery in time and on budget of the products.

Ensure a proper risk management and respective mitigated action all along the Product life cycle.

Maintain the product during its lifecycle:

Ensure the continuous improvement of performance & competitiveness of the Products.

Maintain Product Technical referential: prepare and issue generic technical documents related to the Products, prepare and up-date the list of Product documents, maintain technical product documentation during development execution, maintain documents in engineering database.

Provide support:

Provide solution to commercial team during bidding phase and ensure the product mindset (sustainability/replicability).

Provide guidance and support to teammates to complete all assigned task.

Drive the deployment of the product:

During new prototyping and current product mass production, with the project manager executing the project and ensure that all deliverables are available at the end of the project and that the product is delivering its expected goals.

Cooperation

Internally

Commercial, Project, Service, Quality, Engineering, Procurement, Manufacturing and Operation Planning.
Product management team, regional and globally

Externally 

End customers in the regions

CANDIDATE’S PROFILE

Education / Work Experience

Minimum Bachelor‘s Degree is required with background of Chemical engineering preferred, but related experience in lieu of education may also be considered.
5+ years of working experience in chemistry/gas industry and/or as product engineer.
Good written and oral English.
Experience in project engineering or product management (Must)
Experience in multinational and cross-functional communication (Nice to have)
Experience in Chemistry/Gas industry (Nice to have)
Good understanding of Engineering, Site work and Plant operation.
Experience in technical mechanical drawing and use of CAD tools.
Review P&ID diagram. (capable of P&ID design is plus)
Proficiency in Microsoft application for writing technical report and documentation of procedures, change control and technical specification.
Ability to provide guidance and support to teammates.
Excellent communication and interpersonal skill.
Positive mindset with creativity, good problem-solving and analytical abilities.
Ability to multi-task, organize and prioritize work.
Preferably able to start work with short notice.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Controlling Analyst (Bonifacio Global City, Metro Manila, PH, 1630)

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Your Role:

The Controlling Analyst plays a critical role in delivering high-quality financial reporting, business analysis, and controlling services that support strategic decision-making across the organization.
The role involves close collaboration with global stakeholders to provide accurate, timely, and reliable financial information while driving continuous process improvements and standardization initiatives.
As a trusted Finance Business Partner and Service Expert, the Controlling Analyst is responsible for preparing regular reporting packages, supporting forecasting and budgeting activities, performing financial analysis, ensuring data quality and integrity, and identifying opportunities for process automation and operational excellence.
The analyst is expected to work effectively in a dynamic, fast-paced environment and contribute to finance transformation initiatives.
The role reports directly to the Team Leader and collaborates with local, regional, and global stakeholders on various financial reporting, controlling, process improvement, and project-related activities.

Who You Are:

Bachelor's Degree in Finance, Accounting, Economics, Business Administration, or related field.
Certified Public Accountant (CPA) preferred.
CIMA and/or CMA certifications are advantageous but not required.
Minimum of 5 years of experience in Finance Operations, Financial Planning & Analysis (FP&A), Controllership, or Business Controlling functions in a multinational, local, or shared services environment.

At least 2 years of experience in business controlling, including:

Financial analysis
Management reporting
Budgeting
Forecasting
Performance management

Experience in Shared Services, Global Business Services, or Centers of Excellence is preferred.
Experience in the biotechnology, pharmaceutical, healthcare, or life sciences industry is an advantage.

Technical Competencies

Strong knowledge of Finance, Accounting, and Business Controlling principles.
Advanced proficiency in Microsoft Excel, including complex formulas, PivotTables, Power Query, and financial modeling.
Strong PowerPoint presentation and storytelling skills.
Experience with SAP and other ERP systems.
Working knowledge of:

TM1 / IBM Planning Analytics
Business Intelligence platforms
Business Objects
Power BI or equivalent reporting tools

Experience managing and analyzing large datasets.
Familiarity with automation technologies and Robotics Process Automation (RPA) tools is an advantage.
Knowledge of project management and continuous improvement methodologies is preferred.

Core Competencies

Analytical Thinking

Ability to identify trends, risks, variances, and opportunities through financial and operational data analysis.
Strong problem-solving and critical-thinking capabilities.

Stakeholder Management

Confident in communicating with stakeholders at all organizational levels.
Ability to influence decisions through data-driven insights and recommendations.

Collaboration

Team-oriented with strong interpersonal skills.
Able to work effectively across multiple functions, cultures, and geographies.

Attention to Detail

High degree of accuracy and commitment to data quality.
Strong focus on delivering reliable and error-free outputs.

Adaptability

Comfortable working in a fast-paced environment with evolving priorities.
Open to change and able to manage ambiguity effectively.

Continuous Improvement Mindset

Proactively identifies opportunities for process enhancement and automation.
Champions standardization, harmonization, and operational excellence initiatives.

Work Arrangement

Amenable to work onsite or hybrid in BGC, Taguig City.
Flexible to support morning, mid-shift, or night-shift schedules based on business requirements.
May interact with regional and global stakeholders across multiple time zones.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Manager, US Medical Communications, Oncology (Seaport) (Boston, Massachusetts, US, 02210)

Work Your Magic with us! Start your next chapter and join EMD Serono.

Your Role:

Responsible for leading the development and execution of strategic Medical Publication plans across assigned assets in Oncology. Responsible for all aspects of publication planning while working closely with the AD, Medical Communications, Medical Directors and Congress Planning leads. Receives minimal guidance or works independently. Impacts a range of important customer, operational, project and service activities within own team and other related teams. Guides and influences peers, and middle management regarding technical issues and challenges. Affects the results within own discipline with own contributions and contributes to the technical direction or the strategic direction and operational decision making in the field of specialization. Works effectively in a mixed environment and uses best practices and knowledge or interpretation of internal and external business issues to improve products or services and to define processes and standards. Solves complex problems.

Who You Are

Minimum Qualifications:

Advanced scientific degree (Ph.D., PharmD) strongly preferred (Master’s degree or other scientific or clinical degrees considered) with pharmaceutical industry or medical communications agency experience (required)
6+ years of prior experience working within the pharmaceutical industry or related fields or jobs with a relevant medical/scientific focus
Experience managing medical communications agencies and associated budgets
Scientific and/or clinical experience within Oncology strongly preferred

Preferred Qualifications:

Excellent communication (written and verbal), writing, presentations, interpersonal, organizational, time management, and project management/planning skills
Demonstrated ability to provide strategic input to leadership and influence decision making, particularly on topics regarding publication planning, data dissemination, and data disclosure requirements
Ability to foster collaborative relationships with relevant stakeholder groups to enable development of robust and executable publication plans
Experience in medical writing and/or managing external publication vendors and medical writers
Ability to think strategically to guide communications-related activities in accordance with industry standards and good publication practice, and with scientific integrity and balance

Location: Seaport office

Pay Range for this position: $143,600 - $215,400

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Applied Material Scientist (ICP-MS 경력 필수, 유관 경력 최소 5년 이상, 영어 가능자, 대전 근무) (Daejeon, Daejeon, KR, 34122)

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Your role

Develop and manage the Raw Material Support Program for the global Cell Culture Media sites to include:
Development of risk profiles of chemicals and materials used in the manufacture of cell culture media and related products, for example trace elements or trace impurity profiles.
Providing guidance to customers and internal teams on raw material changes including vendor, sourcing, and manufacturing process changes affecting raw materials.
Working closely with internal R&D, Quality, and Supplier Management Teams to determine potential impact of raw material changes to customer end use
Development and communication of risk mitigation strategies for materials deemed high risk for use in manufacture or for customer end use.
Coordinate the execution of testing of raw materials to support requests for data on high risk materials. This includes liaising with internal testing laboratories and external vendors for sample analysis.
Generate reports and communicate results to internal and external customer stakeholders. Reports may support customer process / product qualification endeavors, risk assessments, and investigations of non-conformances.
Generate or acquire data on raw materials used in the Cell Culture supply chain to develop qualification and / or release testing specifications.
Involvement with industry forums and groups in order to stay informed on market and industry needs regarding the Cell Culture Media supply chain.
Liaise with internal Manufacturing and Quality teams on batch troubleshooting as needed
Provide technical expertise to site Quality and Manufacturing teams during customer audits and investigations as needed.

Who you are

5-7 years Quality Control, R&D, and/or analytical experience. Cell culture manufacture, testing, and/or research desirable
3-5 years demonstrated experience leading projects or 5+ years as a key team member on projects cross functionally focused
3-5 years of risk management, assessment and mitigation experience
Fluent in English
Experienced in external customer facing communications and support.
Demonstrated proficiency writing technical reports, presentations, professional letters and memos
Demonstrated understanding of manufacturing and Quality systems in a GMP or regulated environment
Understanding of industrial large molecule drug production desirable but not required
Equivalent combination of education and experience
Able to analyze data sets and make technical recommendations based on data and knowledge of scientific and / or manufacturing principles
Understanding of sterile liquid and dry powder manufacturing, packaging, and testing for release to the regulated pharmaceutical and life sciences market

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

Solution Architect / Expert Test & Application Life Cycle Mgmt. (Bratislava, Bratislava, SK, 81006)

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We are looking for an experienced Solution Expert–Application Lifecycle Management (ALM) to join our team. In this role, you will be the go-to expert for our ALM toolchain, driving the adoption, governance, and continuous improvement of our testing and quality management platforms. You will work closely with cross-functional teams to ensure that our software delivery processes are efficient, traceable, and aligned with enterprise standards.

Key Responsibilities

Act as the subject matter expert (SME) for ALM platforms, providing guidance, training, and best-practice recommendations to development, QA, and project teams.
Configure, administer, and maintain ALM tools, including user management, project setup, workflows, and integrations with other enterprise systems.
Own and operate the ALM toolchain, with a primary focus on leading Lifecycle and Test management platforms
Drive adoption of standardized testing processes and ALM governance frameworks across the organization.
Collaborate with project managers, developers, and QA engineers to define and implement test strategies, test plans, and quality gates.
Contribute to roadmap planning for the ALM toolchain, evaluating new features, upgrades, and emerging technologies.

Ensure compliance with internal IT policies, data governance standards, and audit requirements.

Required Skills & Qualifications

Bachelor's degree in Computer Science, Information Technology, Engineering, or a related field (or equivalent practical experience).
Excellent communication skills in English (written and spoken); German is a plus.
Strong analytical and problem-solving skills with a structured, detail-oriented working style.
Good ‘hands-on’ Knowledge of established Application Lifecycle Management and Testing tools such as MicroFocus/Open Text ALM, UI Path, Tricentis qTest, etc.

Experience with test management best practices, including requirements traceability, defect lifecycle management, and test coverage analysis.

Provides a wide IT knowledge in various areas such as

Infrastructure, Applications including SAP / SAP-Basis, Compliance and Cypher Security, Service Management

Experience in a regulated industry (e.g., Life Sciences, Pharma) and familiarity with GxP validation or CSV (Computer System Validation) requirements is a strong advantage.
Exposure to the SAP ecosystem or other enterprise ERP platforms.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Assoc Dir., Clinical Quality Mgmt. Lead (Feltham, London, GB, TW14 8HA)

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Your Role

At the heart of global clinical development, quality is not a checkpoint, it is a discipline that shapes every decision. In this pivotal role, you will serve as a subject matter expert in risk-based quality management, guiding cross-functional study teams to embed quality principles from the earliest stages of clinical trial design through to completion. You will lead the implementation and continuous improvement of quality processes across the clinical development lifecycle, ensuring that critical data and processes are identified, risks are proactively managed, and trials are consistently inspection-ready. Working closely with contract research organisations, vendors, and international study teams, you will define quality tolerance limits, maintain quality risk management plans, support risk-based monitoring strategies, and co-lead preparation for regulatory authority inspections. You will also lead the investigation of and response to quality issues, driving accountability and continuous improvement across assigned trials.

The role could be based either in the UK or in Poland.

Who You Are

You hold a degree in medical science, life science, or a related field (a postgraduate qualification is preferred), and bring at least eight years of hands-on experience spanning the full clinical development lifecycle, including trial design, start-up, conduct, analysis, and reporting.
You have deep expertise in clinical quality risk management, Quality by Design principles, risk-based monitoring, and Good Clinical Practice inspection readiness, with a strong working knowledge of international regulatory requirements and harmonisation guidelines.
You have direct experience supporting or co-leading regulatory authority inspections and are confident maintaining inspection-readiness tools and quality risk management plans throughout the trial lifecycle.
You are experienced in working with contract research organisations and external vendors in an international, cross-functional matrix environment, and can effectively oversee third-party quality performance.
You bring strong analytical and project management capabilities, with a proven ability to identify critical-to-quality risks, define meaningful quality tolerance limits, and translate complex quality data into clear, actionable insights for diverse stakeholders.
You communicate with clarity and confidence, are skilled at influencing without authority, and can explain complex regulatory and quality topics to both technical and non-technical audiences across all levels of an organisation.
You are proactive, accountable, and committed to continuous improvement, with the ability to work independently in a complex multinational environment while actively supporting and coaching colleagues.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

(Senior) Software Engineer (all genders, full-/part-time) (Weiterstadt, Hessen, DE, 64331)

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Your Role

Data and AI are reshaping the way global organizations operate, and this role sits at the heart of that transformation. As a Software Engineer within our Enabling Functions Data Office, you will design and deliver high-impact data and AI solutions that power smarter ways of working across the organization. You will be part of a collaborative, internationally distributed team of engineers and architects, working within a Product-Oriented Delivery model to bring Analytics, AI, and data products to life at scale.

In this role, you will:

Design, build, and maintain scalable applications, data pipelines, and platform components that translate complex business requirements from enabling functions such as HR, procurement, and legal into future-ready technical solutions.
Develop robust applications and interfaces that replace manual processes with seamless, intuitive user experiences.
Take ownership of data platforms, ensuring cost efficiency, governance, security, and compliance across the full data lifecycle.
Partner closely with stakeholders across your delivery pod to understand business needs and shape the technical direction of solutions.
Shape the future of data engineering within Enabling Functions, leveraging platforms such as Snowflake, AWS, and Palantir Foundry.
Contribute to a growing Spain-based hub within a global team, with the opportunity to work on diverse and high-visibility AI use cases spanning automation, carbon footprint analytics, procurement intelligence, and more.

Who You Are

You bring several years of proven expertise and experience in software engineering, including application design, development, and delivery within enterprise environments, with a strong foundation in writing clean, maintainable, and secure code.
You are proficient in development platforms and languages such as Python and Spark, and you apply modern engineering practices including version control, CI/CD pipelines, and automated testing as a matter of course.
You have hands-on experience with data platform technologies such as Palantir Foundry, Snowflake, and PySpark, and you are confident designing and delivering end-to-end data pipelines.
You have a solid understanding of data pipeline architecture, data governance, data lineage, privacy and security controls, and compliance standards in enterprise-scale environments.
You communicate complex technical concepts clearly and confidently to non-technical stakeholders, and you are comfortable translating business requirements into actionable technical solutions.
Familiarity with AI workflows, MLOps, AI safety and guardrails, or CI/CD for AI components is a plus
You hold a university degree or equivalent qualification in a relevant technical or engineering discipline.
You are comfortable working in a distributed, international team environment and are open to occasional travel within Europe.
Strong communication skills in English ; proficiency in German is a plus.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Waste Water Treatment Plant Technician 1 (Jaffrey, New Hampshire, US, 03452)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

The Wastewater Technician will provide operational and maintenance support to MilliporeSigma’s wastewater treatment plant in Jaffrey, NH to ensure compliance with discharge permit requirements and the support of manufacturing processes. In addition, the Wastewater Technician will provide will part of a team responsible for treatment systems consisting of anaerobic digestion, aerobic treatment, and membrane bio reactors (MBRs). This includes all associated pumps and lift stations. This technician is responsible for working Sunday – Wednesday, 6AM-4:30PM.

Perform critical sampling and analysis of wastewater facility operations, such as biological oxygen demand, total suspended solids, and pH to evaluate treatment system health and regulatory compliance
Perform preventative maintenance on treatment system components such as pumps, valves, blowers, pH probes, etc.
Collection and preparation of samples for third-party laboratory evaluation
Maintain required wastewater records, logs and checklists of facility operations
Assist in maintaining monthly air emission logs and calculations
Support stormwater and SPCC inspections
Work conscientiously, adhere to EH&S policies and processes, and be aware of safety hazards and participate in 24 hour on-call rotation
Troubleshoot mechanical, plumbing, lighting/electrical issues with assistance from the Facilities group
Collaborates with manufacturing teams to manage wastewater flows and operational conditions, coordinates non-hazardous wastewater shipments to third-party facilities, supports chemical deliveries, performs confined space and elevated work when needed, and reports operational issues or plant changes to management while assisting with additional assigned duties.

Who You Are

Minimum Qualifications

Bachelor’s degree in Environmental Studies (Environmental Science, Sustainability, Environmental Policy, Natural Resources Management, Ecology).
1+ years of experience in wastewater operations

High School Diploma or GED and 3 years’ experience in wastewater operations or environmental position
Valid driver’s license

Physical Attributes

Lift 50 lbs
Stand, bend, walk for 8 hour periods
Comfortable with ladder use and work at heights

Preferred Qualifications

Experience with SCADA systems
Proficiency maintaining electrical systems
Massachusetts Industrial Wastewater License
Powered Industrial Vehicle Operator
Technical and mechanical experience
Works collaboratively with team members
Proficiency with excel, power point, etc.
Familiarity with basic principles of aerobic and anaerobic wastewater treatment

Pay Range for this position: $27- $41 per hour

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Sachbearbeiter Bestandskontrolle (m/w/d) (VZ/TZ) (Schnelldorf, Bayern, DE, 91625)

Ihre Rolle:

In dieser Schlüsselrolle sichern Sie die Verfügbarkeit und Qualität von Waren und Rohstoffen und leisten damit einen direkten Beitrag zur Zuverlässigkeit unserer Lieferkette. Als Teil des Teams der Bestandskontrolle am Standort Schnelldorf prüfen und korrigieren Sie Lager- und Produktionsbestände, bearbeiten Rücksendungen und treffen fundierte Verwendungsentscheide, um Waren schnell und regelkonform wieder in den Verkaufsbestand zu bringen. Dabei arbeiten Sie eng mit angrenzenden Bereichen zusammen, halten alle relevanten Sicherheits- und Qualitätsvorschriften ein und bringen sich aktiv in das tägliche Teammanagement ein. Mit Ihrem Blick für Ordnung, Effizienz und nachhaltige Ressourcennutzung tragen Sie dazu bei, Prozesse kontinuierlich zu verbessern.

Diese Stelle ist befristet auf 12 Monate.

Wer Sie sind:

Abgeschlossene kaufmännische oder logistische Ausbildung in der Industrie sowie mindestens drei Jahre Berufserfahrung in diesen Bereichen
Gute Kenntnisse im Umgang mit SAP sowie MS Office
Sehr gute Deutschkenntnisse (C-Level) sowie gute Englischkenntnisse (B-Level) in Wort und Schrift
Ausgeprägte Teamfähigkeit und klare Kommunikation im Arbeitsalltag
Gültige Zuverlässigkeitsüberprüfung gemäß § 7 Abs. 1 Luftsicherheitsgesetz (LuftSiG)
Kenntnisse in Verpackungscodes oder UN-Containercodes wünschenswert
Kenntnisse im Umgang mit Flurförderfahrzeugen (mindestens Stufe 1) von Vorteil

Bewerben Sie sich jetzt und werden Sie Teil eines Teams, das Neues entdeckt und die Menschheit voranbringt.

(Senior) Manager Auditor Analytics (all genders) (Darmstadt, Hessen, DE, 64293)

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Your role:

As part of the internal audit team, you will gain deep insights into business processes and their related data. You will collect, analyze, validate and interpret those large data sets (for example SAP data) to deliver meaningful audit insights by utilizing common programming languages and analytics tools such as SQL, Python, Power BI or Tableau.

You will be working with a diverse team and will gain process and data insights into various business areas as well as manage stakeholders on all different levels of the hierarchy. Audit related work will ensure varying tasks and great learning and development opportunities.

Who you are:

University degree in Business, Finance, Computer Science, Data Science, Information Technology or equivalent required
Relevant professional experience (minimum 3-5 years in data analytics, Risk advisory, audits or associated fields) in an internationally operating company or in a Big 4 accounting firm is required. Audit specific qualifications (e.g. CPA, CIA or CFE certification) is a plus
Extensive hands-on experience in using data analytics and familiarity with handling SAP system data and data analytics tools (for e.g., Microsoft Power BI, Tableau, Qlik, etc.) as well as programming languages (SQL, Python)
Strong analytical thinking and a structured approach to work, with the ability to translate complex data analyses into clear, actionable insights for both technical and non-technical stakeholders, while maintaining high-quality standards throughout the process
A strong process understanding in the areas of Finance, Order-to-Cash (O2C), Source-to-Pay (S2P), Healthcare Compliance (Marketing & Medical activities) as well as ability to conduct reviews of complex end-to-end processes and related data is an advantage
Industry experience in the Pharma, Biotech, Life Science or Electronics sector is preferred
Ability to be agile, open-minded and to manage audits and stakeholders of different cultures (good intercultural and communication skills), to work in a matrix organization together with a desire to develop your leadership skills; good project management and organization skills with the ability to handle multiple responsibilities at the same time
Business-level fluency in English; additional language skills are an advantage

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Manager, Therapeutic Area Communications (Boston, Massachusetts, US, 02210)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Our Rare Tumors franchise is On a Mission to Improve Lives for patients with desmoid tumors, tenosynovial giant cell tumor (TGCT), and NF1-associated plexiform neurofibromas (NF1-PN). Diseases where progression can mean irreversible loss of function, and where patients often spend years feeling misdiagnosed and unheard.

This role, focused on US product communications sits within Global Therapeutic Area Communications and will also lend expertise to a major potential upcoming launch in Fertility, making it a strong fit for someone who wants exposure across therapeutic areas while anchoring in Rare Tumors.

We are looking for a Senior Manager, US Communications to work closely with the Communications Lead, Rare Tumors to serve as the day-to-day communications liaison across all three US Rare Tumors brands and as the primary communications liaison to US Rare Tumors business leadership.

This is a hands-on role: the person in this position will own tactics end-to-end, from planning through flawless execution, and will be fluent in pharma processes (i.e. vendor contracting, MLR review, Sprinklr management). They will also flex into other product communication needs as business priorities require.

Key Responsibilities:

Serve as the go-to US communications partner and liaison for Rare Tumors business leadership, translating business priorities into communications strategy and keeping leadership informed on plans, risks, and results.
Lead end-to-end execution of communications tactics across the three US Rare Tumors brands (from planning and briefing through drafting, review, and launch) for internal communications, media, patient-facing materials, and executive/spokesperson support.
Actively support the planning and execution of an upcoming Fertility launch, partnering cross-functionally with brand, medical, and other TA communications colleagues.
Own the operational backbone of the work: manage agency and vendor contracts and budgets, and shepherd content through MLR.
Navigate the US healthcare communications landscape fluently: media relations, patient advocacy, congress support, and issues management specific to the US market.
Build strong working relationships across Communications, Brand/Marketing, Medical Affairs, Legal, Regulatory, Patient Advocacy, and Market Access to keep tactics moving without friction.
Flex support to other US therapeutic areas as needed, based on evolving business priorities.

Scope of Focus:

Rare Tumors (~60%): US communications strategy and execution across all three marketed/pipeline brands (OGSIVEO, pimicotinib, GOMEKLI/EZMEKLY), and day-to-day liaison to US Rare Tumors TA Head.
Fertility (~30%): active support of an upcoming product launch, partnering with the Fertility brand teams.
Cross-TA flex (~10%): support for other US-specific therapeutic area needs as they arise, based on business priorities.

Who You Are

Minimum Qualifications:

Bachelor's degree in Communications, Public Relations, Journalism, or related field.
Minimum 7 years of experience in pharmaceutical, biotech, or healthcare communications, ideally with exposure to rare disease and US market dynamics.
Demonstrated hands-on experience managing communications tactics end-to-end, including agency/vendor management, MLR review processes and pharmaceutical compliance requirements.
Experience supporting or partnering with business/brand leadership as a trusted communications advisor.
Strong writing, editing, and project management skills; comfortable managing multiple brands and workstreams simultaneously.
Ability to operate with urgency and integrity in a fast-paced, matrixed environment.
Fluent in English; both verbal and written

Preferred Qualifications:

Experience in rare disease or specialty pharma communications.
Experience supporting a product launch.
Familiarity with patient advocacy engagement in a regulated healthcare environment.

Location: Boston, MA; Seaport Location (Hybrid – 3x week)

Travel: <15%; International and Domestic

Pay range for this position: $122,000.00 - $183,000.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

EHS Specialist (Indianapolis, Indiana, US, 46268)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

We are seeking a proactive EHS Specialist to lead and maintain Environmental, Health, and Safety programs. The role emphasizes environmental compliance and occupational safety, risk mitigation, and continuous improvement in collaboration with operations, quality, and facilities teams to protect employees, the environment, and the business.

Responsibilities include but are not limited to:

Develop, implement, and maintain EHS programs in compliance with US federal, state, and local regulations (e.g., OSHA, EPA, TSCA/REACH, RCRA, Clean Air Act, Clean Water Act) and company policies.

Conduct risk assessments, incident investigations, and root-cause analyses; lead corrective action plans and verify closure.

Monitor and report EHS performance metrics (leading and lagging indicators, near-misses, incident rates) and deliver timely management reports. Maintain EHS documentation, SOPs, forms, and training records, with robust US regulatory traceability.

Lead US-centric EHS training and safety onboarding for employees and contractors; ensure competency, documentation, and regulatory recordkeeping.

Manage chemical safety, waste management, air and water compliance, and Emergency Response Team preparedness (drills, procedures, and equipment readiness) with emphasis on regulatory expectations.

Drive occupational health initiatives, ergonomics reviews, and workstation safety improvements to meet OSHA standards and best practices.

Collaborate with facilities and operations to implement risk controls, audits, inspections, permit requirements, and support site-specific permits and registrations.

Support regulatory inspections, internal audits, and third-party certifications; maintain up-to-date knowledge of US environmental and safety regulations.

Participate in incident response, safety committees, and product stewardship activities as needed.

Lead continuous improvement initiatives to reduce risk, improve compliance, and lower the total cost of risk, with an emphasis on US requirements.

Who You Are:

Minimum Qualifications:

Bachelor’s Degree in any discipline.

5+ years of EHS experience in manufacturing, chemical, or life science industries.

Preferred Qualifications:

6+ years of EHS compliance experience in the chemical, specialty chemical or pharmaceutical industry.

Strong understanding of US EHS regulations and standards (e.g., OSHA, EPA, TSCA/REACH, RCRA, Clean Air Act, Clean Water Act); risk assessment methodologies; incident investigation techniques.

Excellent communication, influencing, and collaboration skills; strong analytical and problem-solving abilities; proficient in EHS software, Microsoft Office, and data management.

Certified Safety Professional (CSP), Certified Industrial Hygienist (CIH), NEBOSH, CHMM, or equivalent; NIOSH credentials.

Attributes: Detail-oriented, hands-on, proactive, and comfortable of working with cross-functional teams; demonstrates ownership of safety culture and continuous improvement.

Master’s Degree.

DOT hazardous material handling.

First Aid / CPR.

Pay Range for this position: $68,800 - $116,600 / year

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Analyst - Material Management/ Inventory Management (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Your Role:

Lead functional design and configuration for MM and IM processes (procure-to-pay, inventory management, movement types, valuation, batch/serial management, MRP, release strategies, pricing).
Configure and optimize master data, material types, vendor master, source list, info records, and configure integration with QM, PP-PI, WM/Extended WM or EWM as needed.
Define and translate business requirements into SAP solutions; create functional specs for integrations, enhancements, reports, and interfaces.
Lead blueprinting, workshop facilitation, and fit-gap analysis; support data migration and cutover activities across all 3 sector’s ERPs
Integration: Strong knowledge of MM integration with SD, PP, FI/CO, QM; experience with data migration and IDOCs/BAPI interfaces.
Develop test scripts, coordinate unit/integration/user acceptance testing, and support issue resolution during go-live and hypercare.
Provide guidance on best practices, system enhancements, and SAP roadmap alignment (S/4HANA MM/IM where applicable).
Collaborate with cross-functional teams (PP, SD, FI/CO, QM, PM, IT security) to ensure end-to-end process alignment.a
Mentor junior consultants; contribute to project estimation, risk assessment, and knowledge transfer.
Ensure compliance with company standards, data governance, and security requirements.
Soft skills: Stakeholder management, workshop facilitation, clear documentation, cross-functional collaboration, mentoring.

Who You are:

Years of experience: 2-5 Years of experience in MM and IM processes.
Must haves:

Material Management, Inventory Management, SAP MM,
Experience in Purchase Order, Sales Order, MRP, InfoRecord, Sourcelist and Master data knowledge.

Nice to haves:

Warehouse Management
Quality Management

Apply now and become a part of our diverse team!

Agentic AI Platform Architect (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

THE OPPORTUNITY

At the intersection of cloud engineering and artificial intelligence, this role offers a rare opportunity to architect the foundational platform that powers the next generation of intelligent, autonomous systems across a global science and technology enterprise. As Agentic AI Platform Architect, you will be actively designing, implementing, integrating and operating cloud-native backend systems that together form a cohesive ecosystem for Agentic AI applications. In particular, you will focus on the evolution of a cloud-based agentic AI platform that enables building and orchestrating agents and is connected into the wider ecosystem. You will be hands-on in writing production code, building pipelines, owning deployments, and taking end-to-end accountability for the solutions you deliver. In addition, you will be able to work with and guide other team members. If you thrive building things that matter, in a team that values quality, ownership, and continuous improvement, this role is for you.

Your key responsibilities:

·Own the platform architecture, technical roadmap and ADRs within the broader agentic AI strategy.

·Design, build and operate the multi-tenant Kubernetes platform using Amazon EKS, Terraform, Helm, Kustomize, Argo CD and Argo Workflows, together with a team of engineers.

·Build repeatable onboarding, promotion, recovery and decommissioning capabilities through Azure DevOps and GitOps.

·Implement identity and tenant isolation across OIDC, Kubernetes RBAC and impersonation, AWS workload identity and secrets management.

·Design secure integrations with models, tools, MCP/A2A services and other enterprise platforms.

·Own operational readiness, including SLOs, telemetry, agent and LLM tracing, evaluation, capacity, cost, incident response, upgrades, backup/restore and rollback.

· Develop and review production Python, Terraform modules, Helm charts and pipeline templates.

· Establish technical standards, documentation and reusable platform patterns, and mentor other engineers.

WHO YOU ARE

Mindset & Ways of Working

· Strong sense of ownership and accountability – you build it, you run it.

· Curious and eager to learn; comfortable adapting to evolving technologies and requirements.

· Collaborative team player in a cross-functional, international environment.

· Ability to influence technical decisions in a fact-based manner, clearly explaining the underlying rationale and gaining stakeholder and technical team buy-in.

Experience & Qualifications

· University degree in Computer Science, Engineering, or equivalent.

· 8+ years of relevant experience building secure, scalable, resilient cloud-native backend systems at enterprise scale.

· Experience in architecting complex cloud-native solutions and in guiding teams in their implementation.

· Hands-on experience designing and operating production Kubernetes platforms, preferably Amazon EKS, including RBAC, networking, ingress, autoscaling, upgrades and troubleshooting.

· Strong AWS platform engineering experience across EKS, ECR, IAM/workload identity, VPC/private connectivity, ALB/WAF, Route 53, Secrets Manager, CloudWatch and S3.

· Strong Infrastructure as Code and GitOps experience using Terraform, Helm, Kustomize, Argo CD and Git.

· Experience building and governing CI/CD pipelines, preferably with Azure DevOps.

· Strong production Python experience, including boto3, API integration, automated testing and operational automation.

· Experience with OIDC/OAuth2/JWT, least-privilege access, tenant isolation, Kubernetes RBAC and secure secrets management.

· Practical experience building or operating GenAI or agentic systems, including tool integration, state and memory, evaluation, observability and failure handling.

· Understanding of MCP and A2A, particularly authentication, authorization, service boundaries and enterprise governance.

· Business-fluent English (written and spoken)

Nice to Have:

AgentCore, Amazon Bedrock
OpenTelemetry, Langfuse or comparable agent and LLM observability platforms.
Aurora PostgreSQL, DynamoDB, SQS or similar distributed state and messaging services.
Argo Workflows, Keycloak or another enterprise identity provider, and External Secrets Operator.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Solution Architect Master Data Mgmt - SAP MDG (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

The Solution Architect is responsible for designing, governing, and implementing scalable Master Data Management (MDM) and Master Data Governance (MDG) strategies across the enterprise to ensure seamless data quality, system integration, and data lifecycle management.This role requires a strong technical knowledge of SAP MDG and particularly all associated strategic capabilities including Cloud and AI components. A good understanding of the SAP strategy based on the BTP platform and SAP Joule are very much required.

Responsibilities

Responsible for providing strategic leadership and technical expertise in designing and architecting Master Data Governance solutions that meet the complex business needs of the organization. This role will drive standardization, reusability, ensure compliance, and provide insight for continuous improvement.

Lead the architecture and design of Master Data Governance (MDG) solutions, including defining system landscapes, data models, governance workflows, and integration points with other SAP modules and non-sap systems.
Collaborate with stakeholders to understand master data requirements, objectives, and translate them into scalable and sustainable MDG architecture and designs.
Elaborate decision paper for different design options to agree on the way forward approach.
Engage with business stakeholders to understand their needs, ensure accurate planning and analysis by integrating business knowledge with technical solutions.
Serve as a subject matter expert (SME) in master data management
Work ‘hands-on’ in the system to implement proposed and agreed system enhancements following the established Change Request process for active MDG domains MATERIAL; BP/Supplier; FINANCE; Reference Data mgmt.

Education/Professional Experience

Master degree or equivalent in Computer Sciences and/or Business Administration
7 years of progressive professional experience with data management leveraging SAP MDG

Languages

English mandatory (written and spoken)

Skills & Competencies

Strong interpersonal and organizational skills
Strong written and oral communication skills
Ability to make difficult decisions and act autonomously
Good understanding of SAP Master Data Strategies and Roadmap / Cloud Ready and AI components along with BTP Integrations and Clean Core principles
Senior SAP MDG expert, 6 years+ ‘hands on’ in SAP Master Data applications including ABAP S/4 HANA
Skills in SAP MDG Data Models, Structures, Enhancing Data Models, Feeder Class, BADIs for doing validation and derivations, Customizing UI's, ALE IDOC's for replicating data to different servers, Creating Database Tables and Maintaining it, Data Elements, Adaptations.
Experience in using BRF+ Rule Based Workflow & Derivation in MDG
Experience in working with Enhancements, Configuration in FPM Feeder Class
Working Experience in S/4HANA Data quality evaluation process
Experience in ODATA concepts to interface MDG to target systems
Development experience in OVS (Object Value Selector)
Good hands-on experience in Data Dictionary Objects (Tables, Structures, Views, Lock objects, Data Elements & Domains).
Experience in established Enhancement Techniques (BADI’s, Exits).
Working Experience in using Business Application Programming Interfaces (BAPI’s) and Function Modules.
CDS View Development and understanding – ABAP RESTful Application Programming Model (RAP)
Good Knowledge On ALE/IDOC’s.
Good Knowledge On WORKFLOW.
Development Experience in Web Dynpro ABAP using MVC (Model View Context) Architecture.
Used Assistance Class & OTR for Accessing Text Elements and Messages in Web Dynpro at Runtime.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Brand Lead Rare Tumors (Maternity Leave) (Rome, Rome, IT, 00145)

Work Your Magic with us!

Your Role

In this role, you will develop and implement integrated marketing strategies across digital and traditional channels, ensuring localized messaging remains aligned with global brand positioning while supporting launch readiness through market research and competitive analysis. You will collaborate with sales, market access, and medical teams to develop promotional materials, manage patient support programs, and execute high-impact presence at key congresses, all while staying within the allocated budget. Leveraging your expertise in data management and business insights, you will track campaign performance using digital analytics to refine strategies and monitor cost expenditure, ensuring full compliance of all activities while leading cross-functional brand planning and driving overall growth objectives.

Who you are:

Minimum 5 years experience in marketing or other relevant role in the rare disease or closely related pharmaceutical industry
Launch experience required, previous sales experience beneficial
Deep knowledge of the local Healthcare system
Strong analytical skills to interpret market data and research findings to inform strategic decisions
Sound project management skills, with the ability to manage distinct and complex requirements, prioritize and execute
Excellent communication and presentation skills, with the ability to engage effectively with diverse stakeholders
Strong sense of urgency, and proven ability to organize, and prioritize for execution and completion
Demonstrable drive for high performance and results
Ability to leverage required technical tools efficiently (e.g., MS Office)BSc or higher in marketing/communication/ business related degree or similar
Fluency in English

Salary Package:

Annual Base Salary (RAL): €50.000 – €70.000
Categoria CCNL: B - A
Variable Compensation (AIP)
Welfare and Benefits Package

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Megasys Project Manager (Santa Clara, California, US, 95054)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Location:

The Project Manager, Megasys is a field-based role located in Santa Clara, CA (or the surrounding Bay Area). Approximately 10% domestic travel is required to meet business needs.

Your Role:

We are seeking a highly skilled and experienced Project Manager to oversee the construction of gas and chemical systems for our customers' semiconductor facilities. In this role, you will serve as both a project leader and people manager, directly leading and developing a team of professionals while managing all aspects of project delivery — including planning, scheduling, budgeting, and ensuring compliance with safety and quality standards.

The Project Manager will work closely with cross-functional operations teams, building a high-performing project team through coaching, mentorship, and clear accountability. You will be responsible for fostering a collaborative and inclusive team culture while driving the successful completion of projects within specified timelines and budgetary constraints.

Key Responsibilities:

Plan, organize, and manage the construction and demolition of gas and chemical systems for the semiconductor facility, ensuring adherence to project timelines and budget with a team of engineers and technicians.
Coordinate with engineering, procurement, and construction teams to ensure the timely delivery of milestones within the project including start up and commissioning of equipment.
Develop and maintain project schedules, resource plans, and budgets, and monitor progress against these plans.
Manage project risks and issues and implement mitigation strategies to ensure successful project delivery.
Ensure compliance with safety, health, and environmental regulations and standards throughout the construction process.
Communicate project status, issues, and risks to stakeholders and senior management on a regular basis.
Lead and motivate project teams to achieve project objectives and deliver high-quality results.
Provide regular updates and reports on project progress, budget, and resource utilization.

Schedule:

The Manager will work a standard Monday through Friday schedule; however, they will be expected to be available for off-hours calls and to coordinate equipment recovery as needed.

Physical Attributes:

75% of time walking throughout the facility (3-5 miles per day).
Climbing of ladders up to 12-foot-tall (utilizing fall protection).
Basic lifting (up to 40lbs).
Bending of the knees and overhead reaching.

Military Veterans:

MEGASYS® is a military-friendly employer that values the skills obtained through military teamwork. Our culture and company value the leadership and focus on safety that is obtained from your service. Veterans from any branch or MOS with hands-on mechanical skill sets are encouraged to apply.

Who You Are

Minimum Qualifications:

Bachelor's degree in Engineering, Chemical Science, Construction Management, or a related field with 5+ years of relevant work experience
3+ years of experience as a Project Manager in facilities, construction, manufacturing, chemicals, or the semiconductor industry, with a focus on gas and chemical systems

High School Diploma or GED with 10+ years of relevant work experience
5+ years of experience as a Project Manager in facilities, construction, manufacturing, chemicals, or the semiconductor industry, with a focus on gas and chemical systems
Demonstrated leadership skills with the ability to coach, mentor, and build high-performing teams

Preferred Qualifications:

Master's degree in Engineering, Chemical Science, Construction Management, or a related field
Project Management Professional (PMP) certification
Experience with Lean Six Sigma methodologies
In-depth knowledge of semiconductor manufacturing processes and equipment
Strong project management skills, including the ability to manage multiple projects simultaneously
Excellent communication, leadership, and interpersonal skills
Proficiency in project management tools and software
Familiarity with industry standards and regulations related to gas and chemical systems in semiconductor manufacturing

Benefits with our team include:

Comprehensive, paid, on the job training program that allows our employees to quickly learn critical technical skills to excel in this role and rapidly progress in their careers.
Excellent benefits including a starting vacation allowance of 3 weeks, 6% 401k match programs and medical, dental and vision benefit coverage on day one of employment!
Tuition assistance program

Pay Range for this position: $144,000 - $170,000

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Director Group Portfolio Execution (all genders) part/full-time (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

Your Role:

As a Director Integration & Carve-Out, you will own the end-to-end integration and carve-out execution for our small to mid-size strategic deals. Reporting to the Head of Portfolio Execution (VP), you will be joining a highly energetic, mission-driven team of experienced integration and carve-out leaders managing these strategic initiatives across the three sectors.

Key Responsibilities

Represent integration interests during due diligence.
Own and lead assigned integration or carve-out projects end-to-end – serving as the primary point of contact with full accountability across all workstreams.
Design and drive a structured, disciplined implementation strategy – from project set-up and timeline planning through milestone delivery – dynamically adapting and recalibrating plans as the situation evolves.
Build trusted partnerships and align with key stakeholders and business leaders, mobilizing necessary cross-functional team members and providing clear direction and oversight for accountabilities and assignments.
Drive creation and sign-off of the future target operating model.
Ensure smooth delivery at country level.
Orchestrate high-impact workstream governance – establishing meeting cadence, creating and deploying common frameworks for feedback, inputs, and deliverables within a business unit and across our company – keeping all teams laser-focused on value drivers and key enablers across the company.
Drive fast decision-making – proactively identifying and resolving risks and pivoting course decisively to protect deal success.
Ensure full compliance with legal and regulatory requirements throughout the transaction lifecycle, safeguarding our organizational and financial interests.
Plan and manage overall integration / separation cost budget.
Ensure people and organizational aspects (culture, org design, retention and engagement, capability identification and preservation) are appropriately considered and managed in integrations.
Lead the end-to-end definition, implementation, and delivery of post-closing services (incl. Manufacturing Supply Agreements (MSAs) and Transitional Service Agreements (TSAs) in carve-out projects. Lead and manage timely and effective post-closing agreement exit in integrations.
Understand and communicate concerns, motivations and needs of all entities to ensure maximum benefit is realized and business momentum is maintained / increased.
Track and report performance against agreed-upon milestones and deliverables (as well as top- and bottom-line synergy / value creation targets in integrations).
Maintain a structured approach for keeping all relevant stakeholders informed – reporting integration / carve-out progress against financial and non-financial targets, surfacing roadblocks, and driving timely escalation to senior leadership.
Create a clear roadmap and transition plan for handover and ongoing ownership.
Actively coach and develop junior team members.
Continuously evolve transaction execution-related best practices and engage in best-practice building.

Who You Are:

Minimum Qualifications:

Master’s degree, e.g., in Business Administration, Economics, Finance or related fields

6+ years of experience with global, matrixed organizations
6+ years of experience in management consulting or similar positions, with demonstrated success in steering large, cross-functional teams and overseeing substantial resources in complex environments
Demonstrated 2+ years of leading operational post-merger integrations and / or carve-outs across various deal types (e.g., share deals, asset deals, standalone / incubator integrations, spin-off).
2+ years of leadership experience
Broad-based knowledge and project experience in the industries in which our company operates (Life Science / Healthcare and / or Electronics) – with curiosity about the technologies shaping our future
Strong analytical and problem-solving skills, with attention to detail
Good balance of strategic and operational strength
Exceptional organizational skills, with ability to work in an agile manner and change course as required; able to systematically work through ambiguity
Skilled at building credibility and networks – from working teams to C-suite – both internally and with external partners
Strong business acumen – deep understanding of business processes / operating models, with knowledge of financial analysis, ROI analysis and key performance indicators
Continuous learning orientation and ability to quickly acquire new skills and domain knowledge in evolving business contexts
Strong drive, especially in fast-paced, complex and high-pressure environments, showing resilience and adaptability
Proven ability to make sound, data-driven decisions with confidence and minimal need for escalation
Culturally and politically savvy, strong in change management and communications

Preferred Qualifications:

MBA degree

Proficient financial literacy and experience in financial due diligence, valuation, and M&A lifecycle

Multi-year experience in strategy, business development, portfolio management, investment banking, or related field is a plus

AI literacy or interest in AI – including critical thinking and experience with AI tools, concepts and prompt engineering to accelerate project execution and drive synergies

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Commercial Specialist (12개월 계약직, 신입 가능, 관련 전공/경력 우대) (Ansan-Si, Gyeonggi-do, KR, 15420)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your Role

We are looking for a Commercial Specialist to support commercial activities with our customers and to initiate order processing procedures with ERP system. The Commercial Specialist’s role is to define an order scope from the customer order, support to processing with and without of ERP system. The Commercial Specialist helps quoting activities for new sales opportunities by organizing order scope definition like as Equipment BOM.

Operate as the point of initiates for any and all specific commercial order to ERP system.
Support commercial activity of customer relationships.
Ensure the timely and successful delivery of our solutions according to customer needs and objectives.
Clearly communicate the progress of customer order requirements to internal and external stakeholders.
Help to develop new business with existing clients and/or identify areas of improvement to meet sales targets.
Help to find a sales forecast and to organize orders list processing (e.g., quarterly and annual forecasts, SOX report).
Create purchase requisition for specific commercial order to ERP system.
Oversee and share feedbacks from internal teams processing customer orders and try effort to resolve any challenges of the timely and successful delivery.
Collaborate with team (production, accounting, project team, product management, marketing, quality, engineering) to process customer order requirements and to develop new opportunities

Who You Are

Education: Bachelor's degree in science or engineering preferred, but not required.
Experience: 2+ years’ experience in the related field preferred, but not required.
Language: Good command of English is a plus.
Ability to communicate, present and collaborate with teams.
Experience MS Office.
Experience ERP solution, Auto CAD, Solidworks preferred, but not required.
Experience delivering client-focused solutions to customer needs
Strong listening, negotiation and presentation abilities
Verbal and written communication skills
Self-motivated with a results-driven approach
Aptitude in delivering attractive presentations

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Expert - K2 Developer (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

We are seeking a seasoned Senior K2 Developer to join our delivery team. The ideal candidate will design, develop, and optimize complex K2-based solutions, lead technical discussions with customers and teammates, and drive best practices in coding, testing, and release management. This role combines hands-on development with collaboration, mentorship, and process adherence.

Key Responsibilities
- Collaborate with customers and team members to discuss requirements and design robust K2-based solutions.
- Provide accurate effort estimates for requirements and clearly communicate technical concepts to non-technical stakeholders.
- Deliver individual contributions while actively supporting team objectives and project milestones.
- Review code, establish coding standards, and ensure quality deliverables.
- Share knowledge through virtual sessions and team forums.
- Adhere to project timelines and change management processes to ensure compliant releases.
- When working from home, align with shift schedules, maintain proper work logs, and present professionally.
- Mentor junior team members to facilitate knowledge transfer and growth in technology expertise.
Required Qualifications
- Bachelor’s degree or equivalent combination of education and experience (preferred: Computer Science, Information Systems, or related field).
Technical Skills (Must-Have)
- 6–10 years of hands-on experience designing and developing applications using Nintex K2 Five.
- Experience creating and configuring SmartObjects, forms, views, and workflows using out-of-the-box features.
- Experience developing custom brokers using .NET assemblies and SharePoint APIs.
- Strong experience integrating with SQL, SharePoint, SAP, Web Services, REST APIs, and Oracle.
- Proficiency in developing and optimizing SQL Server artifacts (tables, views, stored procedures, functions, triggers).
- Hands-on experience with SOAP and JSON serialization/deserialization.
- Experience in performance tuning and optimization of applications.
- SSRS and Power BI for analytics reporting.
- Nice to have: experience with Dox42 and its integration with K2.
- Experience in writing code review guidelines and creating a dummy system for automated testing.
- Hands-on experience with packaging and deployment tools, Visual Studio, and Azure DevOps for release management.
- K2 Certification.
- ServiceNow and Azure DevOps is a plus. (Note: Replaces the previous ServiceNow + HPSM reference.)
- PowerShell integration experience.
Soft Skills
- Strong verbal and written communication skills with customers, teammates, and management.
- Excellent organizational, behavioral, and time-management abilities.
- Effective presentation skills for product knowledge sharing with customers and management.
- High emotional intelligence and the ability to engage empathetically with others.
- Problem-solving mindset and openness to constructive criticism.
- Flexibility to work across technologies as needed.
Certifications (Nice-to-Have)
- K2 Certification (required minimum expectation for this role)
- Any relevant integration or development certifications
What We Offer
- Competitive salary and performance-based incentives
- Comprehensive benefits package (health, dental, vision, retirement plans)
- Flexible work arrangements and a collaborative team environment
- Opportunities for professional growth, training, and certification

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Internship - Microbiology Quality Control (m/f/d) (Corsier-sur-Vevey, Vaud, CH, 1804)

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Start date: July or August 2026

Duration: 6 months

Location: Corsier-sur-Vevey

Role level: Internship

Within the QC Microbiology department, ensuring reliable, efficient, and compliant microbiological testing is essential to support product quality and patient safety. The industry is rapidly evolving toward automation, digitalization, and rapid microbiological methods (RMM). This internship will contribute to our strategic roadmap to modernize and optimize microbiological controls.

Your role :

The intern will participate in the benchmarking, evaluation, and preliminary qualification of alternative rapid and automated microbiology technologies. Activities include:

Mapping available RMM and automated solutions.
Comparing technologies based on performance, regulatory acceptance, cost, and operational fit.
Conducting traditional testing as compendial reference method.
Designing and executing laboratory evaluations by tests in accordance to study protocol (feasibility, robustness, usability).
Supporting data analysis, risk assessment, and decision matrices (SWOTs, scoring grids, ROIs).
Contributing to recommendations for implementation within QC Microbiology.
Preparing technical reports and presenting findings to QC, manufacturing leadership and QA stakeholders.
Contributing to the transformation roadmap.

Your profile :

Currently undertaking studies in a relevant field
Methodical, curious and team spirit
Fluent in English, French is a plus

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Automated Equipment Technician 2- 1st shift (Jaffrey, New Hampshire, US, 03452)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

The Automated Equipment Specialist II is an experienced level position within the Automated Equipment Maintenance team. The Automated Equipment Maintenance team primarily focuses on the maintenance of equipment that operates autonomously or with minimal human intervention, such as robotics, conveyor systems, and automated assembly lines. Maintenance of automated equipment often requires specialized knowledge of software, sensors, controllers, and other components specific to automation technology. Automated equipment maintenance may heavily rely on predictive maintenance techniques, leveraging data from sensors and I/O devices to predict equipment failures and schedule maintenance proactively. Automated Equipment maintenance involves maintaining the integration of automated equipment with other systems, such as data networks, control systems, and software interfaces. Compared to manufacturing maintenance, automated equipment maintenance requires a higher degree of specialization in modern automation technologies.

Duties Include:

Daily intermediate level preventive and breakdown maintenance of automated production equipment - mechanically, pneumatically, and electrically.
Perform intermediate-level maintenance activities on automated equipment including manufacturing equipment and manufacturing equipment control systems, laboratory equipment control systems, robotic systems, etc.
Intermediate level knowledge base of the above systems that require minimal human intervention, the software, controllers, and other components.
Automated Equipment Specialist maintains the integration of automated equipment with other systems, such as data networks, control and safety control systems, and software interfaces.
Utilize predictive maintenance techniques and leverage data from sensors and electronic devices to drive proactive maintenance activities and predict/prevent equipment failures.
Complete tasks that are more specialized than routine maintenance activities due to the modern automation technologies which include integrated data networks, control systems, and software interfaces.
Diagnose and repair intermediate-level automated equipment malfunctions, minimize equipment downtime to support production schedules, and collaborate cross-functionally with Operations, Quality, and Engineering teams.
Optimize preventative maintenance activities, maintain accurate documentation, support new equipment installation and validation, proactively identify and communicate safety, quality, and productivity concerns, collaborate cross-functionally and across shifts to resolve issues, follow all EHS requirements, contribute to continuous improvement and sustainability initiatives, maintain a clean and organized work environment, and work effectively with limited supervision.

Physical Attributes

Physical flexibility to interact with and troubleshoot machinery and equipment.
Exposure to chemical reagents.
Use hand and power tools.
Sit, stand, and walk for extended periods of time.
Frequent lifting/carrying of 26 - 50 lbs.
Bend, squat, stoop, and kneel.
Pinch, grasp, and manipulate objects consistently and regularly.
Fine motor skills.

Who You Are

Minimum Qualifications

3+ years of automated manufacturing equipment maintenance experience.
High school diploma or GED

Preferred Qualifications

5+ years automated manufacturing equipment maintenance or related experience within an ISO certified or cGMP manufacturing environment.
Associate’s degree in mechanical/electrical technology or related technical field.
Intermediate Electro-Mechanical and controls knowledge along with experience applying this knowledge to process/equipment design and troubleshooting.
Proven mechanical, machine tool, and automated equipment repair skills.
Demonstrated ability to pass on-site mechanical and controls aptitude tests, mentor junior Automated Equipment Technicians, and apply robotics experience, including teaching and touch-up of robot points.
Become a Qualified Electrical Worker (QEW), with knowledge of EHS, ISO, cGMP, and manufacturing regulations; ability to read and interpret mechanical/electrical drawings and P&IDs; proficiency with Microsoft Office and familiarity with CAD; and experience following safe work practices, including Lockout/Tagout (LOTO) and electrical safety procedures.
Creating and editing drawings/schematics in CAD.
Lean/Six Sigma experience.

Pay Range for this position: $30-$46 per hour

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Experto en Eficiencia Operativa (Montevideo, Montevideo, UY, 91605)

El Analista en Eficiencia Operativa contribuirá a la identificación, coordinación y ejecución de proyectos de eficiencia, mejora continua, optimización y automatización de procesos, trabajando con distintas áreas del sitio y asegurando el cumplimiento de los requisitos de Calidad, GxP, EHS y sostenibilidad.

Responsabilidades

Participar en la identificación y priorización de oportunidades de mejora. Analizar procesos utilizando herramientas Lean, Excelencia Operacional y análisis de causa raíz. Coordinar y ejecutar proyectos con las áreas involucradas. Realizar el seguimiento de KPIs y medir los beneficios obtenidos. Participar en la actualización de documentación de procesos. Cumplir con las normas y procedimientos de EHS, Calidad y cumplimiento. Promover la simplificación, estandarización y mejora continua.

Quien eres

Estudiante avanzado o egresado de Ingeniería en Producción, Industrial, Ingeniería Química, Química Farmacéutica o carreras afines (excluyente).
Inglés avanzado (excluyente).
Excel avanzado (excluyente).
Experiencia en mejora continua, Lean, optimización de procesos o gestión de proyectos (deseable).
Power BI y SAP (deseables). Conocimientos de GMP y GDP (deseable).
Capacidad analítica, organización, orientación a resultados y trabajo en equipos multidisciplinarios

Clinical Site Management Excellence Lead (all genders) (Feltham, London, GB, TW14 8HA)

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This role requires to be on-site in our office in Feltham, UK for 3 days per week.

Your role:

The Clinical Site Management Excellence Lead is a strategic and operational leader responsible for driving excellence in the planning, execution, and oversight of clinical trial monitoring and site management activities. The role is pivotal in ensuring that clinical monitoring and site management practices are globally harmonized, inspection-ready, and responsive to evolving trial models, including decentralized trials, risk-based monitoring, remote and centralized monitoring, digital health integration, and evolving site-facing coordination needs.

With clinical monitoring strategy as a core focus, the role also defines how site management enables effective implementation of that strategy in practice, from site activation and initiation through site monitoring, ongoing oversight, escalation, issue management, CAPA linkage, and close-out. Site management in this context also includes the coordination of how different functions interact with study sites at country, regional/cluster, and global levels, ensuring clear communication, role clarity, aligned site-facing engagement, and consistent ways of working across GDO and R&D peers, Regional and Cluster Heads, study teams, CROs, vendors, and other functions interfacing with sites.

As an internal consultant and transformation leader, the Site Management Excellence Lead partners closely with Regional and Cluster Heads, GDO peers, applicable study members, and site-facing functions to shape and implement scalable, efficient, and Good Clinical Practice (GCP)-compliant clinical monitoring and site management processes. These processes must align with regulatory expectations, organizational objectives, and the needs of modern clinical trial delivery.

Who you are

You hold an advanced degree in Life Sciences, Medicine, Clinical Research, or a related field, or bring equivalent professional experience.
You bring 12+ years of experience in clinical research, with deep expertise in site management and clinical monitoring across global environments.
You have a proven track record of owning end-to-end clinical processes, including process design, documentation, performance oversight, and continuous improvement in a regulated setting.
You are highly knowledgeable in ICH-GCP guidelines, including ICH E6(R3), and experienced in applying Quality by Design and risk-based quality management principles.
You have led cross-functional initiatives in complex matrix organizations, building alignment across diverse teams, CROs, and vendors without direct authority.
You have partnered with technology and digital teams to shape system requirements and drive adoption of tools that support process compliance and operational efficiency.
You apply a strong analytical and data-driven approach to translate performance metrics into targeted process improvements.
You are comfortable in a global, multicultural setting and willing to travel internationally up to 20% of the time.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

IT Project Manager - Infrastructure (Barueri - SP, Sao Paulo, BR, 06455-035)

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Your Role

Delivering secure, reliable, and scalable technology is at the heart of how a global science and technology company keeps its operations running. As an IT Project Manager within the Foundation Solutions team, you will lead end to end delivery of critical technology projects spanning infrastructure, cloud services, networks, cybersecurity, workplace platforms, and foundational IT services. You will own the full project lifecycle: defining scope, managing budgets and resource plans, mitigating risks, and driving governance and stakeholder communication to ensure every project lands on time, within budget, and to the highest quality standard. Working closely with technical teams, vendors, and business stakeholders across the globe, you will ensure smooth transition of delivered solutions into operational support and continuously improve delivery practices and outcomes. In this role, your work directly shapes the technology foundations that enable the organisation to operate, innovate, and grow.

Who You Are

You bring 8 or more years of experience delivering infrastructure and technology focused IT projects, with a track record of on time, on budget delivery to a high standard.
You have hands on experience managing projects involving cloud platforms, networks, cybersecurity, workplace technologies, data centres, telecommunications, or enterprise infrastructure services.
You are skilled in developing and maintaining project plans, schedules, budgets, and resource plans, and in managing risks, issues, dependencies, and change requests with rigour.
You are comfortable working across Agile, Waterfall, and hybrid delivery methodologies, and with project management tools such as Smartsheet, Jira, or similar platforms.
You communicate clearly and confidently with technical teams, vendors, and senior business stakeholders, and you build strong relationships that keep projects moving forward.
You hold a Project Management Professional certification or equivalent, or are actively working towards one.
Experience in regulated environments and familiarity with GxP requirements is an advantage.
You are proficient in English.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Apprentissage - stagiaire IT (m/f/d) (Corsier-sur-Vevey, Vaud, CH, 1804)

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Date de début : 01.02.2026

Durée : 12 months

Localisation : Corsier-sur-Vevey ou Aubonne

Role : Apprentissage

Nous recherchons un·e stagiaire en informatique, idéalement issu·e du CPNV ou de l'ETML, pour rejoindre notre équipe de support à Aubonne ou Vevey dans le cadre d'un stage d'un an. C'est une excellente opportunité pour les étudiant·es souhaitant acquérir une expérience pratique dans le domaine de l'informatique et du support technique.

Ton role :

Assister l'équipe de support dans la résolution des problèmes techniques rencontrés par les utilisateurs.
Participer à la gestion et à la maintenance des systèmes informatiques.
Contribuer à la documentation des procédures et à la mise à jour de la base de connaissances.
Collaborer avec les membres de l'équipe sur divers projets d'amélioration des services

Ton profil :

Connaissances en systèmes d'exploitation, réseaux et support technique.
Fortes compétences en communication
aptitude à travailler en équipe.
Autonomie
Sens de l'organisation et capacité à gérer plusieurs tâches de front.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

(Senior) AI Engineer - Data & AI Organisation (all genders) 1 (Bangalore, Karnataka, IN, 560100)

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AI Engineer

Location: India

Your Role

Within the Data & AI Organization, a team of data enthusiasts, engineers, and AI specialists, you will design and implement reliable analytics pipelines and enterprise-grade agentic workflows that deliver scalable AI solutions across Enabling Functions such as Finance, HR, Procurement, and Legal. Integrating large language models (LLMs), predictive models, and multi-agent frameworks, you will ensure model reliability, reproducibility, and performance at enterprise scale, leveraging platforms such as AWS, Palantir Foundry, and Snowflake.

Embedding explainability, transparency, and security into every AI solution is a core expectation of this role. You will use agentic engineering tools to accelerate delivery and work closely with Product Owners, Data Engineers, and Data Scientists in agile, cross-functional Product-Oriented Delivery Teams (PODs). You will support business teams in consuming AI outputs through APIs, dashboards, and embedded analytics, while actively contributing to internal AI literacy by sharing knowledge, mentoring peers, and piloting innovative approaches. A genuine curiosity for the latest developments in AI and data science will drive you to continuously identify opportunities to experiment, measure impact, and advance the field within the organization.

Who You Are

You hold a university degree or equivalent qualification in Mathematics, Physics, Computer Science, or a related discipline.
You bring 5 or more years of experience in data science, data engineering, analytics, or application design within a global organization, including exposure to Finance, HR, or Procurement data and business processes.
You have excellent programming skills in Python and SQL, with a strong foundation in machine learning, statistics, predictive modeling, and NLP, combined with practical experience developing LLM-powered applications.
You are familiar with vector stores, reranking techniques, and LLM observability tooling such as Langfuse, LangSmith, or similar, and you have experience using agentic engineering tools effectively and responsibly within enterprise software development workflows.
You have hands-on experience with cloud and enterprise data platforms such as AWS, Palantir Foundry, or Snowflake, and with data transformation frameworks such as Apache Spark, Polars, DuckDB, or dbt.
You have MLOps and DevOps experience, including MLflow, CI/CD pipelines, and Docker, and you apply these practices to ensure model reliability and reproducibility at scale.
You demonstrate AI literacy — a critical understanding of how AI works, its practical applications and decision-making implications, and the ethical considerations around bias, fairness, privacy, and governance — enabling you to build and deploy AI solutions responsibly.
You communicate complex technical concepts clearly in English to diverse audiences; German language skills are a plus, and you stay continuously up-to-date with emerging technologies and the evolving AI landscape.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Process Engineer (Dallas, Texas, US, 75241-7824)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Process Engineer provides day-to-day technical support for blending and chemical manufacturing operations producing CMP slurries and Surface Prep & Cleans (SP&C) products for Tier 1 semiconductor foundries at the Dallas facility. This role executes hands-on troubleshooting, data analysis, and documentation work that supports process reliability, product quality, and continuous improvement objectives, while working closely with Production, Quality, Supply Chain, and Maintenance teams. The position requires regular presence on the manufacturing floor, direct use of process data systems (SAP, LIMS, SCADA/DCS historian trends), and application of structured problem-solving and statistical tools to support operators, monitor process performance, and drive operational excellence in a high-purity, low-variability manufacturing environment with change control.

Key Responsibilities:

Manufacturing Support

Provide daily process engineering support to blending and manufacturing operations, including real-time review of batch records, recipe parameters, and SCADA/DCS process trends (e.g., Rockwell/Allen-Bradley, FactoryTalk, or equivalent control systems).
Support operators and production supervisors in resolving process-related issues affecting blending assets, filtration/purification skids, and UPW systems using process flow diagrams (PFDs), P&IDs, and standard operating procedures (SOPs).
Develop and monitor process performance dashboards against control limits and operating envelopes; identify opportunities to improve efficiency, quality, and throughput using multivariate SPC charts and OEE metrics.
Participate in daily tier meetings and production meetings; communicate process-related performance and investigation updates using visual management boards and shift handover reports.

Process Troubleshooting & Investigations

Conduct troubleshooting activities for process deviations, equipment issues, and manufacturing concerns using first-principles chemical engineering (mass/energy balances, reaction and mixing fundamentals) and structured methodologies (5-Why, Fishbone/Ishikawa, A3).
Support root cause analysis efforts, applying statistical process control (SPC) and basic multivariate analysis techniques (e.g., Pareto analysis, control charts, Cpk/Ppk calculations) using tools such as JMP, Minitab, or Python.
Assist with deviation investigations, 8Ds, and corrective and preventive actions (CAPA) within the site's electronic quality management system (eQMS/QMS).
Collaborate with Quality, Operations, and Maintenance teams to implement corrective actions and verify effectiveness.

Continuous Improvement

Identify opportunities for waste reduction, yield improvement, cycle time reduction, and process optimization using Lean Manufacturing tools (value stream mapping, 5S, standard work).
Support implementation of Lean Manufacturing and Six Sigma continuous improvement initiatives (DMAIC framework); Green Belt certification or working toward certification is a plus.
Participate in Kaizen events and operational excellence projects, quantifying and communicating the business impact of improvements.
Monitor effectiveness of implemented improvements using statistical trending and communicate results to the site leadership.

Documentation & Process Control

Create and revise manufacturing procedures, work instructions, batch records, and process and data maps in accordance with GMP-aligned document control practices.
Support change control activities and document revisions within the site's change management system.
Maintain process engineering records, drawings, technical files, P&IDs and process specification sheets defining operating parameters and control limits.
Assist with development and maintenance of process specifications, recipe management, and operating parameter documentation.
Support SAP-related manufacturing data updates, including bill of materials (BOM) and routing reviews, production order execution, and batch record reconciliation as assigned.

Product Transfers & Engineering Support

Support execution of engineering trials, engineering batches, and product transfer activities for CMP slurry and SP&C formulations.
Collect and analyze process data during validation, qualification (IQ/OQ/PQ), and process capability studies.
Assist senior engineers with manufacturing readiness assessments and process qualification activities for new product introduction (NPI) and technology transfer projects.
Participate in new product introduction and commercialization projects, including scale-up from lab/pilot to full production scale.

Equipment & Reliability Support

Work with Maintenance and Operations teams to troubleshoot equipment-related process issues on blending tanks, filtration/purification skids, pumps, and instrumentation.
Assist with equipment qualification, commissioning, and startup activities, including review of control system logic and instrumentation calibration records.
Support process improvements related to equipment performance and reliability, using CMMS (computerized maintenance management system) data to identify recurring failure modes.
Participate in preventive maintenance reviews and process optimization initiatives in coordination with Automation and Reliability engineering.

Quality & Compliance

Assist with internal and external audit preparation activities for ISO 9001, ISO 14001, and ISO 45001 certified manufacturing systems.
Ensure process documentation remains current and compliant with quality system and change control requirements.
Support CAPA implementation and effectiveness checks within the site's eQMS.
Participate in risk assessments (e.g., FMEA, PHA/HAZOP) and process safety initiatives.

Growth Opportunities

Develop expertise in CMP and SP&C processes.
Gain hands-on experience supporting daily production, troubleshooting process issues on the manufacturing floor, and understanding how engineering decisions impact safety, quality, delivery, and cost.
Lead projects from design to execution and sustaining phases.
Work closely with Production, Quality, Supply Chain, Maintenance, and R&D teams, gaining exposure to the broader manufacturing value chain and developing skills needed for future technical and leadership roles.
Learn digital tools to integrate in production data analytics and automation processes driving the site towards industry 4.0.
Exposure to customer relationship management, and audit programs.

Physical Attributes:

Regular presence in manufacturing and warehouse environments.
Ability to wear required PPE and work safely in production areas, including chemical-handling and cleanroom-adjacent zones as applicable.
Ability to walk production areas daily and support manufacturing activities on the floor.
Occasional lifting and movement of materials consistent with site safety requirements.

Location: Dallas, Texas
Work arrangement: Onsite

Travel: up to 10%

Who You Are:

Minimum Qualifications:

Bachelor’s degree in chemical engineering, Industrial Engineering, or a similar engineering discipline.
2+ years of manufacturing or process engineering experience, ideally in batch chemical, specialty chemical, or semiconductor materials manufacturing.

Preferred Qualifications:

Experience in chemical manufacturing, specialty chemicals, semiconductor materials, or related regulated industries.
Experience in FEED projects with involvement in qualification and validation using DOEs.
Strong analytical and problem-solving skills, including comfort with basic statistical concepts (mean/variance, control limits, Cpk/Ppk).
Ability to analyze process and quality data and develop practical, data-driven solutions.
Proficiency in Microsoft Office applications, AutoCAD and Python.
Familiarity with statistical analysis and process improvement tools such as Palantir Foundry, JMP, Minitab, or Python (pandas/numpy) for SPC and trend analysis.
Experience with SAP or other ERP systems, including BOM, routing, and production order transactions.
Knowledge of Process Safety Management, Lean Manufacturing principles and/or Six Sigma methodology (Green Belt training or certification a plus).
Exposure to quality systems, deviation investigations, and CAPA processes within an eQMS environment.
Experience supporting manufacturing operations in a regulated environment (ISO 9001/14001/45001, GMP-aligned, or semiconductor-industry quality systems).
Familiarity with automation/control systems (e.g., Rockwell/Allen-Bradley, FactoryTalk, SCADA/DCS historians) for reviewing process trend data. Hands on PLC coding experience is a plus.
Ability to analyze process and quality data and develop practical, data-driven solutions.
Effective communication and interpersonal skills for cross-functional collaboration with Production, Quality, Maintenance, and Supply Chain.
Ability to work effectively in a cross-functional manufacturing environment and adapt to shifting production priorities.

Pay Range for this position: $64,400-130,800 per year

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Associate Director, Search and Evaluation Cardiometabolic & Endocrinology (Seaport MA) 1 (Boston, Massachusetts, US, 02210)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Drive access to key external innovations from biotech/biopharma companies globally for Cardiometabolic, Fertility & Endocrinology (CM +F&E), enabling critical advancement of the company pipeline; search and evaluate external opportunities and support scientific and technical assessment process for potential partners, acquisitions, or licensing deals;

Take responsibility for Initial Assessments (IAs) as the initial step in a Due Diligence process with key functional experts and present high quality decision making documents to the Investment Board (IB) and lead respective multi-functional teams
Partner with internal stakeholders to identify search priorities and support defining the CM + F&E partnering strategy
Develop and keep overview of External Innovation landscape within investment priorities in alignment with the CM+F&E Therapeutic Areas;
Drive proactive search to identify assets of interest and potential partners and guide partner selection
Select and prioritize opportunities for further evaluation in close collaboration with Business Development counterparts
Maintain overview of search and evaluation activities in CM+F&E and maintain a longlist of potential opportunities
Oversee and guide filtering of potential opportunities (e.g., unsolicited, VC portfolios, conferences); execute CDA and provide aligned feedback to stakeholders
Benchmarking of potential partners based on aligned criteria to elucidate differentiation
Build and maintain external network (e.g., biotech/pharma/VC) and represent/position us externally towards potential partners
Collaborate with BD colleagues for partnering discussions to assess viability / feasibility of partnership.
Consult on assessment of risks and mitigations and ensure seamless transition of IA projects to DD Lead
Drive identification of big rocks and consolidation of IB decision-making document to make a go/no-go decision
Provide decision making documentation to IB and DRB level senior management to proceed into Due Diligence activities to assess Big Rocks or full data packages of external opportunities

Strategic Impact

Generating strategic value by identifying high value opportunities to develop and expand our innovative pipeline of opportunities in CM+F&E as key strategic therapeutic areas

Scope of People Responsibility:

Develop and mentor talents (e.g. GoGlobal Trainees and Short-Term Assignees)
Lead multi-functional assessment teams to generate IAs, DD scopes

Who You Are

Minimum Qualifications:

University degree ( PhD) in pharmaceutical science or an equivalent qualification with high expertise, strong network, and substantial R&D experience in respective investment priority field

Preferred Qualifications:

5+ years experience with 2+ years in BD&L / EI
Thorough understanding of the pharmaceutical drug discovery/development process
Scientific profile with substantial R&D experience
Strong leadership acumen to lead cross functional teams to develop search scopes, External Innovation strategy and IAs
Strong presentation skills enabling senior management decision making

Location: Seaport MA

Pay Range for this position: $130,600 - $195,900

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Global Head of Scientific Communication (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

At the intersection of science, strategy, and patient impact, this role offers a rare opportunity to shape how medical evidence reaches the people who need it most. As Global Head of Scientific Communications, you will lead a global organization of approximately 90 professionals across Scientific Communication Asset Leads, Scientific Content Creation, and Medical Information, setting the strategic direction for how scientific evidence is communicated accurately, objectively, and compliantly to healthcare professionals, patients, caregivers, field medical teams, and other Medical Affairs stakeholders.

In this pivotal role, you will define and implement the global Medical Affairs scientific communication strategy across therapeutic areas and the full product lifecycle. You will oversee the planning, development, review, approval, localization, and lifecycle management of scientific communication assets, including modular and omnichannel-ready content, while driving a streamlined medical-legal-regulatory review process. You will provide strategic oversight of global publication plans, ensuring adherence to GPP 2022 and ICMJE recommendations, and lead the global Medical Information strategy to deliver timely, accurate, balanced, and non-promotional responses to inquiries.

As a member of the Global Medical Affairs leadership team, you will partner with Clinical Development, Regulatory, Commercial, Compliance, and Communications functions while retaining Medical Affairs ownership of scientific communication and medical information standards. You will champion the responsible adoption of generative AI and advanced analytics across content development and medical information, ensuring human scientific oversight, quality control, and compliance guardrails are maintained throughout. You will protect scientific and medical integrity, manage budgets, resources, vendors, and technology investments, and deliver measurable outcomes including content utilization, medical information response service levels, and team engagement.

Who You Are

Basic/Minimum Qualifications

Advanced scientific degree (PharmD, MD, or PhD); a Master's degree in a life science with equivalent experience will be considered.
12+ years of experience in Medical Affairs, scientific communications, publications, medical information, or medical writing within the biopharmaceutical industry or a similarly regulated environment.
8+ years of experience leading global, matrixed, multi-site organizations, including budget and vendor responsibility.
Experienced in scientific evidence and data interpretation, medical review, scientific writing, and compliant communication.
Working knowledge of GPP 2022, ICMJE recommendations, and applicable industry codes (IFPMA, EFPIA, PhRMA, and local codes).
Working knowledge of AI and analytics applications in Medical Affairs, including compliance and quality implications.
Experience with strategic planning, operating model design, governance, budgets, vendors, digital platforms, and performance measurement.
Demonstrated ability to engage with artificial intelligence technologies, including their practical applications, limitations, ethical considerations, and governance implications, to make informed and responsible decisions in a regulated Medical Affairs environment.

Preferred Qualifications

CMPP certification (ISMPP).
Experience with content and medical-legal-regulatory platforms and omnichannel engagement strategies.
Experience in Oncology, Immunology, Neurology, or Fertility.
Medical education or accredited continuing medical education experience.
Excellent communication and stakeholder management skills across seniority levels, functions, and cultures.
Demonstrated ability to lead change management and business-process transformation, including digital and AI-enabled ways of working.
Patient-centric mindset, including a commitment to health literacy and plain-language communication.

Pay Range for this position: $251,000- $409,300

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Warehouse Operator Team Lead - Weekend Night Shift (Danvers, Massachusetts, US, 01923)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Responsibilities include but are not limited to:

Manage shift coverage, prioritize daily workloads to prevent production disruption, and lead the team to increase throughput and overall efficiency through effective time management and communication. Perform a wide variety of tasks related to shipping and receiving materials, supplies and equipment.
Perform a variety of tasks related to shipping and receiving, including unpacking, verifying items against purchase orders, preparing goods for shipment, posting weights and charges, and managing international shipments. Maintain accurate records of received goods, promptly rejecting unsatisfactory items.
Accurately maintain records of received and shipped goods, promptly rejecting unsatisfactory items, assisting with weekly cycle counts, and transacting and moving material between warehouses. Prepare and maintain records of shipped items.
Perform various tasks using ERP and other computer software (e.g., material/production/distribution/barcoding), and analyze data (LPNs, Min/Max, Aging, Shortage, and Expiring Inventory reports) to identify and improve efficiency trends. Utilizes PC and material/production/distribution/barcoding software.
Safely operate forklifts, Powered Industrial Trucks (PIT), and box trucks for moving materials and performing external logistics as needed. Transacts and moves material from off-site warehouse to main plant as needed.
Adhere to company Environmental Health and Safety (EHS) procedures, and meet all output and targets set by management. Train new operator(s) on Shipping/Receiving processes with high proficiency.
Investigate, escalate, and resolve complex issues, and cooperate/communicate with cross-functional teams (Warehouse, Quality, Production, Engineering, etc.) to meet scheduled targets. Analyzes data to identify and improve efficiency trends.
Train new operators on shipping/receiving processes, participate in process improvement projects, monitor equipment functionality, coordinate maintenance, and complete shift hand-offs. Handle debit memos, expiration dates, Monster Jobs, and other requirements specified by supervisors or managers.
Weekend Night Shift: Friday - Sunday 6pm – 6am.

Who You Are:

Minimum Qualifications:

High School Diploma or GED.
Valid Driver’s License.
1+ years of warehouse experience.

Preferred Qualifications:

Experience with ERP systems (SAP or Oracle).
Forklift experience.

Pay Range for this position: $30 - $46 / hour

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

R&D Engineer / EUV Resine_Electronics(Shizuoka) (Shizuoka, Shizuoka, JP, 437-1412)

メルクと一緒に、あなたの力を発揮しよう！

冒険、限界への挑戦、そして発見に焦がれるあなたへ。あなたの大志を、メルクで羽ばたかせましょう！科学とテクノロジーを駆使したイノベーションに情熱を注ぐメルクのスタッフは世界中で活躍中です。ヘルスケア、生命科学、エレクトロニクスの分野で、メルクのソリューションは人々の暮らしをますます豊かなものにしています。あなたとメルクの力を合わせて、大きな夢を抱きましょう。メルクは、人、顧客、患者、そしてこの地球という惑星が共存する豊かな世界の構築に情熱を注いでいます。このためメルクでは、好奇心にあふれた人材を募集中です。メルクと一緒に、想像を超えた世界を開拓しませんか？

エレクトロニクスでの弊社のすべての行動は、企業を支える企業になることと、デジタルリビングを発展させるという目的を実現させるためのものです。弊社は、エレクトロニクス業界、自動車業界、化粧品業界にとって、ハイテク素材、サービス、特殊化学品の信頼されるサプライヤーになるために全力を尽くしています。弊社は、勝利するための情熱を持ち、お客様のことを常に考え、好奇心を絶やさず、あきらめずに行動する個人によって構成されるグローバルなコラボレーション型組織を育てます。弊社は力を合わせて科学の新境地を開き、お客様のためにさらなる可能性を追求いたします。

English Follows

募集職種：R&D senior engineer

職務内容

・EUVリソグラフィーを含む最先端半導体製造に用いられる電子材料の研究開発業務。

・材料開発だけでなく、顧客サポートを含むグローバルな環境で業務に従事していただきます。

必要なスキル・資格など

・化学、材料科学、またはその他の関連する科学分野の修士号、または博士号を取得されている。

・半導体製造に用いられる材料開発に3年以上の経験。

・日本語、英語での文章および口頭でのコミュニケーション能力

・アイデアを創出し、実施に向けてチームメンバーと推進する能力

推奨

・有機化学のバックグランド

・先端材料開発に伴う、新しい概念、不確実性にチャレンジできる

・チーム、他部署と共に成功するための適応力を持っている。

・プロジェクトリードの経験

・クリーンルーム環境業務の経験

・デジタルツールを利用した業務に長けている

担当業務:

【新規アイデア】材料コンセプト、モデル、組成の設計

【ラボワーク】実験計画に基づき、電子材料サンプルの調製、評価。

【クリーンルームワーク】電子材料の評価。

【報告・ディスカッション】チームディスカッション、顧客との会議

【その他】特許、論文調査

Job title: R&D specialist

Job Description:

Research and development of electronic materials used in advanced semiconductor manufacturing including EUV lithography.
Engage in activities in a global environment that includes not only material development but also customer engagement.

Required skills and Qualifications:

Master's or Ph.D. degree in chemistry, materials science, or other related scientific fields.
Over 3 years of experience in material development for semiconductor manufacturing.
Communication skills in English and Japanese, both written and verbal.
Ability to generate ideas and drive the team towards implementation.

Preferred

Background in organic chemistry.
Ability to challenge new concepts and uncertainties associated with advanced material development.
Adaptability to work collaboratively with teams and other departments for success.
Experience in leading projects.
Experience working in a cleanroom environment.
Proficient in utilizing digital tools in work processes.

Responsibilities:

New idea: Design of material concepts, models, and compositions.
Lab work: Preparation and evaluation of electronic material samples based on experimental plans.
Cleanroom work: Evaluation of electronic materials.
Reporting and discussion: Team discussions and meetings with customers.
Other: Patent and paper research.

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

Head of Site Safety, Health and Environmental Compliance (Kankakee, Illinois, US, 60901)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The site Head of Environmental, Health, Safety & Security (EHSS) is a key leadership role responsible for developing, implementing, and maintaining comprehensive EHS and security programs across the organization. This position ensures regulatory compliance, drives a culture of continuous improvement in safety and environmental stewardship, and oversees contracted security operations. The Head of EHSS will demonstrate expertise in management system standards, process safety, and physical security program oversight.

Key Responsibilities:

Environmental Management

Oversee and maintain the organization's ISO 14001 Environmental Management System (EMS), ensuring ongoing conformance and continuous improvement.
Lead internal audits, management reviews, and third-party certification audits related to ISO 14001.
Identify and manage significant environmental aspects and impacts; develop and monitor environmental objectives and targets.
Ensure compliance with all applicable local, state, and federal environmental regulations.
Maintain environmental permits and manage reporting obligations (e.g., air, water, waste).

Health & Safety Management

Oversee and maintain the organization's ISO 45001 Occupational Health & Safety Management System (OHSMS), driving conformance and continual improvement.
Lead incident investigations, root cause analyses, and corrective/preventive action (CAPA) processes.
Develop and deliver EHS training programs for employees at all levels.
Conduct and facilitate risk assessments, job hazard analyses (JHAs), and safety inspections.
Monitor leading and lagging safety performance indicators and report to management.
Champion a proactive safety culture through employee engagement and behavioral safety initiatives.

Process Safety Management (PSM)

Oversee the facility's Process Safety Management (PSM) program in accordance with applicable regulatory requirements (e.g., OSHA PSM standard 29 CFR 1910.119 and/or EPA RMP).
Coordinate and manage PSM elements including Process Hazard Analyses (PHAs), Management of Change (MOC), Pre-Startup Safety Reviews (PSSRs), Mechanical Integrity, and Operating Procedures.
Ensure PSM documentation is current, accurate, and audit-ready.
Collaborate with engineering and operations teams to identify and mitigate process safety risks.
Track and close PSM action items and recommendations in a timely manner.

Security Program Management

Oversee the day-to-day performance of contracted security officers, ensuring service delivery aligns with contractual obligations and site requirements.
Serve as the primary liaison between the organization and the contracted security provider.
Conduct regular performance reviews of the security contractor; escalate performance gaps and drive corrective actions.
Develop and maintain site security plans, access control procedures, and emergency response protocols.
Conduct security risk assessments and recommend improvements to physical security infrastructure and procedures.
Coordinate with local law enforcement and emergency response agencies as needed.

General EHSS Leadership

Serve as a subject matter expert and internal consultant on all EHSS matters.
Participate in and support emergency response planning, drills, and actual emergency events.
Maintain accurate EHSS records, metrics, and reports; present findings to senior management.
Stay current with evolving regulations, industry standards, and best practices.
Mentor and coach junior EHSS staff and cross-functional team members.
Primarily on-site role with regular presence on the plant/facility floor.
Reports directly to the Site Manager with dotted line reporting into regional EHS leadership.
May involve occasional off-hours availability for emergency response or security incidents.
May involve some travel for audits, training, or multi-site support.

Who You Are

Minimum Qualifications:

Bachelor’s degree in Environmental Science, Occupational Health & Safety, Chemical Engineering, or other EHS field.
3+ years of experience in environmental, health, safety, and/or security roles.
1+ years of experience managing ISO 14001 and/or ISO 45001 management systems through certification and surveillance audits.
1+ years of experience with OSHA PSM and/or EPA RMP program management.

Preferred Qualifications:

Master’s degree in Environmental Science or Occupational Health & Safety.
Experience overseeing contracted security services.
Certified Safety Professional (CSP).
Certified Hazardous Materials Manager (CHMM).
ISO 14001 and/or ISO 45001 Lead Auditor certification.
Physical Security Professional (PSP) certification.
In-depth knowledge of federal, state, and local EHS regulations (OSHA, EPA, DOT, etc.).

Excellent written and verbal communication skills; ability to present complex topics to varied audiences.
Proven ability to manage multiple priorities and projects simultaneously.
Proficiency in EHS management software and Microsoft Office Suite.
Strong interpersonal skills and the ability to influence without direct authority.

Pay Range for this position: $83,300 - $124,900/year.

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Manager of EHS&S and Risk Mgmt. (Hsinchu, Hsinchu County, TW, 300046)

與我們攜手施展你的超能力！

The Site EHS&S and Risk Management Manager is accountable for the safety, security, environmental compliance, and risk management of the site in Hsinchu, Taiwan. This role leads the development, implementation, and continuous improvement of EHS&S policies, procedures, and practices; conducts EHS and Process Safety risk assessments; ensures adherence to local regulations and global standards; and partners with site leadership to foster a strong EHS&S culture.

Your Role

Regulatory & Standards Compliance: Ensure site-wide compliance with applicable Taiwan EHS&S regulations, global EHS&S standards, andCorporate EHS policies, standards, and procedures.
Reporting & Data Integrity: Oversee accurate, timely, and high-quality reporting to local authorities and global systems, ensuring data integrity.
SOP & MOC Management: Collaborate with Production, Facility Engineering, QC, Warehouse, R&D, and other functions to develop and regularly update SOPs, with emphasis on Management of Change (MOC) in line with global Process Safety & EHS guidelines.
Risk Mitigation & Training: Lead regular risk assessments, develop mitigation and prevention plans, and coordinate cross-functional actions to maintain ongoing regulatory compliance and training.
Policy & SOP Maintenance: Develop and maintain local and site-specific EHS&S and Risk Management policies and SOPs to protect employees, customers, and other stakeholders from compliance violations and safety hazards.
Adherence Enforcement: Ensure adherence to policies and regulations across all levels of management, with support from site leadership.
Emergency Response: Lead the site emergency response program, including SOPs, system updates, employee training, and reporting aligned with local regulations and global requirements.
Audits & Oversight: Plan and conduct EHS and process safety audits covering site operations, waste treatment, suppliers, tollers, and 3PL warehouses, while supporting customers.
Cross-Functional Collaboration: Partner with local and global EHS counterparts to drive continuous improvements in EHS&S and Risk Management.
Financial & Project Support: Manage departmental OpEx and CapEx, and support local and global EHS&S projects.
Contractor Safety: Develop and maintain contractor management SOPs and standards.
External Audit SPOC: Act as the single point of contact (SPOC) for external audits; drive performance in EHS&S, Sustainability, and Process Safety.
Process Safety Governance: Serve as the accountable owner for process safety governance; coordinate HAZOPs and periodic revalidations, ensuring timely completion and closure of high-risk recommendations after technical review.
Continuous Improvement: Lead site risk assessment initiatives and process safety improvements, aligning controls with company standards.
Culture Building: Foster a compliant, proactive safety culture through training, communications, and leadership engagement tailored to site operations.

Who You Are

Education: Bachelor’s or higher degree in Engineering, Environmental Science, Occupational Health & Safety, or a related field.
Experience: 3 or more years of experience as an EHS Manager or Process Safety Manager in the chemicals, display, or semiconductor manufacturing industries.
Certifications: Possession of relevant EHS certificates, such as Class A Occupational Safety & Health Manager (甲業) / Class B Occupational Safety Specialist (乙勞), environmental certifications, or Toxic and Concerned Chemical Substances Emergency Response certificates.
Regulatory Knowledge: Strong knowledge of Taiwan environmental, health, and safety regulations.
Leadership Capabilities: Demonstrated ability to lead cross-functional teams, manage audits, incident investigations, and continuous improvement initiatives.
Communication & Languages: Excellent communication, training, and stakeholder-management skills; fluent in English and Mandarin (TOEIC score of 700 or above preferred).

立即申請，成為這個致力於激發探索精神、提升人類未來的團隊一員！

Demand & Supply Planner (Tokyo, Tokyo, JP, 106-0041)

ポジション名

需要計画／IBP担当

部門

Supply Network Operations／需要計画

職務目的

SAP IBPにおける信頼性の高い需要予測データの維持、部門横断的なインプットの取りまとめ、予測精度のモニタリングを通じて、需要計画およびIntegrated Business Planning（IBP）プロセスを支援する。また、事実に基づく需要レビューおよび事業上の意思決定を可能にする。

主な職務・責任

1. 需要予測管理

合意されたスケジュールおよび計画要件に基づき、OP、各種フォーキャストサイクル、月次LBEその他必要な計画更新を含む月次需要予測データをSAP IBP上で作成・維持する。

2. 部門横断的な予測の取りまとめ

Commercialおよび関係する社内部門から需要予測に関するインプットを収集・統合・整理し、レビュー、協議および認識合わせに付す。

3. データレビューおよび課題のエスカレーション

売上実績および予測データをレビューし、差異、不整合、データ品質上の問題を特定するとともに、重要な事項をマネージャーまたは適切な関係者へエスカレーションする。

4. レポーティングおよび予測精度のモニタリング

定期レポートを作成・維持し、予測精度および関連するパフォーマンス指標をモニタリングすることで、需要レビューおよび事業上の意思決定を支援する。

5. IBP会議の支援およびアクション管理

IBP会議資料の作成を支援し、需要計画に関する協議で合意された担当アクションを追跡・フォローアップする。

6. 部門間の連携およびコミュニケーション

必要に応じて、Supply Network Operations、Commercial、Finance、Quality、Regulatory Affairsおよびその他の関係部門との定例コミュニケーションおよび情報連携を調整する。

7. 新製品上市支援

需要計画の観点から、新製品上市に必要なデータを準備し、関連タスクを追跡するとともに、適切な指示・支援のもとで関係部門との調整を行う。

8. 継続的改善

現行プロセスを文書化し、改善機会を特定するとともに、合意された変更の導入を支援することで、継続的改善活動に貢献する。

主な関係部門

Supply Network Operations
Commercial
Finance
Quality
Regulatory Affairs
需要計画およびIBP関係者
マネージャーおよびその他の関係する社内部門

期待される貢献

本ポジションは、予測データを期限どおりに更新し、部門間の認識合わせを促進し、リスクやデータ上の課題を可視化するとともに、効果的なIBP運営および意思決定を支援することで、透明性と信頼性の高い需要計画プロセスに貢献する。

Position Title

Demand Planning / IBP Specialist

Function

Supply Network Operations / Demand Planning

Job Purpose

Support the demand planning and Integrated Business Planning (IBP) process by maintaining reliable demand forecast data in SAP IBP, coordinating cross-functional inputs, monitoring forecast performance, and enabling fact-based demand reviews and business decisions.

Key Responsibilities

1. Demand forecast management

Prepare and maintain monthly demand forecast data in SAP IBP in accordance with agreed timelines and planning requirements, including OP, forecast cycles, monthly LBE, and other required planning updates.

2. Cross-functional forecast alignment

Collect, consolidate, and organize forecast inputs from Commercial and relevant internal stakeholders for review, discussion, and alignment.

3. Data review and issue escalation

Review sales and forecast data, identify variances, inconsistencies, and data-quality issues, and escalate relevant findings to the manager or appropriate stakeholders.

4. Reporting and forecast accuracy monitoring

Create and maintain regular reports and monitor forecast accuracy and related performance indicators to support demand reviews and business decision-making.

5. IBP meeting support and action follow-up

Support the preparation of materials for IBP meetings and track and follow up on assigned actions resulting from demand planning discussions.

6. Cross-functional coordination and communication

Coordinate routine communication and information exchange with Supply Network Operations, Commercial, Finance, Quality, Regulatory Affairs, and other relevant functions as required.

7. New product launch support

Support new product launch activities from a demand planning perspective by preparing relevant data, tracking activities, and coordinating with relevant functions under appropriate guidance.

8. Continuous improvement

Contribute to continuous improvement initiatives by documenting current processes, identifying improvement opportunities, and supporting the implementation of agreed changes.

Key Interfaces

Supply Network Operations
Commercial
Finance
Quality
Regulatory Affairs
Demand Planning and IBP stakeholders
Manager and other relevant internal stakeholders

Role Contribution

The role contributes to a transparent and reliable demand planning process by ensuring timely forecast updates, improving cross-functional alignment, highlighting risks and data issues, and supporting effective IBP governance and decision-making.

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

Internship - ADC modeling (m/f/d) (Corsier-sur-Vevey, Vaud, CH, 1804)

Work Your Magic with us!

Start Date: 1st January 2027

Duration: 6 months

Localisation: Corsier-sur-Vevey

Role Level: Internship

Conjugation of monoclonal antibody with a drug linker is a critical step in the development of antibody-drug bioconjugates. Today, offline analytical methods provide detailed information on the reaction, but they are time-consuming and don’t enable continuous process monitoring.The objective of this project is to develop a proof of concept for a hybrid soft sensor combining UV-Vis spectroscopy to provide fast, information-rich process measurements; a kinetic reaction model to describe the evolution of the conjugation species; an Extended Kalman Filter to combine measurements and model predictions while accounting for their respective uncertainties. The internship will focus primarily on modelling and data analysis, with experimental work performed when needed to support the project.

Your Role:

Support the development and evaluation of the UV-Vis-based soft sensor, including data preprocessing and chemometric data treatment.
Develop kinetic reaction models using gPROMS and/or Python to describe the evolution of the conjugation species.Compare different kinetic model structures, estimate kinetic parameters, and assess the predictive performance.
Validate the kinetic model against independent experimental or offline analytical data where available.Combine kinetic model with the soft sensor data using an Extended Kalman Filter.
Evaluate the ability of the hybrid model to update the estimated reaction state and predict the reaction progress.Identify data gaps and, if required, design and perform additional small-scale conjugation experiments.
Analyze model performance, robustness and limitations.
Plan and execute experiments in collaboration with PAT, modelling and process experts.Ensure that experimental conditions and results are accurately recorded and traceable.
Develop Python-based tools for data preparation, visualization, and analysis.Present your results during project reviews and prepare a final technical report.

Your Profil:

Currently in master’s or Engineering student in data science, analytical chemistry, biochemistry, biotechnology, chemical engineering or a related field.
Strong interest in reaction kinetics, mechanistic modelling, dynamic systems, and data science.
Experience with python and gPROMS or another process modelling tool is a strong plus.
Interest in spectroscopy and chemometrics; knowledge of UV-Vis or PLS is an advantage.
Practical laboratory experience and strong attention to data quality and reproducibility.
Knowledge of Kalman filtering is a plus.
Curious, rigorous, proactive, and able to work independently as well as in a multidisciplinary team.
Fluent in English

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Welder (Indianapolis, Indiana, US, 46268)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

EMD Electronics is looking to immediately hire experienced Welders to support an existing project within the US. Welders will be responsible for operating a TIG Lathe and Orbital welder assembling job orders in a manufacturing environment. This position would be scheduled Monday-Friday 8:00 am to 4:00 pm with potential overtime, and must be able to support a travel schedule that aligns with this project.

MEGASYS® offers specialized services in managing gases, chemicals and slurries, where our technicians and engineers provide critical on-site support in semiconductor manufacturing environments.

Perform orbital GTAW tube welding, assembly, and installation of mechanical components onto sheet metal plates and inside of sheet metal frames and enclosures on equipment

Check raw materials and quantities against a bill of materials and arrange them according to a design drawing

Perform inspection and general tool maintenance

Apply welding symbols and maintain proper sequence of assembly and accuracy of fit-up

Use computer interface for reading/understanding P&ID and mechanical diagrams and drawings

Work with supervision to adjust weld parameters to meet required weld quality

Maintain all required certifications under applicable codes

Physical Attributes:  

Work in Clean/Weld room using heat resistant welding gloves and welding face shield

Sit for up to 6 hours

Maintain hand dexterity and stability for weld quality

Lift up to 50 lbs. 5 times per day and transfer this weight to a cart either at the same level or down at knee height

Push or pull carts on wheels (up to 200 lbs)

Stand and kneel on ergonomic mats over concrete

Use full range of motion with arms and legs

Use hand, power tools, taps, wrenches, sockets, cutting tools, jigs and fixtures and simple measuring instruments

Who You Are:  

Minimum Qualifications:

High School Diploma or GED

1+ years of hands-on TIG Lathe or Orbital welding experience

Preferred Qualifications:

Self-starting and motivated with good written and verbal communication skills

Ability to work effectively in a fast-paced dynamic environment while following safety and process controls

Ability to interpret mechanical and electrical schematics and engineering mechanical drawings

RSREMD

Pay Range for this position: $21-$33/hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Sr. Technical Project/Program Manager (장비_Equipment, Project Management) (Ansan-Si, Gyeonggi-do, KR, 15420)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your role:

The Lead Systems Engineer is responsible for driving system-level engineering execution across multiple concurrent customer projects in a high-mix, low-volume semiconductor equipment environment.

This role combines deep engineering knowledge with strong project and task management capabilities to ensure successful execution of customer programs from concept through deployment.

The position serves as a key technical leader responsible for coordinating cross-functional teams, managing technical risks, aligning customer requirements, and driving project execution while maintaining system-level integrity.

Unlike a traditional Principal Engineer focused on long-term technology strategy, this role emphasizes execution, coordination, technical governance, and delivery of multiple simultaneous projects in a fast-paced customer environment.

Key Responsibilities

System Engineering Leadership
- Maintain system-level ownership of customer solutions and engineering deliverables.
- Understand and assess impacts across Mechanical, Electrical, Software, Manufacturing, and Service functions.
- Translate customer requirements into executable technical plans.
- Drive system-level problem solving and technical decision making.
- Ensure engineering changes and design decisions maintain overall system integrity
Project & Task Management
- Lead multiple concurrent engineering projects with competing priorities and aggressive timelines.
- Develop and maintain execution plans, schedules, milestones, and action tracking.
- Identify project risks and drive mitigation actions.
- Coordinate resources across engineering disciplines to meet customer commitments.
- Escalate critical issues and drive timely resolution.
- Improve project execution discipline through structured governance and reporting.
Customer & Stakeholder Engagement
- Act as a technical focal point for strategic customer programs.
- Lead technical discussions with customers and internal stakeholders.
- Coordinate communication between Engineering, Manufacturing, Quality, Service, Supply Chain, Sales, and Project teams.
- Support customer escalations and complex technical issues.
Compliance & Technical Governance
- Coordinate certification and compliance related activities.
- Ensure regulatory, quality, and customer requirements are incorporated into project execution.
- Support technical reviews, risk assessments, and engineering change processes.
- Drive lessons learned and continuous improvement initiatives.
Operational Excellence
- Establish project visibility through KPI and dashboard reporting.
- Improve engineering workflow efficiency and prioritization.
- Support workload balancing across multiple programs.
- Drive standardization and best practices for project execution.
Who you are:

Minimum Qualifications
- Bachelor's degree in Mechanical, Electrical, Chemical, Systems, or related Engineering discipline.
- 8+ years of experience in semiconductor equipment or industrial equipment engineering.
- Strong understanding of complete system architecture and product lifecycle.
- Proven experience managing multiple engineering projects simultaneously.
- Experience working with cross-functional teams in a matrix organization.
- Strong communication and stakeholder management skills.
- Fluent Korean and business-level English

Preferred Qualifications
- Master's degree in Mechanical, Electrical, Chemical, Systems, or related Engineering discipline.
- Experience supporting Samsung or SK hynix programs.
- Experience in semiconductor systems with fluid behavior.
- Experience with certification, compliance, or regulatory requirements.
- Experience with ECR, MOC, PDM, PLM, and configuration management.
- PMP or equivalent project leadership experience.
- Experience in high-mix, low-volume manufacturing environments.
- Experience coordinating global engineering teams.

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

머크는 구성원들에게 아래와 같은 혜택을 제공하고 있습니다. 머크에서는 모두 호기심을 바탕으로 서로 다른 배경과 가치관, 그리고 경험을 가진 다양한 구성원들과 함께 성장할 수 있습니다. 머크는 다양성을 소중히 여기며, 이를 통해 탁월한 성과와 혁신을 이끌어내 과학 기술의 발전에 공헌하고 있습니다. 머크는 구성원 모두 본인만의 속도로 발전하고 성장할 수 있도록 커리어 개발의 기회를 제공합니다. 머크의 구성원들은 서로 돕는 건강한 기업 문화를 조성하고 있습니다. 머크에서 여러분만의 특별한 재능으로 인류의 진보를 실현하는 마법을 펼쳐보세요!

다양성으로 가득한 머크의 구성원이 되어주세요!

GMP Associate Production Scientist - Rotating Shift (St. Louis, Missouri, US, 63118-3306)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Join our St. Louis Cherokee facility at MilliporeSigma, a leading contract development and manufacturing organization (CDMO) and a recognized Center of Excellence for antibody-drug conjugate (ADC) manufacturing. We are seeking passionate and enthusiastic professionals to contribute to our innovative bioconjugate production, leveraging over 35 years of expertise in the field. As a vital part of our dedicated team, you will play a key role in delivering high-quality ADCs that improve the quality of life for patients suffering from cancer and other debilitating diseases. With our state-of-the-art technologies and commitment to excellence, you will ensure the highest standards of quality and compliance in our ADC manufacturing processes.

As an Associate Production Scientist – Rotating Shift you will manufacture products according to established protocols under ICH Q7 pharmaceutical regulations, provide technical support to others and perform operations in support of the group and department.

Job Duties Include:

12 hour rotating Day (6:00am - 6:30pm)/ Night (6:00pm - 6:30am) shifts with a 20% shift differential
Evaluate products by established protocols, providing technical support and performing operations to meet departmental goals.
Safely conduct routine processes and unit operations, including cleaning equipment and work areas, while ensuring quality expectations.
Maintain required training and qualifications, train team members, and act as a technical consultant.
Support facility functions by maintaining equipment, preparing reagents, restocking supplies, and managing waste disposal.
Maintain accurate records and logbooks according to quality guidelines, communicating operational status and concerns to supervision.
Collaborate with other departments, participate in quality audits and customer interactions, and perform procedures independently or in a team.
Improve processes using scientific knowledge and principles, ensuring compliance with change control.
Address unsafe conditions promptly and troubleshooting challenges related to biological processes and GMP compliance.

Physical Attributes:

Ability to lift to 50lbs.
Ability to wear personal protective equipment, such as respirator or chemical protective clothing, for extended periods.
Expected on-floor time: (70%)

Who You Are

Minimum Qualifications:

Bachelor’s Degree in scientific discipline (e.g., Chemistry, Biochemistry, Biology, etc.)

Associate Degree in Chemistry, Biochemistry Biology or any other Life Science discipline
2+ years of industry Production/Laboratory experience

RSREMD

Preferred Qualifications:

Experience with Antibody Drug Conjugates (ADCs), including knowledge of their formulation and manufacturing processes.
Experience with Automated Tangential Flow and Automated Chromatography systems.
Familiar with laboratory instruments and production equipment
Familiarity with process techniques, unit operations, and safe chemical handling methods.
Experience with Microsoft Office (Word, Outlook, Excel, etc.).
Mechanical and troubleshooting skills.
Knowledge of cGMP and ICH Regulatory and Quality standards.
Knowledge of Operational Excellence.
Clean room experience
Ability to interact professionally in customer-facing meetings, including challenging discussions on process planning and process execution

RSREMD

Pay Range for this position: $25.00 - $45.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Flow Control Services Strategist (San Jose, California, US, 95134)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

Your Role:

MEGASYS® offers specialized services in managing gases, chemicals and slurries, where our technicians and engineers provide critical on-site support in semiconductor manufacturing environments.

In this position, you will have the opportunity to shape and advance the organization’s strategic direction by developing business concepts, evaluating markets, customers, competitors, and growth opportunities, and translating insights into clear, actionable recommendations. Your leadership will be crucial in driving the success of our operations and enhancing customer relationships.

Key Responsibilities:

Lead the development and execution of long-term business strategies.
Provide strategic insights to the President and leadership team.
Oversee major transformation programs, focusing on post-merger integration.
Manage cross-functional teams to achieve transformation goals.
Develop a high-performing team while fostering a culture of accountability and continuous improvement.

Physical Attributes:

Walking throughout the facility (up to 3 miles per day).

Basic lifting (up to 40lbs).

Military Veterans:

Who You Are:

Minimum Qualifications:

B.A. or B.S. degree (or equivalent) in engineering (chemical, mechanical, etc.) with 8+ years of experience in semiconductors, electonics or a closely related industry.

Preferred Qualifications:

Proven experience in the semiconductor or electronics industry
Good commercial and financial skills, ideally experience with financial planning
Great communicator (incl. fluently in English)
Passion for technologies – to shape the technologies of the future
Very good analytical skills and experience with PowerPoint and Excel
Ability to work in dynamic and complex environments, handling multiple projects/ workstreams in parallel while achieving the required outcomes and timelines
Highly motivated team player and ambitious to grow within our organization

Pay range for this position: $166,900 - $240,000

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Counsel -US Rare Tumors (Boston, Massachusetts, US, 02210)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Senior Counsel, Rare Tumors will provide comprehensive legal support to a Therapeutic Area, including both Commercial and Medical functions. Specifically, this role will be part of the legal team supporting Rare Tumors, one of EMD Serono’s key Therapeutic Areas, and will report to an Associate General Counsel.

Key Responsibilities:

Primary Legal Counsel: Serve as lead attorney for a key brand of the Rare Tumors Therapeutic area, including: review of marketing (promotional) materials; advice regarding Marketing and Sales Operations; review of scientific (non-promotional) materials; advice regarding Medical Affairs and Medical Operations; manage outside counsel as specialized advice is required for Therapeutic Area projects; work collaboratively with paralegals.
Compliance & Regulatory Oversight: Ensure all activities comply with FDA, OIG, CMS, and state requirements, as well as company policies and industry codes (e.g., PhRMA Code).
Contracting & Negotiations: Draft, review, and negotiate agreements with advertising, consulting, call center and Therapeutic Area-specific distribution agreements, as well as contracting with healthcare professionals including advisory boards and consulting.
Training & Education: Deliver legal training on relevant healthcare laws and company compliance requirements.
Cross-Functional Collaboration: Partner closely with Commercial, Compliance, Medical Affairs, and Regulatory teams to align business practices with legal standards. Collaborate with US and Global colleagues in order to ensure business strategies and objectives comply with applicable laws, regulations and policies.
Risk Management: Proactively identify, counsel, and communicate potential legal issues to mitigate risk. Manage risks through counseling, training and practical application of relevant legal and regulatory requirements, Company policies and procedures to Therapeutic Area operations.

Who You Are

Minimum Qualifications:

Juris Doctor (JD) degree from an accredited U.S. law school.
Active bar membership in good standing in at least one U.S. jurisdiction.
7-10 years of legal experience in a firm and/or in-house.
Strong ability to interpret and apply laws, regulations, and guidance in a practical, business-oriented manner.
Excellent communication, drafting, and negotiation skills.
Proven ability to work collaboratively across multiple functions in dynamic and fast-paced environment.

Preferred Qualifications:

Prior in-house experience at a pharmaceutical or biotechnology company.
Demonstrated expertise in healthcare fraud and abuse laws, FDA regulatory matters, and patient support program compliance.
Experience supporting commercial business units, including contracting, supporting the development of commercial strategies.
Experience participating in or advising MLR/Promotional Review Committees.
Background in compliance counseling or interaction with government agencies (OIG, DOJ, FDA).

Competencies:

Strategic thinker with strong business acumen.
Excellent judgment and risk-based decision-making.
Collaborative, practical, and solutions oriented.
Ability to manage multiple priorities and stakeholders effectively.
Committed to ethics, compliance, and patient-centered values.

Pay Range for this position: $188,600 - $283,000

Direct link to benefits site if the hyperlink no longer works: https://careers.emdgroup.com/us/en/benefits].

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Medical Science Liaison Rare Tumors (Lombardia, Piemonte, Liguria) (Rome, Rome, IT, 00187)

Work Your Magic with us!

Your Role

As a Medical Science Liaison responsible for the area of Lombardy, Piedmont and Liguria, you bridge the gap between complex science and clinical practice. Operating under the Medical Head and Medical Advisor, you drive scientific exchange and manage medical projects within your therapeutic area. You build and maintain critical relationships with healthcare professionals, delivering precise clinical data and capturing field insights to shape our medical strategies. You own the execution of medical meetings, advisory boards, and congress activities while assisting with clinical research initiatives. Collaborating across cross-functional teams, you ensure all communications align with regulatory standards. Your proactive engagement directly enhances data transparency, supports medical education, and optimizes patient outcomes.

Who You Are

Degree in Life Sciences, Pharmacy, or Medicine (PhD preferred).
At least 3 years of experience in Medical Affairs or Clinical Operations
Strong interest in Medical Affairs and scientific communication.
Excellent presentation and interpersonal skills.
Fluency in both written and spoken Italian and English.
Ability to collaborate effectively in cross-functional teams.
Proactive attitude with exceptional organizational skills.
Prior pharmaceutical industry experience is advantageous.

Salary Package:

Annual Base Salary (RAL): €40.000 - €60.000
Categoria CCNL: B - A
Variable Compensation (SIP)
Welfare and Benefits Package

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Marketing of Rare Tumors /Biopharma (Tokyo, Tokyo, JP, 106-0041)

Marketing Manager, Desmoid Tumor

Position Summary

The Marketing Manager, Desmoid Tumor will lead market development, launch readiness, stakeholder engagement, and commercial execution for the first systemic therapy in Japan for patients with Desmoid Tumor.

The role is responsible for developing disease awareness, shaping treatment paradigms, building multidisciplinary treatment networks, partnering with patient advocacy organizations, and ensuring effective commercial execution.

This position combines Marketing, Market Development, Commercial Excellence, and Field Execution responsibilities and will play a critical role in transforming treatment practices and accelerating patient access.

Key Responsibilities

Brand Strategy & Launch Excellence

Develop and execute annual brand and market development strategies.
Lead launch readiness planning and execution.
Develop promotional materials, disease awareness programs, digital assets, and omnichannel campaigns.
Translate global strategy into actionable local initiatives.

Market Development & Ecosystem Building

Assess patient journey, referral pathways, diagnosis patterns, and treatment barriers.
Develop regional market development plans tailored to local market dynamics.
Build treatment ecosystems that facilitate diagnosis, referral, and treatment access.
Identify and address barriers to treatment adoption.

Stakeholder Engagement & Consensus Building

Establish and maintain relationships with key opinion leaders, treatment centers, and academic societies.
Partner closely with patient advocacy groups and patient communities.
Facilitate alignment among physicians involved in Desmoid Tumor management.
Support multidisciplinary treatment decision-making and referral networks.
Lead initiatives that drive consensus and behavior change across healthcare stakeholders.

Commercial Excellence & Field Execution

Develop field execution strategies and regional action plans.
Partner with Sales Leadership on territory prioritization and resource deployment.
Monitor execution quality and business performance.
Conduct regular business reviews and recommend corrective actions.
Ensure rapid translation of market insights into field actions.

Performance Management & Analytics

Develop KPIs and performance measurement frameworks.
Establish dashboards and business review processes.
Track customer engagement, referral generation, treatment adoption, and business performance.
Monitor launch performance and identify opportunities for optimization.
Support forecasting and business planning activities.

Required Qualifications

Professional Experience

Minimum 5 years of pharmaceutical industry experience.
Proven marketing experience in Specialty Care, Oncology, Rare Disease, Immunology, or Hospital-based products.
Experience leading product launch or pre-launch activities.
Strong project management and cross-functional leadership skills.

Critical Experience

Demonstrated experience working across multiple medical specialties.
Proven ability to build alignment and consensus among healthcare professionals with different clinical perspectives.
Experience supporting multidisciplinary treatment decision-making processes.
Experience developing and executing market development initiatives.
Experience translating strategy into measurable field execution and business outcomes.
Experience developing KPIs, performance metrics, and execution tracking frameworks.

Preferred Therapeutic Area Experience

Candidates should have meaningful experience in multiple of the following specialties:

Orthopedic Surgery
Gastrointestinal Surgery
Medical Oncology
Dermatology
Rare Diseases
Sarcoma or Tumor-related Diseases

Experience working across specialty boundaries and driving collaboration among different clinical stakeholders is strongly preferred.

Critical Success Factors

Ability to influence without direct authority.
Strong stakeholder management and relationship-building skills.
Excellence in consensus building and behavior change leadership.
Strong analytical and business planning capabilities.
Ability to balance strategic thinking with operational execution.
Passion for improving outcomes for patients with rare diseases.

Key Performance Indicators

Launch readiness achievement
Disease awareness growth
KOL engagement and advocacy development
Patient advocacy partnership effectiveness
Referral network activation
Regional execution performance
Treatment adoption and patient starts
Forecast accuracy
Business performance versus plan

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

Tech Electronic (Jerusalem, Jerusalem, IL, 9777613)

Work Your Magic with us!

Within our matrix organization you will be part of the Maintenance and Engineering team and will perform maintenance work at the cGMP facility in Jerusalem. You will provide services to all equipment in the cGMP facility and utilities, as well as housekeeping.

You will be responsible for cGMP process equipment, clean utilities and QC equipment maintenance, fix equipment breakdown and perform preventive maintenance activities

You will be responsible of instrument calibration.

You will also provide technical support to plant employees

Who you are:

Mechanical technician or Mechatronic practical engineer.
Certified electrician – is an advantage.
Experience in maintaining industrial process equipment and utilities.
Experience in product launches in the last 3-5 years.
Computer application (Microsoft office, internet etc.)
Communication and team work skills
Industrious, self-motivated and self-learner
Willing to work overtime
Availability for emergency calls
Reliability and responsibility

Basic English knowledge

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Field sales specialist (Madrid, Madrid, ES, 28006)

Work Your Magic with us!

Objective:

Promotes and sells products and/or services of biomonitoring portfolio and solutions directly to current and new end customers. Closes direct sales of products and/or services. Creates,
monitors and revises lead generation plans to ensure a substantive sales opportunity pipeline.

Key responsibilities:

Typically reports to a South Europe Sales Manager role or to country supervisor

1. Account plans:
• Monitor and take action to close gaps against sales targets, and update forecast as required
• Understand customer’s business, their needs and goals and identify potential new business
• Identify, build relationship with appropriate decision makers within Customers and manage sales negotiations

2. Business analysis/Problem solving:
• Identify general areas for improvements to maximize customer satisfaction & efficiencies, streamline processes, increase sales, improve
delivery and product availability etc.

3. Reporting:
• Provide performance reports and metrics and other data as required to customers and internally
• Use sales-specific systems (like SalesForce.com) to manage own sales pipeline, forecast and monitor sales targets

4. Activity:
• Achieve the sales target for the assigned territory
• Visit existing and potential customers face to face or vitual
• Manage sales opportunities by generating and following leads using the CRM provided
• Manage contract implementation where appropriate
• Support implementation of the tactical plan aligned with the segment strategy

5. Product / Market knowledge updates:
• Identify market and competitor activity, product and industry developments and feedback this information to management and other relevant
functions (e.g. Marketing or Sales Development)

6. Collaboration:
• Work collaboratively with all colleagues across territories, regions, or countries to share best practice as well as participate in important
projects in order to improve the coverage of multi-country customers and improve processes
• Work and collaborate with internal teams to increase customer network and leads/opportunities/sales

Sell macrobiology portfolio products, quality control and assurance and sell the products (macrobiological test) to enterprise

Advance solution business in LifeScience, by biomonitoring, using technical sales to sell macrobiology portfolio, pharmaceutical industry.

Who You Are:

We are looking for a motivated professional who is ready to make decisions and deliver results. You bring:

Microbiology background
Experience in similar functions within the pharmaceutical industry.

Competencies developed in:

Strong communication skills, with the ability to interact effectively with stakeholders at all levels.
Curios mind
Dynamism
Goal-oriented
Positive and solution-oriented attitude

Work location: Spain. Flexible, with a preference for Barcelona or Northern Spain.

Flexible working hours. 80% traveling, and 20% on remote. Reference site: Mollet del Vallès.

Including a company car

Permanent employment

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Experto en Planificación y Gestión de Inventario (Temporal) (Montevideo, Montevideo, UY, 91605)

Tus responsabilidades

Tu principal responsabilidad será la planificación y compra de materiales de empaque e insumos para depósito y empaque, la gestión del inventario y apoyarás en tareas de planificación de producción y master data.

Participarás activamente en el desarrollo y análisis de KPI del sector de Planificación Operativa, apoyarás la optimización de procesos y proyectos de mejora continua y contribuirás a la generación de información clave para la toma de decisiones y la mejora de la eficiencia operativa del sector.

Tu perfil

Te caracterizas por tener iniciativa, proactividad, pensamiento analítico y orientado a procesos, eres una persona con capacidad organizativa y para el trabajo en equipo.

Egresado o Estudiante avanzado de las carreras o tecnicaturas de Producción, Logística o Cadena de Suministro, entre otras.
Experiencia mínima de 1 año en posiciones similares.
Manejo avanzado de Excel y herramientas de Microsoft
Nivel avanzado del idioma Inglés
Power BI (deseable)
Conocimiento en SAP o similares (deseable)

Contrato temporal hasta 28/2/27

¡Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!

En el marco de la Ley 19.691 el llamado comprende a candidatos que estén inscriptos en el Registro Nacional de Personas con Discapacidad que funciona en el Ministerio de Desarrollo Social.

Energieelektroniker oder Mechatroniker (m/w/d) befristet auf 2 Jahre (Gernsheim, Hessen, DE, 64579)

Bei SUSONITY strahlt Ihre Arbeit im Rampenlicht

Aus einer Innovationsgeschichte seit 1959 hervorgegangen, gestalten wir die Zukunft der Materialwissenschaft heute unter einem neuen Namen: SUSONITY. Wir machen Oberflächen intelligenter, widerstandsfähiger und eindrucksvoller – von perlmuttartigen Effekten in Premiumfahrzeugen bis zu leistungsstarken Wirkstoffen in hochwertiger Hautpflege.

Mit tiefem naturwissenschaftlichem Know-how und kreativer Entdeckungsfreude verleihen wir allem, was wir tun, Schönheit und Performance.

Aus Tradition entsteht Zukunft: SUSONITY

Ihre Rolle: Werden Sie Teil von Susonity Production GmbH und tragen Sie zur Optimierung unserer Produktionsanlagen bei!

In der spannenden Rolle als Elektrofachkraft (EFK) (m/w/d) sind Sie verantwortlich für die Instandhaltung unserer Systeme, einschließlich Inspektionen, Wartungen und Instandsetzungen, auch unter Ex-Bedingungen. Sie (m/w/d) installieren, demontieren und reparieren elektrische Anlagen und Motoren, um einen reibungslosen Produktionsablauf sicherzustellen. Darüber hinaus führen Sie regelmäßige Wartungen von Geräten, Maschinen und Anlagen durch und übernehmen Funktionsprüfungen sowie Inbetriebnahmen gemäß allgemeiner Anweisung. Zudem unterstützen Sie (m/w/d) die Weiterentwicklung von SPS-Programmen und dokumentieren die durchgeführten Maßnahmen. Wenn Sie (m/w/d) technisches Know-how und eine Leidenschaft für die Elektrotechnik mitbringen, freuen wir uns auf Ihre Bewerbung!

Die Stelle ist auf 2 Jahre befristet.

Ihre Aufgaben:

Fachkenntnisse auf dem Niveau einer dreijährigen zielführenden technischen Ausbildung z.B. Energieelektroniker (m/w/d) oder Mechatroniker (m/w/d) sowie mehrjähriger Berufserfahrung im genannten Berufsfeld
Mehrjährige fundierte Erfahrung im Bereich der Instandhaltung im Chemie-, oder Pharma Umfeld
Kenntnisse in Arbeits- und Umweltschutz, Unfallverhütung und Qualitätssicherung
Teamfähigkeit, Flexibilität, Problemlösungskompetenz, Eigeninitiative, Bereitschaft zur Wochenendarbeit
Kenntnisse der Grundlagen im Bereich Arbeits- und Umweltschutz, Unfallverhütung und Qualitätssicherung
Sehr gute Deutschkenntnisse, min. C1 Level

Manufacturing Operator 2 - 12 Hour Night Shift (Sheboygan Falls, Wisconsin, US, 53085-2819)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

$5000 Sign on Bonus if Hired

Your Role:

This role is primarily focused on the safe and efficient manufacturing of products that are used by our customers to manufacture the most advanced semiconductors in the world as well as life science products that contribute to quality-of-life enhancements. In this role you will manufacture materials using existing production procedures and maintain a high level of safety and quality in the work environment.

In this role your tasks will include, but are not limited to:

Produce, purify and package chemical compounds to meet the requirements of MilliporeSigma customers
Stage materials utilizing a variety of warehouse equipment including pallet trucks and Powered Industrial Trucks
Verify the quality and integrity of materials and equipment
Perform in-process analytical testing including workups and simple interpretations as described in the Master Production Record
Update batch records, computer systems and SAP per ISO procedures
Demonstrate proper lab, manufacturing and packaging safety practices in accordance with OSHA, EPA, DNR, DOT and other regulatory agency guidelines
Maintain a high level of safety with our pro-active “see something – say something” approach to safety as well as participate in core operational excellence programs including Daily Management System, 6S organization and safety walks
Participate in team-based objectives focused on improving safety, quality and production output of key manufacturing processes
Shift/Hours: 12-hour night shift, 6:00 PM - 6:30 AM - 2/2/3 schedule (M/T on, W/R off, F/S/S on, M/T off, W/R on, F/S/S off, repeat)

Physical Attributes:

Wear an air helmet, respirator mask, safety shoes, rubber apron, chemical protective suits and gloves, safety glasses and goggles to protect from toxic or corrosive chemicals
Work in occasional wet, humid abnormally hot or cold environment
Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, or crouch for long periods of time
Lift and/or move up to 50 pounds
Work with and in proximity of hazardous chemicals
Use close vision, distance vision, color vision, peripheral vision, depth vision and the ability to adjust focust

Who You Are:

Minimum Qualifications:

High School Diploma or GED
3+ years of experience in an industrial or manufacturing setting

Preferred Qualifications:

Experience with chemical handling
Experience with chemical reactions and hazards
Experience with ISO and quality systems
Strong mechanical and technical aptitude
Ability to read and understand written protocols
Experience with multitasking
Strong problem solving and equipment troubleshooting skills
Strong oral and written communication skills

Pay Range for this position: $21/hour - $38/hour
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

Validation Engineer 3 (Jaffrey, New Hampshire, US, 03452)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

The Validation Engineer III is an advanced level validation engineering position responsible for executing complex validations and qualifications of equipment, materials, processes and tests used in the production of high purity filters, prioritizing a focus on quality and safety. Responsible for establishing and maintaining qualification techniques. This position may lead lower-level engineers to ensure their projects meet validation standards. This role requires close collaboration with cross functional teams to assess risk, disposition product, resolve complex problems, and ensure projects and programs meet their expected objectives.

Duties Include:

Expert with Qualification and Validation of Manufacturing Equipment, QC equipment, raw materials, and Supply chain equipment including FAT, SAT, Installation and Operational Qualifications, and Performance qualifications (temperature mapping and process qualification).
Drive validation requirements needed for advanced manufacturing equipment design qualification and risk assessment to ensure that the equipment design is meeting manufacturer's specification and functional requirements.
Coordinate the scheduling of validation execution by collaborating with Manufacturing, Planning and Quality Control departments and analyze the test results against pre-determined acceptance criteria.
Prepare, maintain, and review Validation documentation such as CQV documentation for DQ, FAT, IQ, OQ, PQ, and process qualification.
Perform assessment of vendor change notifications to identify the impact of the change on validated status of equipment and GMP production. Review equipment calibration specifications and any out of tolerance records to determine the extent of failure on the validation test.
Represent the Validation department during internal and external audits.
Brings solution recommendations to management, assesses customer requirements, and studies product characteristics to select validation objectives and standards.
Provide guidance and mentorship to team members and contractors regarding cycle development and validation of complex manufacturing equipment and raw material changes.
Proficient at developing complex project plans to drive process improvements or changes, and capable of leading a cross functional team to meet deadlines. Able to anticipate challenges and roadblocks, and experiments with alternative and innovative solutions to avoid just refining existing solutions.
Highly skilled at building consensus with a cross functional team at all levels and converting vision into clear goals and milestones.
Facilitates effective teamwork by actively managing team dynamics. Anticipates challenges by utilizing knowledge / history to prevent issues from occurring.
Helps develop other experts by giving concrete advice, coaching, and mentoring on how to succeed in a business setting.
Leads Root Cause Analysis (RCA) and Corrective Action Preventive Action (CAPA) actions, implementing robust solutions to address root cause and prevent events from reoccurring.
Expert technical writing skills and strong understanding of Current Good Manufacturing Practices (cGMP).
Proficient at leading complex equipment and process validations activities, including protocol and report writing, review and execution.
Leads strategic or complex change requests in Change Management system, ensuring implementation solutions support operational needs and meet quality standards.
Anticipate roadblocks and challenges and navigate the team through problems to meet deadlines.

Physical Attributes:

Physical flexibility to interact with and troubleshoot machinery and equipment.

Exposure to chemical reagents.

Use hand and power tools.

Sit, stand, and walk for extended periods of time.

Frequent lifting/carrying of 26 - 50 lbs. Occasional lifting 75Lbs.

Bend, squat, stoop, and kneel.

Pinch, grasp, and manipulate objects consistently and regularly.

Fine motor skills.

Who You Are

Minimum Qualifications

Bachelor’s Degree in STEM (engineering, sciences, or computer science, etc.), technical management, business management.
5+ years of experience in an FDA regulated medical device manufacturing facility, pharmaceutical facility or other regulated industry leading the validation of automated and manual assembly processes with working knowledge of ISO, cGMPs and Good Engineering Practices.

Preferred Qualifications

Master of Science Degree in STEM (engineering, sciences, or computer science, etc.), technical management, or business management.
Read and understand complex mechanical and electrical drawings and P&ID’s.
Lean/Six Sigma experience, with a green or black belt certification.
Experience with HMI/PLC and preferred code knowledge.
Strong communication skills.
Manage and lead multiple projects and participate on cross-functional project teams.
Must be self-driven, able to work independently, and in teams with urgency.
Proven ability to analyze complex data sets, apply statistical analysis principles, and clearly summarize conclusions/results.
Familiarity with EH&S, ISO, cGMP, and other regulatory requirements in a manufacturing environment.
Experience with Microsoft products, Minitab, and CAD software packages.
Understand safe work practices and experience in lockout, tag out, electrical safety, etc.

Pay Range for this position: $105,000 -$115,000 annually

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Principal Manager, NA & EU Product Engineering (Breinigsville, Pennsylvania, US, 18031)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Principal Manager, NA & EU Product Engineering is responsible for providing the resources and technical support required for new product development and sustaining engineering programs. This leader manages the regional engineering staff and oversees project management plans, resource modelling, and workload forecasting. The role holds a seat on the global engineering council, contributing to the processes and products that serve a global customer base and its business requirements, and works in close collaboration with the other regional engineering leads.

Key Responsibilities:

Reporting to the Global Head of Engineering, lead a team of equipment, software, and electrical engineers, as well as production engineers, across the North America and Europe regions. This includes the Allentown and Breinigsville, PA, and Chandler, AZ sites, where the focus is on delivering technical leadership and strategic direction.
Own the regional execution of the new product development portfolio, from concept and feasibility through design, prototype build, qualification, and release to volume manufacturing. Hold programs to their agreed deliverables, development timelines and manage risks at each gate.
Promote safety and quality practices within engineering and laboratory environments, with particular emphasis on the safe handling of hazardous gases and chemicals. Establish rigorous safety protocols and quality assurance measures to ensure compliance with industry standards, including SEMI and ISO.
Develop and execute resource plans aligned with workload forecasts, in collaboration with engineering, product development, and other stakeholders. Ensure the optimal allocation of resources across development and sustaining projects involving the design, installation, and maintenance of gas and chemical delivery systems.
Communicate the impact of change and its potential effects on engineering to stakeholders, and recommend solutions that optimize cost without compromising quality or service.
Lead the monthly town hall meetings with regional engineering teams, manage the regional budget and forecast and guarantee compliance with customer and legal standards.
Ensure engineering teams provide day-to-day engineering support across regional manufacturing operations to resolve critical build and installation challenges.
Utilizes robust engineering practices to champion quality initiatives, driving root cause analysis and corrective actions for both internal and customer escapes. Actively participates in FMEAs and process validations while collaborating closely with supplier quality teams to address technical issues.
Implement metrics and data analytics to measure engineering deliverables from global framework, including new product development cycle time and first-pass yield, and use them to inform development priorities.

Who You Are:

The position is based in Breinigsville, PA, and requires some travel to the Chandler manufacturing site and to customer locations within the region. The successful candidate is adaptable to a fast-paced environment and able to manage multiple priorities.

Minimum Qualifications:

BS degree in engineering or a related field; a master’s degree with an electromechanical background is preferred.
8+ years’ experience in operations or engineering roles.
Proven leadership and management skills, with the ability to optimize team performance and development.
Demonstrated experience leading new product development programs through a structured stage-gate or equivalent process.

Preferred Qualifications:

Experience in engineering roles focused on gas and chemical delivery systems within the semiconductor industry.
Experience transferring new products from development into volume manufacturing.
Excellent problem-solving abilities and a strategic mindset.
Knowledge of safety and quality standards in engineering practices, particularly in the context of hazardous materials.
Proven project management and supplier management experience.
Ability to add value, reduce costs, and deliver business improvements.

Pay Range for this position: $156,000 - $200,000

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Solution Lead - Study Design Platform (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your Role: Clinical trials are at the heart of bringing new therapies to patients — and the decisions made in early study design have a lasting impact on their success. As Solution Lead for the Study Design Platform, you will own the end-to-end delivery and continuous evolution of a next-generation Software as a Service platform that enables smarter, data-driven decisions in clinical study planning, protocol authoring, and scenario-based operational feasibility analysis. You will join the Digital, Data & IT (DDIT) R&D team within our Healthcare sector, working at the intersection of clinical operations, digital innovation, and enterprise IT.

During the implementation phase, you will act as the critical bridge between R&D business stakeholders, the IT team, and the software vendor. You will lead solution design activities, translate complex business requirements into clear functional specifications and process flows, support User Acceptance Testing (UAT), facilitate alignment workshops, and drive change management and user onboarding to ensure a successful platform rollout.

Beyond go-live, you will take ownership of lifecycle management: prioritizing enhancements, supporting releases, monitoring solution performance, and ensuring sustainable adoption and business value realization. Working across a global matrix organization, you will collaborate closely with R&D users, IT partners, and the software provider — and may also contribute your analytical expertise to broader digital R&D initiatives in the clinical trial space.

This position is based in Spain, preferably Barcelona or Madrid, but other locations in Spain may also be considered.

Who You Are

You hold a Master's degree in life sciences, computer science, or a related field, or bring equivalent professional experience.
You have 5 or more years of experience as an IT Solution Lead, Application Lead, or in a comparable role within the healthcare or life sciences industry.
You bring in-depth knowledge of clinical trial processes, including protocol design, operational planning (country and site selection), and study conduct.
You have a proven track record of translating complex business needs into functional specifications and communicating effectively with both technical and non-technical stakeholders.
You have hands-on experience contributing to IT solution delivery in regulated environments, with a solid understanding of software development lifecycles and computerized system validation (CSV) in line with GxP requirements.
You are familiar with clinical trial systems and clinical trial data standards, and can navigate a global matrix organization to build trusted relationships across R&D, IT, and external partners.
You are fluent in English (written and spoken) and bring a proactive, solution-oriented mindset — you take ownership, anticipate challenges, and drive issues through to resolution.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

资深生物工艺工程师 (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Your Role:

A senior technical role within MSAT responsible for providing end-to-end technical support and scientific leadership for downstream — primarily chromatography, tangential flow filtration (TFF) and clarification — at manufacturing scale. The Lead BME will support customer site implementations, lead troubleshooting and process optimization, deliver training, and drive technical solutions for bioprocess technologies in China.

Key Accountabilities:

Provide on-site and remote technical support for manufacturing-scale chromatography, TFF and clarification operations, including implementation, troubleshooting and process optimization at customer facilities.
Serve as the recognized scientific expert for chromatography and TFF; develop and deliver internal and external theoretical and hands-on training programs.
Validate and confirm process sizing, process parameters, engineering estimates, design and technical reviews for customer projects.
Perform reviews and audits of process sequences, SOPs, design parameters and operational protocols; lead root-cause investigations and field troubleshooting.
Conduct in-house hydromechanics engineering studies and modelling using a rigorous scientific approach to support process design and scale-up.
Coordinate project activities, track technical milestones, and communicate project status and critical updates to stakeholders.
Prepare and deliver technical seminars and training at customer sites and internally to grow technical capability across teams.
Collaborate closely with China Process Solution colleagues (e.g., Sales, Customer Application teams) to drive successful process solutions and customer outcomes.
Maintain and leverage connections with global MSAT and technical networks; adapt and implement global best practices for the China market.
Proactively identify opportunities for technical improvements and professional development; work with your manager to drive personal and team growth.

Requirements/Qualification:

Master’s degree or PhD in Biological/Biochemical sciences, Bioprocessing, Chemical/Biological Engineering or a closely related discipline.
Hands-on experience with GMP-compliant biomanufacturing processes — downstream and/or upstream — at pilot or commercial scale.
Deep technical expertise in chromatography and tangential flow filtration (TFF); experience with clarification operations is preferred.
Experience with scale-up, process sizing, parameter development and engineering design reviews.
Familiarity with automation platforms and process control is preferred.
Strong problem-solving and troubleshooting skills, with a practical engineering mindset.
Excellent presentation, technical writing and interpersonal communication skills.
Good command of English (oral and written); Mandarin proficiency for customer engagement in China.
Willingness to travel frequently to customer sites.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

ANALISTA DE IMPORTACAO E EXPORTACAO SENIOR - BARUERI/SP (Barueri - SP, Sao Paulo, BR, 06455-035)

Seu Papel
Nesta posição, você será responsável por garantir a excelência operacional e a conformidade das atividades de comércio exterior. Seus principais requisitos técnicos e responsabilidades incluem:

Processamento e Conformidade: Analisar e processar requisições de compras nacionais e internacionais via sistema SAP, assegurando que todas as operações estejam em conformidade com as normas vigentes.
Gestão de Sistemas e Dados: Gerenciar informações nos sistemas ERP internos dedicados ao fluxo de compras internacionais, garantindo a máxima precisão e qualidade na alimentação dos dados.
Controle de Importação: Monitorar e aplicar requisitos mandatórios específicos para a importação de itens, assegurando o cumprimento rigoroso dos prazos acordados com as áreas de interface.
Gestão de Performance (SLA): Administrar a performance operacional dos fornecedores da cadeia de comércio exterior, garantindo que os níveis de serviço (SLAs) sejam atingidos.
Suporte Técnico e Operacional: Prestar suporte técnico especializado às áreas internas sobre o status de processos de importação/exportação e apoiar demandas correlatas gerenciadas pelo departamento.
Liderança de Sistemas (Keyuser): Atuar como Keyuser, liderando a gestão de sistemas e processos críticos para garantir a continuidade e eficácia das operações.
Comunicação de Desvios: Reportar de forma clara e eficiente qualquer desvio no processo de importação através dos canais oficiais de comunicação.

Quem é você
Buscamos um profissional com perfil dinâmico, visão colaborativa e foco em melhoria contínua. Para esta posição, os aspectos comportamentais e requisitos esperados são:

Graduação completa: Comércio Exterior, Relações Internacionais, Administração de Empresas, Logística, Economia, ou áreas correlatas.
Idiomas: O inglês é obrigatório e o espanhol é um diferencial competitivo.
Pró atividade e Gestão de Riscos: Capacidade demonstrada em identificar riscos antecipadamente, tratar desvios e implementar melhorias contínuas nos processos da área.
Liderança Colaborativa: Habilidade para liderar projetos multidisciplinares, colaborando ativamente com stakeholders das áreas de Supply Chain, Jurídico, Financeiro e Comercial.
Orientação a Resultados e Compliance: Foco em entregas de alta qualidade, sempre pautado pelo cumprimento de normas corporativas e integridade nos processos.
Adaptabilidade: Capacidade de atuar em ambientes dinâmicos e disponibilidade para participar de atividades de job rotation, visando o desenvolvimento multifuncional e o fortalecimento da equipe.
Espírito de Equipe: Atitude voltada ao suporte mútuo, auxiliando o time na gestão de demandas e promovendo um ambiente organizado e colaborativo.

Candidate-se agora e torne-se parte de uma equipe dedicada a Despertar a Descoberta e Elevar a Humanidade!

Senior Product Manager (Milwaukee, Wisconsin, US, 53209-3650)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

We are seeking a Senior Product Manager to lead and grow MilliporeSigma's Multiomics portfolio within our Biochemistry business, with a specific focus on metabolomics and glycomics. This is a high-impact, cross-functional role for a strategic thinker and hands-on executor who thrives at the intersection of science, commercial strategy, and business development.

The successful candidate will own the end-to-end product lifecycle, from identifying unmet customer needs and white-space opportunities to building and executing a differentiated innovation pipeline. This role requires a rare combination of deep scientific expertise, P&L ownership, and the commercial acumen to translate cutting-edge omics science into business results. The position sits within the Chemistry business field of Discovery Solutions and reports to Biochemistry business leadership.

Key Responsibilities:

Portfolio Strategy and Innovation Pipeline

Define and own the multi-year product roadmap for metabolomics and glycomics, anchored in a workflow-centric approach spanning sample preparation, derivatization, separation, detection, and data interpretation.
Identify white-space opportunities through VOC programs, market analysis, competitive intelligence, and scientific literature; translate insights into actionable product development briefs.
Prioritize the innovation pipeline in alignment with business goals and resource constraints; champion projects through stage-gate processes from ideation through commercial launch.

Commercial Execution and Go-to-Market

Own full P&L performance for the multiomics portfolio, including revenue, gross margin, market share, and new product vitality index; take data-driven corrective action as needed.
Develop and execute launch plans for new multiomics products and workflow kits, including pricing strategy, positioning, channel strategy, and commercial readiness.
Champion a workflow-based go-to-market framework by building product bundles, application notes, and protocol libraries that drive pull-through across the Biochemistry portfolio.
Partner with the marketing communications team to develop technical content, including application notes, webinars, and conference presentations, that establish MilliporeSigma as the authoritative voice in multiomics.
Support sales and key account teams with competitive briefings, deal support, and customer-facing presentations; monitor the portfolio lifecycle and lead phase-out decisions for underperforming SKUs.

External Partnerships and Business Development

Identify, negotiate, and manage strategic partnerships with instrument manufacturers (MS, LC, CE platforms), software and informatics providers, and academic centers of excellence.
Collaborate with the Business Development team to evaluate in-licensing, co-development, and acquisition opportunities that strengthen the multiomics portfolio.
Build and maintain a network of KOLs, academic collaborators, and industry thought leaders; represent MilliporeSigma at key scientific conferences including ASMS, Metabolomics Society, HUPO, and SLAS.

Cross-Functional Leadership and Collaboration

Serve as business owner and internal champion for the multiomics portfolio, aligning R&D, supply chain, regulatory, quality, and commercial stakeholders around shared priorities.
Partner with R&D and Applications teams to define product specifications and ensure the application relevance of new products.
Contribute to the Biochemistry AOP and mid-term planning processes with data-driven portfolio analyses, revenue forecasts, and opportunity assessments.
Mentor and provide guidance to junior product management and marketing staff on best practices and commercial execution.

Who You Are

Minimum Qualifications:

Ph.D. or M.S. in Biochemistry, Analytical Chemistry, Metabolomics, Glycobiology, or a closely related life science discipline.
Minimum 8 years of experience in product management, strategic marketing, or a closely related commercial role within life science tools, reagents, or analytical chemistry.
Demonstrable expertise in metabolomics and/or glycomics through hands-on research (academic or industry) or commercial management of related portfolios.
Strong working knowledge of LC-MS/MS, GC-MS, NMR, CE-MS, or other analytical platforms used in multiomics workflows.
Proven P&L ownership with demonstrated ability in market sizing, competitive benchmarking, financial modeling, and business case development.
Track record of developing and executing go-to-market plans including pricing, positioning, and channel strategy for life science research tools.

Preferred Qualifications:

MBA or equivalent business training paired with an advanced scientific degree.
Established network within the metabolomics and/or glycomics research community across academia, pharmaceutical, or CRO environments.
Experience in multiomics workflow development, including sample preparation, derivatization chemistries, separation media, reference standards, and data analysis tools.
Prior business development experience including partner identification, term sheet negotiations, and licensing or co-development agreements.
Familiarity with bioinformatics and data analysis tools relevant to metabolomics and glycomics, such as MetaboAnalyst, Skyline, XCMS, or GlycoWorkbench.
Track record of successfully launching products in the life science research tools market.

Pay Range for this position: $82,600 - $177,200

Direct link to benefits site if the hyperlink no longer works: https://careers.emdgroup.com/us/en/benefits].

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Associate Production Scientist - Analytical Development (Sheboygan Falls, Wisconsin, US, 53085-2814)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

We are seeking an Associate Production Scientist - Analytical Development to perform analytical testing in a fast-paced chemical manufacturing environment.

In this role, responsibilities include, but are not limited to:

Execute established analytical methods in support of process development or site production.
Transfer external or internal analytical methods into site QC / analytical development.
Maintain and troubleshoot analytical instrumentation.
Basic analytical method development supporting site operational needs.
Analytical representation at project meetings.
Maintain databases, document work for internal / external communication of experimental outcomes.
Shift/Hours: Monday – Friday, 8:00am - 4:30pm.

Who You Are:

Minimum Qualifications:

Bachelor's Degree in Chemistry, Biology, Chemical Engineering, Electrical Engineering, or other Life Science or Engineering discipline.

High School Diploma or GED and 4+ years of work experience in a chemical production, laboratory or chemical engineering role.

Preferred Qualifications:

1+ years’ experience in an industrial or academic chemical environment.
Experience with chemical measurement technologies such as IC, HPLC, GC, NMR, IR and wet chemistry.
Experience with safe chemical handling.
Experience with ISO or GMP requirements.
Experience with writing experimental procedures and reports.

Pay Range for this position: $30/hr - $47/hr. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of Distribution South Korea (생명과학, Chemical) (Incheon, Gyeonggi-do, KR, 21991)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Position Summary:

Reporting to the Head of Distribution – APAC, this exciting position is responsible for warehousing and distribution for a broad portfolio of Life Science products across South Korea. Leading a diverse team of leaders, the position will be responsible for end to end distribution processes.

The successful candidate will be a hands-on team player with high energy and work as a collaborative leader to achieve operational goals. This person must be highly self-motivated, have an intense customer focus and be able to satisfy both internal and external customer requirements.

Your Role:

Be responsible for driving performance across all operational aspects—safety, customer delivery, quality, and cost management.
Substantial experience in all technical areas of logistics operations, including procurement, transport/distribution, warehousing and stock management, fleet management, asset management, communications, and security.
Attracts, develops, and retains top performers through networking, training, coaching, development, and assigning stretch goals. Leads with a clear vision and drives achievement of goals and objectives.
Acts as a mentor to establish a learning organization.
Suitable candidate will demonstrate strong analytical skills and the ability to translate raw information into actionable strategies and initiatives.
The candidate plays a highly collaborative role and will routinely work with cross-functional teams to enable commercial growth strategies. Able to utilize a robust toolbox of influence skills to effectively manage across a matrixed organization and foster teamwork.
Key role requiring alignment across multiple levels of the organization with strong communicator, both verbally and in writing.
Develop and implement Life Science Distribution strategies and procedures for the management of transport, import/export, logistics, warehousing, and for the management of vehicle fleets, communications, systems, and assets.
Ensure that Life Science logistics flow is appropriate and cost-effective, based on budget, markets, infrastructure, global and regional distribution guidelines, and the need for timely delivery and reporting functions.
Ensure compliance with statutory provisions pertaining to environmental, safety, and security (including data protection) matters at the Songdo site.
Comply with the rules set forth by the Quality and EHS management systems and Corporate our Standards, Code of Conduct, and procedures pertaining to site activities.

Who you are

Bachelor’s degree or higher
+ 10 years of experience in a supply chain and distribution role
Proven track record in managing and supervising others in logistics, including training and capacity building
Experience with frequent visibility and interaction with senior-level managers
Strong understanding of biotech and pharmaceutical customer expectations of Life Science suppliers is a plus
Knowledge of QMS, ISO (cGMP is a plus)
Experience in the chemical industry (life science, medical devices, pharma, biotech a plus)
Related certificates are preferred (Black Belt or Green Belt, PMP, CPM or CPIM)
Fluent in Korean and English
Demonstrated strong leadership skills with the ability to motivate and inspire cross-functional teams
Experience with structured problem-solving techniques is desired
Commitment to continuous improvement
Good listener with an inclusive mindset
Collaborative and likeable team player who shares and advances best practices
Ability to drive change and challenge the status quo in a respectful, professional manner

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Packaging Operator 1 (Sheboygan Falls, Wisconsin, US, 53085-2814)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

$5000 Sign on Bonus if Hired

Your Role:

In this role your tasks will include, but are not limited to:

Precisely weigh and transfer hazardous and non-hazardous chemicals into specified containers and compare filled quantities against consumed bulk quantities to ensure quality standards are met.
Complete all required paperwork, document cleaning procedures, and populate electronic process orders following Good Documentation Practice (GDP).
Set up, operate, dispensing equipment, including assembling, disassembling, and cleaning tools and utensils according to safety protocols.
Verify room ventilation and safety equipment functionality, obtain and scan process orders, and confirm electronic balance calibration prior to starting any operation.
Verify bulk container, batch, and material numbers against process order specifications before use to ensure accuracy.
Actively participate in promoting a proactive safety culture, identifying hazards, and maintaining equipment, tools, and facilities according to 6S standards.
Safely operate powered and manual pallet and drum movers, and ensure proper disposal of waste according to both company and government regulations.
Participate in the testing and implementation of process and equipment changes to enhance efficiency and maintain an incident-free work environment.
Shift/Hours: Monday - Friday, 2:00pm-10:30pm or Sunday-Thursday 10pm-6:30am

Physical Attributes:

Wear appropriate protective gear, (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protection equipment "PPE" to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles.
Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl.
Lift and move up to 50 pounds unassisted.
Close vision, distance vision, color vision, peripheral vision, depth perception, and adjust focus.

Who You Are

Minimum Qualification:

High School Diploma or GED.

Preferred Qualifications:

Strong oral and written communication skills.
Strong attention to detail and problem-solving skills.
Strong math skills, including using the metric system.
Strong mechanical and technical aptitude

Pay Range for this position: $20/hour - $31/hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Megasys Technician (Santa Clara, California, US, 95054)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

EMD Electronics in Santa Clara, CA is adding Megasys Technicians to their team! MEGASYS® offers specialized services in managing gases, chemicals and slurries, where our technicians and engineers provide critical on-site support in semiconductor manufacturing environments.

Megasys Technicians will work with Engineers and Operations teams in a wafer fab cleanroom environment to ensure that existing semiconductor processing equipment is repaired and maintained in a timely manner.

Responsibilities:

Perform Safety Protocol check on all equipment before maintenance or service work
Assist with equipment upgrade or installation projects as needed
Maintain and improve equipment performance by providing timely repair and maintenance for critical products deliverables
Foster the adoption of continuous improvement as a way of life; creating a culture of execution
Handle the task of installing and upgrading tools to ensure the control of cost and delivery of quality work
Conduct thorough troubleshooting of equipment problems and report detailed findings
Analyze equipment malfunctions and failures and accordingly develop corrective actions
Maintain record of all equipment serviced, next due date, remarks for follow up, etc.
Work safely with hazardous chemicals and materials

Technicians are scheduled 12-hour compressed shifts, including nights and weekends.

Physical Attributes:

Lifting of a minimum of 50 lbs.
Working with toxic materials requiring the use of a respirator
Crouching, climbing a stepstool, reaching, twisting

Who You Are:

Minimum Qualifications:

High School Diploma or GED with 5+ years of experience in a semiconductor fab environment

Preferred Qualifications:

Associate Degree in Electrical Engineering, Mechanical Engineering, Electronics Engineering, or other Engineering or Technical discipline
Vacuum experience with UHV on PVD and/or CVD systems as well as ALD Chambers
Ability to debug systems with the help of schematics and manuals
Ability to work without supervision
Excellent troubleshooting and analytical skills
Familiarity with engineering drawings and the materials used for maintenance
Motivated, focused self-starter with high energy
Excellent computer skills

Benefits with our team include:

Comprehensive, paid, on the job training program that allows our employees to quickly learn critical technical skills to excel in this role and rapidly progress in their careers.
Excellent benefits including a starting vacation allowance of 3 weeks, 6% 401k match programs and medical, dental and vision benefit coverage on day one of employment!
Tuition assistance program

RSREMD

Pay Range for this position: $49-$75/hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

业务开发专家 (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Your Role

As Sales Development Expert – China, you will play a key role in driving new business growth by identifying and capturing emerging market opportunities across China's dynamic life science landscape. You will engage closely with key customers to foster collaboration and innovation, uncover new market segments, and maximize revenue and sustainable growth for Discovery Solutions business.

Key Responsibilities

Identify and develop new business opportunities across Pharma & Biotech, AGH, and I&T segments in China to drive sustainable growth for Discovery Solutions.
Build strategic relationships with key customers, scientific stakeholders, and ecosystem partners to enable long-term collaboration and value creation.
Conduct market research and customer needs analysis to identify emerging trends, unmet needs, and high-potential applications.
Collaborate with Commercial, Marketing, Technical, and global teams to translate insights into market development initiatives and go-to-market strategies.
Develop customer presentations, business proposals, and solution narratives aligned with customer priorities and scientific challenges.
Manage the sales development pipeline, ensuring timely lead qualification, follow-up, stakeholder alignment, and accurate CRM updates.
Provide customer insights, market intelligence, and competitive feedback to support product positioning and business strategy.
Ensure all activities comply with local regulations, industry standards, and policies.

Who You Are

PhD in Life Sciences, Cell Biology, Molecular Biology, Biochemistry, Pharmacology, Biotechnology, or related field.
Strong understanding of drug discovery and translational research workflows.
Biopharma R&D experience, 6+ years of hands-on experience in drug discovery, biologics development, cell biology, preclinical research, translational medicine or advanced research platforms.
Knowledge of emerging discovery technologies in one or more of Organoids / Organoid-on-chip, 3D cell culture, Stem cell biology, Cell & gene therapy, High-throughput screening and Advanced biochemical or molecular biology platforms
Experience in management consulting, strategic planning, business development, or market development.
Strong analytical and business case development skills.
Excellent presentation and stakeholder management capabilities.
Track records in strategic business development including build new markets, establish partnerships, create sales pipelines and launch new technology platforms.
Willingness to travel extensively within China (up to 50%) and occasionally internationally (must-have).

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Process Engineer, MSAT（シングルユース/統合プラットフォーム担当） _Life Science (Tokyo, Tokyo, JP, 106-0041)

Senior プロセスエンジニア– （シングルユース & 統合プラットフォーム）

ポジションの概要

MSAT分野の上級プロセスエンジニアとして、大規模生物製造プロセスの専門知識を活かし、特にタンジェンシャルフローフィルトレーション（TFF）、澄析、ウイルスろ過、そしてプロセス分析技術（PAT）に注力します。深い科学的知識と顧客志向のアプローチを通じて、技術サポートの高度化・思想的リーダーシップを推進し、日本のバイオ医薬市場における商業的成功を支援します。

主な職務内容

技術専門性とプロセスサポート

TFF、澄析、ウイルスろ過、PAT技術（例：ラマン分光分析装置、オートサンプリング）をカバーする大規模生物プロセスの専門家として活動
ProCellics™ ラマンアナライザー、Bio4C™ Raman Software、MAST® Autosampling Solution などを用いた高度な分析機器の開発・スケールアップ・導入を設計・実行
プロセス・機器に関するトラブルシューティング、根本原因分析、スケールダウン/スケールアップ試験の主導

CapEx投資・プロジェクトコンサルティング

顧客の技術・エンジニアリングチームと密接に連携し、CapEx投資計画や施設設計に対する助言と実務支援（質量収支計算を含む）を提供
科学的知識・モデリング・設計スキルを活用した意思決定支援

思想的リーダーシップ・顧客エンゲージメント

シングルユース系、PAT統合、先端機器に関するカンファレンス、トレーニング、ウェビナー等での発信
顧客と直接関わり、長期的な機器・プロセス戦略に沿った高品質なサポートを提供

商業・横断的コラボレーション

コマーシャル組織内の技術エキスパートとして代表・貢献
VOC（Voice of Customer）をR&D、フランチャイズ、商業チームと共有
顧客ニーズに対応するため、内部ステークホルダーと協働

その他

新規ライセンスイン化合物の毒性・安全薬理評価に関するグローバルビジネス開発への協働
学会・学術団体の年次総会への参加を通じた基礎医薬の情報収集
製品の基礎知識を臨床・医薬部門・商業部門へ提供

応募条件

バイオ製造・MSAT領域での実務経験（5年以上の実績が望ましい）
化学工学・生物工学・バイオテクノロジー等の学士以上
大規模生産・パイロット・ラボスケールでの経験
複雑な技術情報を多様な聴衆に伝える優れたコミュニケーション能力
グローバルなチームでの協働経験、英語での業務遂行能力

歓迎条件

プロセス制御（PLC/PCS等）、バイオファームの自動化・データインテグリティの実務知識
質量収支、PFD/P&IDの作成経験
複数のワークストリームと異なる利害関係者を統括したリーダーシップ経験

勤務地・雇用形態

勤務地：日本国内（本社または事業所）
雇用形態：正社員（試用期間あり）

待遇・福利厚生

経験・能力に応じた年収レンジ
各種社会保険、福利厚生、教育研修制度、フレックスタイム制など

求める人物像

顧客志向で戦略的思考を併せ持ち、統合ソリューションの実現を推進できる方
グローバルチームと協働し、異文化環境で結果を出せる方
複数部門を跨ぐプロジェクトを推進できる協働力とリーダーシップ

POSITION SUMMARY

The Senior Process Engineer (MSAT) serves as a subject matter expert in large-scale bioprocessing and biomanufacturing, with a specialized focus on Tangential Flow Filtration (TFF), clarification, virus filtration, and Process Analytical Technology (PAT). This role is responsible for delivering advanced technical support, driving thought leadership, and enabling commercial success through deep scientific expertise and customer-centric engagement across the Japanese biopharmaceutical market.

Position Title

Senior Process Engineer, MSAT – Single Use & Integrated Platform Solutions

Position Summary

The Senior Process Engineer (MSAT) serves as a subject matter expert in large-scale bioprocessing and biomanufacturing, with a specialized focus on Tangential Flow Filtration (TFF), clarification, virus filtration, and Process Analytical Technology (PAT). This role delivers advanced technical support, drives thought leadership, and enables commercial success through deep scientific expertise and customer-centric engagement across the Japanese biopharmaceutical market.

Key Responsibilities

Technical Expertise & Process Support

Act as a recognized expert in large-scale bioprocessing with emphasis on TFF, clarification, virus filtration, and PAT technologies (e.g., Raman spectroscopy analyzers, auto-sampling systems) across the full bioprocessing workflow.
Design and execute hands-on process development, scale-up, and implementation work for advanced analytical equipment (e.g., ProCellics™ Raman Analyzer with Bio4C™ Raman Software and MAST® Autosampling Solution) following best-practice protocols.
Lead troubleshooting, root-cause investigations, and scale-down/scale-up studies related to processes and equipment.

CapEx Investment & Project Consulting

Collaborate with customers’ technical and engineering teams to provide consultative and hands-on guidance for CapEx investment projects and facility design, including mass balance calculations.
Provide complex technical consultation to support clients’ capital investment decisions, leveraging scientific knowledge, modeling, and engineering design expertise.

Thought Leadership & Customer Engagement

Deliver thought leadership activities including conference presentations, customer trainings, and webinars focused on single-use systems, PAT integration, and advanced biomanufacturing equipment.
Build and maintain trusted partnerships with customers through direct engagement, offering high-level technical support aligned with their long-term equipment and process strategies.
Ensure high-quality customer communication via teleconferences and face-to-face meetings regarding equipment performance and process details.

Commercial & Cross-Functional Collaboration

Represent our company as a technical expert within the commercial organization and drive best-in-class capabilities to enable winning commercial outcomes.
Proactively capture and share Voice of Customer (VOC) insights with R&D, franchises, and commercial teams.
Collaborate with internal stakeholders including the commercial team and system manufacturing teams to address customer needs and ensure successful deployment.
Identify and capture commercial opportunities using sales effectiveness tools.

Key Accountabilities

Drive our product adoption, competitive conversion, and seeding wins to ensure business growth and market leadership in Japan.
Defend our position with customers and provide strategic understanding of customer programs and plans (e.g., technology transfer).
Share technical and process knowledge acquired from customers with internal teams to advance commercial opportunities into strategic impact.
Lead and influence cross-functional teams without direct authority to deliver customer-centric outcomes.

Scope of Collaboration

Internal: Regional Commercial Organization, Global TSS Peers, R&D, Franchise, Field Service, GSA, ISCO, Quality Teams.
External: Customers, Industry Forums & Associations, Conferences, Regulators.

Candidate Profile

Minimum Qualifications

B.S., M.S., or Ph.D. in Chemical Engineering, Biotechnology, or related engineering/science field.
Minimum 5 years of proven biopharmaceutical technical experience in manufacturing, pilot, and/or lab-scale environments.
Strong foundation in science/engineering with hands-on engineering design sense.
Substantial experience in scaling and implementation for biopharmaceutical processes.
Excellent written and oral communication to diverse audiences.
Commercial acumen with understanding of market needs/trends.
Open-minded, customer-focused, and effective team player with experience in multicultural, matrix organizations.
Essential competencies: customer centricity, strategic thinking, and an integrated mindset.

Preferred Qualifications

Technical mastery in one or more bioprocess applications, including process requirements, best practices, and industry standards.
Functional knowledge of process controls (PLC, PCS), biopharma automation, and FDA data integrity guidelines.
Experience with mass balance calculations, process flow diagrams (PFDs), and P&IDs.
Demonstrated leadership in multi-workstream projects with diverse stakeholders.

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

People Development Partner (Madrid, Madrid, ES, 28006)

Work Your Magic with us!

Your role: The People Development Partner is essential in shaping the talent development portfolio across our organization. This role serves as the main point of contact for learning consulting, facilitating alignment with a high-impact organizational culture and global learning initiatives. Responsibilities include developing and implementing learning strategies based on comprehensive needs analysis and managing the annual Learning & Development portfolio to align with business priorities. This role will be deeply involved in designing customized learning solutions, evaluating training program effectiveness while ensuring regulatory compliance, and collaborating with internal teams and external vendors to create and distribute training materials. This position provides a exciting opportunity to significantly influence employee development and enhance organizational effectiveness.

Who you are:
You have a minimum of 10-12 years of progressive experience in Learning & Development or Organizational Development, ideally within a global, matrixed environment.
You demonstrate end-to-end ownership of learning programs, including needs analysis, design of customized solutions, content development, vendor management, and impact evaluation.
You possess proven consulting experience with senior stakeholders, effectively translating business strategies into capability roadmaps and delivering multi-region projects on time and within budget.
You have strong learning technology and data fluency, with hands-on experience using LMS platforms (e.g., SAP SuccessFactors Learning) and virtual delivery tools.
You are skilled in using analytics and dashboards to report outcomes and drive continuous improvement in training initiatives.
You have experience in regulated, science-led industries, which is an advantage for this role.
You are adept at building and maintaining strong relationships with external trainers and vendors, ensuring alignment with the company’s culture and development goals.
You are proactive in responding to inquiries related to Learning & Development topics and customizing training requests from the business.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Tax Intern (Jakarta Timur, Jakarta Raya, ID, 13760)

Work Your Magic with us!

About The Role

Prepare withholding tax slips (Bukti Potong) and distribute them to vendors on a monthly basis.
Prepare nominative lists and prepaid for CIT purposes.
Assist to fixed asset tagging.
Assist in reconciling Witholding tax and VAT in every month.
Manage the e-Faktur and e-Bukpot systems for tax-related processes.

Who You Are

Accounting or Fiscal Major.
Fresh graduate or in last year semester.
Experience in handling e-Faktur and e-Bukpot systems would be a plus.
Proficient in processing data in MS Excel (Must).

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Account Manager (3년 이상의 경력, 분석경험, Life Science, 서울) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your role:

Sales Target & Business Delivery

Execute sales strategy and deliver monthly, quarterly, and yearly sales achievement for assigned territory and major accounts according to established sales policies.
Monitor sales performance, identify risks and opportunities, and take proactive actions to achieve or exceed targets.

Territory & Market Coverage

Expand market coverage within assigned territory by managing both direct customers and distributor-linked end customers.
Identify growth opportunities across Pharma, Biotech, CxO, QC, academia, research institutes, and emerging accounts where relevant to the territory.

Major Account Management

Develop and execute Major Account plans by analyzing current revenue structure, end-customer purchasing data, workflow context, and initiative-based growth opportunities.
Explain account business beyond run-rate by clarifying who bought, what they bought, for which workflow, and where additional growth can be created.

Workflow-based Solution Selling

Understand customer workflows and decision-making processes, and position our solutions to solve workflow challenges and reduce customer decision risk.
Move beyond product explanation by helping customers make the next decision through insight discovery, opportunity qualification, de-risking, and execution.

Initiative Execution & Growth Conversion

Convert strategic initiatives into measurable sales outcomes by linking customer needs, workflow opportunities, product portfolio, and execution plans.
Build customer-level action plans for relevant initiatives and track progress through pipeline, conversion, and revenue impact.

Forecast Accuracy & Data Discipline

Improve forecast accuracy by managing Base, Risk, Project, and Growth Driver assumptions with clear evidence.
Maintain customer information, opportunity records, purchasing insights, and relevant documents in SFDC and other appropriate databases.

Customer Relationship & Stakeholder Management

Build and manage positive relationships with customers and distributors.
Share sales leads, customer feedback, competitor information, and market insights with Marketing, Sales Specialist, Tech Service, Global/Regional stakeholders, and other relevant teams.

Commercial Execution & Risk Management

Respond to complex customer inquiries, negotiate within authority, manage strategic pricing discussions, and monitor receivables and credit conditions to minimize business risk.

Who you are:

Bachelor’s degree or above in Life Science, Chemistry, Biotechnology, Pharmacy, Business, or related fields.
Experience in analytical testing, QC, laboratory workflows, or relevant customer applications is preferred.
3 - 5 years of Sales experience in Life Science, Pharma, Biotech, Diagnostics, or related industries is preferred.
Experience in account management, territory management, distributor collaboration, workflow-based solution selling, or technical sales is preferred.
Fluent in Korean and proficient in English is preferred.

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Data Scientist (유관 경력 2년 이상, 영어 가능자, Python, 서울) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your role:

You want to develop AI solutions that have a tangible impact on our Electronics business?

Join our international team of digital experts as a Data Scientist! In this role, you will work on transformative use cases achieving measurable impact for our Integrated Supply Chain business functions. You will help translate business requirements into the right solution design and implement effective and robust tools on our internal Data & Analytics platform powered by Palantir Foundry and AWS. Throughout the use case journey, you will collaborate closely with other digital roles (product owners, data analysts, data engineers) and domain experts. As part of a broader team of Data Scientists within our department, and an active community of digital and AI experts across our company, there are many opportunities to grow and continuously learn from each other.

Who you are:

Bachelor or Master in Computer Science, Mathematics, Physics, Chemistry, Engineering, Operations Research, or a similar field
2+ years of professional experience applying Data Science outside academia, preferably in Supply Chain related fields
Proficiency in English is a must, knowledge of Korean, Japanese, or Mandarin is a plus
Good knowledge in a broad range of Data Science methods (for example, tabular data ML, time series forecasting, simulation & optimization, generative AI) with hands-on experience in some areas
Very good coding skills in Python with experience in collaborative development and rapid prototyping
Initial experience in building end-to-end applications with basic knowledge in cloud-based stacks for ML Engineering and CI/CD
Excellent communication skills to interact with diverse stakeholders and ability to present complex technical concepts to non-expert audiences, paired with a curious mindset and a spirit of taking initiative

<유의사항>

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글 크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Associate Director, Clinical Trial Lead (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Manage multiple studies, projects, and work streams with
high complexity, risk, impact and reach, typically Phase III and registrational/sourcing models.
Demonstrates skills in successfully leading large-sized global project teams in a matrix organization and directs, influences and motivates stakeholders from closely related areas and beyond, creating a positive working climate.
Leads the development of the clinical trial strategy while accountable for successful project execution and delivery of clinical operational budget, timelines and quality standards agreed upon by Governance Committees.
As a core member of the Clinical Operations Team and leader of the Clinical Trial Team, aligns clinical trial team with organizational goals, Clinical Operations Team, and/or Global Program Strategy Team.
Filters, prioritizes, analyzes and validates complex and dynamic information from a diverse range of external and internal sources to respond to operational and organizational challenges in a holistic manner to mitigate risks.
Exhibits Subject Matter Expert level understanding of multiple functions and functional processes. Familiar with and considers overall company strategy.
Acts as a senior advisor and mentor within the team and beyond and serves as best practice resource within own discipline or as technical functional teams or projects.
Ensure all study management activities will be completed in accordance with SOPs/WI, local regulatory guidance including ICH-GCP; audit leadership- interviewee & responses.
Contribute to non-study -related initiatives in addition to study assignments. Provide reports to senior management, including updates and timelines independently.
Demonstrates creativity and innovation to support projects from a strategic perspective, able to predict the result of action in advance and achieve goals.

Who You Are

Minimum Qualifications:

Bachelors degree with minimum 8 or more years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment
Minimum 7 years of in-depth experience in clinical trial management
Demonstrated experience in managerial responsibility

Preferred Qualifications:

Advanced degree desirable (MPH, MS, MA, MBA, PharmD); PM cPMP) desirable.
Proven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing study activities, from startup through final study report.
Experience in multiple Therapeutic Areas (oncology and immunology preferred)
Requires substantial to extensive professional experience in relevant disciplines and substantial project management experience. Required and experience in own discipline and beyond which may also require good market and competitor knowledge.
Strong leadership competencies and influencing skills.
Proven team dynamic knowledge and skills and ability to foster partnerships across projects and multidisciplinary teams.
Growing expertise in drug development, including some knowledge of interfaces and interdependencies of clinical development with other nonclinical & pharmaceutical development, regulatory, commercial/marketing)

Location: Billerica MA, Onsite

Travel: <10%; International and Domestic

Pay range for this position: $122,200 - $202,900

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

高级质量体系工程师 (Nantong, Jiangsu, CN, 226010)

Work Your Magic with us!

Your role：

Overall Objectives of the Position ：

The QS Engineer role will entail ensuring compliance with all regulatory and corporate requirements in support of regulatory（ISO, Chinese GMP, EU GMP and applicable agencies）and customer expectations, by carrying out quality management system and quality control tasks and activities.
Conduct internal and external audits of manufacturers, laboratories, supplier, etc. to assure compliance to cGMPs/ISO.
Resolve quality concerns and implement quality improvements with other department Managers, Supervisor to assure current methods, procedures or SOP’s meet current standards.
Comply with company EHS safety regulations and master skill of safety work and emergency rescue knowledge.

Main Tasks：

Develop and implement consistent processes and systems that assure quality, GMP and compliance. The main responsibility includes:

1) Prepare the quality related procedure according to company requirement.

2) Review and approve the SOPs.

3) Prepare the quality related procedure according to company requirement.

4) Follow up the progress of documentation system building up.

5) Build up the quality related electronic systems.

6) Participate in GMP training program in the plant to ensure the training management meeting the requirements of site and global.

Participate in training-need feedback and implement GMP training activities at the factory, enhancing employees' quality awareness and skills.
Responsible for preparing and handling of quality complaints and ensure timely closed loop handling of complaints.
Change control management
Responsible for factory quality certificate declaration cycle management and certificate system maintenance.
Organize customer audits and official certification audits to ensure that the company's quality management system continues to be effective and meets customer requirements and official certification standards.
Responsible for customer audit/ internal GMP/ISO audits and follow up of CAPA’s with internal department and make sure the audit closed in time.
Responsible for communicating external quality related matters to the factory to ensure effective communication and coordination with suppliers, customers and regulatory authorities.
Support for quality related tasks of transferring products from different giving sites to Life Science Nantong.
Complete other quality systems related work assigned by superior.
Be a valuable team member of Quality organization through close teamwork and cross functional/sectional activities.
Actively participate in quality culture building and quality related activities.
Actively report quality related events and participate in continuous quality improvement activities.

Who you are：

Bachelor or above
Minimum 10 years of working experience in pharmaceutical or GMP/ISO environment with some auditing experience.
In-depth knowledge of Quality Systems and related norms (e.g. ICH7/ 8/9/10, ISO 9000 series)
Good experience in product release and Good experience in deviations investigation and root cause analysis.
Experience of E-Quality System like Trackwise, SAP system is preferred.
Experience of lead customer audit is preferred.
Fluent in English. Good reading, writing and communication skills.
New project experience is preferred.
Can work under pressure, handle and overall manage multiple tasks.
Excellent communication, problem-solving, planning and organization skills.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Pflegefachkraft (m/w/d) Arbeitsmedizin (Gernsheim, Hessen, DE, 64579)

Entfalte das Besondere mit uns!

Pflegefachkraft (m/w/d) für Arbeitsmedizin

Ihre Rolle
In Ihrer Rolle arbeiten Sie in einer arbeitsmedizinischen Praxis mit angeschlossener Ambulanz am Standort unseres Unternehmens. Sie betreuen Mitarbeitende vor Ort und im Werk, führen eigenständig technische Untersuchungen, Vorsorgen und medizinische Vorsorgemaßnahmen durch und unterstützen Gesundheits-tage. Darüber hinaus planen und organisieren Sie medizinische Maßnahmen in der Ambulanz, übernehmen Verantwortung im Bestellwesen, Praxisqualitätsmanagement und Rechnungswesen, dokumentieren medizinische Daten sorgfältig und arbeiten eng mit dem Betriebsarzt sowie der weiteren Pflegekraft zusammen. Sie handeln vertrauensvoll im Sinne der Betriebs- und Patientensicherheit und kommunizieren kooperativ mit externen Ärztinnen/Ärzten.

Wer Sie sind
• Abgeschlossene Ausbildung als Gesundheits- und Krankenpflegerin, Pflegefachkraft (m/w/d) oder vergleichbar
• Mindestens 2 Jahre Berufserfahrung in einer Ambulanz oder auf einer Intensivstation
• Mindestens 1 Jahr Erfahrung in der Arbeitsmedizin oder idealerweise Fachkunde Arbeitsmedizin
• Sicherer Umgang mit MS Office
• Grundkenntnisse Englisch
• Freundliches, professionelles und serviceorientiertes Auftreten
• Organisationstalent, selbstständige Arbeitsweise und Teamfähigkeit
• Zuverlässigkeit, Diskretion und Verantwortungsbewusstsein

Bewerben Sie sich jetzt und werden Sie Teil eines Teams, das Neues entdeckt und die Menschheit voranbringt.

应用工程师-EL-上海 (Shanghai, Shanghai, CN, 201206)

Work Your Magic with us!

Key Individual Job description：

Work as technical sales to support Thin Film business, handle technical issues or projects by coordinating cross-functions.
Maintain communication with global semiconductor equipment companies to support the promotion with their new tools and materials.
Drive the adoption of alternative container parts of thin film materials to safeguard operations against international geopolitical alignment shifts.

Coordinate and manage the whole NBDs (New Business Development) and product tuning processes for key accounts, ensure to achieve POR position and drive to upgrade existing products for customer needs with risk management sense collaborating closely with Sales.
Work with global OEM team and customer application team to solve a range of straightforward problems through technical experience.
Work closely with local R&D team and product team to drive new product development and manufacturing to satisfy our customers‘ requirement.’

Focus on improving DOEs (Design of Experiments) and analytical skills to provide good technical service to the customers.

Provide accurate monthly report and contribute to Weekly Sales & Applications Meeting.
Monitor KPI in timely manner.

Key Skills/Knowledge：

Bachelor’s degree or above majored in Chemical, Physics, Material Science, electrical etc.
3–10-year experience, Semiconductor industry experience, and hands-on thin film processes, CVD/PVD/ALD etc.
Good coaching, interpersonal, and communications skill.
Skilled at SPC (Statistical Process Control), DOEs.
Literate in common software.
Ability to work in a matrix/cross-functional setting.
Willing to travel up to 50% of time.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

General Ledger Expert (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

Your Role:

You will drive operational excellence and financial integrity for your assigned entities.
Moving beyond routine execution, you will own complex accounting treatments, lead Month-End Close (MEC) orchestrations, ensure strict compliance with local and Group policies, and serve as a key business partner to local entity finance teams.
You will also act as a mentor to junior accountants and a catalyst for continuous process improvement.
Key Responsibilities
Financial Ownership & Reporting Excellence
Lead and orchestrate the Month-End Close (MEC) process for complex assigned entities, ensuring all activities are executed accurately and within strict deadlines.
Prepare, review, and analyze high-quality financial statements and management reports for both local entity finance and Group Accounting.
Perform deep-dive process analysis, variance commentary, and balance sheet reviews to provide actionable insights into financial health.
Complex Accounting & Master Data Governance
Manage high-complexity GL activities, including specialized accruals, complex payroll/benefits accounting, and sensitive journal entries.
Oversee and approve the reconciliation of critical, high-risk accounts, ensuring timely resolution of open items.
Act as a gatekeeper for GL master data integrity, ensuring compliance with global charting and reporting standards.
Audit, Compliance & Risk Management
Serve as the primary liaison for internal and external auditors (working with ABPs); prepare comprehensive audit schedules, pre-audit analyses, and resolve complex audit queries.
Ensure all processes strictly adhere to internal controls (SOX/ICFR), Group accounting policies, and local statutory regulations.
Process Optimization & Technology Driving
Identify, design, and implement process excellence initiatives (automation, standardization, and workflow simplification) to reduce MEC cycle times.
Lead User Acceptance Testing (UAT) and serve as a Subject Matter Expert (SME) for ERP upgrades, migrations, or GL-related system implementations.
Track, analyze, and report on team operational metrics and Key Performance Indicators (KPIs).
Stakeholder Management & Escalation Resolution
Act as the first point of escalation for complex operational issues, collaborating effectively with local entity CFOs/Finance Directors to drive swift resolutions.
Foster strong, consultative partnerships with cross-functional teams (ABP, Subledger, P2P, I2C, Treasury) to ensure end-to-end process alignment.
Leadership & Capability Building
Provide guidance, mentorship, and technical support to junior GL accountants, fostering a culture of continuous learning.
Develop and maintain up-to-date Standard Operating Procedures (SOPs) and training documentation.
Location: Manila Shared Service Center
Reports To: GL Team Lead / Manager

Who You Are:

Bachelors degree holder in finance, accounting or any related field required
Master’s Degree in Finance / Accounting or CPA accreditation highly preferred
At least 8 or more years of experience in General Ledger Accounting Operations
Profound accounting knowledge required (IFRS, GAAP, Tax)
Experience within a Shared Services Center preferred
Experience with Oracle and SAP
Fluent English language skills required
Willing to be based in BGC, Taguig
Amenable to work on a mid shift / night shift schedule (varying shifts every MEC and NONMEC)
With automation experience (VBA, other automation tools)
MS Excel Proficiency - Expert

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Data Scientist / Integrated Supply Chain_Electronics (Tokyo, Tokyo, JP, 106-0041)

Your role:

You want to develop AI solutions that have a tangible impact on our Electronics business?

Who you are:

Bachelor or Master in Computer Science, Mathematics, Physics, Chemistry, Engineering, Operations Research, or a similar field
2+ years of professional experience applying Data Science outside academia, preferably in Supply Chain related fields
Proficiency in English is a must, knowledge of Korean, Japanese, or Mandarin is a plus
Good knowledge in a broad range of Data Science methods (for example, tabular data ML, time series forecasting, simulation & optimization, generative AI) with hands-on experience in some areas
Very good coding skills in Python with experience in collaborative development and rapid prototyping
Initial experience in building end-to-end applications with basic knowledge in cloud-based stacks for ML Engineering and CI/CD
Excellent communication skills to interact with diverse stakeholders and ability to present complex technical concepts to non-expert audiences, paired with a curious mindset and a spirit of taking initiative

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

Associate Production Scientist - 12 Hour Night Shift (Sheboygan Falls, Wisconsin, US, 53085-2814)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

In this role responsibilities include, but are not limited to:

Independently and accurately sets up equipment to manufacture chemical compounds—including existing items, new product introductions, lost supplier replacements, takeovers, and custom orders—and executes corresponding analytical testing.
Ensures end-to-end quality throughout the manufacturing process, verifying that final products meet strict specifications, and thoroughly documents all data and observations per department guidelines.
Rechecks analytical results for any out-of-specification (OOS) data, selects alternative testing methodologies, and proactively escalates issues for management assistance when necessary.
Leads the department during supervisor absences or directs a small production group; dynamically balances responsibilities to shift focus toward chemical production or process improvement if supervisory duties exceed 10% of total time.
Assists with workforce scheduling and task assignments to ensure completion; leads small teams during shift changeovers to guarantee seamless, clean handoffs across all shifts.
Mentors and trains new hires while assisting with the cross-training of current personnel; creates and maintains detailed equipment calibration logs and employee training records.
Serves on specialized committees dedicated to driving continuous improvement across the department, site, or company, focusing on safety, quality, inventory, output, and cost reduction.
Reviews established operational protocols to suggest proactive changes for management review, maintains exemplary attendance/adherence to schedules, and executes miscellaneous tasks as assigned.
Shift/Hours: 12-hour night shift, 6:00 PM - 6:30 AM - 2/2/3 schedule (M/T on, W/R off, F/S/S on, M/T off, W/R on, F/S/S off, repeat).

Physical Attributes:

Wear appropriate PPE.
Lift up to 50 lbs.
Use close vision, distance vision, color vision, peripheral vision, depth vision and adjust focus.
Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, or crouch for long periods of time.

Who You Are

Minimum Qualifications:

Bachelor's Degree in Biology, Chemistry or other Life Science discipline.
1+ years of experience in a laboratory setting in chemical production.

Preferred Qualifications:

Experience with ISO and quality systems.
Experience with reading and understanding written protocols.
Strong problem solving and equipment troubleshooting skills.
Strong oral and written communication skills.

Experience with chemistry and math.

Strong mechanical and technical aptitude.

RSREMD

Pay Range for this position: $27/hr - $48/hr.
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Sales Director BioMonitoring - Pharmaceutical Industry, West & North Europe (f/m) (Guyancourt, Yvelines, FR, 78280)

Work Your Magic with us!

Your role:

As Sales Director for West & North Europe (f/m), you will lead the commercial strategy for BioMonitoring solutions that help pharmaceutical manufacturers protect patients and bring life-saving medicines to market. You will manage and inspire a high-performing team of Field Sales Specialists and Line Managers across a strategically important region.

You will own short- and long-term sales targets, commercial KPIs, forecasting accuracy, and sustainable revenue growth. By setting clear goals and providing focused coaching, you will turn performance ambitions into measurable results. You will build a culture of accountability, customer focus, and continuous development that attracts, retains, and grows exceptional talent. You will create career development plans that strengthen the team today while preparing future leaders for tomorrow.

As a member of the wider EMEA leadership community, you will shape commercial strategy, tactical planning, and local execution. You will turn market intelligence into action and unlock synergies across Advanced Solutions, Supply Chain, Customer Excellence, distributors, and local commercial teams. You will cultivate trusted relationships with senior pharmaceutical customers and ensure seamless coordination across regional and global accounts.

This is an opportunity to combine sales leadership, scientific expertise, and strategic influence to build lasting commercial impact.

This is a field-based position that may be filled in France or in other strategic European markets, such as the United Kingdom, Ireland or the Benelux region.

Who you are:

You have at least five years of experience leading commercial teams in the pharmaceutical microbiology quality-control market, with a strong understanding of customers, buying cycles, and the competitive landscape.
You have a proven track record of delivering sales growth, expanding margins, and managing commercial performance through clear targets, rigorous forecasting, and decisive action.
You are an inspiring people leader who coaches actively, develops talent, promotes from within, and creates a culture where high standards and collaboration go hand in hand.
You hold a Master's or PhD in a Life Science discipline and/or a Master's degree in Business, enabling you to connect scientific value with commercial strategy.
You build credible, long-term relationships with senior pharmaceutical stakeholders and know how to align distributors and cross-functional partners around shared priorities.
You bring a hands-on, customer-centric mindset and are willing to step in, solve problems, and support your team when it matters most.
You communicate fluently in business English and in at least one relevant regional language, such as French, Dutch, or another local language.
You are comfortable travelling regularly across the region and hold a valid driver's license.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Upstream Field Application Scientist (Hyderabad, Andra Pradesh, IN, 500003)

Work Your Magic with us!

Your Role:

As part of the Customer Application (CA) team within Process Solutions, you are responsible for offerings under Process Materials and Cell Culture Franchise (e.g., cell culture media, cell lines, biopharma materials) and Single-Use and Integrated Platform Solutions Franchise (e.g., upstream perfusion systems).

Act as the technical expert for upstream process development and biomanufacturing, partnering with customer’s technical teams to deliver consultative guidance and hands-on support.
Design, execute, and validate process development, scale-up and implementation studies with customers, aligned with best practices; translating customer needs into technical outcomes.
Communicate findings clearing through reports, meetings, and training; build trusted customer relationships and support technical onboarding.

Key Responsibilities:

Technical expertise and thought leadership

Act as subject matter technical expert in commercial and technical discussions; drive best-in-class capabilities and thought leadership to enable desired outcomes and impact.
Represent the company as subject matter technical expert and industrial events; delivery thought leadership activities
Apply scientific knowledge, experimental designs and hands-on process design to address complex customer needs and troubleshooting.
Capture technical findings and contribute to case studies, references and innovation roadmaps.
Maintain up-to-date technical collaterals, catalogs and point of views; track competitor activities and customer insights to influence portfolio positioning and strategy.
Deliver training to customers and internal teams on upstream bioprocesses and our upstream innovative offerings.
Develop and share customer-facing materials to support sales enablement.

Customer engagement and value realization

Engage customers on challenges, trends and activities around upstream bioprocesses.
Provide technical consultative guidance, technical training and best practice recommendations to accelerate adoption and implementation
Support, nurtures and helps to close sales opportunities

Collaborations with internal stakeholders

Partner with upstream sales development experts and account managers for customer centric upstream buying journey.
Coordinate with franchise, R&D and other internal stakeholders to address customer needs and roadmap impacts.
Serve as escalation point for technical issues during evaluation, adaptation, scale-up and implementation; drive timely resolution and customer satisfaction.
Propose internal and external process improvements (simplify and act with urgency) and contribute to technical programs and seminars
Proactively identify and capture opportunities using sales effectiveness tools
Support M Lab Collaboration Center activities

Who You Are:

B.S., M.S. or PhD in Biochemistry, Biotechnology, or a related science or engineering discipline
6+ years’ experience in biopharmaceutical technical roles in upstream bioprocesses, in lab, pilot and/or manufacturing scale environments. Extensive years of proven experience and knowledge in upstream bioprocesses.
Technical mastery in upstream bioprocesses; strong hands-on upstream cell line, media and process development, scale-up and implementation studies.
Proven abilities to translate customer needs into technical outcomes; proficient in data analyses and design of experiments.
Excellent written and oral communication; capable of delivering reports, presentations and training to diverse audiences including senior internal stakeholders and management.
Commercially astute; understands market needs and trends, processes and how technical solutions map technical and business impact.
Collaborative; effective team player, in a cross-functional, multicultural matrix environment; strong stakeholder management.
Fluent in English, and local language, where applicable

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Associate Director, Statistical Programmer (Hyderabad, Andra Pradesh, IN, 500003)

Work Your Magic with us!

Statistical programming sits at the heart of clinical evidence generation — and in this role, you will be instrumental in turning complex data into the high-quality deliverables that advance medicines from development to patients. As a Statistical Programmer at the Senior or Principal level, you will contribute to and lead statistical programming activities across one or more clinical trials and global project sub-tasks within clinical development programs. Working within a matrix organization and under the oversight of a Project Statistical Programmer, you will coordinate programming workstreams, provide oversight of Contract Research Organization (CRO) activities, and ensure the timely, accurate delivery of analysis datasets and outputs in line with regulatory standards. You will apply and deepen your expertise in CDISC SDTM and ADaM standards, contribute to integrated databases and submission-ready deliverables, and bring a proactive, solutions-oriented mindset to complex technical and operational challenges. Beyond project delivery, you will play an active role in advancing best practices and process improvements within the global Biostatistics function — sharing knowledge, guiding colleagues, and helping to shape the programming standards that underpin the organization’s clinical pipeline.

Who You Are:

- You hold a Bachelor’s or Master’s degree in a numerate discipline — such as Statistics, Mathematics, or Computer Science — or equivalent professional experience.
- Location - Bangalore OR Hyderabad
- You bring 8+ years of directly relevant statistical programming experience within clinical development at a pharmaceutical, biopharmaceutical, or CRO environment.
- You have hands-on experience working with SDTM datasets and creating ADaM datasets and specifications — and at the more senior level, integrated databases for regulatory submissions.
- You are very proficient in R and demonstrate solid knowledge of ICH and CDISC SDTM and ADaM standards, with the ability to interpret and apply relevant regulatory guidance from ICH, FDA, and EMEA.
- You have a sound understanding of drug development processes and the interfaces between statistical programming and other clinical development functions, including familiarity with relevant therapeutic areas and regulatory submission requirements.
- You work effectively in international, multicultural, and cross-functional matrix teams, with strong organizational, communication, and interpersonal skills and the ability to manage multiple priorities with accuracy and attention to detail.
- You demonstrate leadership capability — whether coordinating programming activities, guiding colleagues on processes and regulatory requirements, or driving project commitments with composure and clear decision-making under pressure.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Sub-Fab Equipment Specialist (Fremont, California, US, 94538)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

MEGASYS® offers specialized services in managing gases, chemicals and slurries, where our technicians and engineers provide critical on-site support in semiconductor manufacturing environments.

In the Subject Matter Expert (SME) role, you will provide technical expertise and support to the Total Gas & Chemical Megasys (TGCM) Team and customer. This role ensures the safe and efficient operation of gas and chemical distribution systems, offering solutions and training to enhance customer service and operational effectiveness.

Join us in delivering exceptional service and driving flawless execution. If you’re ready to embark on an exciting career in the semiconductor industry and are open to travel and mobility, we have opportunities available nationwide. We seek individuals who are adaptable and willing to travel, with potential relocation options for the right candidates. We would love to hear from you!

Key Responsibilities:

Train and develop technicians, evaluating performance and improving skills
Identify and implement technical solutions to improve equipment performance
Evaluate business operations and provide expert consultation
Develop and verify technical documentation, including user guides and training materials
Lead the development and implementation of technical solutions
Diagnose and resolve equipment alarms, supporting customer modifications as needed
Prepare and conduct onboarding and continuous training programs

Physical Attributes:

75% of walking throughout the facility (3-5 miles per day)
Climbing of ladders up to 12-foot-tall (utilizing fall protection)
Basic lifting (up to 40lbs)
Bending of the knees and overhead reaching

Schedule:

Monday-Friday 7am-3:30pm

Military Veterans:
MEGASYS® is a military-friendly employer that values the skills obtained through military teamwork. Our culture and company value the leadership and focus on safety that is obtained from your service. Veterans from any branch or MOS with hands-on mechanical skill sets are encouraged to apply.

Who You Are:
Minimum Qualifications:

High School Diploma or GED
5+ years of experience in a semiconductor, chemical or other manufacturing setting
1+ years of experience with BCD/PCD and gas-related equipment
1+ years of experience with gas and/or chemical delivery systems in ultra-high purity operation

Associate Degree in Chemistry, Mechanical Engineering, or other technical discipline
2+ years of experience in a semiconductor, chemical or other manufacturing setting
1+ years of experience with BCD/PCD and gas-related equipment
1+ years of experience with gas and/or chemical delivery systems in ultra-high purity operation

Preferred Qualifications:

Bachelor’s Degree in a Chemistry, Mechanical Engineering, or other technical discipline
5+ years of experience working in the semiconductor industry
Proficiency in MS Office Suite

Benefits with our team include:

Comprehensive, paid, on the job training program that allows our employees to quickly learn critical technical skills to excel in this role and rapidly progress in their careers.
Excellent benefits including a starting vacation allowance of 3 weeks, 6% 401k match programs and medical, dental and vision benefit coverage on day one of employment!
Tuition assistance program

RSREMD

Pay range for this position: $35-$53/hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

应用销售专家-药物早研产品，北京 (Beijing, Beijing, CN, 100016)

Work Your Magic with us!

Sales Specialist — Discovery & Early Research Workflow

We are looking for a Sales Specialist to drive business growth for our discovery & early research workflow solutions in Beijing. This role will focus on products and solutions related to chemical synthesis, bioactive small molecules, metabolism assay kits, retrosynthesis software and integrated early drug discovery workflows.

The successful candidate will be responsible for developing new business opportunities, managing strategic accounts, delivering technical seminars and consultations, and positioning innovative workflow solutions to customers in pharma, biotech, CRO, academia and research institutions.

Key Responsibilities

Drive sales growth and business development for discovery and early research workflow products.

Promote portfolios including chemical synthesis products, bioactive small molecules, metabolism assay kits and retrosynthesis software.

Develop new business opportunities in pharma, biotech, CRO, academic and research accounts.

Deliver targeted seminars, workshops, product presentations and one-on-one technical consultations.

Understand customer workflows across chemical synthesis, biochemical assays, metabolism studies and early drug discovery.

Position workflow-based solutions to address customer pain points and support business conversion.

Build multi-level relationships within strategic accounts and collaborate closely with local and regional account managers.

Gather market intelligence, monitor competitive activities and support strategic product initiatives.

Requirements

Master’s degree or PhD preferred in chemistry, organic chemistry, medicinal chemistry, biochemistry, life sciences or related fields.

3–5 years of experience in sales, business development, technical sales, application support or solution selling in pharma, biotech, CRO, life science or research-related industries.

Technical understanding of one or more areas: chemical synthesis, biochemical assays, cell/protein research, metabolism studies, ADME/DMPK, drug discovery or retrosynthesis software.

Strong communication, presentation, negotiation and consultative selling skills.

Ability to understand customer workflows and translate technical value into business opportunities.

Self-motivated, result-oriented and able to work independently.

Fluent in Chinese and English.

Advanced computer skills – Microsoft Outlook, Excel, Word, PowerPoint.

Willingness to travel domestically.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Maintenance Mechanic - 3rd Shift (Indianapolis, Indiana, US, 46268)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Under general supervision, the mechanic independently overhauls, troubleshoots and repairs machinery, equipment and the facility at large as well as installing new equipment. The Mechanic shall be required to perform work in one or more of the following manufacturing areas: component preparation, compounding, filling, capping, packaging, and machine shop. In this role you will work with the area Production Supervisor to determine work and repair priorities that may impact their operation.

3rd Shift: Sunday - Thursday 11pm - 7:30am.

Responsibilities include but are not limited to:

Performs Preventive maintenance on equipment and plant systems.
Performs setup and installation of equipment and training for production employees on machine operation.
Diagnoses malfunctions of production equipment and utility systems and makes necessary repairs.
Completes work orders, special projects, and other duties as assigned.
As a part of the employee’s job requirements, the employee may be required to handle waste including hazardous waste.

Physical Attributes:

Lift and/or move up to 50 pounds.
Use ladders regularly.

Who You Are:

Minimum Qualifications:

High School Diploma or GED.
5+ years of work experience in electrical, pipe fitting, machinist, or other trade.

Preferred Qualifications:

Experience interpreting drawings and schematics.
Strong verbal and written communication skills.
Must be proficient in maintaining documentation.
GMP pharma experience.
Strong mechanical and electrical skills; repairing, diagnosing, and troubleshooting.
Boiler and/or steam experience.
Documentation and CMMS experience.

Pay Range for this position: $70,600 - $111,000 / year

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Director, Real World Evidence Scientist (Oncology) (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

Your Role:

The Director, Real World Evidence Scientist is a highly experienced scientific expert who develops and owns the RWE strategy at the program(s) level, leads PRWE and CMS cross-functional initiatives, and interfaces directly with Global Program Teams (GPTs) and sub-teams. This role provides deep scientific leadership for the RWE strategy for one complex/high-priority product or group of products — leading and executing end-to-end RWE activities, providing expert oversight of studies, and representing our organization externally — without formal line management responsibilities.

Location: This position located in Billerica, MA with a hybrid (3x/week in office) schedule.

Key Responsibilities:

Develop and own the RWE strategy at the program(s) level; interface directly with Global Program Teams (GPTs) and the subteams to integrate RWE into clinical development and regulatory strategies.
Lead PRWE and CMS cross-functional initiatives
Ensure planning and management of outsourced deliverables are effectively performed to the highest quality and in a timely manner.
Ensure objective results interpretation and adequate internal communication in support of informative decision making at GPT, PST, and Senior Management level.
Lead and execute the RWE strategy for assigned product(s) without supervision. Provide leadership in the development of RWE strategy in Integrated Evidence Plans (IEPs) in close collaboration with cross-functional teams; ensure RWE generation needs are included in the IEP and secure budget for strategy execution.
Collaborate closely with development team functions (GPS, GRA, GMU, GVD, GCD) and commercial teams (Market Access, Marketing, GVAP) as well as within PRWE.
For one complex/high-priority product or group of products: adequately and timely design, plan, initiate, monitor, and finalize NIS (including protocol development and study report writing); peer review key documents (protocol, study report, briefing books for Health Authorities).
Ensure the identification and selection of fit-for-purpose RWD sources for given research questions; contribute to the RWD strategy of the assigned therapeutic area.
Solves complex or novel problems by analyzing research findings. Interprets critical internal or external business issues and develops innovative solutions to help sustain competitive advantage
Represent PRWE in cross-functional governance bodies; direct the RWE contribution for publications.
Represent Company in external interactions requiring RWE expertise; represent PRWE at international conferences and consortia, contribute to peer-reviewed publications, conference presentations and scientific communications.
Research and implement state-of-the-art RWE methodology; develop RWE standards focusing on efficient study designs to support sound R&D decision making.
Lead process improvement to gain efficiency in current SOPs/WIs, and develop new ones as needed; promote lean concepts; encourage and foster collaboration at all levels within PRWE.
Ensure methodological intelligence on appropriate regulations, guidance documents, and methodological developments; provide sound and up-to-date recommendations to NIS conduct.
Handle interactions with Health Authorities and manage difficult issues with limited supervision; represent the company during approval processes including defense of RWE aspects with regulatory agencies.
Provide high quality input to critical review assessments, expert statements, publications, and study proposals from internal and external sources.
Develop new processes and SOPs relevant for PRWE at Company and customize existing ones according to lean concepts.
Manage budget associated with program-level RWE projects; maintain overview of budget spend by functional and program budget.
Act as scientific mentor for less senior scientists within the function.

Who You Are:

Minimum Qualifications:

Master's or PhD in Epidemiology, Public Health, Health Economics and Outcomes Research, or Biostatistics.
8-10 years of RWE experience in CRO, or pharmaceutical/biotechnology industry settings.
Demonstrated strong experience in studies based on secondary data use (claims, EMR, registries) across different healthcare environments (Europe, US, Asia).
Experience in studies based on primary data collection.
Knowledge of federated data networks (CPRD, Optum, IQVIA, TriNetX) and OMOP CDM or FHIR data standards.

Preferred Qualifications:

Strong methodological skills; medical/pharmacological/pharmacovigilance knowledge.
Experience in project management as a global RWE leader, preferably in multi-cultural environments.
Strong expertise in drug development, including interfaces and interdependencies of clinical development with other functions.
Experience in global regulatory and/or payer submissions and interactions.
Experience in at least one key therapeutic area (Oncology, Neurology & Immunology).
Excellent understanding of the regulatory environment and standards.
Track record of thought leadership (publications, conference presentations, advisory roles).
Experience with AI/ML applications in RWE, including NLP.
Experience with patient-reported outcomes (PROs) and health technology assessment (HTA).
Experience in budget oversight and vendor management in global organizations.
Knowledge of health equity and DEI principles in evidence generation.
Involvement in industry working groups, regulatory advisory committees, or professional society leadership

Pay Range for this position: $172,000 - 258,000
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

#LI-hybrid

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Microbiology Supervisor (QC Lab) (St. Louis, Missouri, US, 63118-3306)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

The Microbiology Supervisor leads the GMP Quality Control Microbiology department, ensuring full compliance with ICH Q7 and 21 CFR regulations for active pharmaceutical ingredient (API) testing. Key responsibilities include overseeing microbiological test methods, method validations, and tech transfers; managing OOS/OOT investigations, deviations, and CAPAs; and conducting routine training on aseptic techniques and testing procedures.

Supervise, manage, and develop a QC Microbiology team of 8–10 employees, holding full accountability for meeting business quality performance metrics and KPIs
Oversee the Environmental Monitoring Program and the Bioburden and Endotoxin Testing laboratories
Manage and prioritize laboratory testing schedules to ensure all products are released in a timely manner
Develop and implement programs to establish and maintain quality systems and product/service standards, while driving quality improvement initiatives and establishing policies, procedures, and methods to enhance product, material, component, process, and operational quality
Support and participate in client and regulatory audits
Interface with internal and external customers on a regular basis to communicate project status, resolve issues, and implement methods, techniques, and evaluation criteria for products and processes
Perform other duties as required by management

Who You Are

Minimum Qualifications:

Bachelor's Degree in Microbiology, Biochemistry, Biology, or other Life Science discipline
3+ years of experience as a quality control manager, supervisor, or lead

Preferred Qualifications:

Master’s degree in a Life Sciences discipline
Experience as a Quality Control Supervisor or Manager at a Life Sciences organization
In-depth knowledge of health authority (FDA, EMA) expectations for pharma/biotech bulk and finished product manufacturing, alongside microbiological testing requirements
Proficiency with analytical instrumentation and laboratory software
Comprehensive knowledge of ICH Q7, 21 CFR 210/211, USP, and EP pharmacopeia requirements
Proven experience working in a highly matrixed organization, preferably within a GMP manufacturing environment
Strong written and verbal communication skills, with a demonstrated ability to translate complex issues into straightforward, succinct explanations
Advanced root cause analysis and problem-solving skills
Strong computer skills, including proficiency in word processing and Quality Systems databases
Subject matter expertise in aseptic principles and practices
Strong understanding of microbiological methodology and laboratory techniques, specifically USP <85>, USP <61>, and USP <62>

Salary range for this position: $77,400 - $116,100 annually

技术员 (Suzhou, Jiangsu, CN, 215021)

与我们携手施展你的超能力！

探索未知、打破壁垒、勇于发现，你准备好了吗？你有宏图大志正待实现，我们同样雄心勃勃。我们遍布全球的员工热爱科技创新，以医药健康、生命科学和电子科技领域的解决方案，切实改善人类生活。我们怀揣远大梦想，热忱关爱员工、客户、患者和人类居住的这颗星球。因此我们一直在寻找永葆好奇心的你，与我们一路同行、敢想敢做，把不可能变为可能！

在电子科技，我们所做的一切都是为了成为众多企业推进数字化生活的幕后推手。我们致力于作为值得信赖的供应商，为电子、汽车和化妆品行业提供高科技材料、服务和特种化学品。我们培养了一个全球协作的组织，我们的员工热情好胜、秉持客户至上、充满好奇心且行动敏捷。我们齐心协力突破科学的极限，为客户创造更多可能。

职位描述：

根据安排进行生产相关作业。
配合班长管理生产现场的5S和安全工作
根据生产指令进行适时生产，包括1#栋所有作业：如光刻胶和化学品的调制、充填、包装、包材准备等。
及时发现并解决生产中出现的问题。
提供合适的改善提案。
维护并提高现场的5S和安全控制水平。
完成班长安排的其他工作。

任职要求：

高中及以上学历
1年以上相关工作经验或化工技校应届毕业生
有铲车驾驶证优先
仔细认真，有高度的责任心和团队意识

我们提供的机遇：我们是一群充满好奇心的伙伴，有着不同的背景、视角和生活经历。我们相信，多元化将推动卓越与创新，从而提升我们在科技领域的领导力。我们致力于为所有人创造平等的发展机会，让每个人都能按照自己的节奏成长。加入我们，共同打造一个具有包容性与归属感的文化，影响数百万人，助力每个人推动人类进步！

立即申请，加入这个致力于点燃创新火花，提升人类福祉的团队！

Technicien Métrologue f/h (Saint-Ismier, Auvergne-Rhône-Alpes, FR, 38330)

Exprimez votre talent avec nous !

Toutes les activités du secteur Electronics visent à nous aider à atteindre notre objectif : être l’entreprise qui soutient toutes les autres en faisant progresser la vie numérique. Nous nous engageons à être le fournisseur de confiance de matériaux, de services et de produits chimiques spéciaux de pointe destinés aux industries de l’électronique, de l’automobile et des cosmétiques. Notre organisation de collaboration mondiale est composée d’individus qui ont la passion de gagner, placent le client au cœur de leurs actions, exploitent sans cesse leur curiosité et agissent rapidement. Ensemble, nous repoussons les limites de la science afin d’élargir le champ des possibles pour nos clients.

Votre rôle

Au cœur de nos opérations de fabrication, vous jouez un rôle déterminant dans la qualification et la validation des équipements de production. En appliquant des techniques de métrologie optique avancées, notamment l'interférométrie et la réflectométrie, vous garantissez que chaque machine répond aux exigences de performance définies dans les cahiers des charges, en mesurant avec précision la justesse et la dispersion des équipements. Vous utilisez et gérez des étalons de calibration afin d'assurer la traçabilité et la fiabilité des mesures effectuées. Lorsque des dérives sont détectées, vous les analysez avec rigueur et, dans la mesure du possible, proposez des solutions correctives adaptées. Vous rédigez et mettez à jour des procédures techniques claires, accessibles à l'ensemble des équipes concernées. En collaboration étroite avec les équipes de production et d'ingénierie — aussi bien côté matériel que logiciel — vous contribuez activement à la fiabilité, à la qualité et à l'amélioration continue de nos procédés industriels.

Qui vous êtes

Vous avez une expérience ou une formation de type Technicien en métrologie, optique, physique appliquée ou dans un domaine technique équivalent.
Vous maîtrisez les techniques de métrologie optique, en particulier l'interférométrie et la réflectométrie.
Vous êtes à l'aise avec les outils statistiques de base (mesure de justesse, dispersion, analyse de dérive).
Vous avez été exposé à l'industrie technologique, idéalement dans le secteur des semi-conducteurs ou de l'électronique.
Vous savez utiliser des étalons de calibration et rédiger des procédures techniques avec rigueur.
Vous communiquez efficacement en français et en anglais professionnel dans un environnement international.
Vous faites preuve d'autonomie, d'un fort esprit d'équipe et d'une sensibilité aux normes de qualité et de performance.

Postulez dès maintenant et devenez membre de notre équipe dont la vision est de stimuler les découvertes pour élever l'humanité !

Senior Associate (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Your Role:

Key responsibilities will include:

Batch Operations: Follow the Master Production Record (MPR) and perform batch operations using PLC/SCADA systems.
Data Management: Accurately record critical information (ingredients, weights, temperatures) into the database during batch execution, ensuring compliance with regulations.
Troubleshooting: Identify and resolve issues related to production equipment and processes effectively.
Safety Compliance: Observe and adhere to all safety and quality regulations, reporting any accidents or safety violations.
Process Improvement: Assist in planning and enhancing processes and product quality.
Team Collaboration: Work collaboratively with team members to ensure the successful completion of the production process.
Physical Requirements: Meet the physical demands of the role, including extended periods of walking, standing, or sitting, lifting heavy objects, climbing, crouching, operating tools, and wearing appropriate safety gear.

Who You Are:

Basic/Minimum Qualifications:

Experience: 3 to 7 years in a similar operational role.
Must-Haves: Manufacturing or Production, PLC or Scada, Troubleshooting
Nice-to-Haves: Safety Certification.
Education: Diploma/ B. Tech in Chemical Engineering.
Technical Skills: Proficiency in operating PLC/SCADA systems.
Data Accuracy: Ability to accurately record and input data into databases.
Regulatory Knowledge: Familiarity with safety and quality regulations in a production environment.
Preferred Qualifications:
Documentation Skills: Strong documentation skills in line with Good Manufacturing Practice (GMP) requirements.
Troubleshooting Ability: Excellent problem-solving skills for addressing production equipment and process challenges.
Team Player: Ability to work collaboratively in a team setting.
Communication Skills: Effective verbal and written communication abilities.
Process Improvement Experience: Demonstrated experience in initiatives aimed at improving operational processes.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Platform Engineer/资深平台工程师 (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

About the role: You will turn architecture into working production paths: implement integrations, automate quality and operations, harden day-2 operability, and help grow internal engineering capacity. You will be a key technical counterpart to architects, security, and external partners throughout design, delivery, and run.

Your role:
• Design, implement, and maintain platform foundations (integration layers, identity hooks, environments, automation)
• Improve reliability through CI/CD, infrastructure-as-code, monitoring, alerting, and operational runbooks
• Build reusable engineering assets (templates, test harnesses, smoke/E2E checks, quality gates) that reduce manual effort and create repeatable evidence of readiness
• Partner with architects and vendors to harden production paths, clarify acceptance standards, and improve day-2 operability
• Troubleshoot complex cross-component issues spanning applications, APIs, data services, and cloud infrastructure
• Contribute to secure-by-default engineering practices (secrets management, access control, auditability).
• Support environment readiness and production handover for platforms delivered with external partners.
• Coach junior engineers/interns and help grow internal engineering capacity.

Who you are:
• Solid experience (typically 6+ years) in platform, backend, and cloud engineering
• Hands-on experience with China cloud providers is required
• Practical skills with cloud services, APIs, automation, and observability tooling
• Experience with identity/access integration and secure service-to-service communication
• A production mindset: quality gates, incident readiness, maintainability, and clear run documentation
• Strong debugging and collaboration skills with architects, security, and external partners
• Comfortable working in a global–local matrix; English and Mandarin required.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Megasys Maintenance Technician (Austin, Texas, US, 78754-1908)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

MEGASYS® at EMD Electronics is seeking Maintenance Technicians in Austin, TX.

MEGASYS® offers specialized services in managing gases, chemicals and slurries, where our technicians and engineers provide critical on-site support in semiconductor manufacturing environments.

In the MEGASYS® Maintenance Technician role, you will be performing daily maintenance on a variety of equipment that ensures consistent supply of chemicals and gases necessary for producing semiconductor chips used in various electronic devices. This position provides a challenging and rewarding opportunity for individuals eager to contribute to a dynamic and expanding business.

In this role, you will work full-time, ensuring 24/7 operations and handling periodic service calls during your shift. Your responsibilities include maintaining advanced gas and chemical blending equipment, chemical reprocessing, and life safety systems. You will perform repairs on distribution system equipment and address chemical system leaks. Collaborating with your team, you will focus on key performance metrics related to safety, quality, and productivity. Your work's reliability and accuracy will enhance team performance, and you'll provide high-level technical support during troubleshooting and maintenance activities.

Join us in delivering exceptional service and driving flawless execution. If you’re ready to embark on an exciting career in the semiconductor industry and are open to travel and mobility, we have opportunities available nationwide. We are seeking individuals who are adaptable and willing to travel, with potential relocation options for the right candidates. We would love to hear from you!

Key Responsibilities:

Conduct daily maintenance of chemical, gas, and slurry distribution systems
Write technical documentation for process development
Ensure accurate documentation of all activities performed
Read, interpret, and create Piping and Instrumentation Diagrams (P&IDs)
Execute technical repairs on equipment

Physical Attributes:

75% of time walking throughout the facility (3-6 miles per day).
Climbing ladders up to 12 feet tall utilizing fall protection.
Lifting up to 40lbs.
Bending of the knees and reaching overhead.

Military Veterans:

Who You Are:

Minimum Qualifications:

High School Diploma or GED
3+ years of industrial maintenance or trades (e.g. plumbing, welding, oil field work, etc.) work experience

Preferred Qualifications:

Completion of trade/vocational school (e.g. Plumbing, Electrical, etc.) or Associate Degree in a technical discipline (e.g. Chemical Engineering, Automation Systems, etc.)
Proficiency with PLCs, to include troubleshooting
Extensive experience with startup and commissioning
Experience with installation and maintenance of plumbing systems
Experience in continuous improvement
Ability to read P&IDs and PFDs
Familiarity with gas and chemical delivery systems in ultra-high purity operations
Previous safe work practices and experience in lockout, tag out projects
Technical aptitude to identify parts needed for a repair
Strong overall mechanical aptitude
Ability to read gauges, understand units of measure and use precision measuring equipment
Understanding materials of construction and chemical compatibility
Proficient with MS Office Suite
Excellent teamwork and interpersonal skills

Benefits with our team include:

Comprehensive, paid, on the job training program that allows our employees to quickly learn critical technical skills to excel in this role and rapidly progress in their careers.
Excellent benefits including a starting vacation allowance of 3 weeks, 6% 401k match programs and medical, dental and vision benefit coverage on day one of employment!
Tuition assistance program

RSREMD

Pay Range for this position: $24-$40/hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Fixed Assets Specialist (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

Your Role:

To perform Fixed Assets, Projects Accounting and Capital Expenditure /Order Accounting for diverse and complex business operations.
Maintain an accurate fixed asset register, including tracking the acquisition, depreciation, and disposal of fixed assets.
Work closely with other departments including local finance organizations and support ensuring the integrity of the Fixed Assets accounting data.
Support the recording of all related financial activity in the Financial Services Statements and the ERP Fixed Asset sub ledger system.
Conduct reconciliations and provide reporting and analysis services to internal customers as assigned.
You are responsible for accounting and reporting all activity in accordance with generally accepted accounting principles, internal controls and company policies and procedures.
Provide training and support to fixed asset accountant on fixed asset processes and best practices.
Help develop and implement policies and procedures for fixed asset management, ensuring adherence to regulatory requirements.
Assist in internal and external audits by providing documentation and explanations regarding fixed asset transactions and valuations.

Who You Are:

Educational Background: Bachelor’s degree in accounting, Finance, or a related field. CPA or equivalent accounting license is a nice to have but not required.
Experience: Minimum of 1-3 years of experience in fixed asset accounting.
Technical Skills: Proficiency in fixed asset management software and ERP systems (e.g., SAP, Oracle) is essential.
Regulatory Knowledge: Strong understanding of local and international accounting standards related to fixed assets (e.g., IFRS, GAAP).
Analytical Skills: Strong analytical and problem-solving skills, with the ability to interpret financial data and provide actionable insights.
Communication Skills: Excellent verbal and written communication skills, with the ability to effectively present information to various stakeholders.
Global Perspective: Experience working in a global environment with an understanding of different regional practices and regulations.
Work Environment: Willingness to work at BGC, Taguig, during day shifts (9 AM - 6 PM) or mid shifts. Shifts change due to MEC.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Controls Engineer (Cork, Cork, IE, T23 A5NR)

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimaginable with us.

The Role

The Automation and Controls Specialist is responsible for designing, programming, and implementing control strategies to optimize manufacturing processes using advanced automation technologies. This role requires proficiency in configuring and troubleshooting systems such as PLCs, SCADA, DCS, and HMI.
While the role focuses on Smart Manufacturing and CapEx projects implementation, on a day-to-day it may also support diagnosis and resolution of issues related to control systems.

Duties

• Design, develop, install, modify and test the programming of PLC's, Robotics, vision systems as well as supporting the sites SCADA systems.
• Responsible for repairing, fault finding, and troubleshooting automation issues on production equipment as part of a team working in a live production environment.
• Collaborate with team members to implement effective repairs and improvements.
• Develop knowledge of on-site systems and equipment such as PLC's, Servo motors, vision systems and robotics to become the Site SME for these technologies. Lead or manage the development of GAMP documentation with the project team e.g. URS, FDS, FAT, SAT etc...
• Participate and in some cases lead projects, provide technical support and make informed decisions on hardware and architecture selection.
• Monitor and analyze opportunities for the development of new or improved tools for process improvement activities. Define the equipment and technologies to be used in the department based on experience in the area.
• Support the site during out of hours with automation issues as part of the Automation Oncall service as part of the Automation On-call team rota.
• Have a keen ability to fault find complex automation equipment including interrogation ofprogram code to identify issues.
• Coach area technicians and junior control engineers as required and support problemsolving and continuous improvement efforts across all areas of Biotools.
• Carry out justification for capital projects for the site and lead all elements of the projectwithin schedule and costs
• Manage all Requisitions and financial needs to ensure site discretionary budgets and capitalbudgets are met.
• Give input to the budgeting process for controls \ automation needs to allow the correctfinance to be put in place for execution.
• Ensure project design and installations meet the requirement of EU directives such as the Machinery Directive and CE compliance.
• Ensure Electrical Control Panels are built to standard and adhere to Safety of Machinery –EN60204-1.
• Develop critical spares list for site controls and automation hardware & ensure that criticalspares are in stock or are readily available at all times. Ensure that an effective program is then maintained.
• Investigate EHS incidents, lead RCAs and complete EHS actions as appropriate.
• Perform all tasks with due recognition of safety, environment, GMP & plant procedures.

Who You Are

• BEng degree in electrical/electronic/automation engineering or equivalent, with particularemphasis in the automation discipline.

• Minimum of 7 years + industry experience in an FDA or GMP environment as an automation\ controls engineer. Electrician experience and qualification is desirable.

• Experience with Robotic/pick &place Machines with high speed assembly operations required.
• Knowledge of interfacing with and controlling of servo drive and Motion Control systems.
• Knowledge of Vision Systems is preferable. [Cognex and other Vendors]
• Experienced with Rockwell, Siemens S7, Telemecanique and other types of PLC Controllers.
• In depth knowledge of automation network protocols including EtherNet IP, DeviceNet,ControlNet, Modbus and Profibus.
• Knowledge of control systems integration with plant MES (Manufacturing Execution System).
• Excellent problem solving and analytical ability and the ability to work as part of a team.
• Be familiar with planned preventative maintenance approaches.
• Excellent awareness and experience in relation to Quality and Health, Environment andSafety.
• Management of projects through their full life-cycle.
• Knowledge of CE marking and declaration of conformity reviews and approvals.
• A knowledge of IT systems that support manufacturing equipment.
• Lead Machine Improvement Initiatives to increase reliability or productivity.
• Electrical and machine control system problem solving
• Familiar with GMP requirements within a regulated industry.
• Excellent verbal, written & interpersonal communication skills.
• Motivated team player with pro-active and flexible approach to work.
• Ability to deliver on time and meet tight deadlines.
• The ability to work effectively within a team environment.
• Capable of working on several projects with different businesses, priorities and designrequirements.
• Self-motivated.
• Keen to learn & take responsibility within a fast paced environment.
• Training and professional development of maintenance technicians
• Strong organisational, time management and planning ability.
• Computer Literate in Excel, Word etc.
• Methodical Work Approach

• Support production teams in attaining all targets set out in the production schedule.
• Responsible for the supervision and control of all documentation / back up systems relatedto plant controls and PLC's.
• Responsible for negotiating and maintaining all associated support contracts.
• Responsible for keeping all controls related equipment up to date and conforming to all internationally recognised standards.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!

Staff Pathologist (St. Louis, Missouri, US, 63103-2355)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Staff Pathologist

Onsite in St. Louis

Your Role

As a staff pathologist at MilliporeSigma, you will oversee the development of new immunohistochemistry markers and play an active role in managing the current portfolio of immunohistochemistry markers, working under limited supervision and in collaboration with other members of the Pathology team and colleagues in Research and Development, Operations, and Quality. You will provide anatomic pathology expertise to the regulatory team to meet in vitro device (IVD) regulatory standards. You will also play a crucial role in strategic planning and the overall direction of pathology products and services.

Primary Responsibilities

• Score and interpret immunohistochemistry stains.

• Review H and E slides, pathology reports, and immunohistochemistry stains for new tissue blocks and maintain tissue block inventory.

• Research and provide pathology expertise in choosing new antibodies to develop for immunohistochemistry.

• Provide pathology expertise to quality and to regulatory departments to support in vitro diagnostic regulatory approval.

• Stay current on new immunohistochemistry applications in pathology with attendance of pathology conferences as needed.

Who You Are

Requirements:

MD/DO degree and residency training in pathology
A minimum 5 years’ broad experience in anatomic pathology with experience in immunohistochemistry, in situ hybridization, and other histopathology stains.

Preferred Qualifications:

• ABP board-certified/eligible in AP or AP/CP

• Advanced communication and presentation skills focused on training and/or teaching various audiences are desired.

• Strategic thinking about future directions for immunohistochemistry products and services.

• Highly motivated and can work with limited supervision.

Pay Range for this position: $149,300-$279,200

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

FP&A Lead Analyst (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Your Role:

The FP&A Lead Analyst – Headcount Planning & Controlling is responsible for planning, monitoring, and analysing workforce costs and headcount. The role provides accurate financial insights to support workforce decisions, budget control, forecasting, and business performance management.
Lead the annual headcount planning, budgeting, and forecasting process.
Monitor actual headcount and personnel costs against budget, forecast, and prior-year results.
Prepare monthly management reports and explain key variances and cost drivers.
Partner with HR, Finance, and business stakeholders to validate workforce plans and assumptions.
Support workforce scenario modelling, cost-saving initiatives, and business cases.
Ensure data accuracy, reporting consistency, and compliance with financial controls.
Improve reporting processes and automate recurring analyses where possible.
Present clear financial insights and recommendations to senior stakeholders.
Provide guidance and support to junior analysts and contribute to FP&A improvement initiatives.
Beyond technical competence, success in this role depends on how the work gets done:
Proven experience managing senior business and finance stakeholders, including at leadership level, with confidence and credibility.
Ability to unbox complex, ambiguous problems and structure them into clear, actionable solutions.
Strong collaboration skills, working effectively across Finance, HR, and business functions to reach shared outcomes.
Comfortable navigating dilemmas and competing priorities, and able to balance trade-offs with sound judgement.
Skilled at driving transparent, open discussions, surfacing issues early and addressing them directly rather than avoiding them.
Builds trust through consistency, honesty, and clear communication, even in difficult or sensitive conversations.

Who you are:

8-12 Years of experience:
Strong knowledge of FP&A, controlling, budgeting, Accounting, Business Partnering, E2E view of things.
Advanced Excel and financial-modelling skills.
Experience with ERP, planning, reporting, or business intelligence tools.
Experience in a multinational organisation, shared-services environment, or large and complex business. Knowledge of SAP, SAC, TM1.
Strong analytical, communication, stakeholder-management, and problem-solving skills.
High attention to detail and the ability to manage deadlines in a complex environment.

Apply now and become a part of our diverse team!

Pharmaceutical Manufacturing Technician Weekday Overnight Shift (Verona, Wisconsin, US, 53593-8510)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

Employee is responsible to adhere to the GMP requirements defined within 21 CFR parts 210 &211, 820, ICH Q7, Safety standards set under ISO 14001 & 45001. This position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API’s) according to current Good Manufacturing Practice (cGMP) requirements. The role of Pharmaceutical Manufacturing Technician is a lab-based role primarily focused on supporting and executing activities in the manufacturing environment, including but not limited to: equipment cleaning and setup, verification tasks during GMP manufacturing, maintaining the safety and quality of the manufacturing environment, and other production tasks as directed.

The shift for this position is: Monday-Thursday 6:30pm-7:00am, then Monday-Wednesday 6:30pm-7:00am.

Ensure safety and cleanliness in production areas, focusing on potent compound handling techniques.
Utilize and update various written procedures, including batch records and operating procedures.
Serve as a primary or secondary operator for cGMP production of APIs and intermediates.
Operate production equipment effectively during production, cleaning, and maintenance.
Communicate production status clearly using shift pass-off tools and computer systems.
Address safety and process issues identified during inspections and audits promptly.
Participate in a collaborative, multi-shift manufacturing environment and support departmental responsibilities as directed by leadership.

Physical Attributes:

Stand for long periods of time, lift and move up to 50 pounds with the assistance of equipment or teammates as necessary.
Utilize proper personal protective equipment (PPE), including respiratory protection, lab coats, and full-body protection.
Work with highly potent/hazardous materials and understanding chemical hazards
Work in Class 1 / Div 2 areas and near moving mechanical parts.
Operate hand tools, calculators, and weighing/measuring devices.

Who You Are

Minimum Qualifications:

High School Diploma or GED
2+ years of pharmaceutical manufacturing, chemical manufacturing, or analytical lab experience

Preferred Qualifications:

Read and understand written protocols.
Basic computer literacy (Microsoft Word, PowerPoint, Email, etc.) and strong problem-solving skills
Effective oral and written communication skills.
Basic mathematical skills.
High degree of motivation and self-starter attitude.
Ability to multi-task while paying close attention to detail.

Pay Range for this position: $25.00-$41.00 per hour

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Megasys Technician (Fremont, California, US, 94538)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

MEGASYS® offers specialized services in managing gases, chemicals and slurries, where our technicians and engineers provide critical on-site support in semiconductor manufacturing environments.

In the MEGASYS® technician role, you will be essential in ensuring the supply of chemicals and gases necessary for producing chips used in various electronic devices. This position provides a challenging and rewarding opportunity for individuals eager to contribute to a dynamic and expanding business.

As a MEGASYS® technician, you will work full-time, with responsibilities that include 24/7 operations and periodic service calls. You will work with advanced gas and chemical blending equipment, chemical reprocessing, and life safety systems, ensuring compliance with all operational and maintenance procedures, as well as emergency preparedness protocols.

Key Responsibilities:

Safe operation of assigned chemical and/or gas distribution systems.
Handling and change-out of gas, chemical, and slurry containers.
Gas and chemical equipment troubleshooting and preventative and repair maintenance.
Computer operations to support job functions and customer needs.
Support of quality systems.
Adhering to site protocols and demonstrating a safety-conscious approach.
Primary communication point to customer.

Physical Attributes:

75% of time walking throughout the facility (3-5 miles per day).
Climbing of ladders up to 12-foot-tall (utilizing fall protection).
Basic lifting (up to 40lbs).
Bending of the knees and overhead reaching.

Military Veterans:

Who You Are:

Minimum Qualifications:

High School Diploma or GED and 2+ years of experience in a semiconductor, chemical, or other manufacturing setting

Preferred Qualifications:

Associate Degree in Chemistry, Mechanical Engineering, or other technical discipline
Understanding of safe work practices and experience in lockout, tag out projects
Effective communication skills (both verbal and written) 
Technical aptitude to identify parts needed for a replacement or repair
Ability to read flow transmitters, pressure transducers, understand units of measure and use precision measuring equipment
Understand materials of construction and chemical compatibility
Awareness to identify unsafe work conditions and report them to management
Excellent teamwork and people skills

Benefits with our team include:

Comprehensive, paid, on the job training program that allows our employees to quickly learn critical technical skills to excel in this role and rapidly progress in their careers
Excellent benefits including a starting vacation allowance of 3 weeks, 6% 401k match programs and medical, dental and vision benefit coverage on day one of employment!
Tuition assistance program

Pay Range for this position: $26-$40/hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Account Manager _ Life Science (Tokyo, Tokyo, JP, 144-0041)

Work Your Magic with us!

Job Title: Account Manager Process Solutions Japan.

Location: Japan Tokyo or Osaka.

Reports To: Head of Region, Process Solutions.

The Process Solutions division provides systems and equipment, filtration solutions, consumables, services, and pharmaceutical raw materials to pharmaceutical companies for use throughout drug development and manufacturing.

With a broad portfolio of solutions, the division partners with customers to support the development of innovative medicines and enable reliable, high-quality production—ultimately contributing to improved patient health and society.

The team builds strategic partnerships with a wide range of customers, from global pharmaceutical companies to venture-backed biotechnology organizations. By delivering high-quality solutions that respond to evolving customer needs, we help advance the pharmaceutical industry.

Your role

As Account Manager, Process Solutions, you will manage and grow strategic customer relationships across Japan. You will work closely with customers and internal stakeholders to understand business needs, develop effective solutions, and advance projects from opportunity identification through execution. You will:
- Deliver annual sales growth of 10% in a market expected to grow by 8%.
- Manage and develop customer relationships to strengthen customer experience, retention, and revenue growth through continuous engagement and value creation.
- Identify and capture new business opportunities aligned with customer requirements and market needs.
- Drive competitive conversions through solution selling and value-based selling.
- Develop and execute account and sales strategies that support sustainable business growth.
- Collaborate with internal and external stakeholders to move customer projects forward and deliver effective solutions.
- Build trusted relationships with key opinion leaders and senior customer stakeholders.
- Maintain a strong understanding of customer priorities, industry developments, and competitive dynamics.
- Engage customers with a consultative approach, translating their challenges into relevant products, services, and solutions.
- Work on complex, high-impact projects while benefiting from comprehensive training and strong internal support.
Who You Are:
- Bachelor’s degree in science, chemistry, engineering, biotechnology required; an MBA or equivalent advanced degree is preferred.
- At least 7 years of experience in commercial sales role, with at least 10 years of professional experience in the biopharmaceutical, pharmaceutical, or broader life sciences industry.
- Good knowledge of biopharmaceutical products, processes, and business applications.
- Strong project management skills and the ability to coordinate complex initiatives.
- Experience developing and implementing sales strategies.
- Strong execution discipline and persistence in achieving assigned targets.
- Ability to engage effectively with key opinion leaders and senior external stakeholders at an appropriate strategic level.
- Strong negotiation skills, particularly in difficult or complex business situations.
- Proven ability to influence collaboratively and lead stakeholders effectively, including without direct authority.
- Clear, inclusive, and adaptable communication skills.
- Demonstrated potential and motivation to develop into future leadership roles.
- Ability to communicate effectively by email, deliver presentations in English, and participate actively in English-language training and meetings.
- Intermediate English communication skills, equivalent to a TOEIC score above 700.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

云设施开发运维工程师-上海 (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

About the Role
We are building a new cloud landing zone on Tencent Cloud (Domestic China) within a GxP-regulated environment. As a Cloud Infrastructure DevOps Engineer at Level 2, you will grow into a hands-on cloud practitioner – contributing to infrastructure automation, platform operations, and CI/CD pipelines. This role is well-suited for engineers who have a solid foundation in DevOps or infrastructure engineering and are ready to deepen their cloud expertise, including those who are newer to Tencent Cloud or public cloud platforms. You will be part of a global team responsible for multi-cloud infrastructure across AWS, GCP, and Azure, with a primary focus on the Tencent Cloud platform in China.
What You’ll Do
• Support the build and maintenance of the Tencent Cloud landing zone infrastructure using Infrastructure as Code (IaC) – contributing to a no-manual-changes culture
• Assist in deploying, operating, and troubleshooting TKE clusters (Tencent Kubernetes Engine), including networking, RBAC, scaling, and monitoring
• Contribute to CI/CD pipelines for infrastructure deployment using GitHub Actions and GitOps workflows
• Support automation efforts – provisioning, configuration, testing, compliance checks, and drift detection
• Monitor infrastructure health and participate in incident response, supporting high availability
• Assist in implementing and maintaining network security controls: firewall rules, security groups, and VPN connectivity
• Learn and leverage AI-powered tooling at the infrastructure level to improve automation, monitoring, and alerting
• Support Qualification activities in the GxP-regulated environment under guidance of senior engineers
• Participate in on-call rotations covering the global multi-cloud environment (AWS, GCP, Azure)
• Collaborate with the Infrastructure Architect and senior engineers to implement designs and develop your cloud expertise
What You Bring
Must Have
• 2–4 years of experience in infrastructure engineering, DevOps, or a related discipline (Level 2 / Mid-level)
• Basic to intermediate understanding of cloud concepts – candidates newer to Tencent Cloud or public cloud are welcome; willingness to learn is key
• Foundational knowledge of Kubernetes (e.g. kubectl, pods, deployments, services) – hands-on TKE experience is a plus but not required
• Exposure to Infrastructure as Code concepts (Terraform or similar); willingness to build deeper expertise
• Experience with Git and basic CI/CD principles; some exposure to GitHub Actions is beneficial
• Interest in automation and eliminating manual operational tasks
• Basic understanding of networking concepts: VPCs, subnets, firewalls, and security groups
• Willingness to participate in global on-call rotations
• Fluent in English (written and spoken) – our team language is English
Nice to Have
• Hands-on experience with Tencent Cloud services (VPC, CCN, CVM, CLB, COS, Security Groups)
• Knowledge of TKE (Tencent Kubernetes Engine) cluster operations
• Experience with observability tools (Prometheus, Grafana, Loki, or Tencent Cloud Monitor)
• Experience with an additional cloud platform: AWS, GCP, or Azure
• Familiarity with GxP/regulated environments or compliance frameworks (CSV, GAMP5)
• Experience with PaloAlto firewalls, Akamai, or Tencent WAF
• Cloud or Kubernetes certifications (e.g., Tencent Cloud TCA, CKA/CKAD, AWS Cloud Practitioner)
• Mandarin language skills (beneficial for local vendor interactions)
What We Offer
• Hybrid working model (40% remote)
• Structured onboarding and mentoring from senior cloud engineers to accelerate your cloud journey
• Work in a global, diverse team with colleagues across multiple regions
• Opportunity to build a greenfield landing zone from the ground up
• Access to cutting-edge AI tooling for infrastructure automation
• Career development pathway in a regulated, enterprise-scale cloud environment
• Competitive compensation package

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Process Engineer (Hsinchu, Hsinchu County, TW, 300)

與我們攜手施展你的超能力！

Location:

South Taiwan ( Tainan city is preferred )

Skills:

Strong organization and execution skills

Ability to set and manage multiple priorities in ambiguous and/or changing environments

Excellent verbal and written communication skills. Ability to communicate effectively with all levels within the MERCK business unit and within our manufacturing partner’s organizations.

EXPERIENCE / EDUCATION DESIRED:

A BS or MS in Chemistry / Chemical Engineering related. A degree in other engineering disciplines may be considered if accompanied by direct experience in chemical manufacturing or chemical product development.
A minimum of 3 years experience with at least 1 years direct experience with chemical manufacturing & quality control, chemical process engineering, or chemical product development.
Demonstrated capability in process modeling and process troubleshooting
Direct experience using Statistical Process Control (SPC) and Design of Experiments (DOE) to troubleshoot and/or improve chemical processes & quality.
Electronics industry experience & quality expertise is a plus

POSITION SUMMARY:

The Toll Manufacturing process Engineer is responsible for developing, deploying, troubleshooting, improving and optimizing the processes, equipment, analytical systems and quality controlled necessary to manufacture PLA and SP&C products to the exacting and ever increasing standards of semiconductor manufacturing industry. This position will provide key technical support for development and commercial products throughout their life cycle, including but not limited to improving their quality, consistency, productivity, Environment, Health, Safety , Engineering projects , daily operations at Toller site, SAP, material management and production cost improvement, as well as participating in the resolution of customer quality issues or product performance excursions.

The incumbent will work in laboratory, pilot plant, and manufacturing site settings supporting both MERCK and our Toll manufacturing partners.

PRINCIPAL ACCOUNTABILITIES:

Take new product development data, NPIs and/or small volume manufacturing (SVM) data and define the technology and manufacturing processes necessary to translate these products to full scale manufacturing. If SVM data does not exist , will work with Technology to create data set to be used for scale up to HVM
Create Work instructions and Batch Sheets for any new product and define Process of Record (POR) for that product in HVM. Will monitor compliance to POR at designated manufacturing site.
Define key process steps and trend performance to POR in those steps. Will be responsible for identifying and managing all out of control process parameters.
Provide process engineering support for the commissioning and start-up of new equipment and/or production facilities
Establish and implement process models and statistical process control schemes to monitor process inputs and outputs, and conduct designed experiments to and reduce the sources of process or product variability.
Day to day production related management of manufacturing site, including but not limited to manufacturing activity, material management , Environment, Health, Safety…etc . .
Support the Technology and Product Management teams in resolving customer quality issues and product performance excursions.
Collect and report on key Operational metrics for the designated manufacturing site and identify areas for continuous improvement.

立即申請，成為這個致力於激發探索精神、提升人類未來的團隊一員！

Senior Benefits Strategy Partner (Burlington, Massachusetts, US, 01803)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Senior Benefits Strategy Partner supports the execution of our North America benefits strategy and leads assigned areas of focus across health and welfare and retirement programs. The role receives strategic guidance from the Head of Benefits Strategy while independently leading assigned initiatives and collaborating across the organization to optimize benefit programs that attract, retain, and engage talent while managing cost and compliance.

Core Responsibilities:

Develop, refine, and execute benefit strategies within assigned areas of focus including health and welfare and/or retirement programs.
Contribute to the development and refinement of short- and mid-term benefit strategies aligned to our High Impact Culture.
Manage the tools that measure our benefit program costs and identify efficiency opportunities; assist with cost tracking and year-over-year reporting.
Build effective partnerships with HR, Finance, Legal, Benefits Operations, and external vendors to support strategic benefit objectives.
Conduct market benchmarking and competitive analysis to support benefit program recommendations.
Support vendor management activities, including partnering with Benefit Operations and external vendors to ensure service quality and compliance.
May assist in due diligence activities related to acquisitions and initial stages of integration of benefit plans under direction.
Prepare and present data-driven analyses, business cases, and recommendations to support benefit program decisions.
Monitor industry trends, competitive practices, and regulatory developments and recommend program enhancements as appropriate.
Review contract terms and ensure alignment with company expectations.
Evaluate vendor performance metrics and identify opportunities to improve service delivery and participant experience.
Support additional strategic benefit initiatives and special projects as business needs evolve.

Who You Are

Minimum Qualifications:

BA/BS in Human Resources, Business, or a related field.
Minimum 5 years of experience developing, managing, or consulting on employee benefits programs.
Working knowledge of health and welfare, retirement, leave programs, and regulatory requirements relevant to the US and Canada.
Demonstrated ability to collaborate, influence, and independently manage effective relationships with internal teams and external partners.
Strong analytical and problem-solving skills; ability to translate data into actionable insights.
Excellent communication, time management, and organizational skills.

Preferred Qualifications:

Experience supporting M&A activities, including benefits due diligence, program gap assessments, and purchase agreement reviews, is preferred.
Experience with ERISA, COBRA, HIPAA, and regional regulatory considerations for the US and Canada, including the US leave landscape.
AI literacy: experience applying AI-enabled tools to review data, scenario planning, and automation.
Ability to support multiple projects with competing priorities.
Ability to work independently, take ownership of assigned initiatives, and drive to completion.
Detail-oriented with strong execution focus.
Comfort working in a fast-paced, evolving environment.

Experience supporting benefits communications and benefits operations.

Location: Burlington, MA; Hybrid

Travel: <10%, International and Domestic

Pay Range for this position: $113,300.00 - $169,900.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Clinical Data Manager (all genders) (Maroussi, Attiki, GR, 15123)

Work Your Magic with us!

This role requires to be on-site in our office in Maroussi, Greece for 3 days per week.

Your role

As a Senior Clinical Data Manager, you will be accountable for the delivery, quality, integrity, and submission-readiness of clinical trial data for assigned global Phase I–IV studies. In this role, you will implement risk-based data collection, cleaning, review, reconciliation, and quality activities across electronic data capture (EDC) and external data sources, while representing Clinical Data Management on the Core Trial Team for assigned studies. You will lead the project management of all study-level data management deliverables, including timeline planning, resource coordination, risk identification, issue resolution, and stakeholder communication across internal and external partners. You will oversee day-to-day CRO/vendor activities, support compliance with regulatory requirements and industry standards such as CDISC, and help ensure that clinical data packages are complete, accurate, and submission ready. Beyond study execution, you will contribute to the evolution of data management standards, SOPs, best practices, and process improvements, including the effective use of automation, advanced analytics, and AI-enabled solutions where appropriate, while sharing knowledge and supporting the development of colleagues within Clinical Data Management.

Who you are

You hold a Bachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related field.
You have a minimum of 8 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry, with a demonstrated track record of delivering end-to-end data management activities for global clinical trials.
You bring strong project management, communication, collaboration, and problem-solving skills, with the ability to work independently and proactively on studies and projects of varying complexity.
You have experience coordinating global, cross-functional teams in a matrix organization, including managing day-to-day CRO/vendor activities and resolving operational issues.
You are proficient in clinical data management systems and tools, with sound knowledge of regulatory requirements, industry standards, and good practices in clinical data management.
You have experience with clinical trial data standards, including CDISC, and understand the requirements for complete, accurate, and submission-ready clinical data packages.
You are committed to continuous personal and professional development and bring relevant external insights to support innovation, process improvement, and the effective implementation of data management standards and processes.
Experience with Risk Based Data Monitoring and Management is preferred. Experience using or supporting the implementation of automation, advanced analytics, and/or AI-enabled solutions in clinical data management is an advantage.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Regulatory CMC Senior Manager _ Biopharma (Tokyo, Tokyo, JP, 106-0041)

YOUR ROLE

This role provides a unique opportunity to make a significant impact in the pharmaceutical industry while working in a dynamic and supportive environment.

As the CMC Regulatory Senior Manager, you will serve as a pivotal liaison between global and Japan teams, ensuring effective coordination of CMC and regulatory science issues. Your key responsibilities will include leading discussions and actions towards shared goals within the team, preparing critical documents such as the AAF, QOS, and Module 3 for Japan submissions, and crafting comprehensive responses to CMC inquiries from the PMDA. You will maintain close communication with global Regulatory CMC colleagues to ensure that the most up-to-date CMC status and information are shared. Additionally, You will assess the adequacy of CMC information (API, excipients, drug product) content based on Japanese regulatory requirements and provide key CMC information to our counterparts around the world, as well as propose and coordinate development strategies in Japan. Your role is crucial in identifying potential scientific challenges and regulatory scientific gap early to mitigate risks in development plans, thereby supporting the company's mission of delivering innovative healthcare solutions. Currently, our team consists of three people, and this position will be a playing manager with no direct reports. This position is based in Japan and offers flexible remote work options up to two days a week.

WHO YOU ARE

You have 7-10 years of experience in CMC NDA dossier preparation (CTD Module 2 and Module 3) and supplemental NDA submissions, including partial changes and PMDA CMC-related consultations.
You possess professional experience in CMC activities, such as formulation development, analytical development, and API and drug product manufacturing.
You have a solid understanding of ICH guidelines and Japanese CMC-related regulations, particularly for regulatory submissions.
You are familiar with global pharmaceutical product development processes and possess strong business acumen.
You have experience leading global projects and fostering collaboration among diverse teams.
You demonstrate excellent communication skills, both written and verbal, in English and Japanese.
You have a proactive mindset, with the ability to influence and encourage colleagues to work cohesively towards common objectives.
You are skilled in collecting and sharing scientific and technical information from various internal and external resources to enhance project outcomes.

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

Working Student Commercial Excellence (Santa Fe de Bogota, Bogota, CO, 9896)

Tu rol:

Daras apoyo operativo en SFE para manejo de Veeva-CRM, tickets y dashboards de MM Cono Norte. Bajo supervisión, garantiza precisión de datos y seguimiento.

1. Desempeñarás un papel clave en la provisión de apoyo tanto operativo como estratégico al departamento de Commercial Excellence.
2. Serás responsable de analizar información, gestionar documentación interna y manejar cambios en categorías y territorios, de la mano con el SFE Business Partner
3. Asistirás con solicitudes masivas, revisando adiciones y eliminaciones del panel en Veeva, creaciones de Planes de Ciclo y apoyarás a la fuerza de ventas con la gestión de tickets.
4. Colaborarás en la creación de encuestas en Veeva, tabulación de datos, gestión del tiempo fuera de territorio, aprobación de cuentas, merge de cuentas en Veeva, cargas masivas, mantenimiento de la plataforma y generación de informes y paneles de control.
5. Apoyarás al equipo de SFE con la actualización del Dashboard de Muestra Médica, le elevarás las alertas necesarias a los gerentes de distrito y le harás el respectivo seguimiento

¿Quien eres?

Estudiante de Ingeniería Industrial, Ingeniería de Negocios, Negocios Internacionales, Ciencia de Datos, Tecnologías de la Información o carreras afines enfocadas en análisis de datos, Mercadotecnia, adiministracion de empresas.
Experiencia básica en Excel intermedio (tablas dinamicas, fintros, busquedas, formulas, macross), Power Bi (deseable).

Familiaridad con tecnologías de inteligencia artificial aplicadas al análisis de información.
Inglés técnico intermedio o avanzado (deseable)
Habilidad para comunicar hallazgos de forma clara y trabajar en equipo.
Proactivo, capaz de trabajar de forma autónoma y con facilidad de aprendizaje rápido en entornos dinámicos y multiculturales, habilidades numericas y analiticas, y atencion al detalle.

¡Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!

Chemical Packaging Operator 1 (Sheboygan Falls, Wisconsin, US, 53085-2814)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

$5000 Sign on Bonus if Hired

Your Role:

In this role your tasks will include, but are not limited to:

Precisely weigh and transfer hazardous and non-hazardous chemicals into specified containers and compare filled quantities against consumed bulk quantities to ensure quality standards are met.
Complete all required paperwork, document cleaning procedures, and populate electronic process orders following Good Documentation Practice (GDP).
Set up, operate, and troubleshoot all automated dispensing equipment, including assembling, disassembling, and cleaning tools and utensils according to safety protocols.
Verify room ventilation and safety equipment functionality, obtain and scan process orders, and confirm electronic balance calibration prior to starting any operation.
Verify bulk container, batch, and material numbers against process order specifications before use to ensure accuracy.
Actively participate in promoting a proactive safety culture, identifying hazards, and maintaining equipment, tools, and facilities according to 6S standards.
Safely operate powered pallet and drum movers, and ensure proper disposal of waste according to both company and government regulations.
Participate in the testing and implementation of process and equipment changes to enhance efficiency and maintain an incident-free work environment.
Shift/Hours: Monday - Friday, 2:00pm-10:30pm

Physical Attributes:

Wear appropriate protective gear, (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protection equipment "PPE" to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles.
Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl.
Lift and move up to 50 pounds unassisted.
Close vision, distance vision, color vision, peripheral vision, depth perception, and adjust focus.

Who You Are

Minimum Qualification:

High School Diploma or GED.

Preferred Qualifications:

Strong oral and written communication skills.
Strong attention to detail and problem-solving skills.
Strong math skills, including using the metric system.
Strong mechanical and technical aptitude.
Experience operating a forklift.

RSREMD

Pay Range for this position: $20/hour - $31/hour

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

ERP Integration Lead (all genders) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

Your Role:

As the ERP Integration Lead for the our Life Science business, you will lead the governance, design, and continuous evolution of the application integration landscape supporting our global SAP S/4HANA transformation program. Working closely with Business Process and IT Solution Owners, the ERP Design and Build organization, the Deployment Leads, Integrated Enterprise Solutions as well as our implementation partners, you will drive the delivery of scalable, standardized, secure, and compliant integrations between SAP S/4HANA and connected business applications. You will provide technical leadership throughout the integration lifecycle from architecture and solution design through implementation, deployment readiness, and cutover support. Your leadership will ensure a robust and resilient integration landscape that enables successful global deployments while preserving enterprise architecture principles and clean core standards.

Key Responsibilities

Lead the end-to-end ERP Integration function within the global SAP S/4HANA transformation program.
Own the governance, quality, and continuous evolution of the application integration landscape supporting the global ERP template.
Define and govern enterprise integration principles, interface standards, API strategies, middleware architecture, and integration patterns across SAP and connected business applications.
Govern technical integration decisions and ensure alignment with enterprise architecture principles, clean core strategy, and global technology standards.
Provide leadership and governance for the design, implementation, testing, and deployment of application integrations across functional workstreams and implementation partners.
Ensure integration consistency and technical solution integrity across multiple concurrent deployment programs while balancing global standardization with justified local requirements.
Partner closely with Deployment Leads to enable technical deployment readiness, interface validation, cutover planning, technical issue resolution, and successful deployment execution.
Collaborate with ERP Design and Build, Data Migration, Testing, Validation, Security, Enterprise Architecture, Digital Manufacturing, and other technology teams to deliver an integrated enterprise solution.
Ensure application integrations are designed, built, tested, and delivered in compliance with validation requirements, and global quality standards by partnering closely with Validation organizations to support deployments into regulated environments.
Drive planning and governance for integration readiness, interface testing, technical defect resolution, deployment preparation, and cutover activities across all integrated applications.
Identify technical risks, interface dependencies, and architectural constraints early and proactively manage mitigation plans to support successful program delivery.
Provide leadership and direction to internal teams, external implementation partners, SAP, and technology vendors while driving accountability, delivery excellence, and effective collaboration.
Leverage SAP Integration Suite, SAP Business Technology Platform, APIs, event driven architecture, and emerging SAP technologies to continuously improve the enterprise integration landscape and accelerate future deployments.

Who You Are:

Bachelor's or Master's degree in Information Technology, Computer Science, Engineering, or a related field, or equivalent professional experience.

10 or more years of experience leading SAP integration, enterprise application integration, or large scale SAP S/4HANA transformation programs.
Extensive experience designing and governing enterprise application integration landscapes supporting SAP and non SAP business applications.
Strong understanding of SAP S/4HANA technical architecture, SAP Integration Suite, SAP Business Technology Platform, APIs, middleware technologies, and modern enterprise integration patterns.
Proven leadership experience managing global technical teams and implementation partners across multiple concurrent initiatives.
Strong knowledge of enterprise integration governance, enterprise architecture, clean core principles, cybersecurity, and SAP implementation methodologies.
Demonstrated experience leading integration solution delivery in GxP regulated Life Science, Pharmaceutical, Medical Device, or similarly regulated industries is highly desirable.
Deep understanding of deployment readiness, integration testing, interface validation, technical cutover planning, and transition from build to deployment.
Excellent stakeholder management skills with the ability to influence senior business and IT leaders across global organizations.
Outstanding communication and presentation skills with the ability to translate complex technical concepts into business value.
Strong analytical and strategic thinking skills with the ability to balance technology strategy, business value, operational stability, risk, and delivery timelines.
Demonstrated ability to lead cross functional teams without direct authority in a matrix organization.
Experience leading multiple concurrent initiatives within a global ERP transformation program.
Fluent in English. German or another European language is considered an advantage.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in Germany.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Analytical Scientist (St. Louis, Missouri, US, 63118-3306)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

In this Sr. Analytical Scientist role you will be involved with problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing. Key responsibilities include the following:

Serve as a subject matter expert in analytical development, perform troubleshooting / provide efficient and innovative solutions, and support transfer of analytical methods to GMP QC labs
Utilize customer-facing skills, document experimental results, communicate results to all stakeholders, author method development and qualification documents, contribute to information for customer proposals
Serve as a project lead and ensure project deliverables are on quality and on time, develop multiple technical approach plans as needed to solve problems and mitigate risk, ensure process and methods are in place for efficient GMP start
Lead project teams, influence exemplary work in other team members, lead process improvement initiatives, scout for new technologies / emerging trends, proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities

Who You Are

Minimum Qualifications:

Bachelor’s degree in chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 6+ years of research in an industrial or post-graduate setting

Master’s degree in chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 2+ years of research in an industrial or post-graduate setting

PhD in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 1+ years of research in an industrial or post-graduate setting

Preferred Qualifications:

Experience with protein characterization via ELISA, SPR, Isoelectric Focusing, CE-based methods, UV-Vis, and/or chromatography (HPLC/GC/IC/UPLC/SEC/HILIC)
Experience with advanced laboratory techniques; theory and practice to enable the development of novel approaches to solve complex process and analytical problems on fast-paced projects with changing priorities
Knowledge of small molecule or bio-therapeutics drug development process
Experience with antibody-drug conjugation
Knowledge in Biochemistry or Organic Chemistry
Experience in automation in analytical settings and instrument maintenance and troubleshooting
Knowledge of Microsoft Word, Excel, and PowerPoint
Experience with advanced data acquisition and/or statistical software systems
Ability to coordinate information exchange and manage data generated by contract testing labs

RSREMD

Pay Range for this position: $75,700 - $113,500 annually

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Compliance Officer, Rare Tumors (Boston, Massachusetts, US, 02210)

Work Your Magic with us! Start your next chapter and join EMD Serono.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

As Compliance Counsel, Rare Tumors, you will serve as a trusted advisor to the Rare Tumors franchise and partner with business leaders to promote ethical decision-making and compliance with applicable laws, regulations, industry standards, and company policies.

You will provide practical, risk-based guidance across commercial and medical activities, helping to identify and mitigate compliance risks while supporting business objectives. You will contribute to training and awareness initiatives, support investigations, and help shape compliance strategies and responses to emerging risks while fostering a culture of integrity and accountability across the organization. You will also support broader compliance initiatives designed to strengthen ethical business practices and promote a culture of integrity across the organization.

Who You Are

Minimum Qualifications:

BA/BS degree
Minimum of 7 years of work experience in a Legal or Compliance function with a multi-national organization with specialization in pharmaceutical compliance, law and regulations.
Senior level collaborator with ability to influence and gain buy in at the leadership level
Established reputation for excellence in traits such as credibility, integrity, confidentiality, and trust
Collaboratively work across department and geographies and encourage teamwork that respects backgrounds and culture diversity
Innovative approach, creative thinker
Participate in feedback culture and take responsibility
Embracing new opportunities that will shape the future

Preferred Qualifications:

J.D. degree or LL.M. degree from an accredited law school, admission to practice law in a U.S. jurisdiction
US & Global experience strongly preferred

Location: Boston, MA, USA; Onsite (Hybrid)

Travel: <15%; International and Domestic

Pay range for this position: $134,700.00 - $202,000.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Field Service Engineer (Madrid, Madrid, ES, 28006)

Work Your Magic with us!

Your Role : The function of the Field Engineer is to perform the service activity strategy, acting as the mobile Field Service Engineer on an assigned geographical Service area. He has to perform assigned Work.The Field Engineer installs, troubleshoots and maintains an extensive variety of products and equipment. Identifies, analyzes, and repairs product failures, orders and replaces parts as needed.

He is working with all personnel contacts, internally and externally, to drive the “go to market strategy” with a high "Service Excellence value“.Perform assignments as directed by Inhouse Service Center or senior technical staff.

Who you are:

Technical degree. A degree in Engineering is desirable.
1 - 3 years of experience in the field or in a related area.
You are fluent in English and Spanish
You are familiar with a variety of the field’s concepts, practices, and procedures. Relies on experience and judgment to plan and accomplish goals.
Be proactive to promote Service activities, products and solutions, lead generation.
You adapt and are flexible in any situation or unforeseen event.

Permanent employment

100% remote position

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Field Service Engineer (all genders) Dresden (Dresden, Sachsen, DE, 01099)

Work Your Magic with us!

Your Role

As a Field Service Engineer (all genders) you will be affiliated with our Dresden office while providing field service support to customer sites across Germany and, when required, throughout Europe. In this role, you will install, maintain, troubleshoot, and repair production material systems used in semiconductor manufacturing. These systems enable the production of chips found in technologies such as smartphones, LEDs, and flat-screen TVs. You will ensure the reliable operation of gas and chemical distribution systems, blending equipment, critical monitoring, and life-safety systems while delivering excellent customer service. In this role, you will perform preventive maintenance, equipment inspections, technical troubleshooting, and accurate service documentation, while providing practical solutions for equipment operation and configuration. This position requires up to 85% travel and a strong commitment to quality, safety, and operational excellence.

Who you are

Associate’s or Bachelor’s degree in Mechanical Engineering, Electrical Engineering, or another technical discipline
2+ years of experience in the semiconductor, chemical or other manufacturing setting is an advantage
Strong analytical and troubleshooting skills with the ability to interpret technical documentation
Experience in performing preventive maintenance, equipment troubleshooting, and documenting service activities
Committed to quality, safety, and following established procedures and escalation processes
Strong communication and customer service skills with the ability to work independently and remotely; Excellent written and verbal communication skills in English; basic German language skills are required
Physically able to perform the essential duties of the role, including lifting equipment, climbing ladders, working in confined spaces, and wearing and using required personal protective equipment (PPE)
ISO 9000/9001 awareness or knowledge of semiconductor manufacturing processes is an advantage; A valid passport and driver’s license with a clean driving record (past 36 months) are required

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Analyst - Dangerous Goods (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Your Role:

As a Dangerous Goods Analyst, you will play a critical role in ensuring the safe, compliant, and efficient movement of goods across global supply chains. You will serve as a subject matter expert, drive process improvements, and collaborate across functions to uphold the highest standards of regulatory compliance.
Collaborate with cross-functional teams to ensure safe and uninterrupted global goods flow.
Continuously identify and drive process improvements in day-to-day activities, contributing to a culture of operational excellence.
Support on 3rd party processes, New Product Introductions and Change management.
Support global projects and audit activities.

Who You are:

Master’s degree in chemistry, with 0-3 years of experience in Dangerous Goods.
Strong analytical skills with the ability to critically evaluate scientific data and regulatory information.
Maintain expert knowledge of Dangerous Goods regulations and global frameworks, including IATA, ADR, IMDG, and 49 CFR.
Motivated and detail-oriented individual with a passion for Dangerous Goods, and a drive to make a real impact.
Ability to work effectively and professionally with international colleagues across different cultures and time zones.
Purposeful and result-driven, with a proactive approach to identifying and solving problems.
Collaborative team player who contributes positively to group dynamics and shared goals.
Comfortable navigating and delivering results in a highly complex and fast-paced environment.
High learning agility, with the curiosity and openness to quickly acquire new knowledge and skills.

Apply now and become a part of our diverse team!

Sr. Investigator (Indianapolis, Indiana, US, 46268)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

Reports to QMS Manager and Quality Systems Team.
The Sr Deviation Investigator is responsible for providing timely resolution of assigned deviations and complaints, ensuring that the investigations are thoroughly investigated to determine root cause, and that robust CAPA’s are implemented whenever necessary. The investigator will be assigned specific areas for which they will be responsible for deviation investigation.
The investigator will coordinate with the area, technical support, and other personnel to facilitate completion of deviation investigations.
The investigator will keep track of deviations for assigned area(s) and help to ensure deviations are evaluated and closed per timing requirements.
Sr Deviation Investigators are generally assigned the more complex deviations as they require more experience and coordination to complete investigation.

Major Position Activities & Responsibilities:

Deviation Investigation:

Process deviations and complaints within the quality management system and conduct thorough root cause investigations. This will require interviewing personnel involved and interacting with technical support and other personnel to determine root causes of the deviations and to assess impact. Deviation investigation will also require reviewing instructions, reference material, and documentation to understand the processes being investigated and what went wrong.

Deviation Tracking:

Track deviations for area assigned to help ensure on-time completion of each step.

Scope:

Tracking and completing deviation investigations for areas assigned and assisting manager in improving the quality of investigations.

Who You Are

Minimum Qualifications:

Bachelor’s degree in a science or engineering field
Minimum of 5 years of experience required in a pharmaceutical manufacturing site environment with at least 2 of those years directly supporting deviation investigations

Preferred Qualifications:

Advanced user of Microsoft Office products, including Excel, Word, Access, and PowerPoint
Use and system knowledge and experience of Quality Management Systems
Ability to interface with personnel from multiple areas to deliver results (e.g., complete deviation investigation)
Demonstrated ability to write through, clear, concise, and logically organized technical documents

Pay Range for this position: $104,100- $156,100 / year

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Head of US HRBPs and Global HRBP, Electronics (Allentown, Pennsylvania, US, 18106)

Work Your Magic with us! Start your next chapter and join EMD Electronics.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Who You Are

A strategic, credible, and hands-on HR leader with strong business acumen, leadership capability, and deep understanding of the people implications of operating in a global semiconductor business.

You bring strong experience in labor relations, HR operations, and country HR leadership, combined with the ability to partner effectively with senior leaders in a complex matrix environment.

Your Role:

Senior HR leader for the United States within the Electronics business of Merck KGaA, Darmstadt, Germany and member of the Electronics HR Leadership Team.

Lead the HR agenda for an organization of approximately 2,000 employees in the US and manage a team of 5 direct reports.

Drive the country people agenda across organization effectiveness, workforce planning, talent, succession, leadership development, employee relations, and change management.

Act as strategic HR partner to senior leaders in the US, ensuring strong alignment between business priorities, country needs, and people strategies.

Hold a double-hat role as Global HR Business Partner for one Semiconductor Business Unit, reporting in this capacity to the Head of HR Semi Solutions.

Operate effectively in a matrix environment, balancing country HR leadership responsibilities with global business HRBP accountabilities.

Use data, business insight, and external perspective to shape people decisions and position the organization for future needs

Minimum Qualifications:

Bachelor’s degree required with minimum 8 years of relevant HRBP experience

Experience in HR operations and/or a Global HRBP role in a fast-changing and matrix environment is required, ideally in the semiconductor industry.

Proven experience leading an HR team and driving the people agenda for a sizeable country or regional organization.

Proven experience as a strategic HR partner on organizational design, talent strategy, succession planning, leadership development, and change management.

Demonstrated ability to operate successfully in a complex matrix structure, balancing country leadership and global business HRBP responsibilities.

Strong understanding of the US business, people environment and labor laws

Strong analytical, strategic thinking, and execution skills in a high-change business setting.

Location: One of EMD Electronics hub cities in the USA (Allentown, PA, Tempe or Chandler, AZ); Hybrid

Travel: <15%; International and Domestic

Pay range for this position: $177,600.00 - $266,400.00

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Director, Head of Clinical Delivery and Monitoring Unit II (all genders) (Eysins, Vaud, CH, 1262)

Work Your Magic with us!

Your role

As Director, Head of Clinical Delivery and Monitoring Unit II, you will oversee the assigned Delivery and Monitoring teams to ensure high-quality, risk-based, and efficient delivery of the entire clinical portfolio (Phase I–IV, RWE, ISS, and other studies). In this role, you will provide strategic and operational oversight, governance representation, cross-functional and CRO collaboration, and continuous improvement of systems, processes, and performance across GDO/CDPC. Additionally, you will manage a diverse team, ensuring high-quality execution of clinical studies while driving the delivery and quality of Phase I-IV studies, epidemiology, real-world evidence studies, and early access programs within the clinical portfolio. You will oversee a team of Trial Clinical Delivery Leads (TCDLs), Program Clinical Delivery Leads (PCDLs), and Regional Clinical Delivery Leads (RCDLs) to ensure high-quality execution of clinical studies. You will engage with internal partners across GDO, Global Medical Affairs, and CROs to ensure seamless trial execution and performance accountability. You will represent the Clinical Delivery team at internal governance boards, ensuring operational feasibility and delivery considerations are evaluated.

Key responsibilities:

Clinical Delivery Oversight
Operational Excellence
Risk Management
Collaboration and Networking
Performance Improvement

You will be expected to travel domestically and internationally up to 20% of the time. This is an office-based position that requires to be on-site in Eysins for 3 days per week.

Who you are:

You have a proven track record of 10+ years in clinical research and operations, focusing on managing complex studies and teams.
You possess a strong ability to interpret and anticipate business challenges, driving process improvements and innovative solutions.
You have demonstrated the ability to sponsor and drive transformation initiatives within clinical operations.
You hold a graduate degree (Medical or Life Sciences) in a clinical research-related discipline or equivalent.
You have at least 5 years of experience in people and resource management.
You exhibit outstanding leadership capabilities to direct, influence, and motivate diverse teams across functions and geographies.
You have strong analytical skills, enabling you to assess risks, solve problems, and make informed decisions.
You possess a high degree of cultural awareness and are adept at working in a multicultural environment with global teams.
You are skilled in implementing operational excellence strategies by leveraging expertise from Global Development Operations (GDO) and collaborating with partner functions.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

MSL Rare Tumor_BioPharma (Tokyo, Tokyo, JP, 106-0041)

Roles providing expertise on scientific topics regarding relevant disease areas and Company assets to ensure their safe and appropriate use by patients.

Acts as a field-based expert, building relationships with External Experts as trusted scientific partners. Exchanges credible scientific information to ensure the optimal use of Company assets and to improve patient care. Gathers and provides insights back to the Company to inform strategy and activities.

IMPACT: Impacts the results of own team or even influences a range of customer, operational, project or service activities of closely related teams with own contributions. Explains complex or even difficult/sensitive information to others in straightforward situations and interacts across business areas. May even advance discussions and build consensus across the business and with external parties regarding own technical area.

COMPLEXITY: Performs a range of routine or even non-routine assignments to solve problems of low to moderate complexity that require working knowledge and experience in own job discipline. Analyzes factual information and possible solutions to make independent judgement, recommendations and decisions. May also use best

practices to improve products or services.

ACCOUNTABILITY/ INDEPENDENCE: Accountable for the quality of own work. Works independently and receives a moderate to low level of guidance and direction within clear or even broad guidelines.

EXPERIENCE: Requires a graduate background plus some to substantial relevant professional experience, and good knowledge and experience in own discipline and beyond.

ORGANIZATION: Typically reports to a Manager role, Project Manager role for a defined period of time based on organizational set-up (there is not necessarily a difference in role level between a manager and its direct reports - same level or lower level reporting is possible, provided job scope and responsibilities are clearly distinct); typically no direct reports.

University degree (Bachelor’s) required, preferably in scientific field of relevance to position

Secondary/ advanced scientific degree (e.g., MSc, PharmD, PhD, DO, MD) required

Scientific and/ or clinical training in area of relevance to position strongly preferred

Proven experience in oncology Medical Affairs, with preferred exposure to rare tumors, sarcomas, or other rare/orphan disease areas

Professional, clinical or research experience in a scientific or related field required (minimum of 5 years)

Knowledge and experience of methodology of clinical research and Good Clinical Practice preferred

Advanced English language competency and fluency in local language

Advanced scientific knowledge, relationship building and networking skills

Strong analytical skills and ability to think strategically

Strong ability to evaluate publications on scientific content and communicate peer to peer on the scientific content with external stakeholders

Master communicator to external stakeholders and peers, in both small and large group settings

Ability to build ongoing and productive relationships throughout the organization to achieve strategic goals

Excellent organizational and time management skills

Highly developed interpersonal and teamwork skills

Excellent presentation and communication skills, for both in-person and virtual environments

Good knowledge of computer tools and software (MS Office), including virtual interaction platforms (MS Teams, Zoom, etc.)

Good conflict resolution/management skills

今すぐ応募して、発見を促し、人類の発展を高めることに専念するチームの一員になりましょう！

HR Services & Resolution Specialist with German (Wroclaw, Dolnoslaskie, PL, 53-616)

Work Your Magic with us!

YOUR ROLE

In your role as an HR Services & Resolution Specialist, you will deliver personnel administration and employee lifecycle support for our Swiss operations. You will ensure high data accuracy across employee records, monitor data entry procedures, update work instructions, and handle queries promptly. Working alongside coordinators, team leads, and HR partners, you will support administrative tasks, assist with audit requests, and help drive continuous process improvements. This role offers a great environment to build your HR skills, expand your operational knowledge, and grow your career in international HR services.

Work model: 2 days per week from the office in Wrocław.

WHO YOU ARE

1–2 years of experience in HR administration or a Shared Services environment
Fluency in German (written and spoken) and good command in English
Practical knowledge of HR systems such as Employee Central
High attention to detail, conscientiousness, and care when handling confidential documentation
Bachelor’s degree in HR or a related discipline
Familiarity with ticketing systems (e.g., ServiceNow) is a plus

YOUR MAIN BENEFITS:

Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card
Work-Life balance: Enjoy additional paid days off, flexible working hours.
Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.

Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Field Service Engineer - West London (Feltham, London, GB, TW14 8HA)

Work Your Magic with us!

Your Role:

As a Field Service Engineer, you will be the technical backbone of our Life Science business. Your role is crucial in ensuring our customers receive the highest quality service and support.

Here's a glimpse of your exciting responsibilities:

Installation & Commissioning: Expertly install and commission instrumentation, predominately lab water purification systems at various client sites, ensuring optimal performance from day one.
Maintenance & Servicing: Perform regular maintenance and servicing to keep systems running smoothly, preventing downtime, and ensuring reliability.
Repairs: Diagnose and repair any issues with precision and speed, minimizing disruptions for our clients
Validation: Validate and calibrate equipment to ensure compliance with industry standards and client specifications.
Customer Support: Provide exceptional support and training to customers, empowering them to utilise our systems to their full potential.
Travel: Enjoy a dynamic role with travel predominantly around the West London area, offering new challenges and experiences every day.

Who you are:

Minimimum HNC or equivalent, in either an Engineering or Scientific discipline.
Technical Expertise: 2+ years' experience in a hands on engineering role.
Problem Solving Skills: Ability to diagnose and troubleshoot issues efficiently.
Customer focus: Excellent communication skills and customer-centric approach.
Adaptability: Flexibility to travel and adapt to varying work environments.
Team Player: Collaborative mindset and the ability to work independently.
Experience: Previous field service experience is a plus, but not mandatory. Comprehensive training and onboarding will be provided.
Generate leads for new hardware, consumables, accessories, and service contracts via the current CRM tool.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Regional Sales Director, West (Burlington, Massachusetts, US, 01803)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Regional Sales Director (RSD) is responsible for driving revenue growth within a designated area in North America by leading a sales team, establishing regional targets, executing strategic initiatives, analyzing market trends, and nurturing key client relationships. This role serves as a vital connection between field sales and corporate leadership, enhancing performance and achieving company objectives. Additionally, the RSM will oversee approximately $60+ million in business, ensuring effective management and growth. The ideal candidate should be a strong leader capable of coaching the team on effective selling tactics. Core responsibilities include strategic planning, motivating and training the team, forecasting sales, and tailoring company offerings to meet local market demands.

Key Responsibilities

Strategy & Planning: Formulate and implement regional sales strategies, establish quotas, and project sales to align with business goals.
Team Leadership: Recruit, train, mentor, and inspire a team of sales representatives to achieve high performance.
Performance Management: Track sales metrics, evaluate performance, and ensure that targets are consistently met or surpassed.
Client & Market Relations: Develop and sustain relationships with key accounts, identify new market opportunities, and collect customer feedback for continuous improvement.
Operations: Manage regional sales operations, oversee budgets, and coordinate distribution activities.

Location: United States – preference for candidates to be located in states within the territory - CO, WA, OR, ID, WY, SD, NE, KS, MN, WI,MI

Travel: 50% travel within the assigned territory, emphasizing the geographically based nature of the role

Who You Are

Minimum Qualifications:

Bachelor’s degree in sciences, business, marketing, or a related discipline.
8 years of demonstrated experience in sales management, preferably within the pharmaceutical, biotechnology, or healthcare industries.
Proven ability to lead, motivate, and develop a sales team, fostering a high-performance culture.
Strong verbal and written communication skills, with the ability to present effectively to diverse audiences, including internal stakeholders and clients.
Proficient in data analysis and sales forecasting, with the ability to interpret market trends and adjust strategies accordingly.
Ability to think strategically and solve problems effectively, both internally and externally.

Preferred Qualifications:

Minimum bachelor's degree in relevant fields of study, preferred Advanced degree in a relevant field.
Minimum of 8 year's experience in the pharmaceutical, biotechnology, or healthcare sectors, with a strong understanding of market dynamics and customer needs.
Track record of exceeding sales targets and driving revenue growth in a regional or national capacity.
Experience in coaching sales representatives on effective selling tactics and strategies, with a focus on professional development.
Demonstrated success in building and maintaining relationships with key clients and stakeholders, with a focus on long-term partnerships.
Familiarity with CRM software and sales analytics tools to manage sales processes and data effectively.
Experience in formulating and implementing strategic sales initiatives that align with overall business goals.
Experience in managing budgets and overseeing regional sales operations to ensure financial targets are met.

Pay Range for this position: $166,400 - $307,100

Direct link to benefits site if the hyperlink no longer works: https://careers.emdgroup.com/us/en/benefits].

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Senior Expert Cloud Data & AI Architect - Healthcare (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your Role: As a Senior Cloud Data & AI Architect within the Healthcare Architecture Team, you will design and govern cloud-native architectures that enable scalable data, analytics, AI/GenAI, and agentic AI solutions across the healthcare portfolio. You will partner with Data & AI, Security, Platform, and cross-functional Healthcare teams to define standards, drive reference architectures, and enable governed solutions across AWS, Snowflake, Palantir Foundry, and related technologies. This role combines deep cloud engineering with data, AI/ML, and agentic workflow architecture to accelerate value delivery while ensuring compliance, security, reliability, and responsible AI.

• Design end-to-end cloud architectures on AWS and connected data platforms, including Snowflake and Palantir Foundry.

• Define and govern reusable patterns for data ingestion, storage, processing, analytics, and AI/ML workflows.

• Lead the architecture of AI/ML and GenAI capabilities, including MLOps, model monitoring, and risk controls.

• Embed security, privacy, data governance, resilience, and cost management into solution designs from the start.

• Evaluate platform and integration choices to improve performance, scalability, and total cost of ownership.

• Promote architecture standards and best practices; create reference architectures, design documents, roadmaps, and runbooks; and mentor engineers and architects on automation and infrastructure as code.

• Collaborate with cross-functional Healthcare teams to translate business priorities into scalable, secure, and compliant data and AI solutions.

• Define reusable architecture patterns for agentic AI solutions, including agent orchestration, retrieval-augmented generation, tool integration, human-in-the-loop controls, evaluation, observability, and governance.

Who You Are – Minimum Qualifications

• Bachelor’s degree in computer science, information technology, engineering, or a related field.

• 6+ years of experience in cloud architecture, cloud engineering, or a closely related technical role.

• Hands-on expertise designing solutions on AWS, including identity and access management, storage, compute, serverless, data, and security services.

• Experience with at least one enterprise data platform, such as Snowflake or Palantir Foundry.

• Experience designing and delivering AI/ML or GenAI infrastructure, including data pipelines, deployment, monitoring, and governance.

• Knowledge of data governance, data quality, privacy, security, and regulated-data considerations, including PII/PHI and GxP-relevant contexts.

• Proficiency in Python and SQL, plus infrastructure-as-code tooling such as Terraform or CloudFormation.

• Experience designing or delivering GenAI and agentic AI solutions, including large language model application architecture, retrieval-augmented generation, agent orchestration, tool integration, evaluation, monitoring, and responsible-AI controls.

Preferred Qualifications

• Master’s or doctoral degree in a related discipline.

• AWS certifications, such as Solutions Architect, Data Analytics, or Machine Learning Specialty.

• Experience with clinical, research, manufacturing, regulatory, commercial, or supply-chain data in a healthcare or life-sciences environment.

• Experience leading architecture governance forums and developing enterprise standards, data lineage, metadata, or integration practices.

• Experience delivering scalable, multi-service data and AI platforms in regulated environments.

• Experience applying agentic workflows to regulated healthcare or life-sciences use cases, with security, privacy, auditability, and human-oversight controls.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Chemical Packaging Operator 1 - 2nd Shift (Milwaukee, Wisconsin, US, 53209-3650)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

At MilliporeSigma, the Chemical Packaging Operator 1 – 2nd shift will manually and semi-automatically portion chemicals into containers using safety equipment and following protocols.   Job duties include:

2nd Shift: Monday – Friday, 2:00pm – 10:30pm
Verify hood and safety equipment function, obtain process order, scan into computer system, verify electronic balance is calibrated.  
Verify match of process order and bulk container lot numbers.  
Obtain correct type and quantity of containers for process order.  
Operate powered pallet and drum movers.  
Verify weighed bottles and determine if quantity matches process order requirements.
Pull samples for customers and/or quality control.  
Complete paperwork including tray tags, process orders, and computer PKRV scan.  
Document process order for specific required data, inclusive of weighing accountability to assure the accuracy of the weighed material using Good Documentation Practices (GDP).  
Fill out data for tray tags and affix to each tray or case of filled bottles.  
Complete production logs.  
Maintain equipment, tools, and facilities in safe, clean environment.  
Assemble, disassemble semiautomatic powder or liquid dispensing equipment, and replace worn or disposable parts as necessary.  
Clean semi-automatic dispensing equipment according to manufacturer recommendations and chemical safety protocols. 
Clean tools and utensils with appropriate material in hood according to chemical safety protocols.  
Clean hood/workstation according to method and protocol for specific chemical weighed.
Assemble, test, maintain, and use appropriate safety equipment.  
Clean and maintain reusable safety equipment for next use.  
Facilitate packaging operations by providing support for weighers and moving material within the department.  
Procures bulk and package components for weighers.
Maintain, clean, and safe work areas and equipment following 5S standards.  
Take necessary steps to ensure we provide our customers with the highest quality product possible.  
Immediately report any situation that could compromise safety or quality

Physical Attributes:

Work near moving mechanical parts. 
Wear Personal Protective Equipment, “PPE”, including but not limited to hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes
Work in wet, humid, or abnormally hot or cold environments.
Lift, push, and or pull up to 50lbs

Who You Are: 

Minimum Qualifications:

High School Diploma or GED

Preferred Qualifications:

Ability to read instructions and understand oral and written instructions. 
6 + months of experience weighing hazardous and non-hazardous chemicals using precision equipment into specific containers
Experience of safety equipment and semi-automated equipment
Excellent communication and problem-solving skills

RSREMD

Pay Range for this position: $20.00-$32.00/hourly

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Customer Service Supervisor (San José, San José, CR, 10101)

Work Your Magic with us!

Customer Service Supervisor

Your Role

As a Customer Service Supervisor, you will lead and develop a team of 10–12 customer service representatives in a fast-paced environment that directly supports our Sales organization. You will be responsible for managing team performance across the order-to-fulfillment cycle, ensuring service levels are met, and driving continuous improvement in processes, policies, and training. Your day-to-day will include coaching team members of varying seniority levels, setting individual and team goals, and using performance data to make operational decisions. You will oversee functions such as sales support administration, logistics coordination, key account management, and customer escalation resolution. You will also be accountable for contact center KPIs—including phone abandonment rate, speed to answer, schedule adherence, and login time—and will regularly report results and strategic updates to senior leadership. This role requires a minimum of 3 years of experience directly supervising teams in customer service or operations environments.

Who You Are

You have demonstrated experience directly supervising and coaching customer service or operations teams of 10 or more people.
You have a proven track record of managing contact center KPIs such as phone abandonment rate, speed to answer, unavailability, schedule adherence, and login time.
You bring hands-on experience with the order-to-fulfillment cycle, including sales support, logistics coordination, or key account management.
You are proficient in Microsoft Office, particularly Excel, and have used data and reporting tools to drive team performance decisions.
You have experience building individual development plans (IDPs), conducting regular coaching sessions, and providing structured performance feedback.
You have exposure to Oracle, SAP, or similar Web-Based Order Management and Call Center systems (training on internal systems will be provided).
A B.S. in Business Management, Operations, or Logistics is preferred.
English requirment - C2

Employment Details

Location: Costa Rica.
Travel: Occasional travel may be required based on business needs.
Scope: This position reports to the Customer Service Manager and supports the regional Sales organization.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Manufacturing Automation Engineer (The Woodlands, Texas, US, 77380-3677)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

In the role of Manufacturing Automation Engineer you will develop, enhance, and maintain manufacturing equipment and automation systems at a nucleotide manufacturing site. In this role you will drive engineering improvements that strengthen safety, quality, reliability, and operational efficiency in a regulated ISO 13485 environment. The operation consists of a 37,000 sqft facility operating a wide variety of robotic equipment including automated handling of labware, vision systems and small scale precision liquid handling.

In this role you will lead or contribute to automation projects from concept through implementation, commissioning, documentation, operator training, and handoff to operations.

Program manufacturing equipment such as Festo and ACS Motion control platforms, Panasonic FP0H, Visual Studio C# Windows applications, and PIC microcontrollers to control motion platforms, valves and end effectors.
Analyze production and equipment data to identify and implement improvements in uptime, throughput, cycle time, quality and safety.
Collaborate closely with safety and quality teams to maintain adherence to regulatory requirements and industry standards.
Use SolidWorks and PDM to create, revise, and maintain engineering drawings and BOMs.
Create accurate SOPs and maintenance documentation.
Train operators on safe, effective use of new or modified systems.
Implement good engineering practices as well as adherence to management of changes policies.
Work safely and effectively in a live manufacturing environment using standard laboratory PPE.
Effectively communicate and collaborate across Manufacturing, Quality, Safety, Maintenance, and Engineering teams to deliver robust solutions.
This position involves less than 5% travel.

Who You Are

Minimum Qualifications:

Bachelor’s Degree in an Engineering discipline (Electrical, Mechanical, Computer, etc.).
2+ years of experience programming or configuring automation systems using PLC, PC-based, microcontroller, or comparable control platforms.
1+ years of experience in technical documentation, work instructions, or training materials.
1+ years of experience designing, troubleshooting or prototyping electromechanical systems in a laboratory, manufacturing, industrial, or comparable environment.

Preferred Qualifications:

Strong communication and collaboration skills across operations, quality, safety, maintenance, and engineering teams.
Ability to develop clear technical documentation, work instructions, and training materials.
Experience with equipment qualification, validation, change control, risk assessment, and/or technical investigations.
Proficiency with source control and documented software release practices.
Experience using Foundry, Tableau, Power BI or similar tools to provide quality and cost savings insights.
Lean, Six Sigma, or structured continuous-improvement experience.

Pay Range for this position: $69,500- $104,200

RSREMD

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Responsable Affaires Réglementaires (F/H) (Lyon, Rhone, FR, 69008)

Exprimez votre talent avec nous !

Votre rôle :

Rattaché au Directeur des Affaires Réglementaires France, vous rejoignez une équipe experte et contribuez à la gestion d’un portefeuille diversifié de médicaments matures et innovants.

Vous êtes le référent réglementaire d’un portefeuille de produits commercialisés en France et accompagnez leur maintien ainsi que leurs évolutions tout au long de leur cycle de vie. Vous garantissez l’optimisation des Autorisations de Mise sur le Marché (AMM) dans le respect des exigences de l’ANSM et de la réglementation européenne. Vous pilotez les soumissions réglementaires locales, notamment les variations, renouvellements, changements administratifs et activités liées au Module 1.

Vous participez aux lancements de nouveaux produits et accompagnez les équipes projet à chaque étape réglementaire clé. Vous veillez à la conformité des articles de conditionnement et des documents associés, tout en assurant une veille réglementaire proactive et l’évaluation de ses impacts.

En tant que Pharmacien expérimenté, vous contribuez à certaines activités déléguées du Pharmacien Responsable, notamment la revue, l’approbation et la certification des communications promotionnelles et non promotionnelles destinées aux professionnels de santé. Partenaire stratégique des équipes Marketing, Médicales, Qualité et Globales, vous coordonnez les activités réglementaires et favorisez l’alignement des stratégies locales et internationales.

Basé au siège à Lyon, vous bénéficiez d’une forte visibilité, d’une réelle autonomie et de l’opportunité d’influencer des sujets stratégiques dans un environnement à taille humaine et en constante évolution.

Qui vous êtes :

Vous êtes Docteur en Pharmacie et êtes inscriptible auprès de l'Ordre afin d'exercer les activités pharmaceutiques requises en France.
Vous justifiez d’au moins sept années d’expérience en Affaires Réglementaires dans l’industrie pharmaceutique ou biopharmaceutique.
Vous maîtrisez les procédures d’enregistrement des médicaments aux niveaux national et européen ainsi que les exigences applicables au marché français.
Vous êtes autonome dans la gestion d’un portefeuille réglementaire et savez piloter des projets complexes en respectant les priorités et les délais.
Vous avez idéalement contribué au lancement de produits et à des projets réglementaires à forts enjeux.
Une expérience dans la revue de matériels promotionnels et non promotionnels ou dans des activités relevant de la responsabilité pharmaceutique constitue un atout significatif.
Vous faites preuve de rigueur, d’esprit d’analyse, de collaboration et d’influence dans un environnement matriciel.
Vous maîtrisez le français et l’anglais professionnel, à l’écrit comme à l’oral, et êtes à l’aise dans un contexte international.

Postulez dès maintenant et devenez membre de notre équipe dont la vision est de stimuler les découvertes pour élever l'humanité !

Geschäftsführende Intendanz, Deutsche Philharmonie Merck (m/w/d) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Über uns

Die Deutsche Philharmonie Merck, rechtlich als Verein geführt und unterstützt von Merck KGaA, Darmstadt, Deutschland, gehört zu den leistungsstärksten freien Orchestern der deutschen Musiklandschaft und ist kulturelles Aushängeschild der Rhein-Main-Region mit 30–40 Auftritten im Jahr und erfolgreicher Kulturbotschafter auf nationaler und internationaler Ebene. Unser Spektrum reicht von Sinfonie- und Neujahrskonzerten über Open-Air-Events und Filmmusik bis hin zu Cross-Over-Projekten, Kinderkonzerten sowie Gastspielen im In- und Ausland.

Ihre Aufgabe

Als geschäftsführende Intendanz tragen Sie die künstlerische und betriebswirtschaftliche Gesamtverantwortung. Sie schärfen das Profil des Orchesters im Wettbewerb, sichern die finanzielle Stabilität, führen ein eigenes Team und unterhalten ein hochkarätiges Netzwerk aus freiberuflichen Musikerinnen und Musikern sowie Kooperationspartnern. Eine zentrale Säule Ihrer Arbeit ist der kreative Dialog als Schnittstelle zwischen dem Vereinsvorstand und unserem Förderpartner. Wir suchen eine profilierte Führungsperson, die strategisch steuert, künstlerisch inspiriert und im Alltag tatkräftig mitgestaltet.

Gesamtleitung & Strategische Planung

Strategische und operative Gesamtverantwortung für Spielplangestaltung, Disposition und Personalführung.
Saisongestaltung: Konzeption, Disposition und Koordination des Spielplans in enger Abstimmung mit den Dirigentinnen und Dirigenten.
Kuration & Formate: Weiterentwicklung innovativer Konzertreihen, Tourneen und digitaler Angebote.
Qualitätsmanagement: Sicherstellung eines international wettbewerbsfähigen Niveaus des Orchesters und Auswahl exzellenter Solistinnen, Solisten und Gastkünstlerinnen und Gastkünstler.
Spielstätten Management: Vorausschauende Planung und Buchung geeigneter Spielstätten.
Steuerung der Organisation und des Personals.
Planung und Durchführung von internationalen Konzertreisen.

Betreuung des Musikerinnen- und Musiker-Netzwerks & Ensembleleitung

Netzwerkpflege: Erhalt und Erweiterung unseres qualifizierten freien Musikerinnen- und Musikerstamms.
Orchesterkultur: Zusammenführung wechselnder Projektbesetzungen zu einer musikalischen Einheit mit unverwechselbarer Identität und gemeinsamer Klangkultur.
Besetzungsmanagement: Bedarfsgerechte und künstlerisch kohärente Besetzungsplanung für alle Projekte in Abstimmung mit dem Orchestermanagement.
Vertragswesen: Rechtssichere Gestaltung von Honorarverträgen.

Kaufmännische Geschäftsführung

Finanzverantwortung: Erstellung, Monitoring und Kommunikation des jährlichen Wirtschaftsplans in Abstimmung mit dem Vorstand, inklusive der operativen Buchhaltung, des Rechnungswesens und der Kassenführung.
Repräsentation: Souveräne Vertretung des Orchesters gegenüber Medien und Fachöffentlichkeit sowie Leitung vor Ort bei Konzerten und Gastspielen.

Ihr Profil

Abgeschlossenes Hochschulstudium (Kulturmanagement, Musikwissenschaft, BWL) oder eine vergleichbare Qualifikation, z.B. durch einen einschlägigen Quereinstieg.
Mehrjährige Praxiserfahrung im Orchestermanagement oder in leitender Funktion in Kultureinrichtungen.
Fundiertes Wissen im klassischen und zeitgenössischen Repertoire.
Führungsperson: Empathischer und professioneller Umgang mit einem hochspezialisierten Team. Kommunikative Persönlichkeit mit sehr gutem Organisations- und Improvisationstalent, Flexibilität und der Fähigkeit zum ergebnisorientierten Arbeiten im Team, hohes Maß an Eigenverantwortung.
Sicherer Umgang mit Kulturrecht (insbesondere freiberufliche Beschäftigung).
Erfahrung in Management- und Budgetverantwortung.
Strategische und operative Gesamtverantwortung für Spielplangestaltung, Disposition und Personalführung.
Umfassende Kenntnisse der Konzertliteratur und ein starkes, etabliertes Netzwerk in der deutschen und europäischen Musiklandschaft.
Verhandlungssicheres Deutsch und Englisch.
Verhandlungssouveränität: Diplomatisches Geschick im Umgang mit Agenturen, Künstlerinnen und Künstlern sowie Gremien.
Strategisches Denken: Fähigkeit, Visionen in wirtschaftlich tragfähige Konzepte zu übersetzen.
Kompetenz im Umgang mit unterschiedlichen Kulturen und Erfahrung im internationalen Umfeld; Freude an Reisen und Neugier auf Neues.
Freude am Kulturbetrieb mit allem, was dazu gehört.

https://philharmonie-merck.de/

Bewerben Sie sich jetzt und werden Sie Teil eines Teams, das Neues entdeckt und die Menschheit voranbringt.

Healthcare Business Process Architect (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your Role: In this pivotal role, you will guide the global healthcare business through its digitalization journey by shaping efficient, consistent end to end processes supported by enterprise resource planning systems. You will act as a technical authority for SAP TM (Transportation Management) connect related supply chain processes, and independently solve complex business and technology challenges. By using process analytics, monitoring, benchmarking, configuration, and master data insights, you will identify opportunities, guide improvement and deployment initiatives, define measurable business value, and influence stakeholders across functions and external partners to deliver sustainable improvements for customers and patients.

Who You Are

You have a university degree or equivalent experience in industrial engineering, information technology, business administration, data science, supply chain, or a related discipline; a relevant professional qualification is an advantage.
You bring deep knowledge of supply planning and related supply chain processes in fast moving consumer goods, life sciences, pharmaceuticals, or comparable industries.
You have deep expertise in SAP TM (Transportation Management) and its integration with SAP EWM (Extended Warehouse Management), SAP O2C (Order to Cash), and SAP Inbound to Outbound logistics processes within ERP (enterprise resource planning environments).
You have deep expertise within SAP TM Freight Order, Carrier selection, Shipment execution and Exception alerts, Freight settlement and Invoice processing & Reporting.
You have strong experience with process analytics, process mining, benchmarking, configuration, master data, and reporting, including implementation at production or distribution sites.
You solve complex problems independently, shape technical direction, and translate global and local priorities into measurable process improvements.
You have experience guiding improvement or deployment projects, influencing stakeholders across business and technology functions, working internationally, and traveling up to 30%.
You have experience managing and driving the team of business Key users and external partners for the solution of end to end logistics processes. Also have extensive experience with Business stakeholder communication and management reporting.
You communicate clearly in written and spoken English and bring a collaborative, curious, accountable, and value focused approach; Spanish or another language is an advantage.
You understand how artificial intelligence works, including core concepts and limitations; can evaluate practical applications and decision implications; and apply ethical judgment covering bias, fairness, privacy, governance, and accountability. Any further experience with SAP Joule or AI tools for Transportation integration would be a plus.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

助理客户经理 (Beijing, Beijing, CN, 100016)

Work Your Magic with us!

Responsibility

Responsible for liaising with major clients in the panel industry regarding product development needs, coordinating internal development resources to meet these needs, and driving project progress.
Continuously monitor project progress, maintain active communication with relevant client departments, and ensure the project qualification.
Understand the semiconductor display industry, keep abreast of industry developments, and identify business breakthrough opportunities.
Stay informed about clients' development trends and prepare products in advance to meet their needs.
Continuously monitor the competition landscape and respond quickly.
Identify client needs, establish long-term stable partnerships, and enhance client satisfaction.
Strive to achieve business targets set by the company and maintain a positive and optimistic attitude.
Complete internal company reports with care and accuracy, providing an objective and truthful reflection of client conditions.
Assist the customer service department in communicating about product delivery, payment, and other matters.
Actively address technical issues raised by clients, coordinate internal resources, and complete relevant tests.

Qualifications

Education Background

Bachelor's degree or above.

Work Experience

Over 5 years of experience in the Semi/Display industry.
Preference for candidates with hands-on experience in panel manufacturing.

Professional Skills

Familiarity with the market characteristics and technological trends of the semiconductor display industry.
Proficiency in using office software (such as Word, Excel, PowerPoint, etc.).
Strong spoken and written English communication skills.

Personal Qualities

Excellent communication skills, market analysis capabilities, and customer service awareness.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Product Manager - Fertility & Endocrinology (Singapore, Singapore, SG, 118222)

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What You Do

Develop and execute the annual brand and marketing plans for the Fertility & Endocrinology portfolio, aligned with business objectives, regional strategy and market dynamics.
Translate market, customer, competitor and patient insights into clear brand priorities, differentiated positioning, key messages and competitive strategies.
Drive end-to-end execution of marketing initiatives, campaigns, customer programs and product launches, with clear objectives, KPIs and performance tracking.
Identify portfolio growth opportunities to strengthen market share, product adoption, patient access and sustainable business performance.
Develop a deep understanding of the Fertility & Endocrinology patient journeys and identify opportunities to improve diagnosis, treatment initiation, adherence and overall patient experience.
Build and maintain strong relationships with key opinion leaders, fertility specialists, endocrinologists, paediatric endocrinologists and other relevant healthcare stakeholders.
Partner with Sales and Medical to develop customer engagement strategies and account-specific initiatives for priority institutions and healthcare networks.
Drive initiatives to strengthen product access, institutional listings and adoption across relevant public and private healthcare channels.
Develop compelling scientific and promotional messages, educational materials, campaigns, congress activities and customer engagement programs to strengthen brand differentiation.
Design and implement omnichannel engagement strategies, leveraging face-to-face, digital, CRM and other channels to enhance customer experience and engagement effectiveness.
Partner closely with the Sales team to translate brand strategy into effective field execution, including product, disease and competitive training.
Capture and integrate field insights, customer feedback and competitive intelligence to continuously refine brand strategy and execution.
Collaborate cross-functionally with Sales, Medical, Market Access, Regulatory Affairs, Quality, Supply Chain, Finance, regional and global teams to ensure integrated portfolio execution.
Monitor sales performance, market share, customer behaviour, competitive developments and key performance indicators to identify opportunities, risks and corrective actions.
Lead demand forecasting and inventory planning in collaboration with Sales and Supply Chain to optimize product availability and business continuity.
Manage promotional investments and resources effectively, ensuring allocation is aligned with strategic priorities and business impact.
Contribute to annual business planning, budgeting, forecasting and longer-term portfolio planning for Fertility & Endocrinology.
Ensure all business and marketing activities comply with relevant HSA, SAPI, company policies and Code of Conduct requirements.
Recognize and appropriately report Adverse Events, pharmacovigilance information and product quality complaints according to company procedures

Who You Are

Bachelor’s Degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, Medicine, Business, Marketing or related field; MBA is an advantage.
Minimum 5 years of pharmaceutical experience in product management, marketing and/or commercial roles.
Experience in Fertility, Endocrinology, Women’s Health, Paediatrics or hormonal therapies is preferred.
Strong commercial acumen and analytical skills, with the ability to translate market, customer and clinical insights into actionable strategies.
Strong brand management, marketing execution and project management capabilities.
Excellent communication, stakeholder management and cross-functional collaboration skills.
Familiarity with the Singapore healthcare environment and relevant HSA/SAPI requirements.
Experience with digital marketing, CRM and omnichannel engagement is an advantage.
Fluent in written and spoken English, with proficiency in Microsoft Office applications.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Validation Specialist (12개월 계약직, 2년 이상 유관 경력자, 제약/바이오) (Daejeon, Daejeon, KR, 34122)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your role:

The Validation specialist role will perform site qualification& validation and ensure that qualification& validation activities consistently comply with all regulatory and corporate requirements in support of regulatory requirements and customer expectations.

This position will also entail validation Management system operation and maintenance, to ensure the system compliance with all Domestic and Global regulatory and corporate requirements.

Ensure validation employees are hired, trained, and qualified to support project execution and conduct daily operational activities.
Develop site validation management procedures for equipment qualification, computerized system validation, process validation, cleaning validation, transportation verification, and HVAC/Clean Utilities ensure that site validation management procedure complies with regulatory requirements and global standards.
Prepare Validation Master Plan, Validation Plans for Equipment qualification, process and cleaning validation, and Computerized Systems (PCS, MES, EMS, WMS, ASRS, LIMS) in place on schedule in collaboration with Subject Matter Experts.
Conduct site qualification& validation, ensure that processes, procedures, equipment, facility, systems and methods are validated, and ensure that qualification& validation activities consistently comply with GxP/ISO regulatory requirements, corporate standards and customer expectations.
Collaborate process owner/relevant dept for validation activities such as URS, risk assessment, FAT/SAT document review, validation protocol/report preparation, and execute DQ/IQ/OQ/PQ including test execution witness and result review.
Carry out periodic validation status review and perform site requalification and revalidation.

Who you are:

Minimum bachelor’s degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, or a related discipline.
+ 2 years in the pharmaceutical, biotechnology in quality assurance, GMP compliance, operations or validation, ideally in a multinational company.
Experience in handling sterile product required.
Experience in developing CCS and APS/APV preferred.
Good communication in English.
Good decision-making and problem-solving capability

<유의사항>

•여러분이 찾고 계시는 채용 포지션이 없으신가요? 그렇다면 인재풀(클릭)에 여러분의 이력서를 등록해주세요! 향후 인력 수요가 있을 경우 최우선으로 안내드리겠습니다.

•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.

•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.

•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.

•지원서의 기재사항이 사실과 다른 것으로 확인되거나 Reference from previous employer 상에 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.

•(The company reserves the right to withdraw the offer, it if discovers subsequently that a candidate has given false information in application or has provided false or fraudulent documentation in support of his/her application. The offer is conditional upon satisfactory results of reference checks.)

•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Category Manager & Global Sourcing Manager Site Services (all genders) (Weiterstadt, Hessen, DE, 64331)

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Your role
As a Global Category Manager for Site Services, you will sit at the heart of a worldwide Technical Sourcing organization, shaping the procurement strategies that underpin some of the most significant capital and operational investments across a global science and technology enterprise. This is a high-
visibility, high-impact role for an experienced procurement professional who thrives on complexity, drives value at scale, and influences outcomes across organizational boundaries without relying on direct authority.
You will own and continuously evolve the global category strategy for Site Services – spanning Equipment and Components, Construction, and Energy – directly aligned to capital investment plans and long-term business priorities. Applying a spend entrepreneurship mindset, you will lead rigorous end-to-end sourcing programs: from market analysis, supplier segmentation, and total cost of ownership modeling through to contract conclusion and claim management.
You will build and govern a high-performing strategic supplier portfolio, establish structured supplier relationship management programs with clear key performance indicator frameworks and governance cadences, and ensure resilient, multi-region supply continuity. Acting as a trusted counterpart to
Manufacturing, Engineering, Operations, Finance, Legal, and Compliance stakeholders across all business sectors, you will coordinate virtual global category teams across the Americas, Europe, and Asia – generating cross- project synergies and delivering quantifiable, sustained value improvements with full transparency to senior leadership

Who you are
• Bachelor’s or Master’s degree in Economics, Supply Chain Management, Engineering, Business Administration, or a related field; equivalent professional experience is equally valued.
• 8–12+ years of progressive experience in strategic sourcing and category management, with a strong track record in indirect, technical, or engineering-related procurement within complex, multinational environments – ideally in life sciences, healthcare, or electronics.
• Demonstrated expertise in developing and executing global category strategies, including capital expenditure and operational expenditure procurement, supplier relationship management, contract negotiations, and multi-region supplier governance.
• Exceptional analytical and commercial acumen: fluency in total cost of ownership modeling, spend analytics, should-cost analysis, and advanced negotiation strategies, with the ability to translate technical requirements into compelling procurement solutions.
• Outstanding stakeholder management and influencing skills; proven ability to lead without formal authority in a matrixed global organization and to present data-driven business cases to senior leadership.
• Solid understanding of compliance-intensive environments, including Good Manufacturing Practice standards and sustainable procurement practices aligned to environmental, social, and governance principles.
• Demonstrated ability to engage with artificial intelligence tools and concepts – including their practical applications, limitations, and ethical implications – to support informed, responsible decision-making in a procurement context.
• Business fluency in English is required; proficiency in German, French, Mandarin, or other languages is a distinct advantage.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Manufacturing Operator 2 - 12 Hour Night Shift (Sheboygan Falls, Wisconsin, US, 53085-2814)

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

$5000 Sign on Bonus if Hired

Your Role:

In this role your tasks will include, but are not limited to:

Produce, purify and package chemical compounds to meet the requirements of MilliporeSigma customers
Stage materials utilizing a variety of warehouse equipment including pallet trucks and Powered Industrial Trucks
Verify the quality and integrity of materials and equipment
Perform in-process analytical testing including workups and simple interpretations as described in the Master Production Record
Update batch records, computer systems and SAP per ISO procedures
Demonstrate proper lab, manufacturing and packaging safety practices in accordance with OSHA, EPA, DNR, DOT and other regulatory agency guidelines
Maintain a high level of safety with our pro-active “see something – say something” approach to safety as well as participate in core operational excellence programs including Daily Management System, 6S organization and safety walks
Participate in team-based objectives focused on improving safety, quality and production output of key manufacturing processes
Shift/Hours: 12-hour night shift, 6:00 PM - 6:30 AM - 2/2/3 schedule (M/T on, W/R off, F/S/S on, M/T off, W/R on, F/S/S off, repeat)

Physical Attributes:

Wear an air helmet, respirator mask, safety shoes, rubber apron, chemical protective suits and gloves, safety glasses and goggles to protect from toxic or corrosive chemicals
Work in occasional wet, humid abnormally hot or cold environment
Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, or crouch for long periods of time
Lift and/or move up to 50 pounds
Work with and in proximity of hazardous chemicals
Use close vision, distance vision, color vision, peripheral vision, depth vision and the ability to adjust focust

Who You Are:

Minimum Qualifications:

High School Diploma or GED
3+ years of experience in an industrial or manufacturing setting

Preferred Qualifications:

Experience with chemical handling
Experience with chemical reactions and hazards
Experience with ISO and quality systems
Strong mechanical and technical aptitude
Ability to read and understand written protocols
Experience with multitasking
Strong problem solving and equipment troubleshooting skills
Strong oral and written communication skills

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Graduate/Junior Field Service Engineer - West London (Feltham, London, GB, TW14 8HA)

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Your Role:

As a Graduate/Junior Field Service Engineer, you will be the technical backbone of our Life Science business. Your role is crucial in ensuring our customers receive the highest quality service and support.

Here's a glimpse of your exciting responsibilities:

Installation & Commissioning: Expertly install and commission instrumentation, predominately lab water purification systems at various client sites, ensuring optimal performance from day one.
Maintenance & Servicing: Perform regular maintenance and servicing to keep systems running smoothly, preventing downtime, and ensuring reliability.
Repairs: Diagnose and repair any issues with precision and speed, minimizing disruptions for our clients
Validation: Validate and calibrate equipment to ensure compliance with industry standards and client specifications.
Customer Support: Provide exceptional support and training to customers, empowering them to utilise our systems to their full potential.
Sales: Generate leads for new hardware, consumables, accessories, and service contracts via the current CRM tool.
Travel: Enjoy a dynamic role with travel predominantly around the West or North West London area (depending on your location), offering new challenges and experiences every day.

Who you are:

Education: Degree, Apprenticeship or equivalent level qualification in either an Engineering or Scientific discipline.
Location: Candidates must be located on territory on the West or North West side of London within the M25.
Problem Solving Skills: Ability to diagnose and troubleshoot issues efficiently.
Customer focus: Excellent communication skills and customer-centric approach.
Adaptability: Flexibility to travel and adapt to varying work environments.
Team Player: Collaborative mindset and the ability to work independently.
Experience: Previous field service experience is a plus, but not mandatory. Comprehensive training and onboarding will be provided.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Advanced Packaging Principle Integration Technologist (Principal Engineer, 10 years+ experience) (Hsinchu, Hsinchu County, TW, 300)

與我們攜手施展你的超能力！

Internal Job Title: High Performance Packaging Principle Integration Technologist

Summary:

In this role, you will be instrumental in developing our Advanced Packaging opportunity definition, ecosystem engagement strategy, and program development. By connecting across key business unit partners and leveraging our core competencies, you will drive business and product development from idea to proof of concept for transfer to high-volume manufacturing.

The ideal candidate will combine deep equipment, process, and integration knowledge of Advanced Packaging technologies — including Wafer Level Packaging, Hybrid Bonding, Fusion Bonding, and adjacent technologies — with a vast ecosystem network of equipment suppliers, Integrated Device Manufacturer, Foundry, and Memory customers, as well as consortia partners.

Your Role:

Through technical expertise, identify and stay ahead of key Advanced Packaging technology inflection points and roadmaps
Through industry and ecosystem connections, continuously acquire in-depth strategic knowledge of customer and Original Equipment Manufacturer(OEM) roadmaps
Transfer knowledge and educate peers — both laterally and upward — on Advanced Packaging roadmaps
Leverage industry knowledge to identify process, equipment, and integration challenges
Work across business units and the Chief Technology Office to identify material solutions and developments that address industry challenges
Leverage industry networks and connections to engage the ecosystem on collaborative development opportunities
Apply deep technical knowledge to ensure development programs identify and meet industry-standard datasets
Ensure development programs leverage industry expertise to deliver relevant datasets in the most timely manner

Who You Are:

Minimum Qualifications:

Master of Science degree or higher in Mechanical Engineering, Electrical Engineering, Chemical Engineering, or a related engineering field
10 or more years of experience developing integration and process flows
10 or more years of hands-on 300mm process and equipment R&D experience
Experience as an Advanced Packaging 300mm Equipment Tool Owner
Experience in Advanced Packaging Thin Film Deposition, Chemical Mechanical Planarization, Bonding, or Patterning process development
7 or more years of collaborative external business development experience
Experience defining Scope of Work, Proof of Concept, and Design of Experiments for equipment and material definition

Preferred Qualifications:

5 or more years of experience engaging with Advanced Packaging consortia — such as IMEC, ITRI, and A*STAR — including engagement model definition, Scope of Work development, and Proof of Concept execution
Demonstrated ability to work effectively in highly ambiguous environments
Demonstrated ability to work across matrixed organizations and deliver results
Demonstrated ability to influence senior stakeholders in order to secure resources
Entrepreneurial mindset with a drive for innovation
Ability to distill complex material into clear, actionable items
Ability to engage and align resources to deliver successful outcomes
Demonstrated knowledge of customer and supplier interactions, with the ability to extract meaningful insights from those conversations
Self-starter with the ability to operate with minimal direction

Work Location: Based in Taiwan (Open to: Taipei, Hsinchu, Tainan, or Kaohsiung offices)

立即申請，成為這個致力於激發探索精神、提升人類未來的團隊一員！

Senior Cloud Engineer - AI-ML Platform (Bangalore, Karnataka, IN, 560100)

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Senior Cloud Engineer – AI/ML Platform (f/m/d)

Your Role

As a Senior Cloud Engineer specialising in AI/ML Platform infrastructure, you will be at the heart of building and operating the cloud-native foundation that powers data, analytics, and artificial intelligence workloads across the organisation. In this pivotal role, you will design, deploy, and continuously improve scalable, resilient infrastructure on AWS — enabling AI/ML engineers and data scientists to develop, deploy, and monitor machine-learning models and AI services at production scale. You will own critical platform components end-to-end: from containerised workloads and streaming pipelines to networking, security, and CI/CD automation. Working at the intersection of cloud engineering, data platforms, and AI/ML operations, you will solve complex infrastructure challenges with a pragmatic, reliability-first mindset and directly shape the technical direction of a platform that drives meaningful business outcomes.

Who You Are

You bring 5 or more years of hands-on cloud engineering experience, with strong expertise in AWS services including Elastic Container Service, Elastic Kubernetes Service, Virtual Private Cloud networking, and managed streaming solutions.
You have proven experience provisioning and managing cloud infrastructure as code using Terraform and/or CloudFormation, and you are comfortable owning production environments end-to-end.
You are skilled in building and maintaining CI/CD pipelines (for example using Azure DevOps) and apply disciplined version-control practices in collaborative engineering environments.
You have hands-on experience designing and operating streaming platforms such as Apache Kafka or equivalent cloud-managed alternatives, with a focus on scalability and resilience.
You implement platform security with confidence — including Transport Layer Security, secrets management, access controls, and authentication mechanisms such as JSON Web Tokens, OAuth, and LDAP.
You have experience deploying, scaling, and monitoring AI/ML workloads and model-serving APIs, and you collaborate effectively with AI/ML engineers and data scientists to bring models into production.
You hold a degree in Computer Science, Software Engineering, or a related field, or bring equivalent professional experience; familiarity with multi-cloud environments or Azure AI/ML services is a plus.

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Regional Regulatory Manager (Billerica, Massachusetts, US, 01821)

Work Your Magic with us! Start your next chapter and join EMD Serono.

The Regional Regulatory Manager is responsible for the execution of the regulatory strategy for their assigned projects and for supporting local regulatory activities in their region / country.

Represent and provide input for your respective region at the GRST.

Lead or support the respective regional regulatory sub-team.

Drive the regulatory submission in your respective region. Ensure optimal planning in alignment with cross-functional team, and execution to plan for both development submissions and maintenance submissions to ensure ongoing compliance. Partner with Regulatory Project Management and Submission Management.

May act as direct contact to a local HA (e.g. FDA). Lead the direct interactions with the respective local HA in this case.

Contribute to the global regulatory strategy with local / regional strategy for assigned projects.

Matrix leadership role of respective Regional Regulatory sub team.

Participate in cross-functional and GRA initiatives.

Required Background

Advanced degree (e.g., PhD, PharmD, MD, or equivalent).
At least 1 year of regulatory affairs strategy experience in drug development in the US
Demonstrated successful interactions with FDA related to strategy and execution of development and maintenance activities.

Demonstrated matrix leadership skill.

Location: This is an onsite role based in our Billerica, MA facility requiring and onsite presence at least 3 days per week.

Pay Range for this position: $103,900 - $155,900. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here: https://careers.emdgroup.com/us/en/benefits

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

CMC & GM Sales Representative - Cuenca (Quito, Pichincha, EC, PISO 11)

Tu Rol

Promocionarás y comunicarás las especificaciones de nuestros productos en cardio metabólica (cardiovascular, tiroides y diabetes) a clientes, asegurando que conozcan precios y disponibilidad. Implementarás técnicas de ventas efectivas y optimizarás el perfilamiento del cliente. Te comprometerás con los médicos en la prescripción de nuestros productos mediante la adaptación de planes de mercadeo. Realizarás seguimiento a inversiones y ejecuciones, analizando desviaciones. Colaborarás con el gerente de distrito para segmentar adecuadamente a los médicos. Cumplirás con KPIs y planes de visitas predefinidos. Capacitarás a dependientes de farmacias sobre nuestros productos clave y te auto capacitarás constantemente. Se requieren de 3 a 8 años de experiencia como representante médico.

Quien Eres

Tienes experiencia en línea cardio metabólica.
Posees relaciones con médicos generalistas, cardiólogos, internistas, familiares y endocrinos.
Manejas herramientas como DDD, POWER BI, Close Up, iQVIA, VEEVA y Microsoft.
Cuentas con habilidades analíticas para entender tu territorio y sus dinámicas.
Tienes un título universitario en un campo relacionado. (Indispensable)
Eres proactivo y orientado a resultados.
Tienes habilidades de comunicación efectiva y trabajo en equipo.

¡Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!