Careers at Merck KGaA, Darmstadt, Germany

Access Strategy Manager (Hanoi, Ha Noi, thu do, VN, 110001)

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.

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.

Report to: Head of Market Access and Pricing

Base in: Hanoi

Your roles:

National Reimbursement Drug List (NRDL): Convince Health Authorities to include company products in the NRDL by presenting robust, evidence-based data on their efficacy and cost-effectiveness.
National Centralized Tender in National Centralized Procurement Center (NCPC): Support the Distributor for a securing an appropriate quota plan for the market demand, good price approach and a securing supply plan.
PAP (Patient Assistant program): Design a program to provide support to patients who may have difficulty accessing medications or healthcare services.
Policy (related to NRDL, Pricing, Drug Procurement, Orphan drugs): Keep track of relevant policies to ensure the company's actions are well informed ahead & be compliant.

Who You Are:

Over 3 years of experience in multinational pharmaceutical companies, focusing on Access area (NRDL, PAP, Pricing, Policy).
In-depth understanding of healthcare systems and relevant policies.
Strategic thinker with a customer-oriented mindset, effectively engaging both internal and external stakeholders.
Proficient in verbal and written English at an upper-intermediate level or higher.

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!

Engineer Field Services - Toscana (Milano, Milan, IT, 20149)

Work Your Magic with us!

Your Role:

As a Field Service Engineer, you will be responsible for the maintenance and repair of the Biomonitoring equipment at the customer site. You act as the interface between customers and internal departments to develop business opportunities by promoting service activities, products, and solutions.

You will install, repair, and maintain an extensive variety of products and equipment. You will identify, analyze, and repair product failures. You will recommend which products or services would best fit customer’s needs and provide trainings to customers. You will perform service activities that align with all applied regulations (EHS) and advise customers on this topic. You will follow current company procedures and SOPs/guidelines. You will update timely the CRM (Service Max) and report regularly to the Management. You will order and replace parts as needed. You will handle own spare parts in stock & car to enhance first time fix rate without impacting the non-moving parts' list. Besides that, you will also be involved with other duties aligning with the company strategy.

Who You Are :

You are preferably located in the central part of Italy (Tuscany)
A completed vocational training or bachelor’s degree in Technical Professions with preferred practical experience as Field Service Engineer
Good level of English and Italian to communicate in a professional manner
Good knowledge in digital literacy (Word/Excel/CRM) & experienced in project management
Willingness to travel, at least 85% of the time. Will be mostly in Italy but could be from time to time in other countries in Western Europe. A valid Italian driving license is mandatory.
Ability to work independently and develop personal initiatives with strong interpersonal and problem-solving skills

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

安全工程师 (Liaoning, Liaoning, CN, 21 116600)

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：
制定并实施企业环境健康安全管理体系（EHS),统筹管理生产现场的安全风险防控、职业健康管理及环境保护工作；
负责安全事故调查分析与整改闭环管理，定期组织应急演练及隐患排查，确保零重大事故目标达成；
推动EHS法规合规性审查，建立标准化操作流程(SOP）及应急预案体系，提升全员安全意识；
协调跨部门资源推进环保项目落地（如危废处理、节能减排等），完成政府监管机构检查迎检工作；
监控安全生产指标数据，编制月度／年度安全报告，提出持续改进方案以降低运营成本；
参与新员工岗前培训及特种作业人员资质审核，构建覆盖全层级的安全文化宣教机制。

任职要求：
本科及以上学历，安全工程、环境科学、化工类相关专业优先，持有注册安全工程师证书；
熟悉《安全生产法》《职业病防治法》等法律法规，掌握ISO14001/OHSAS18001体系标准；
具备基础数据分析能力，能运用Excel/PPT进行安全管理报表制作及可视化呈现；
拥有良好的沟通协调能力，可独立推动多部门协调。

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！

质量体系技术员 (Wuxi, Jiangsu, CN, 214033)

与我们携手施展你的超能力！

职位描述：

岗位目标:

该职位将负责投诉调查实验室的日常投诉调查测试，协助解决投诉报告并参与产品质量改进分析。

岗位职责：

按照SOP、质量标准和分析方法等进行检测，及时并合适的对各相关活动进行记录。
跟踪工作进度并按时完成以确保团队/部门目标及时达成。
按照指导进行投诉调查并支持投诉报告撰写，并追踪投诉调查的关闭和CAPA的执行。
对于投诉进行登记，并能使用电子工具登记/分析调查结果。
根据工作指令的紧急程度，对紧急测试进行优先排序。
根据计划执行分析设备的校验和维护。
跟踪工作表的进度。完成团队/部门目标所需的大量工作并在期限内完成。
根据需要为实验室提供支持。
在EHS部门的指导下，确保实验室日常操作的安全。
负责主管安排的其他工作。

任职要求：

本科及以上学历，微生物或者制药相关专业。
1年以上生命科学或制药行业QC或同等工作经验。
基本的英语听说读写能力。
良好的团队合作精神，优秀的交流，问题处理，计划和组织能力。
GMP/ISO9000背景。

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！

Production Manager (화학 산업군, 10년 이상 경력, 시화 근무) (Siheung-Si, Gyeonggi-do, KR, 15094)

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.

생산팀 매니저 (화학 공정, 10년 이상 경력, 시화 근무)

주요 업무

시화 사이트의 담당 단위 생산 공정을 운영 관리 및 최적화하여 시장 수요를 효율적이고 안전하게 충족합니다.
EHS 규정, ISO 표준(9001/14000/18001) 및 회사 규율을 준수합니다.
생산 일정 관리로 납기일을 준수하며, 비용을 통제하고 품질 기준을 유지합니다.
생산 문제에 대한 원인을 분석하고, 예방 조치를 포함한 문제를 해결합니다.
공정 개선 및 생산 용량 확장을 위한 CAPEX 프로젝트를 개발 및 실행합니다.
EHS, QA 등 관련 팀과 협력하여 공정 안전을 유지하고, 고객 요청에 대응합니다.
공정 최적화를 통한 제조 우수성을 촉진합니다.
유지보수 팀과 협력하여 안전한 셧다운 실행을 보장합니다.
목표 설정, 직원 코칭, 성과 평가, 지식 교류 촉진 등을 통해 팀원들의 성장을 촉진합니다.

자격 요건

공학 또는 관련 분야 학사 이상의 학위 소지자
화학 또는 제조 공정에서의 최소 10년 이상의 생산 업무 경험
EHS 규정, 엔지니어링 표준, 글로벌 안전 프로그램(BSP)에 대한 이해도
예산 관리, 자원 배분, 재고 관리 시스템 및 조달 프로세스 성공적 운영 경험
매니저로서 팀 관리 경험
생산 문제 해결, 원인 분석(RCA), 예방 조치 실행 경험

<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.

Rare Tumour Medical Science Liaison Rare Tumors Portugal (Alges, Alges, PT, 1495-190)

Work Your Magic with us!

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.

As the (Senior) Medical Science Liasion for our newly acquired company, SpringWorks, you will play a pivotal role in driving operations and strategicgrowth within your designated country or cluster.

The (Senior) Medical Science Liaison, (hereafter (Sr.) MSL) will be responsible for managing a company product(s) within a defined territory. This entails establishingand maintaining key scientific relationships with Key Opinion Leaders (KOLs) within their territory and serving as a scientific expert to the medical community andfacilitating the appropriate exchange of scientific information.

Key expectations include the Sr. MSL being able to develop and maintain an advanced scientific, medical, and product knowledge base, ability to communicate keyinsights learned, and disseminate critical scientific data to external stakeholders; including but not limited to academic/scientific/clinical experts and patient organizations.

The (Sr.) MSL will be responsible for ensuring timely and appropriate input on the field medical engagement plans in support of our clinical development andcommercialization programs and activities. In addition, the (Sr.) MSL will assist, lead, and drive the support of the company’s clinical trials in partnership with theclinical development team and with researchers as appropriate.

The (Sr.) MSL will be expected to master the MSL responsibilities and be able to take on additional leadership roles on projects and initiatives within the country orregion. The (Sr.) MSL will be expected to work independently with little direction/oversight, be accountable, and assist the Regional Medical Director as needed.

Key Responsibilities will include:

Identify KOLs and establish and maintain strong and deep scientific relationships with KOLs across multi-specialty disciplines, connecting to KOLs in academic andnon-academic centers at the local, regional, and national level.
Serve as a scientific expert to the medical community and facilitate the appropriate exchange of scientific information
Communicate experts’ opinion and feedback on new data and clinical trends to Medical Affairs and translate this information into strategic recommendations toenhance science and advance patient care
Act as primary liaison to investigators interested in developing and performing investigator-initiated research
Collaborate with the Clinical Operations organization to enhance patient enrollment in company-sponsored clinical trials by identifying appropriate clinical trialsites, supporting clinical trial awareness, and interacting with investigators in ongoing studies
Serve as medical lead and provide scientific support at medical congresses, support national and European medical booths staffing, participate and lead clinicalsupport, and facilitate medical discussions at advisory boards and local scientific/medical programs
Lead national projects such as national congresses, PAG engagement, as delegated by Country or European medical leadership
Be familiar with country specific pharma rules and regulations, particularly as they apply to MSL activities
Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, non-academic, and healthcare provider settings
Develop and execute territory plans in alignment with regional and national strategy
Develop and maintain strong and deep relationships with clinical decision makers at local and national institutions
Partner with cross functional teams, including HEOR/market access to develop the strategy and generation of health economic and outcomes data as needed, andpresentation of such data to relevant audiences
Serve as mentor for other new hires and/or less-experienced MSLs
Manage/lead relevant medical activities/projects including, but not limited to:
Facilitate and lead field medical onboarding programs, and support training of commercial (including sales) colleagues
Support Country Medical Director in translating the medical affairs strategy to a national KOL engagement plan and ensures the KOL development translates toindividual territories
Partner with Global Medical Information colleagues to continuously improve Standard Response Letters and efficiency of MIRF process
As a senior member of the medical team, contribute to the national, and as needed regional, medical strategy and medical plan
Provide scientific support to Regional Medical Director and facilitate medical discussion for national medical advisory boards
Other duties as assigned

Who you are:

Advanced Scientific degree or equivalent experience required. (MD, PhD, PharmD)
Minimum of 5 years MSL experience in the pharmaceutical industry
Rare disease experience preferred, particularly in Oncology and/or Neurosciences
Demonstrated mastery of effectively presenting clinical/scientific information

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

Senior Planner (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Your role:

Supply planning:

Perform replenishment based on demand requirements by MRP and APO forecasting transfer and monitor potential stock-outs and take preventive measures to ensure business stability.
Analyze the performance of the suppliers (e.g Leadtime, service level) and work with global SCM to improve the performance of vendors.
Manage inventory DSI levels to target expectations while ensure service level agreements.
Balance the supply and demand over a monthly planning horizon to achieve optimum product availability and supply chain efficiencies.
Managing necessary planning parameters to ensure system functionality can be performed as business expected.
Planning reporting related to key KPIs, analyze on monthly trend and work on continuous improvement.

Demand planning:

Managing S&OP process. Drive monthly Local Demand Review with business stakeholders, get alignment on forecast.
Develop and verify rolling forecast and work with global demand planners to ensure a smooth region-to-global handover is conducted.
Tracking data on forecast management tool and handover to validate purchasing requisitions and monitor replenishment triggered by demand forecast.
Responsible for in-charge BU sales quarterly/yearly landing and close contact window with BU with regard of demand management topics.
Managing forecast accuracy, monitoring results on both monthly and quarterly base, take necessary action to improve forecast accuracy to ensure a balance between demand and supply.

Project management/additional technology:

Experience 3+ years on project management.
Initial process setup by cross functional communication with sales, marketing, production planning, supply planning.
Knowledge of tableau, power BI and other digitalization tools will be a plus.

Who you are:

Requirements:

Bachelor’s degree with 6+ years of related SC working experience.
SAP experience 4+ years, demand planning experience with APO DP/SNP is required. Oracle experience will be a plus.
Good interpersonal and Cross functional communication skills.
Good at verbal and written English.
High sense of responsibility. Working under pressure and with passion for continuous improvement.

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

区域产品经理-心血管代谢及内分泌- (Shanghai, Shanghai, CN, 201203)

与我们携手施展你的超能力！

在医药健康领域，我们团结一致，齐心为病患，帮助孕育、改善和延长生命。这是我们的目标，也是我们每天不懈努力的原因。默克在肿瘤、神经变性疾病和辅助生殖等领域不断开发创新药物、智能设备与创新科技。我们的团队遍布全球六大洲，在共同的理念与好奇心驱动下，我们全力以赴地为处于生命各个阶段的患者提供拥抱新生活的机会。加入我们，成为这个多元、包容、灵活工作文化的一份子，并获得在全球范围内的个人职业发展机会。

职位描述：

1.掌握产品和疾病基本知识，掌握和运用市场学知识和市场营销的基本原则和工具。

2.分析市场，了解区内市场潜力及竞争情况，并及时反馈。

3.理解和贯彻产品的推广策略和信息，配合区内情况，提出修改建议。

4.跟进和强化销售队伍的产品和疾病知识，跟进销售队伍对产品信息的传递及推广策略的执行。

5.统筹进行区内推广资源分配，制定推广活动计划。

6.跟进及监控推广活动的执行，分析投入产出，发挥最大效益。

7.定期拜访学术带头人，建立区域各学科专家队伍，取得专家的支持。

任职要求：

教育背景/语言:

医药及相关专业本科以上学历，具备工作所需要的一定英语听说读写能力

专业技术能力:

熟练掌握产品知识，了解相关医学知识，具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

有相关领域经验为佳

HR： 95601

职能：商务

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！

外部创新和合作经理 (Shanghai, Shanghai, CN, 201203)

与我们携手施展你的超能力！

Your Role

As the (Sr.) Manager of External Innovation & Partnerships, you will play a pivotal role in identifying, developing, and managing collaborations with startups, research institutions, and technology providers in laboratory automation and other emerging technologies. Your efforts will drive value and business impact across company’s three sectors—Healthcare, Life Science, and Electronics—both locally and globally, with China market for global impact.

1.Drive Innovation Collaborations
Identify, evaluate, and develop collaboration opportunities that generate value across Healthcare, Life Science, and Electronics, with a primary priority on laboratory automation and a secondary priority on any other relevant emerging technologies.

2.Lead Strategic External Innovation Projects
Act as the project lead for key external collaborations, ensuring effective project management, timely milestone delivery, and alignment with Science & Technology (S&T) innovation priorities.

3.Build and Develop the External Innovation Ecosystem
Establish and maintain strong relationships with startups, technology providers, research institutes, and industry partners within the life science and laboratory technology ecosystem.

4.Stakeholder Management and Cross-Functional Coordination
Collaborate closely with internal stakeholders, global S&T colleagues, and external partners to ensure alignment of innovation initiatives with business priorities and seamless project execution.

5. Ecosystem Intelligence and Technology Trend Monitoring
Continuously monitor developments in laboratory technologies and other emerging technologies within the China innovation ecosystem to inform S&T innovation strategy.

Who You Are

Master’s or PhD in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Life Sciences, or a related scientific discipline.
6–10 years of experience in life sciences, laboratory technologies, or related fields.
Proven experience in business development, innovation partnerships, or ecosystem collaboration roles.
Familiarity with laboratory automation technologies.
Experience managing cross-organizational collaboration projects.
Prior experience in large multinational organizations is strongly preferred.

Strong understanding of the life science and laboratory technology ecosystem.
Excellent interpersonal and relationship-building abilities.
Effective stakeholder management and cross-functional collaboration skills.
Proficient in evaluating emerging technologies and identifying partnership opportunities.
Native-level Mandarin and strong English communication skills.

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！

Eumseong Production Operator (Eumseong, North Chungcheong, KR, 27721)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

��담당 업무

생산 공정 운전 (Operation): 반응, 정제, 분리 등 화학 합성/정제 공정 설비 조작 및 운전
원부재료 투입 및 조작: 제조지시서에 따라 정확한 원재료 계량 및 투입, 혼합
용기 잔량처리 및 세정: 작업지시서에 따라 용기의 잔량처리 및 세정 작업
용기 조립 및 검사: 작업지시서에 따라 용기를 조립하고 검사
품질 및 공정 관리: 생산 중 온도, 압력 등 주요 변수 모니터링 및 제어, 샘플링 및 품질 규격 확인
안전환경 준수 (EHS): MSDS(물질안전보건자료) 숙지, 위험 물질 취급 시 안전 보호구 착용, 공장 환경안전 수칙 준수
설비 점검 및 유지보수: 생산 설비 일일 점검, 이상 발생 시 즉시 보고 및 조치(Troubleshooting)
생산 기록 관리: 생산 일지, 자재 사용 현황 등 데이터 정확히 기록 및 관리

��자격요건

고등학교 졸업 이상 (화학, 화공, 공업계열 전공자 우대)
신입 가능
경력직의 경우, 3년 이내의 화학품 제조 및 생산 경력
필수 요건: 화학물질 취급 안전 교육 이수, 교대 근무 가능자
안전 의식: 철저한 수칙 준수 마인드
커뮤니케이션 능력: 생산 기술, 정비 부서와 원활한 소통 능력
문제해결 능력: 설비 트러블 발생 시 침착한 대처 능력

��우대사항

위험물기능사, 화학분석기능사, 산업안전기사 등

<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.

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!

客户主任-甲状腺-杭州 (杭州, Shanghai, CN, 310006)

与我们携手施展你的超能力！

职位描述：

1. 制订有挑战性的和可行性的区域计划，并能成功地实施。

1）根据自己对所辖市场的了解, 制订区域计划和医院销售目标,活动计划和费用预算。

2）在工作中定期的回顾和修正行动计划, 以更高的达到销售目标。

3）计划和执行每天的拜访活动, 确保有效拜访时间符合公司的要求

4）建立和维护与临床医生和学术带头人的关系

5）定期拜访药剂科以保证良好的供货

6）组织GSA和其他销售和市场活动

7）如果有需要，应当协助销售经理处理经销商供货和医疗保险目录的申报

2. 发展和拓宽市场, 了解市场潜力和维护销售的持续稳定的增长

1）执行销售和市场策略并对执行后情况进行反馈

2）提供竞争对手,医疗保险目录和商业供货等信息

3. 工作态度端正，执行公司的行为要求，树立自身良好形象，维护公司品牌形象

1）体现公司的学术形象，掌握产品及相关知识并在每天的工作中运用。

2）掌握销售技巧和演讲技巧并运用到工作中。

3）工作积极努力,有责任感，保持衣冠整洁，对待客户礼貌周到

4. 报告和培训

1）按时和准确的提交各种报告和报表。

2）认真参加公司组织的各项培训和会议。

任职要求：

1. 医药及相关专业本科以上学历。

2. 熟练掌握产品知识，了解相关医学知识

3. 具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

4. 有相关领域经验为佳

5. 具备RDPAC认证资格优先考虑

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！

Capital Project Engineer (Martin, South Carolina, US, 29836)

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 Capital Project Engineer is an onsite role located in Martin, SC with 10% domestic and international travel required to meet business needs.

Martin, South Carolina is in Allendale County bordering the beautiful Savannah River. A community rich in history with over 50 historical sites to visit. Stunning farms cover the landscape in this agricultural community.

Your Role:

EMD Electronics is a leader in the Silica business, dedicated to delivering innovative solutions and exceptional quality. EMD is currently seeking an experienced Capital Project Engineer to join our team at the Martin, SC plant. This critical role will focus on planning, coordinating, and executing engineering projects, ensuring they meet technical specifications, budgets, and established quality standards. You will collaborate with cross-functional teams and ensure the successful delivery of projects while prioritizing high-quality standards and driving innovation through advanced technologies.

Key Responsibilities:

Collaborate with teams and coordinate with contractors, suppliers, and regulatory authorities to ensure designs meet technical specifications and facilitate smooth project execution.
Manage budgets, timelines, and resources effectively for all project components while monitoring progress and providing regular reports to identify and address potential issues.
Conduct risk assessments and implement safety measures throughout each project phase, ensuring compliance with relevant codes and standards through quality inspections.
Offer technical support and guidance to maintenance and engineering teams, staying informed about the latest engineering technologies and industry best practices.
Participate in the development of CAPEX requirements for annual budgeting and long-term planning (5-year outlook).
Drive continuous improvement and operational excellence by identifying and implementing process enhancements within the engineering and manufacturing environments.
Oversee construction activities, ensuring that capital projects are delivered safely, meeting quality and performance objectives while adhering to cost and schedule commitments.
Direct interface with construction general contractors during the bidding, award, execution, and project closeout phases.
Support project management with construction document management including submittal review, change orders, and invoicing.

Who You Are:

Minimum Qualifications:

Bachelor’s Degree in Mechanical Engineering, Chemical Engineering, Civil Engineering, Electrical Engineering, or related field and 5+ years of experience in capital project management, project management, engineering or maintenance project management.

In lieu of a degree, 8+ years of experience in Capital Project Management, Project Management, Engineering or Maintenance Project Management.
Working knowledge of capital project engineering, construction, construction contract administration, and commissioning in a semiconductor, chemical or large-scale industrial manufacturing industry setting

Preferred Qualifications:

Strong knowledge of engineering principles, systems, and components, along with construction management practices.
Experience in project management skills, including budgeting and cost management.
Ability to manage multiple tasks or projects simultaneously while demonstrating exceptional problem-solving skills.
Excellent communication skills, with a proven ability to collaborate effectively with cross-functional teams.
Understanding of industry-specific codes and regulations.

Pay Range for this position: $116,600 - $174,800

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!

Senior R&D Scientist (Hsinchu, Hsinchu County, TW, 300)

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。

Senior Scientist in Abrasive Technology, Chemical Mechanical Planarization (CMP)

Your role:

As a Senior Scientist in abrasive technology within the Planarization business, you will play a crucial role in advancing the development of nanoparticles for chemical mechanical planarization (CMP). You will lead key initiative including multiple projects focused on the design, synthesis, characterization of innovative nanoparticle technologies, and its application in CMP slurries. Your responsibilities will include develop abrasive technology roadmap, manage projects with detailed milestone and success criteria, develop laboratory experiments and metrology, and analyzing data to derive actionable insights. You will collaborate with cross-regional, cross-functional teams and central units to accelerate the development and implementation of newly developed particles. This role offers the opportunity to present your ideas. findings to diverse audiences, including Sales, Marketing, and Management, thereby influencing strategic decisions. Effective collaboration across departments is crucial for success of your role. We are seeking a highly inquisitive and innovative individual who thrives in both independent and collaborative environments. Excellent communication skills are essential as you will engage with various stakeholders. This position offers a unique opportunity to contribute to cutting-edge research and make a significant impact in the field of nanoparticle formulation for CMP applications.

Who you are:

M.S. or Ph.D in Chemistry, Chemical Engineering or Material Science
5+ years’ experience in particle related research, development, application

Preferred Qualifications:

Ph. D degree within abrasive/inorganic nanoparticle research area, is a plus
Proven expertise in nanoparticle synthesis, characterization and development through publication and commercialization
Working experience in abrasive/inorganic nanoparticle RD, metrology and application in an industrial setting, is a strong plus
Previous exposure to the semiconductor industry, particularly in CMP formulation and/or applications, is a strong plus
Excellent leadership and interpersonal skills that support a diverse team environment
Hands-on experience in project management is highly desirable
Excellent verbal and written communication skills in English

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！

Area Sales Manager - Ahmedabad (Ahmedabad, Gujarat, IN, 380009)

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:

Responsible for achieving sales goals, from strategic customer accounts. Develops and executes strategic Account Management plan. Identifies customer needs and develops solutions. Resolves customer issues. Maintains a pipeline of short and long-term growth opportunities. Collaborates and coordinates with appropriate stakeholders.

Responsible for driving key account sales, key initiatives, strategic projects.
Successfully increased market share in a new product portfolio by end-to end support to customer, technical and marketing activities, deep dive analysis and market research
Responsible for seamless management of inter-company projects for customer deliveries, modality driven approach for market capture.
Responsible for achieving assigned sales goals both primary & secondary.
Develop account plans and coordinate activities with appropriate internal stakeholders.
Analyze accounts and territory and identifies opportunities to accelerate revenue growth.
Managing end-to-end sales process for assigned products & accounts
Resolving customer issues by regular interaction with internal stake holders.
Maintaining an in depth understanding of the competitive landscape within assigned accounts and territory
Learning new technical product and scientific knowledge.

Who you are:

You have 5 to 10 years of proven experience in sales or business development.
Your educational background is in Chemistry or Biology
Job location: Ahmedabad

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!

应用技术专家-上海 (Shanghai, Shanghai, CN, 201206)

与我们携手施展你的超能力！

Key Individual Job description：

Identify customer process or application, interpret technical insights and translate material requirement to Marketing/GPM/R&D/Technical Service/Sales.
Handle technical issues or projects by coordinating cross-functions.
Analyze Applications of IC Lithography and clean process, insights to facilitate market opportunities in cooperation with Sales

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.
Solves a range of straightforward problems through technical experience and using lab facilities in JP/US/Taiwan/Korea etc.

Establish good communication and maintain good cooperation with working level of k module & fab levels.
Focus to improve 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.
Skilled at SPC (Statistical Process Control), DOEs.
Over 5 years, Semiconductor industry experience, and hands-on with Lithography process.
Good coaching skill, interpersonal, and communications skill.
Literate in common software.
Ability to work in a matrix/cross-functional setting.

Willing to travel up to 50% of time.

我们能够提供：我们对未知充满好奇，我们的员工有着多样化的背景、多维度的视角和个性化的经历。作为一家前沿科技企业，我们欣赏全方位的多元性，坚信这能驱动卓越和创新，从而强化我们“科技先锋”的底色。同时我们致力于为所有员工提供机会和资源，支持他们按各自的节奏充分成长和发展。加入我们，共建充满包容性和归属感的企业文化，让每一位志同道合的伙伴能够施展自己的超能力，共同推动人类迈向进步的未来!

立即申请，成为我们多元化团队的一员！

Warehouse Manager (Shanghai, Shanghai, CN, 201203)

Work Your Magic with us!

Your Role:

Manage and provide leadership to improve capability, engagement & motivations for our self-running warehouse in Shanghai ZJ SiAL Warehouse
Liaise with other departments including manufacturing site, purchasing, CSR, planning and IE to coordinate warehouse activities
Smooth and efficient warehouse operation to improve customer satisfaction, operation safety and compliance, continuous improvement.
Project management including CAPEX and Opex for expanding distribution capability in LS China
Implementing lean and 6-sigma concept to drive operation excellence

Main Tasks:

Strategy Development & Implementation

Understand the company’s mission and vision and the distribution’s contribution to them
Assess the strengths and weaknesses of the distribution network with corresponding mid/long-term plans, and lead and support the network’s optimization, particularly for the new China distribution center.
As the site change leader to roll out corporate strategic initiatives including safety, quality, Operation Excellence, especially for LSPS (Life science production system) in Distribution China
Developing site operation cost and capital investment projects for next 1-3 years and manage under the budget
Drive warehouse team organizational & talent strategy implementation, build talent echelon and competency system to align team capabilities with long-term business goals

Operational Management

He/she will provide leadership and direction to drive high safety/quality/service standard in warehouse operation
He/She will lead continuous improvement for cost reduction, raising bar for safety & quality, and service improvement.
Monitor warehouse performance to ensure the smooth inbound, outbound operation and meet site KPI
Maintain safety, security and comfortable warehouse environment via 6S, “Be-safe behavior “
Optimize the warehouse space utilization and ensure all warehouse procedures comply with ISO and GDP requirements
Manage the warehouse budget, schedule expenditures, analyze budget variances and take corrective action
Ensure SOP meets EHS, Quality and Compliance’s requirements.

Organizational Development, Relationship Management & Team Leadership

Lead and develop warehouse organization structure, training plan, and talent pipeline to support future development of distribution /ISCO in China and APAC.
Ensure proper planning and allocation of assigned warehouse resources and tasks
Lead (+40 people) WH team to improve capability, engagement, motivations etc.
Staffing planning based on history productivity and tasks forecast
Liaising with customers and other department (customer excellence, supply chain, Quality management, EHS, etc) to achieve LS /Distribution business /service goals

Who You Are:

Education:

Bachelor degree or above in logistic, supply chain, Bio-Pharm, Chemical background with CSCP/CLTD is preferred.

Working Experience:

10+ year related operation experience including warehouse, transportation, planning

Proven experience on project management

Strong people management skills by leading a mid-size team

ERP (SAP)knowledge and implementation experience

Technical &Professional Knowledge

Good leadership, lean six sigma concept

Strong problem-solving capability

Strong communication skills, teamwork, initiative and willing to work under pressure

Fluent English in spoken and written, familiar with office software (Excel, PPT,etc.)

Logical reasoning, numerical skills, technical skills

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

资深分析师 I-Semi-上海 (Shanghai, Shanghai, CN, 201206)

Work Your Magic with us!

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.

PRINCIPAL ACCOUNTABILITIES

Customer Quality Support: Accountable for and support customer quality troubleshooting requests, ensure timely, accurate and effective analytical insights to maintain customer satisfaction and trust.
Raw Material Analysis & New Product Development Support: Execute and deliver high-quality internal material analysis for raw material validation and new product development, ensuring consistency, reliability, and adherence to analytical standards.
Metrology & Characterization Enablement: Identify, evaluate, and apply appropriate metrology and characterization techniques to support commercial and new products, with strong technical understanding of key performance and quality factors.
Data Analysis & Reporting: Analyze experimental data and prepare clear, detailed technical reports to support decision-making, root-cause analysis, and project milestones.
Method Development & Optimization: Develop, refine, and optimize analytical methods to enhance material characterization capability, data quality, and laboratory efficiency.
Technical Documentation & Compliance: Maintain comprehensive technical documentation of methods, procedures, and results, ensuring traceability and compliance with quality management systems.
Collaboration: Collaborate with global analytical laboratories and cross-site teams to share best practices, align methodologies, and support multi-site projects.
Laboratory Safety & Compliance: Ensure laboratory activities comply with applicable safety, regulatory, and operational standards.
Intellectual Property Support: Contribute to intellectual property generation through method development, technical insights, and innovation activities.

PREFERRED QUALIFICATIONS:

Master’s degree or above in science or engineering disciplines; chemical engineering, chemistry, materials science, or electronics preferred.
Minimum 2+ years of research or industry experience in the chemical or semiconductor industry.
Demonstrated capability in NMR method development for structural identification, quantitative analysis, and impurity analysis, with proficiency in relevant data analysis software is preferred. Experience integrating complementary analytical techniques is a strong advantage.
Strong analytical thinking and problem-solving skills, with the ability to plan, execute, and complete analytical tasks and project reports independently.
Self-motivated, detail-oriented team player with a proactive, can-do attitude and strong learning agility.
Effective interpersonal and collaboration skills in a cross-functional, multicultural environment; good English communication skills (written and verbal) for internal collaboration.

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

高级工程师 I-Semi-上海 (Shanghai, Shanghai, CN, 201206)

Work Your Magic with us!

PRINCIPAL ACCOUNTABILITIES

Lead R&D projects for thin film materials development. Conduct experiments, collect data, optimize process parameters and complete R&D reports.
Fulfill materials processing, sampling, analysis and application demo requests from customers.
Develop system operation and troubleshooting procedures. Maintain equipment performance and establish quality standards. Conduct continuous improvement projects to enhance safety, quality, and productivity.
Provide technical support to commercial teams. Develop and maintain relationships with internal global labs.
Enable cross sharing of learning, insight and experience between team members.
Participate in intellectual property development.

PREFERRED QUALIFICATIONS:

Ph.D in chemical engineering/material science/chemistry/electronics or relevant fields, 2+ years of working experience related to chemical/semiconductor industry OR MS in chemical engineering/materials science/chemistry/electronics or relevant fields, 4+ years of working experience related to chemical/semiconductor industry.
In-depth understanding of chemical reaction and process. Solid knowledge and experience on material handling and equipment operation for one or more domains, including synthesis, purification, sampling, formulating, analysis, etc. Relevant experience on thin film deposition materials is a plus.
Demonstrate creativity and strong problem-solving skills. Ability to coordinate resource, lead project independently, and complete RD report.
Excellent interpersonal and teamwork skills that support a diverse, cross-functional, multicultural team environment.
Effective English skills (verbal and written) for internal communication.
Flexibility for domestic and international traveling.

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

OLED中国业务负责人 (Shanghai, Shanghai, CN, 201206)

与我们携手施展你的超能力！

As the Head of OLED Sales for China, you will play a pivotal role in aligning global OLED growth strategy with the unique needs and dynamics of our key account customers. Your role encompasses developing strategic initiatives that align with our objectives and addressing the unique needs of key accounts. You will cultivate deep, trusting relationships at various decision-making levels within customer organizations.

Your Role

Strategic Vision and Customer-Centric Approach: Develop and implement strategies that not only align with company’s OLED growth objectives but also reflect a comprehensive understanding of customers' businesses, challenges, and market environments. Tailor solutions that drive mutual success.
Relationship Management and Communication Excellence: Build and maintain strong relationships with key account customers, facilitating alignment between R&D, sales, and key functions in Korea and headquarters to ensure cohesive efforts.
Analytical Skills and Performance Orientation: Analyze sales data and market trends to identify growth opportunities, assess account performance, and inform strategic decisions. Maintain a results-driven mindset focused on achieving sales targets and driving revenue growth while ensuring high customer satisfaction.
Leadership and Team Development: Inspire, mentor, and develop a Key Account Management team, fostering a culture of high performance, accountability, and continuous improvement.
Negotiation Expertise and Adaptability: Negotiate contracts and agreements that achieve win-win outcomes for both company and key accounts. Demonstrate flexibility in adapting strategies to changing market conditions and customer needs, with proactive problem-solving capabilities.
Collaboration Skills: Work cross-functionally with marketing, product development, and customer service to deliver comprehensive solutions to key accounts.

Who You Are

-Minimum 10 years of commercial experience in China, including significant exposure to OLED technology and extensive managerial experience in sales roles.

- Proven experience leading a team 3yrs above, fostering a collaborative and high-performance culture.

-Excellent communication skills in English to effectively engage with diverse stakeholders.

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！

Software Engineer (Shanghai, Shanghai, CN, 200031)

Work Your Magic with us!

Role

The Software Support Engineer's primary mission is to resolve IT problems as closely as possible to the client. Proactive and methodical, their goal is to identify malfunctions and quickly implement solutions.

Responsibilities

As a SW support engineer, your responsibility will be around technical stuff mosly independently during field interventions. The list of responsibilities and tasks required will be as follows :

To be readily available to client companies in case of IT problems.
To be able to diagnose and resolve issues as quickly as possible. The Software Support Engineer then assists with the implementation of the solution at the client's site.
To document malfunctions and communicate with development teams to improve the product as needed.
To implement certain fixes and install them directly at the client's site.
To communicate with development teams to synchronize the software platform.
To train users on how to use new features.

Environment

As a true technical support for the client, the Software Support Engineer works in a dynamic and stressful environment. They must be able to manage their stress while remaining responsive to client requests. Methodical, organized, and rigorous, the role of a software support engineer requires strong analytical skills and excellent listening abilities.

Requierement

Experience in industries software environment.

Experience with legacy code and also retro engineering software skill.

Fluency in English is essential for understanding and accessing technical documentation when troubleshooting and work in APAC region

Chinese speaking mandatory.

Technical Skills

Training and/or experience in industrial computing.

Good understanding of MutliThreading application

Object-oriented programming languages such as C++/C# (ideally)/Java.

Proficiency with Git.

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

Global Technical Support-semiconductor (Shanghai, Shanghai, CN, 200131)

Work Your Magic with us!

Are you looking to grow in a dynamic, multicultural, and people-centric environment? Join fast-growing leader in semiconductor metrology and inspection technologies - and be part of our growth by joining our technical support team as GTS Engineer on Metrology system

We are looking for a motivated talent to support our development and take on new challenges together. If you're eager to learn, innovate, and actively contribute to our projects, this opportunity is for you!

Your profile :

Master degree in technical domain or Degree with high experience of >7years in electronic, mechanical, robotic, SW.
Experiences in microelectronics, 3 to 5 years.
Knowledge on metrology and optics
Customers management skills
Communication skills
Analytical and problem-solving capabilities
Ability to travel

You will be joining a team of technical expert to support global field engineer -GTS team
Location: China (Shanghai)

The GTS engineer will be in charge off

Technical Support:

Supervise technically all installation
Link between Field and HQ functions (Engineering, Manufacturing, Apps)
Participate to NC process by providing expertise
Participate to the devellopment of new system
Manage spare parts obsolescence
Develop global training programs

Service Business Development:

Manage Customers escalation, on technical and comunicaton side
Develop catalogue Service Products CIP
Develop spare parts improvement program
Develop Repair/ Refurbish programs
Provide training and participate to training documentation
Insure the cross sharing of the knowledge in the team
Develop maintenace and trouble shooting document

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

售后服务主管-半导体设备 (Shanghai, Shanghai, CN, 200131)

Work Your Magic with us!

Location: Pudong / Shanghai

Coverage: China Service

Responsibilities

Support equipment, hardware and applications qualifications/trouble shooting during installation.
Account management & tools situation update.
Tool installations / FAT signoff and service supports for all tools of China region.
Manage customers relationships and escalations.
Manage HQ relationship and escalations.
Lead meeting for technical discussion; host weekly or monthly customer meeting etc.
Support the system sales and penetration in China.
Increase and maintain a healthy service and spare business in China
Take care of the FSE team in China in term of technical.

Prerequisites:

Good attitude in working and good team-work ability.
Some experience in maintaining and supporting semiconductor M&I (Metrology and Inspection) equipment is preferred.
Team management experience is preferred.
Willingness to travel.
Languages (both written and spoken): Chinese and English.

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

Account Manager (Chennai, Tamil Nadu, IN, 600098)

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:

Strong technical aptitude with demonstrated ability to learn complex product applications and workflows and know pharma/food QC environment.
Excellent communication, presentation and negotiation skills.
Demonstrated ability to build and maintain long-term customer relationships
Proficiency in CRM systems (preferably Salesforce) and Microsoft Office Suite
Strong territory management and strategic account planning capabilities
Strong analytical and problem-solving skills for developing effective sales strategies
Ability to work both independently and collaboratively in a matrix environment
Needs to achieve sales target within assigned territory
Division to be catered- Advance solution Biomonitoring
Travel up to 75% - 100% within assigned territory- Chennai, Kerela, Tamil Nadu and some part of Andhra Pradesh
Fluency in English required; additional language skills based on territory needs

Who you are:

Graduate from life science/microbiology background with 2-6 years of experience in life science sales field.
Management education will be an added advantage

Apply now and become a part of our diverse team!

Senior Warehouse Operator (Ho Chi Minh City, Ho Chi Minh, VN, 70000)

Work Your Magic with us!

Report to: Warehouse Supervisor

Location: Nhon Trach 3 - Dong Nai Province.

Your Roles:

Daily operation to manage inbound/outbound procedure, physical stock count, put away, goods receipt with scanner, pack & pack, stock movement…
Collaborate with transportation vendor to manage truck arrangements and related cost for outbound activities
Warehouse operational report (weekly/monthly) to follow KPI, target
Follow safety rules, EHS mindset strictly
Apply 6S in daily operation.
Follow and carry out other assigned tasks, reports from WH supervisor.
Actively supports and participates in projects/ campaign/activities

Who You Are:

Secondary/high school education.
Fork-life driver certificate
Computer literacy on Microsoft office, WMS (Warehouse Management System)
At least 3 years’ experience on warehouse operation: physical stock count, put away, goods receipt with scanner, pick & pack…, prefer experience in chemical products handling.
General English speaking & writing

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

Delegue Specialiste Fertilite f/h (Lyon, Rhone, FR, 69008)

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.

Votre rôle :

Vous êtes en charge de la promotion des produits et des services auprès des Gynécologues, endocrinologues et biologistes hospitaliers et libéraux sur votre secteur. Vous travaillez en synergie avec votre DR ainsi qu’avec les équipes médicales, marketing et Affaires Publiques pour développer votre secteur. Vous définissez et mettez en place le plan d’action sectoriel (y compris les actions digitales) en analysant les pratiques des centres clés du secteur et leur environnement interne et externe (réseaux de soins, lien ville hôpital…). Vous proposez des projets de partenariats en collaboration avec les fonctions transverses (ventes, médical, marketing, market access, juridique, compliance…), vous suivez l’efficacité de ces projets et proposer des actions correctives. Vous organisez et animez des staffs et réunions, dans le respect de la stratégie de l’entreprise et du cadre réglementaire. Vous réalisez un plan d’actions sectoriel annuel. Vous assurez la remontée des informations utiles aux équipes siège.

Départements : 78/92/93

Poste en CDD

Qui vous êtes :

Diplômé de la VM (ou équivalent) et expérience dans une aire thérapeutique en fertilité
Capacité à interagir/négocier avec toutes les parties prenantes du parcours de soin notamment le lien ville hôpital
Capacité à animer des réunions et à convaincre dans un environnement très concurrentiel
Maitrise de l’anglais oral et écrit
Maitrise du pack office et des outils digitaux ayant la capacité de s’adapter à l’évolution de la visite médicale avec un mix d’activités présentielles et digitales. A ce titre vous serez détenteur de la carte APM

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 !

Indirect Procurement Expert Israel (Rehovot, Central, IL, 7670603)

Work Your Magic with us!

Role Purpose

Lead Strategic Indirect procurement transactions. Oversee quality and compliance across all procurement processes within the organization. Ensures that material purchases are executed in an optimal economic and strategic manner, in full compliance with global corporate procurement policies, while maximizing cross-functional synergies.

Key Responsibilities

Lead end-to-end procurement processes for strategic transactions (above NIS 200,000).
Provide professional support to business units (R&D, Production, Marketing) in managing negotiations with major suppliers.
Conduct ongoing reviews and controls of procurement processes to ensure compliance with global procurement policies.
Keep Procurement policies updated.
Identify and drive synergies across different procurement domains to achieve cost savings and operational efficiency.
Manage relationships with strategic suppliers and establish long-term framework agreements.
Support and assist the CFO in cross-functional projects and related assignments, as required.
Work with Global Procurement Coordinator

Key Stakeholders & Interfaces

Direct reporting line to the CFO
Ongoing collaboration with Purchasing Managers within the Business Units.
Close partnership with core functions: R&D, Production, and Marketing.

Tools, Systems & Infrastructure

SAP
Ariba
Excel excellent knowledge (data analysis and reporting)

Success Metrics

Savings: Achieving measurable and documented cost savings from led strategic transactions.
Compliance: Zero material deviations from global procurement policies in periodic audits.
Cycle Time: Meeting defined timelines for the closure of strategic procurement deals.
Internal Satisfaction: Positive feedback from business units regarding the quality of support and added value delivered.

Reporting Structure

Reports to: CFO
Direct reports: None (Individual Contributor / Headquarters role)

Requirements

Bachelor’s degree – mandatory
Relevant experience in a global organization – advantage
Minimum of 5 years of relevant professional experience – mandatory
High level of English – mandatory
High level of Excel – mandatory
Working with SAP and Ariba - advantage

PERSONAL SKILLS & COMPETENCIES

Time management
Self-starter
Good interpersonal relationships
Reliability and integrity
Proactive, accurate, Team player

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

Head of Site Quality Life Science Operations Darmstadt (all genders) (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.

Your Role:

You will be responsible for quality assurance and quality management of our product range. You will lead a large quality team (approximately 400 employees) and ensure that all products meet the highest quality standards.

Main Responsibilities:

Lead and coordinate the team for the production of a diverse portfolio within Life Science Operations.
Ensure compliance with legal regulations as well as internal standards (ICH Q7, EXCiPACT, ISO 13485, ISO 17025, ISO 17034, ISO 9001).
Develop and implement quality strategies, policies, and procedures.
Identify areas for improvement within the Quality Management System (QMS).
Collaborate with relevant stakeholders, authorities, and customers to ensure product quality.
Cooperate with management to define strategic organizational goals and plans.
Comprehensive responsibility for the quality assurance and control of raw materials, intermediates, and finished products.
Implementation of strategies to actively involve employees in decision-making processes and continuous improvement initiatives; fostering a culture of trust and open communication.

Who you are:

Scientific degree, preferably in natural sciences, particularly in chemistry, pharmacy, or engineering.
10+ years of professional experience in the pharmaceutical or chemical industry, ideally in a leadership position within the quality area of the pharmaceutical or life science sector.
Excellent knowledge of GMP regulations and practical experience in dealing with the FDA and other health authorities during inspections.
Experience in leading large teams of managers and specialists.
Strong problem-solving skills and robust analytical abilities to identify and resolve challenges. Ideally, a qualification as a Lean & Six Sigma Black Belt.
Proven experience in managing change processes to promote the acceptance of new procedures and standards.
Demonstrated ability to lead large teams in a dynamic production environment and create a motivating and supportive work environment.
Solid knowledge of modern production systems (e.g., Lean Management, Six Sigma) for process optimization and efficiency enhancement; experience in building autonomous teams and promoting continuous improvements.
Strong capabilities in identifying and analyzing improvement opportunities.
Excellent verbal and written communication skills for interacting with various stakeholders.
Ability to process and communicate detailed scientific, quality, and regulatory information.
Good understanding of the life science market, especially in the manufacturing and distribution of pharmaceutical active ingredients and excipients.
Fluent in German.

Location: Darmstadt, Germany

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.

Pharmaziepraktikum in DPE ab Mai 2026 (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 Pharmaziepraktikums ab Mai 2026 sind Sie in der pharmazeutischen Entwicklung in der Abteilung Drug Product Excellence tätig. Der Fokus unserer Abteilung liegt auf der Fertigung neuer und innovativer fester und steriler Arzneiformen zum Einsatz in klinischen Studien.

Während Ihres Praktikums erhalten Sie vielfältige Einblicke in die verschiedenen Tätigkeitsgebiete eines Apothekers in der pharmazeutischen Industrie. Bei uns erwarten Sie Aufgaben in den Bereichen der Fertigung fester und parenteraler Arzneimittel. Die Implementierung und Begleitung von Herstellungsprozessen in internen Pilot Plants sowie die Koordination der Herstellungen bei externen Kooperationspartnern sind mögliche Einsatzbereiche. Sie haben die Chance in einer der modernsten Herstellplants mitzuarbeiten und die Herstellung hochpotenter Arzneimittel in Isolatoren kennenzulernen.

Darüber hinaus wirken Sie bei der Gestaltung, Optimierung sowie Anwendung von GMP-Routineprozessen, der Durchführung von Qualifizierungs- und Validierungsaktivitäten und crossfunktionalen Qualitätsthemen mit.

Während Ihres Praktikums arbeiten Sie in interdisziplinären Teams und nehmen eine relevante Schnittstellenfunktion ein.

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
Organisationstalent
Exakte, zuverlässige und selbstständige Arbeitsweise, belastbar und flexibel
Fit im Umgang mit MS Office

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

Rechtsreferendar in der Konzernrechtsabteilung (m/w/divers) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Ihre Aufgabe

Während Ihrer Station als Rechtsreferendar (m/w/d) sind Sie Teil eines Teams von 20 Rechtsanwälten und Rechtsanwältinnen in der Konzern-Rechtsabteilung eines weltweit tätigen Unternehmens der chemischpharmazeutischen Industrie. Wir bilden Sie umfassend aus und bieten Ihnen die Möglichkeit, Ihre Rechtskenntnisse in der Praxis gewinnbringend einzusetzen. Abhängig von Ihrer Schwerpunktsetzung kümmern Sie sich insbesondere um Anfragen aus dem Bereich des allgemeinen Zivil- und Wirtschaftsrechts, des Gesellschaftsrechts, des öffentlichen Rechts oder des Arbeitsrechts. Sie werden aktiv in die Tätigkeiten der Rechtsabteilung eingebunden und bearbeiten Ihre Fälle weitgehend selbstständig - in enger Abstimmung mit den Rechtsanwälten.

Ihre Qualifikationen

• Referendar (m/w/d) mit überdurchschnittlich gutem ersten Staatsexamen
• Idealerweise Erfahrung in einem Wirtschaftsunternehmen, einer Anwaltskanzlei oder einem Verband
• Sehr gute Englischkenntnisse
• Versiert im Umgang mit den gängigen EDV-Anwendungen
• Teamfähig und engagiert
• Analytisches Denkvermögen und schnelle Auffassungsgabe

Start: Grundsätzlich flexibel

Bitte laden Sie alle relevanten Dokumente (Zeugnisse, Noten, Leistungsnachweise, etc.) in Ihrem Profil hoch und geben Sie bitte das Rechtsgebiet Ihrer Wahlstation an.

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

Senior Device Development Engineer for active medical implants (all genders) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

Your role:

As part of the Bioelectronics department, you will work on novel selective implantable Vagus nerve stimulators with a focus on design, verification, feasibility and technical transfer until regulatory submissions. You will work closely with our partners to ensure translation of requirements into the device development flow, give design as well as testing input and contribute hands-on to inhouse and external experiments.

As a Senior Device Engineer, you will work within our interdisciplinary and vibrant team of engineers, physicians, scientists, program managers, and external partners to develop and optimize next generation neurostimulators. Join us on our exciting journey at the frontier of bioelectronic medicine to bring novel therapies to patients!

Who you are:

PhD or MSc in biomedical engineering, electrical engineering, microsystem technologies or a similar field
7-10+ years of industry experience with class III medical device development
Familiarity with applicable standards, regulatory frameworks, and risk management (e.g., 21CFR820.30, ISO13485, ISO14971, IEC60601, IEC62366)
Working knowledge of mammalian physiology and experience with large animal studies
Ability to communicate complex technical concepts to and translate between multiple stakeholders
Can-do entrepreneurial mentality coupled with effective project management skills
Interest in (neuro-)physiological data acquisition and interpretation; ideally knowledge of Python and/or Matlab
This job requires working onsite at our Darmstadt facility, as well as frequent traveling to external sites and partners

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

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

Entfalte das Besondere mit uns!

Ihre Rolle & Aufgaben

Während Ihres sechsmonatigen Praktikums ab November 2026 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.

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

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

Work Your Magic with us!

Your Role:

An exciting opportunity awaits you within the Patient Focused Real World Evidence (PRWE) Team. As passionate leaders of patient focused real world data, evidence generation, and epidemiology, we are uniquely placed to enable fit-for-purpose visionary solutions with real world and patient focused data from early development and throughout the drug life span. Our team operates with a proactive and agile approach, as a trusted partner in qualitative and quantitative sciences, all while striving towards the common goal to deliver more medicines to more patients faster.

As a key member of our team, you will drive the Real-World Evidence and Data (RWE/D) strategy and studies across the lifecycle of drugs, with a particular focus on drug development and excellence in integrated evidence planning. You will provide scientific leadership and expertise to ensure that fit-for-purpose RWD are integrated in evidence generation plans and available in a timely manner to support regulatory submissions and program´s decision-marking.

You will lead the quantitative strategy of RWE/D for your therapeutic area and to provide evidence for Integrated Evidence Plans You will lead the design, implementation and oversight of disease or drug-specific Non-Interventional (NIS) / RWE studies, encompassing safety related studies, external control arm studies, and regulatory grade studies. Your work will involve inspiring cross-functional collaboration, in a unique partnership with other quantitative scientists while maintaining and expanding our external collaborations.

Who You Are

Minimum Qualifications:

Doctoral and/or master’s degree (e.g., PhD, MSc) in Epidemiology, Public Health or related field
Strong experience in RWE/D within the pharmaceutical industry, particularly in the application of RWE in drug development for rare indications

Preferred Qualifications:

Preferably a background in health and life sciences (MD, pharmacist epidemiology, public health), or quantitative data sciences, biostatistics
Demonstrable experience in leading RWE generation plans and studies end-to end, including application of innovative designs and methods
Excellent oral and written communication skills and demonstrated ability to engage and communicate scientific evidence to peers and at scientific meetings
Collaborative, proactive working style, with ability to work independently.

Position can be filled either in Switzerland or Germany (in a hybrid format).

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

Pharmaziepraktikum im Bereich der Herstellung klinischer Prüfpräparate ab November 2026 (m/w/d) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Ihre Rolle & Aufgaben

Während Ihres sechsmonatigen Pharmaziepraktikums ab November 2026 sind Sie in der pharmazeutischen Entwicklung in der Abteilung Drug Product Excellence tätig. Der Fokus unserer Abteilung liegt auf der Fertigung neuer und innovativer fester und steriler Arzneiformen zum Einsatz in klinischen Studien.

Während Ihres Praktikums arbeiten Sie in interdisziplinären Teams und nehmen eine relevante Schnittstellenfunktion ein.

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 mit erfolgreich abgeschlossenem 2. Staatsexamen
Kommunikationsstärke in Deutsch und Englisch
Spaß an der Arbeit im Team
Organisationstalent
Exakte, zuverlässige und selbstständige Arbeitsweise, belastbar und flexibel
Fit im Umgang mit MS Office

Bitte beachten Sie, dass wir nur vollständige Bewerbungsunterlagen inklusive Anschreiben, Lebenslauf und relevanten Zeugnissen berücksichtigen können. Praktikumsstart ist der 1. November 2026.

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

Pharmaziepraktikum gemäß §4 Approbationsordnung für Apotheker im Bereich Qualitätssicherung (m/w/d) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Ihre Rolle

Je nach Einsatzbereich werden Sie mit der Erstellung von Dokumenten zu den Qualitätssystemen und zur Implementierung der Anforderungen von Good Manufacturing Practice betraut und in die Bearbeitung aktueller Vorgänge eingebunden. Neben dem Kennlernen der Abläufe in der Qualitätskontrolle/-sicherung erhalten Sie Einblicke in die Zusammenarbeit mit deren typischen Schnittstellen in einem arzneimittelherstellenden Betrieb, z.B. Herstellung, Qualitätskontrolle/-sicherung, Logistik und Einkauf. Sie gewinnen einen guten Überblick über die Aktivitäten am Pharmaproduktionsstandort Darmstadt und über das dort implementierte pharmazeutische Qualitätsmanagement-System. Dies fördert Ihre Mitarbeit an einem oder mehreren Systemen, wie z.B. Inspektions-, Dokumentations-, Risiko- und Änderungsmanagement sowie die aktive Teilnahme an Inspektionen und Audits.
Es erwarten Sie außerdem Themenbereiche wie die inhaltliche Bearbeitung von Risikoanalysen, Änderungsanträgen oder Abweichungen und die Erstellung von Trendberichten.

Ihre Qualifikationen

• Student (m/w/d) der Pharmazie im Hauptstudium mit 2. Staatsexamen bei Beginn des Praktikums

• Gute EDV-Kenntnisse

• Teamgeist

• Exakte und zuverlässige Arbeitsweise

• Kommunikationsstärke in Deutsch und Englisch

Zeitraum für die Ausschreibung: 01.05.2026-31.10.2026

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

Manager / Senior Manager Inhouse Consulting - Life Science Sector (all genders) (full-/part-time) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with 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 primarily for our Life Science sector, before transitioning to the next exciting career step within our company after approximately 2-4 years. Our Life Science sector is a leading global provider of products, solutions and services for a wide range of customers, including research and diagnostic labs, biotech and pharmaceutical companies, as well as the industrial sector. We are known for our Life Science portfolio brands Millipore, Milli-Q, Sigma-Aldrich, Supelco, BioReliance, and SAFC. Typical Inhouse Consulting projects in the Life Science sector include strategy development (e.g., on sector or franchise level), commercial excellence or operations. 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:

Master’s degree in natural sciences, engineering, pharmaceutical science, medicine or business. PhD or MBA is a plus
Work experience of 2-5 years in management consulting with deep industry-related experience in biotech, diagnostics, bioprocessing, biology, chemistry or similar
Functional expertise in at least one of the following areas: data & digital, strategic marketing, supply chain management, R&D innovation, transformation
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 and with a passion for working in teams
Proficiency in English and preferably also in German
Willingness to relocate to Rhine-Main-Area (e.g., Darmstadt, Frankfurt) to allow for regular office presence (2-3 days per week) for close collaboration and network building

Working student (all genders) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

Your Role:

You will be responsible for customer quality and regulatory inquiry support. As a member of a global team, you will serve as a second level support contact for the Commercial organization. You will interact with various internal contacts to coordinate the provision of quality documentation.
Candidates must be available to work on-site in Darmstadt, Germany, for 3-4 days per week. Remote work is not an option.

Who you are:

Advanced student in Life Science, Chemistry, or related field
Strong communication skills (C1) in English
Willingness to acquire or extend knowledge of quality and regulatory topics
Proactive approach to problem-solving
Ability to navigate a cross-cultural environment

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

Sechsmonatiges Pharmaziepraktikum im Bereich Orals Development ab November 2027 (m/w/d) (Darmstadt, Hessen, DE, 64293)

Entfalte das Besondere mit uns!

Ihre Rolle & Aufgaben

Die Abteilung Orals Development begleitet aktuelle Projekte von Forschung, über Entwicklung bis hin zu Launch und Life Cycle Management. Dabei stehen pharmazeutische Formulierungsentwicklung und Prozessoptimierung nach neustem Stand der Wissenschaft im Mittelpunkt.
Es erwarten Sie spannende Aufgaben in den Bereichen Formulierung, Charakterisierung und biopharmazeutischer Beurteilung früher Wirkstoffkandidaten, sowie Hot Melt Extrusion, Continuous Manufacturing und klassischen galenischen Technologien zur Herstellung fester oraler Darreichungsformen, die unseren Medikamenten den Weg in die Klinik ebnen.

Während Ihres halbjährigen Pharmaziepraktikums gemäß § 4 Abs. 2 Approbationsordnung erhalten Sie die Chance durch die selbstständige Arbeit an einem eigenen Projekt einen wertvollen Beitrag zur Entwicklung zukünftiger Therapieoptionen für unsere Patienten zu leisten. Zusätzlich haben Sie die Möglichkeit am Hauptquartier eines forschenden Arzneimittelunternehmens auch Einblicke in angrenzende Bereiche zu erhalten (z.B. das Technical Development Center, einen modernen state-of the-art GMP-Betrieb für die Herstellung hochpotenter klinischer Prüfpräparate unter Einsatz von High-Containment-Technologien).

Wer Sie sind

Pharmazeut mit erfolgreich abgeschlossenem 2. Staatsexamen
Sehr gute Leistungen in Schule und Studium
Besondere extracurriculäre Leistungen sind von Vorteil
Kommunikationsstärke in Deutsch und Englisch
Exakte und zuverlässige Arbeitsweise, Belastbarkeit und Flexibilität
Solide Kenntnisse im Umgang mit MS Office sind Voraussetzung, weitere Kenntnisse z.B. in Programmierung von Vorteil

Bitte beachten Sie, dass wir nur vollständige Bewerbungsunterlagen inklusive Anschreiben und Zeugnissen über Abitur und das bestandene 1. Staatsexamen berücksichtigen können.

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

Working Student - EL Manufacturing Cluster - Strategy & FP&A (all genders) (Darmstadt, Hessen, DE, 64293)

Work Your Magic with us!

Location: Darmstadt, Germany

Your Role:

In your role as a Working Student (all genders) in Strategy & FP&A Controlling, you will support our production controlling organization on its digital transformation journey. You will work closely with Site Controllers, the Finance Data & Analytics team, and the Strategy & FP&A Controlling team to support and enhance our financial planning and analysis routines.

Key Responsibilities:

Digital Transformation:
- Create, enhance and maintain dashboards in Power BI
- Support the further development and daily operation of our performance and reporting application “Performance Factory”
- Help maintain and improve automated reporting routines, ensuring data is prepared accurately and on time
- Assist in validating data quality and improving data accuracy
- Contribute ideas on how to simplify processes and increase efficiency through digital tools and automation

Financial Planning & Analysis Support
- Support financial analyses related to manufacturing operations (e.g. cost analysis & forecasting tasks)
- Help prepare standard reports, performance reviews and presentations for management
- Consolidation and analysis of financials for production sites / clusters
- Assist in the preparation of standard-price calculations and related controlling processes
- Conduct ad-hoc analyses to support strategic and operational decision-making within the team.

You will be integrated into the day-to-day work of the team and gain insights into production controlling, supply chain, and financial planning processes in an international environment.

Your Qualifications:

You are currently enrolled in a Bachelor’s or Master’s program in Finance, Accounting, Business Administration, Economics, Industrial Engineering, Data/Business Analytics, or a related field
First experience or strong interest in controlling/finance, ideally related to manufacturing or supply chain
Solid knowledge of MS Excel; experience with data analytics / visualization tools (e.g. Power BI) and ERP systems
Strong analytical skills, a structured and reliable way of working, and attention to detail
Curiosity for digitalization and automation in controlling and willingness to learn new tools and concepts
Fluency (C1) in English & good communication skills and a collaborative mindset; you enjoy working in cross-functional and international teams

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

Field Service Engineer (Tainan, Tainan City, TW, 74160)

與我們攜手施展你的超能力！

You Role

- 依各工作區資深工程師安排，就工作範圍區為鋼瓶更換專責工程師、客戶服務廠區負責人、技術支援工程師、氣體系統操作服務工程師，各自負責所屬範圍的技術服務工作，並得隨時依照各區工作需求彼此相互協調支援
- 公司內部工作聯繫協調
1. 協助並接受北中南各區工作小組主管執行客戶端操作服務工作的指派
2. 遵守操作紀律及時回報各項工作問題
3. 各項公司產品品質維護與異常通報，維持零受傷安全目標及零斷氣、零污染品質目標以提升團隊價值

- 公司內部工作聯繫協調
1. 與客戶聯繫窗口建立良好關係與溝通管道。協助業務部門掌控及時知訊，推升公司營業規模
2. 確實遵從客戶標準化文件執行之規範並適時查核
3. 遵循客戶廠區安全之規定，落實工安理念
4. 提供客戶安全與專業的操作服務品質

Who You Are

1. 無經驗可，歡迎應屆畢業生
2. 積極主動企圖心強願意學習，有基礎英文即可
3. 大專(含)以上，主修化學、電子及相關科系為佳。
4. 有無塵室工作經驗佳

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！

Field Service Engineer (Tainan, Tainan City, TW, 74160)

與我們攜手施展你的超能力！

You Role

Who You Are

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！

Stagiaire Coordinateur Distribution f/h (Molsheim, Bas-Rhin, FR, 67120)

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.

Votre rôle :

Coordonner les opérations de traitement de commande, d’entreposage, d’expédition et de transport avec les prestataires de service : 3PL et transitaires. Contact principal pour les partenaires internes de l'entreprise (Service client, Supply Chain, Usines, etc.) pour toute question relative aux opérations d’expédition au départ du prestataire logistique.

Tâches et responsabilités :

Assurer la coordination du traitement des commandes, de l’entreposage, de l’expédition et de l’exécution du transport entre les fournisseurs de services et les collaborateurs en Europe (Customer Excellence, filiales), en lien avec les procédures existantes et de manière à contribuer à l’atteinte des objectifs fixés.

S’assurer que les expéditions soient réalisées physiquement et informatiquement dans les délais prévus.

S’assurer que les documents d’expédition pour l’exportation soient complets, conformes et transmis à temps aux transitaires, et que la traçabilité et l’archivage soient assurés dans les outils définis.

S’assurer que les capacités de transport nécessaires soient réservées à temps, avec un possible choix de solution et arbitrage.

Veiller à ce que les expéditions soient livrées aux clients dans les délais prévus.

S’assurer que les notes de crédit soient gérées dans les délais.

Collaborer avec l’ensemble des partenaires en interaction avec l’équipe.

Assurer la gestion des événements spéciaux (jour férié, grève, météo, etc.), en communiquant avec les parties prenantes et en définissant avec eux un mode de gestion dégradé.

Contribuer à une démarche d’amélioration continue au sein de la distribution : remontée et analyse des problématiques, identification des tâches à non-valeur ajoutée, propositions d’améliorations via les plateformes d’échange en place, participation à la mise en place de projets distribution, etc.

Connaître, appliquer et faire respecter les règles en vigueur liées à la sécurité et à l’environnement ; promouvoir la culture de la sécurité et la politique environnementale

Stage à partir de mai 2026 pour une durée de 4 mois.

Qui vous êtes :

Organisé, multitâche, ouvert d'esprit, vous avez une réelle orientation satisfaction client et vous êtes flexible dans un environnement multiculturel en constante évolution.
Excellente communication orale et écrite, vous soignez vos relations professionnelles et vous avez une appétence pour le travail en équipe.
Connaissances dans le domaine de l’import/export : compétences réglementaires et douanières.
Outils informatiques : Pack Office, utilisation d’un ERP.
Capacité à évoluer dans un environnement digital complexe
Anglais courant oral et écrit

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

Technicien de maintenance f/h (Molsheim, Bas-Rhin, FR, 67120)

Exprimez votre talent avec nous !

Votre rôle :

Dans le cadre du projet d’extension de l’activité Mobius, avec l’intégration de nouvelles lignes de production automatisées à la pointe de la technologie (Robotique, contrôles numérique, vision 2D 3D, aides aux assemblages, etc..), votre mission principale consistera à garantir le bon fonctionnement des équipements de production. Cela inclut le réglage, la maintenance et le dépannage des machines utilisées pour la fabrication (découpe, scellage) de poches en plastique et de sous-ensembles destinés au transfert de fluides, de principes actifs et de produits bio-pharmaceutiques.

Vous serez également responsable de la gestion de projets d'amélioration des processus en collaboration avec nos divers partenaires internes et externes. Vous contribuerez à votre développement de compétences ainsi qu'à celui du personnel de production grâce à des actions de formation et de tutorat.Vous évolurez au sein d’équipes pluridisciplinaires en tant que membre de la maintenance et vous aurez la responsabilité de gérer les actions ou plan d’actions de maintenance, de garantir la qualité des produits fabriqués en fonction des normes de fabrication en vigueur et de la satisfaction client.

Vous devrez également respecter et faire respecter les normes (ISO 9001, ISO 14001, de sécurité, GMP) ainsi que connaître, appliquer et faire appliquer les règles de sécurité et d'environnement en vigueur.Vous interviendrez dans un environnement de salles classées.

Le poste est basé à Molsheim (67), en CDI, en 2x8.

Qui vous êtes :

Issu d’une formation Bac + 3 Type Génie Electrique et Informatique Industrielle ou Systèmes Automatisés, Génie Industrielle et Maintenance ou d’un BTS MAI / CRSA.
Compétences techniques confirmées : robotique, vision, automatisme, électrotechnique, régulation, …
Maitrise des outils informatiques type Word, Excel, Outlook. La connaissance de la langue anglaise et/ou Allemand serait un plus
Idéalement issu d’un parcours d’alternance et/ ou une première expérience dans le domaine de la maintenance serait un plus
Compétences en maintenance préventive et curative acquises lors d’expériences réussies en environnement de production ; vous utilisez un outil de la GMAO

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

Technicien Qualite Environnement f/h (Molsheim, Bas-Rhin, FR, 67120)

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.

Votre rôle :

En développant vos compétences d'organisation et d'analyse, vous contribuerez à la maitrise de la qualité des zones à atmosphère contrôlée et des bons comportements en zone de production.

Vous serez en charge de réaliser et analyser les contrôles environnementaux en zone de production BioMonitoring et S&SU ainsi que les tests de biocharge microbienne de nos produits, conformément aux spécifications établies et dans les délais en veillant au respect des procédures. Vous aurez en charge la lecture et l'enregistrement des résultats dans notre système LIMS et réaliserez les investigations en cas de non-conformité en collaboration avec les équipes Qualité production, afin des déterminer les causes et des actions d'améliorations.

Vous aurez la charge de former les relais formations et les opérateurs aux contrôles de prélèvements, à l'habillage en production et aux bonnes pratiques environnementales pour garantir la maitrise des zones de production.

Vous supporterez la production sur les questions relatives à la Qualité environnementale microbiologique et apporterez votre expertise en apportant des solutions innovantes. Vous aurez la responsabilité de réviser et revoir la pertinence des documents en lien avec l’activité sous le système documentaire Mango.

Vous participerez au développement de l'équipe et de l'activité en proposant et en mettant en place des améliorations par le biais d'audit "Be Quality", de "6S", audit sécurité...

Qui vous êtes :

Vous justifiez d’une formation scientifique minimum Bac +2, avec une bonne connaissance en microbiologie
Vous êtes familier avec les exigences des normes ISO 9001, ISO 14644, GMP, …
Vous avez le sens de l’organisation et des priorités, vous êtes réactif et avez de réelles capacités d’analyse et de synthèse
Vous appréciez le travail en équipe
Une expérience en zone classée serait un plus

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

Ingenieur Chiffrage f/h (Molsheim, Bas-Rhin, FR, 67120)

Work Your Magic with us!

Your role :

Your role will focus on supporting pre-sales activities by leveraging your technical and process expertise to prepare detailed, accurate, and competitive technical quotations in response to customer inquiries and RFPs, which requires a strong technical background, a keen eye for detail, and effective collaboration with cross-functional teams. You will analyze opportunity scope and requirements to determine accurate pricing and technical feasibility of proposed solutions, including evaluating the feasibility of customizations and new concepts or technologies on Multi-Uses (MU) and Single-Uses (SU) systems, and you will develop detailed technical quotations based on customer specifications, project requirements, and industry standards. This involves calculating costs for materials, labor, and overhead to provide competitive and accurate pricing models, and quoting complex opportunities that involve multiple equipment with a high level of customization. You will work closely with engineering, sales, and project management teams to gather necessary information and ensure alignment on technical aspects and pricing. Furthermore, you will engage with customers to clarify technical requirements, provide support during the quotation process, and attend customer meetings to define and challenge opportunities. Your role also requires maintaining organized records of quotations, including technical specifications, pricing justifications, and a complete costing package such as P&ID designs, system specifications, cost sheets, planning, and lists of deviations for future reference and audits. Finally, you will collaborate with stakeholders (Marketing, Field Service, R&D, sponsors) to develop and sustain a strategic plan that aligns with organizational goals, and act as a Lean advocate by identifying quick wins, proposing and executing Continuous Improvement (CI) projects, and contributing to the development of standard operating procedures.

Who you are :

Bachelor’s degree in Engineering (Electrical, Mechanical, Automation, or related field) or equivalent experience.
Proven experience in a technical role, preferably in the biopharma, life sciences, or related industries.
Strong understanding of biopharmaceutical processes and regulatory requirements.
Excellent analytical skills and attention to detail.
Proficient in tools such as Salesforce (SFDC), SAP, or similar quotation management software.
Demonstrated interest in continuous learning and self-development, with a commitment to improving autonomy, impact, and performance.
Strong communication and interpersonal skills, with the ability to work effectively in a team environment.

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

Alternant Coordinateur Distribution f/h (Molsheim, Bas-Rhin, FR, 67120)

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.

Votre rôle :

Tâches et responsabilités :

S’assurer que les expéditions soient réalisées physiquement et informatiquement dans les délais prévus.

S’assurer que les capacités de transport nécessaires soient réservées à temps, avec un possible choix de solution et arbitrage.

Veiller à ce que les expéditions soient livrées aux clients dans les délais prévus.

S’assurer que les notes de crédit soient gérées dans les délais.

Collaborer avec l’ensemble des partenaires en interaction avec l’équipe.

Assurer la gestion des événements spéciaux (jour férié, grève, météo, etc.), en communiquant avec les parties prenantes et en définissant avec eux un mode de gestion dégradé.

Connaître, appliquer et faire respecter les règles en vigueur liées à la sécurité et à l’environnement ; promouvoir la culture de la sécurité et la politique environnementale

Alternance à partir de septembre 2026.

Qui vous êtes :

Organisé, multitâche, ouvert d'esprit, vous avez une réelle orientation satisfaction client et vous êtes flexible dans un environnement multiculturel en constante évolution.
Excellente communication orale et écrite, vous soignez vos relations professionnelles et vous avez une appétence pour le travail en équipe.
Connaissances dans le domaine de l’import/export : compétences réglementaires et douanières.
Outils informatiques : Pack Office, utilisation d’un ERP.
Capacité à évoluer dans un environnement digital complexe
Anglais courant oral et écrit

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

Field Service Coordinator f/m (Molsheim, Bas-Rhin, FR, 67120)

Work Your Magic with us!

Your role:

You will work with our EMEA Field Service team, making sure everything runs smoothly and efficiently across the entire region. Your primary job is to be the central communicator: you will coordinate all service requests, manage the schedules for our field engineers, and keep customers and our internal teams (Sales, Support, Logistics) perfectly aligned. Beyond coordinating, you will help grow the business by partnering with Sales to renew contracts and propose new service agreements. You will also maintain accurate service records and help implement better ways of working so we can consistently deliver exceptional support.

Please note this is an opportunity for a CDD (Fixed-Term) contract.

Who you are :

Proven experience in administrative tasks for Service Coordinaation. It is an office-based role with no Research & Development (R&D) components.
A master of organization and multitasking who knows how to prioritize tasks.
An excellent communicator, skilled at building strong working relationships with customers, engineers, and cross-functional teams.
Technically proficient with the Microsoft Office Suite and experience using a service management system like Salesforce.
Must be fluent in English and French; any additional EMEA languages are a bonus.
A Bachelor's degree in a relevant field or equivalent professional experience.

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

Senior Supplier Quality Engineer (Lenexa, Kansas, US, 66215)

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, you will be pivotal in upholding the highest quality standards throughout the product life cycle. Your responsibilities will encompass evolving a meticulously organized approach to product releases, labeling approvals, and ensuring process consistency. This will involve rigorous reviews of executed batch records, raw material documentation, and product release records, which are essential for maintaining compliance with industry standards.

As a key contributor to collaboration with Quality Control, you will engage in batch release and testing processes, addressing out-of-specification (OOS) and out-of-trend (OOT) scenarios. With a focus on fostering strong internal relationships, you will drive excellence within the External Manufacturing Quality group while supporting MilliporeSigma's quality systems, including participation in audits and the implementation of corporate policies. Your role will not only be to ensure compliance and quality but also about innovating customer service approaches and problem-solving methodologies to meet both regulatory and customer expectations.

Key Responsibilities:

Write/revise and review Operating Procedures and other QA controlled documents under an ISO 9001 quality system. Become point of contact with QC for serum specific topics.
Support MilliporeSigma quality systems, e.g., corporate, internal & external audits and corporate policy implementation(s).
Participate in deviation, corrective and preventative actions, and change control.
Become a role model for customer service and forward-thinking approaches to problem solving.
Opportunity to track, trend, and action complaints depending on experience.
Independently manage and engage in day-to-day interaction with suppliers to ensure on-time delivery of goods and solving quality/production related issues.
Evaluation, monitoring, and quality improvement of external suppliers.
Cultivate and maintain positive, collaborative relationships with key suppliers based on trust, open communication, and mutual respect.
Work closely with cross-functional teams including Supply Chain, R&D, Procurement, and Trade Compliance to ensure product delivery and quality standards, customer, and regulatory requirements.
Develop qualification and validation documentation to support changes to existing products and/or processes.
Support NPI and Project teams to ensure procedures are available, accurate, and adhered to appropriately.

Be amenable to various project assignments
Ensure each NPI project aligns to the LS and Site level procedures in place including the needed documentation for each step.

Who You Are

Minimum Qualifications:

Bachelor’s Degree or higher in science related majors
5+ years of quality related experience in engineering, biotechnology, and/or life sciences

Preferred Qualifications:

Demonstrated Life Science, Chemicals or Healthcare industry knowledge
Knowledge of manufacturing processes and product life cycles
Working knowledge of SAP; Mango, TrackWise, Falcon are a plus
Excellent communication skills with business-fluent English
Mindset and skills for continuous improvement initiatives
Experience managing chemical and biological suppliers is a plus.
Experience with new product introduction and buy/resell processes is a plus.
Experience in cross-functional projects
Strong understanding in ISO 9001:2015
Excellent oral and written communication skills, ideally with experience in Quality communications
Capable of working across a variety of systems, ERPs, electronic platforms, and Quality Management Systems
Self-directed and self-motivated with strong organizational skills and ability to continually prioritize projects and tasks with varying requirements and deadlines
A desire and ability to connect with people at all levels of the organization and external partners, building trust and rapport while collaborating

Pay Range for this position: $97,800 - $157,200.

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

Cyber Protection Expert Electronics / Part-Fulltime/ all Genders (Weiterstadt, Hessen, DE, 64331)

Work Your Magic with us!

Your role: As a vital member of the Cyber Protection & Digital Asset Security team, you will play a crucial role in safeguarding our Electronics Cyber Security operations. You will collaborate with the global Cyber Security team and the Electronics business to ensure the implementation of robust technical security controls. Your expertise will be instrumental in developing and enhancing our technical capabilities, particularly in operational technology environments. You will consult on security measures for networks and endpoints, ensuring effective system hardening and patch management. Additionally, you will contribute to the creation of incident response and recovery plans tailored for IT and OT assets. Your role will involve working closely with engineering teams to identify vulnerabilities and oversee penetration testing efforts. By maintaining a strong Cyber Security posture, you will help protect our software-based products and applications. This position offers the opportunity to make a significant impact on our Cyber Security strategy and contribute to the overall safety of our digital assets. Join us in our mission to secure our technological landscape.

Who you are:

Bachelor’s degree or equivalent in intelligence studies, computer science, engineering, or a related field.
Minimum of 5 years’ experience focused on Cyber Security, adhering to industry standards and regulatory requirements (e.g., ISO27000, NIST CSF, NIS2, PCI DSS, KRITIS / B3S PHARMA).
Strong analytical and interpersonal communication skills, with the ability to build consensus across teams.
Proven experience in developing and implementing security controls within infrastructure, with knowledge of networking, IDS/IPS, and NDR/EDR.
Demonstrated experience in creating and executing incident response and recovery strategies.
One or more industry-recognized security or audit professional certifications (e.g., CISA, CISM, CISSP, CCSP).
Understanding of security challenges and regulatory requirements specific to the chemical and semiconductor industries is a plus.
A professional with a positive attitude, capable of thriving in a dynamic, team-oriented culture, and excellent verbal and written communication skills in English (German is a plus).

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

Senior Network Engineer (all genders) - Network (Datacenter & Connectivity) (Weiterstadt, Hessen, DE, 64331)

Work Your Magic with us!

Your role:

An exciting opportunity has arisen to join our global Network Team, based at our headquarters in Darmstadt. In close collaboration with colleagues across regions, you will help ensure the stability, integrity, and continuous improvement of our enterprise network services.

This is an individual contributor role with a strong focus on data center connectivity, network security controls, and integration patterns with cloud connectivity. Beyond hands-on engineering, you will help define, ensure, and enforce global standards and align with architects and technical leaders across infrastructure and business domains.

You will provide support primarily during Germany business hours, handle escalation activities via support tickets/monitoring/user reports, and participate in an on-call rotation. Occasional work outside normal business hours may be required.

Key responsibilities:

Design, implement, and operate enterprise network solutions with focus on data center networking and related services.
Contribute to architecture and standardization: create/review technical documentation, reusable patterns, and reference designs; support design governance and exception handling.
Align with infrastructure and business architects to ensure end-to-end consistency across domains (including on‑prem/private cloud and public cloud connectivity integration).
Engineer and operate network security components (e.g., segmentation, policy controls, secure connectivity patterns) in line with security and compliance requirements.
Improve reliability and operational efficiency through automation, standard changes, and enhanced monitoring/observability.
Participate in incident handling, troubleshooting, escalation management, and on-call duties; collaborate with internal teams and external partners.

Who you are:

10+ years of experience in IT infrastructure / networking, including designing and operating enterprise network environments.
Strong practical experience with common enterprise networking and security platforms (e.g., DC fabric, routing/switching, firewalls, load balancing, DNS/IPAM), ideally including technologies such as Cisco ACI/Nexus and enterprise firewall solutions (e.g., Firepower/ASA or equivalents).
Strong network automation skills, ideally including Python scripting against network/ACI APIs, Ansible‑based automation for Cisco ACI/Nexus and firewalls, solid Linux/Bash skills, and working with Git‑centric workflows (code review, CI/CD‑like pipelines for network changes).
Solid understanding of core networking concepts and protocols (e.g., BGP, OSPF, MPLS, VXLAN, VLAN/802.1Q, QoS).
Experience in hybrid or multi-cloud environments (AWS, Azure, GCP) is beneficial, especially in connectivity and integration contexts.
Strong documentation skills (concepts, diagrams, and structured design/implementation documentation).
Able to work independently, drive topics end-to-end, and influence through standards in a global, federated environment.
Strong communication and stakeholder management skills.
English required; German is a plus.
Willingness to travel (up to 10% domestic and 10% international).
Willingness to participate in an on-call rotation.

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

Experte Farbmetrik Qualitätskontrolle (m/w/d) VZ / TZ (Gernsheim, Hessen, DE, 64579)

Entfalten Sie Ihr Talent in einem aufregenden Umfeld der Brillanz!

Werden Sie Teil eines visionären Teams, das die Chemiebranche mit frischen Ideen und glänzenden, innovativen Lösungen neu definiert. Als Teil eines marktführenden Weltkonzerns, strahlen wir die Energie und den Enthusiasmus eines Start-ups aus. Mit einem klaren Fokus auf hochwertige Effektpigmente für die Kosmetik-, Automobil- und Bauindustrie bieten wir Ihnen die Möglichkeit, Ihre Fähigkeiten in einem inspirierenden Umfeld zu entfalten. Unsere Produktpalette umfasst renommierte Marken wie Iriodin®, Colorstream® und Ronastar®. Dabei respektieren wir den Chemie-Tarifvertrag mit einer fairen Vergütung, umfassenden Sozialleistungen und gezielte persönliche Förderung. Kommen Sie zu uns und gestalten Sie die Zukunft der Oberflächenlösungen – bringen Sie Farbe in die Welt und setzen Sie Ihre Ideen in die Tat um!

Ihre Rolle:

Zur Verstärkung unseres Teams suchen wir eine engagierte Persönlichkeit mit einem ausgeprägten Gespür für Farbe und hoher Qualitätsorientierung.

In dieser Position übernehmen Sie die visuelle Beurteilung von Farben unter definierten Lichtbedingungen sowie die instrumentelle Bewertung von Farbdaten in verschiedenen Farbräumen. In enger Abstimmung mit der Produktion stellen Sie sicher, dass die geforderten Farb- und Qualitätsstandards zuverlässig eingehalten werden. Bei Abweichungen oder besonderen Fragestellungen arbeiten Sie eng mit dem Troubleshooting-Labor zusammen und unterstützen farbmetrische Projekte, etwa bei Versuchsreihen, der Optimierung von Farbräumen oder der Einführung neuer Messmethoden.

Im Rahmen betrieblicher Erfordernisse bringen Sie zudem die Bereitschaft mit, auch an Wochenenden und Feiertagen zu arbeiten.

Eine sorgfältige, strukturierte Arbeitsweise sowie ein ausgeprägtes Qualitätsbewusstsein zeichnen Sie ebenso aus wie die Fähigkeit, auch unter Zeitdruck konzentriert, zuverlässig und lösungsorientiert zu agieren. Teamfähigkeit, Freude an der Zusammenarbeit mit Produktion und Labor sowie eine hohe Service- und Kundenorientierung runden Ihr Profil ab

Wer Sie sind:

Abgeschlossene Ausbildung als Physik-/Chemielaborant/Chemisch-technischer Assistent (m/w/d) oder vergleichbare Qualifikation
Idealerweise Berufserfahrung in der Abmusterung von Farben und Qualitätssteuerung von Pigmenten
Sicherer Umgang mit Laborsoftware Tableau, gute MS Office (insbesondere Excel) und Kenntnisse in LIMS-Systemen und SAP von Vorteil
Sicherer Umgang mit etablierten Troubleshooting-Methoden wie Root Cause Analysis (RCA)
Sorgfältige und strukturierte Arbeitsweise, hohes Maß an Verantwortungsbewusstsein
Uneingeschränktes Farbsehvermögen
Teamfähigkeit, Eigeninitiative und lösungsorientiertes Denken
Sehr gute Deutschkenntnisse (mind. C2) in Wort und Schrift
Gute Englischkenntnisse in Wort und Schrift (mind. B1)

Technischer Facharbeiter / Industriemechaniker (m/w/d) (Gernsheim, Hessen, DE, 64579)

Entfalten Sie Ihre Talente in einem aufregenden Umfeld der Brillanz!

Werden Sie Teil eines visionären Teams, das die Chemiebranche mit frischen Ideen und glänzenden, innovativen Lösungen neu definiert.

Als Teil eines marktführenden Weltkonzerns, strahlen wir die Energie und den Enthusiasmus eines Start-ups aus.

Mit einem klaren Fokus auf hochwertige Effektpigmente für die Kosmetik-, Automobil- und Bauindustrie bieten wir Ihnen die Möglichkeit, Ihre Fähigkeiten in einem inspirierenden Umfeld zu entfalten. Unsere Produktpalette umfasst renommierte Marken wie Iriodin®, Colorstream® und Ronastar®.

Dabei respektieren wir den Chemie-Tarifvertrag mit einer fairen Vergütung, umfassenden Sozialleistungen und gezielte persönliche Förderung. Kommen Sie zu uns und gestalten Sie die Zukunft der Oberflächenlösungen – bringen Sie Farbe in die Welt und setzen Sie Ihre Ideen in die Tat um!

Ihre Rolle:

Sie arbeiten im Bereich der Technik der Susonity GmbH als Technischer Facharbeiter / Industriemechaniker (m/w/d) in einer agilen Einheit der Technik. In dieser Funktion arbeiten Sie in einem Team, das für die Ausführung von Wartungs-, Montage-, Optimierungs- und Instandhaltungsarbeiten an Anlagen, Geräten und Maschinen am Standort Gernsheim verantwortlich ist. Weiterer Bestandteil der Tätigkeit ist die Störungssuche und -beseitigung, um einen sicheren Anlagenbetrieb zu gewährleisten. Sie pflegen die technische Dokumentation und sorgen für die Einhaltung der einschlägigen Vorschriften. Sie bilden sich fortlaufend weiter und freuen sich neue Technologien einzusetzen.

Wer Sie sind:

Fachkenntnisse auf dem Niveau einer dreijährigen zielführenden Ausbildung z.B. Industriemechaniker (m/w/d) oder Metallverarbeitung
Methoden und Fachkompetenz, Teamfähigkeit, Eigeninitiative und Flexibilität
Technisches Verständnis, Sauberkeits- und Ordnungssinn
Instandhaltungs-Erfahrung in der Chemie und Pharmaumfeld von Vorteil
Erfahrungen im Umfeld der Zerspannung (Drehen, Fräsen)
Grundkenntnisse in Arbeits-und Umweltschutz, Unfallverhütung
Freude am selbstorganisierten eigenverantwortlichen Arbeiten in einer agilen Organisationsstruktur
Gute Deutschkenntnisse in Wort und Schrift minimal auf B2 Level

RM Digital & Business Excellence Manager (Sanpada New Mumbai, Maharashtra, IN, 400705)

Job Summary:

The Business Excellence Lead will be responsible for driving commercial strategies & digital marketing initiatives as a part of Business excellence within the Asia region. This role focuses on monitoring business performance, increasing forecast accuracy, enhance brand visibility and engagement through innovative digital strategies, cross-region initiatives & strategic pillars. for the Asia region. This is a man management role reporting into the Head of RM Asia.

Key Responsibilities:

Develop and implement commercial strategies that align with overall business goals.
Monitor business performance, analyze market trends and competitor activities to identify opportunities for growth.
Increase forecast accuracy through robust analytical methods and data interpretation.
Collaborate with sales teams to enhance performance through trainings, workshops and best practices.
Lead cross-region initiatives to streamline processes and improve operational efficiency.
Propose new ideas and strategies to enhance the Asia business, demonstrating strong analytical skills and critical thinking.
Manage digital campaigns across various platforms, including social media, email, and search engines, ensuring alignment with overall business goals.
Analyze campaign performance and optimize strategies based on data-driven insights to maximize impact across the team.
Collaborate with the content team to create compelling digital content that resonates with target audiences and strengthens brand presence.
Stay updated on digital marketing trends and technologies to ensure best practices are implemented and shared across the team.
Monitor, report KPIs of the regional team to measure effectiveness and ROI, providing insights that drive continuous improvement.
Foster a culture of excellence and accountability within the commercial team.

Qualifications:

Bachelor’s degree in business administration, Marketing, or a related field; MBA preferred.
Extensive knowledge of digital marketing tools and analytics platforms, with a proven track record of impactful campaigns.
Strong creative and strategic thinking abilities.
Excellent communication skills and ability to work in a fast-paced, collaborative environment.
Minimum of 8 years of experience in commercial excellence or process improvement roles; An experience in a commoditized market would be an added advantage.

Skills:

Strong analytical and problem-solving skills, with a self-driven approach to proposing innovative solutions.
Excellent communication and interpersonal skills.
Ability to work collaboratively in a cross-functional team environment.
Successful program implementation @ business process improvements, problem solving - 5 Why's , Risk Assessment & Business continuity planning would be an asset for the position.

Business Executive (Navi Mumbai, Maharashtra, IN, 400706)

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!

Your Role :

Generate or convert doctors for our product portfolio.
Secondary sales – Ensuring to achieve secondary sales targets through prescription generation by each of his BE.
Good at relationship with KOLs (Top Physicians, Endocrinologists & Cardiologists)
Day to day sales reporting
Effective query handling and customer queries.
Ensuring 100% Implementation of Company’s strategies
Pharmacovigilance (Adverse Event Reporting) – To collect adverse drugs reaction (ADR) incidences including lack of efficacy related to medicinal products up to the maximum possible level of completeness and forward to local Patient Safety team immediately within 24 hours of ADR awareness. The additional information can be submitted as soon as possible

Who you are:

Any graduate
Freshers or minimum of 1-2 years of experience in any pharma company
Should have strong product knowledge & communication skills
Location: Goa

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.

Sales Executive (Petaling Jaya, Selangor, MY, 46100)

Key Responsibilies:
• Drive sales growth and achieve revenue objectives by identifying and capitalizing on new business opportunies for Industrial & Cosmetic segment in Malaysia.
• Strategically manage regional and local accounts to maximize profitability and ensure alignment with customer needs.
• Proactively build a healthy opportunity pipeline through robust opportunity tracking and monthly reviews.
• Develop and maintain long-term, trust-based relationships with key customers, partners, and internal stakeholders.
• Collaborate with Regional Marketing, Innovation Lab, and Business Development teams to drive high-value projects and co-create solutions with leading brands.
• Ensure impactful communication with customers to convey value propositions effectively.
• Conduct customer profiling, segmentation, and categorization to tailor solutions and prioritize growth opportunities.
• Analyse market trends, competitor activities, and product performance to identify growth opportunities and stay ahead of the comptition.
• Gather and incorporate customer feedback to enhance satisfation and strengthen partnerships.
• Forecast demand and supply to optimize inventory levels and ensure seamless customer delivery.
• Ensure timely management of receivables and adherence to financial targets.
• Accurately maintain and report sales activities through Salesforce.com or equivalent CRM tools.
• Foster teamwork, transparency, and collaboration across internal teams to deliver superior customer experiences.
• Act as a liaison between customers and internal functions, including supply chain, finance, and to ensure smooth operations.
• Inspire a goal-oriented, competitive mindset within the team to achieve shared objectives.
• Partner with R&D and technical teams to introduce innovative, high-value solutions tailored to customer needs.

Required Skills and Qualifications:
• Minimum 2-3 years or more on sales experience in the area of colorants, active ingredients and specialty chemicals.

• Proven track record in sales and customer development within the Industrial & cosmetics or related industry in the region.
• Strong stakeholder management and relationship-building skills.
• Analytical mindset with the ability to leverage market data for decision-making.
• Proficiency in CRM tools (e.g., Salesforce.com) and sales reporting.
• Ability to work collaboratively across functions and drive results in a dynamic environment.
• Excellent communication, negotiation, and problem-solving skills.

Quality Control Specialist (Singapore, Singapore, SG, 118222)

Work Your Magic with us!

Your Role:

Quality Control (QC) Specialist is to promote and integrate quality into every aspect of our BioReIiance biologics safety testing business in Singapore. Duties of the role include the support of QC operations (environmental monitoring and release of critical raw materials), data integrity and systems administration to ensure that laboratory testing operations are in full compliance with sound scientific practice, GxP and Standard Operating Procedures (SOPs). As a QC Specialist, you will ensure quarantine materials are received and released for use as per appropriate quality procedures. The ability to develop and maintain effective working relationships with operational, support services and quality assurance personnel will be critical for success in this role.

Who You Are:

Graduate degree in life sciences or microbiology or higher related degree
Minimum of 4 years of experience
Demonstrable scientific expertise in microbiology related works
Previous experience working in a Quality Control materials release environment
Previous Pharmaceutical experience would be ideal; however, other industry backgrounds would be considered
You will have previous work experience within a GLP / GMP regulated environment would be highly desirable
You are strongly focused on quality and safety, with strong planning and organisational skills
You have good communication and interpersonal skills and are highly self-motivated, with strong initiative and drive

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

Scientist I - Biosafety Testing (Singapore, Singapore, SG, 118222)

Work Your Magic with us!

Your Role

The Scientist will possess scientific expertise in biologics safety testing, with a focus on Virology, Detector Cell Culture, and Client Cell Culture. This role involves ensuring that all projects are executed in accordance with the necessary scientific and regulatory compliance standards. The Scientist will leverage their expertise to support investigations and client meetings, providing valuable insights and guidance.

The Scientist will be able to perform the following functions independently, with minimal guidance.

What You Do

Lead new assay and technology transfer
Serve as the Study Director or Responsible Scientist for routine and complex assays, holding overall responsibility for the conduct of GLP or GMP studies.
Plan, organize, and prioritize workloads to ensure timely and effective testing, including the issuance of Certificates of Analysis (COA) for studies.
Ensure that routine and complex client studies are completed on schedule and meet the necessary scientific and regulatory standards.
Work with the Lab Manager to develop testing schedules for laboratory personnel.
Provide hands-on support, training, guidance, and mentorship to laboratory personnel in virology, detector cell culture and Client Cell Culture.
Provide hands-on support, training, guidance, and mentorship to laboratory personnel in molecular studies.
Leads by example, acts as subject matter expert, offers scientific coaching and mentoring to other laboratory staff.
Author, review, and approve study-related and technical scientific documents, including amendments, scientific protocols, Standard Operating Procedures (SOPs), workbooks, and technical specifications.
Ensure that trending spreadsheets for all studies are completed promptly and in accordance with relevant SOPs.
Author and reviewer of assay risk assessments related to your area of expertise
Ensures all assays / processes are in a validated state in line with current regulations
Responsible for maintenance and scientific integrity of routine and non-standard assays methods by monitoring assay performance and advising and implementing on improvements where necessary
Leads process improvements within the laboratory to improve quality and performance
Performs regular housekeeping laboratory check and Health and Safety audits
Host internal Quality Audit representing the laboratory; participate in client or regulatory audit
Responsible on audit observations response through the BioReliance Integrated Quality System (Trackwise)
Lead and ensure deviation and Corrective or Preventative Action (CAPA) records in a timely manner
Raise and progress Change Control for new service, testing, assay validation introduction
Acts as scientific consultant to support departmental investigations, client product queries, supplier audits and client/regulatory inspections
Liaises with Commercial, Development Services, Programme Management and other Laboratory Operations to provide technical support for ongoing and upcoming projects/studies, as required
Ensures a safe and healthy work environment at all times by not only complying with but actively embracing health and safety policies and procedures, ensuring the safety of yourself and others within the workplace
Conduct relevant bench work for client studies as assigned.

This list of job duties is not exhaustive, and the post holder may be required to undertake additional tasks as reasonably expected within the scope of the role. Job descriptions will be reviewed regularly to ensure they accurately reflect the position.

Who You Are

Minimum Degree in Biological Sciences or higher qualification in relevant scientific subject.
Minimum 5-8 years of experience in a scientific laboratory role, ideally within a GLP / GMP contract testing laboratory environment
Proven scientific expertise in virology, detector cell culture and client cell culture-related work.
Experience of working in Biosafety Level 2 laboratory

Knowledge & Skills:

Computer literacy and entry of data into databases (LIMS, ELN, SAP, Oracle, etc.)
Ability to complete documentation (both handwritten and electronic) neatly and accurately
Strategy and business knowledge
- Demonstrates customer centricity
- Thinks and acts strategically
- Can troubleshoot effectively
- Understands the business
Operating skills
- Puts safety first by adhering to health and safety procedures and actively takes necessary action when encountering unsafe situations
- Orchestrates multiple activities in parallel to accomplish goals
- Plans workload by assigning tasks appropriately depending on length and difficulty of task
- Through effective communication, provides the information people need to know to do their jobs
Professional and Technical skills
- Has the functional and technical knowledge and skills to do the job at a high level of accomplishment
- Can learn new skills and acquire knowledge rapidly
- Uses logic to solve complex problems with effective solutions
- Shows sound judgement in decision making
- Comes up with new and unique ideas and adds value in brainstorming settings
Energy and Drive
- Self-motivated; is action-orientated and full of energy for the things he/she sees challenging, seizes more opportunities than others
- Pursues everything with energy, drive and the need to finish, especially in the face of resistance or setbacks
- Can be counted on to achieve goals, constantly and consistently, pushes self and others for results
- Deals effectively with pressure; remains optimistic and persistent, even under adversity
Personal and interpersonal skills
- Relates well to all kinds of people in the organization, builds constructive and effective relationships using diplomacy and tact
- Is seen as a team player, cooperative, easily gains support of peers, encourages collaboration
- Communicates effectively with others
- Handles conflict effectively

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

Manager, Inhouse Consulting (Singapore, Singapore, SG, 118222)

Work Your Magic with us!

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!

Channel Sales Representative (APAC) (Singapore, Singapore, SG, 118222)

Work Your Magic with us!

Your Role
The Channel Sales Representative will manage Mirus Bio portfolio. Mirus Bio is a leading provider of life science products, committed to advancing research, development, and healthcare solutions. We work with top-tier organizations in the life sciences field, providing cutting-edge technologies and expertise. You will be critical in driving sales and expanding the market share for our life science products. This individual will be responsible for building and maintaining strong relationships with distribution partners, managing sales strategies, and identifying new opportunities for growth in the life science sector. The ideal candidate will have experience in sales within the life sciences or healthcare industry and a proven track record of success in channel sales management.

What You Do

Develop and Manage Direct and Distribution Channels: Drive sales for Life Science Discovery and manage relationships with distribution partners in key markets, ensuring alignment with company goals and product offerings. Where appropriate identify and recruit new distributors.
Sales Strategy Execution: Work closely with internal teams to develop and implement sales strategies aimed at achieving revenue targets and expanding market presence within the life science sector for both distribution and direct business
Product Knowledge: Maintain in-depth knowledge of the company’s product portfolio, staying up to date on product advancements and market trends to provide valuable guidance to distributors and clients.
Customer Engagement: Provide exceptional support to distribution partners, offering training, troubleshooting, and guidance to ensure their success in selling life science products. Where appropriate, support our direct customer base.
Sales Reporting and Forecasting: Track sales performance, provide regular updates, and manage forecasts to ensure accurate revenue predictions and market penetration.
Market Analysis: Monitor and assess competitor activities, industry trends, and customer feedback to inform sales strategies and product improvements.
Promotional Support: Assist with the creation and execution of marketing and promotional campaigns to enhance product visibility and distributor engagement.
Travel: Regular travel to meet with distributors, attend industry events, and gather customer feedback.

Who You Are

Bachelor’s degree in life sciences or relates field
Minimum of 3-5 years of sales experience, focusing on life science products or related industries like Academia, Biotech, and Pharma
Ideally have a proven track record in managing distribution channels and achieving sales targets.
Strong understanding of life science product offerings and their applications.
Excellent communication, negotiation, and presentation skills.
Ability to work independently and as part of a team in a fast-paced environment.
Proficiency with CRM software and MS Office Suite (Excel, Word, PowerPoint).
Willingness to travel (up to 30% of the time).

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

Biomonitoring Account Manager (Singapore, Singapore, SG, 118222)

Work Your Magic with us!

Your Role

An exciting opportunity to join a vibrant and technology company. You will be responsible for sales management of our BioMonitoring portfolio for our existing client portfolio and developing new segments for our product range dedicated to microbiological control.

If you are self-reliant with an entrepreneurial spirit and natural drive to be successful, then this position may be perfect for you.

Establish and maintain a record of all customer details with contact names and other pertinent information through Customer Relationship Management System (CRM)
Regularly advise management regarding potential methods of business improvement.
Perform all work with consideration to the economical use of resources.

What You Do

Develop objectives, strategies and tactics to expand sales within your customer base.
Monitor sales results against budgets within the allocated customer base and take appropriate action.
Maintain an awareness of market trends and competitor activities and report these to the Sales Manager regularly.
Maintain a record of all customer visits, and feedback information to the Biomonitoring Sales and Marketing staff on Products promoted to these customers through the Customer Relationship Management System (CRM) on a regular basis.
Comply with the face to face call rate as requested by the Biomonitoring Sales Manager.
Provide monthly reports on activities and sales results to the Biomonitoring Sales Manager.
Prepare small quotes for customers and forward to the Quotes Officer.
Attend company meetings, exhibitions, sales conferences and training courses as requested.
Report on key achievements relating to objectives on a weekly basis.

Who You Are

Must have a Bachelor of Science or equivalent experience.
Must have previous scientific sales experience, preferably in pharmaceutical, environmental or food industries.
Experience in a laboratory will be well regarded.
Highly self-motivated and energetic individual with good interpersonal and communication skills.
Able to demonstrate excellent communication and negotiation skills.

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

Associate Scientist III (Singapore, Singapore, SG, 118222)

Work Your Magic with us!

Who We Are

We are a leading science and technology company. Its life science business offers a broad range of innovative products and services to biotech and pharmaceutical drug therapies businesses. Through dedicated collaboration with the scientific and engineering communities, and as one of the top three R&D investors in the life science tools industry, the brand serves as a strategic partner to customers and helps advance the promise of life science.

Your Role

The Associate Scientist III – Biosafety Testing is responsible to perform a wide variety of routine tasks to support GMP operations and primarily focusses on Molecular Biology, NGS, Virology and Cell Culture work related to Biosafety Testing. Responsibilities include performing either PCR-based assays, NGS testing or Cell Culture/Virology assays in Biosafety laboratories which required to characterize product, maintenance of cell culture detector cell lines, preparing and qualifying of reagents, monitoring stock levels, and conducting general equipment maintenance to sustain seamless workflow and optimal performance of laboratory equipment.

The Associate Scientist III may require to provide training and / or mentoring junior members of lab personnel. The ability to maintain effective working relationships with Scientists, Lab Scientists, support services, and laboratory personnel will be critical for success in this role.

What You Do

Works within the Molecular Biology, NGS, Virology, and Cell Culture laboratories following Standard Operating Procedures and compliance regulations.
Adherence to Standard Operating Procedures (SOPs) and Compliance Regulations: Ensure all work is carried out according to established protocols and regulatory standards.
Learning Management System: Ensure zero overdue LMS records, timely complete training required to perform the assay or task.
Timely Completion of Studies and Record Keeping: Complete routine and custom studies on time, maintaining accurate records that meet scientific and Good Manufacturing Practice (GMP) standards.
Assays transfer: Perform assays transfer following relevant protocols as required.
Document Control: Maintain SOPs, laboratory books, and forms, ensuring outdated versions are removed promptly. Review and improve working documents through document control processes.
Stock Control and Procurement: Manage stock levels, order consumables, and handle procurement through designated systems.
Laboratory Maintenance: Conduct housekeeping, equipment checks, and environmental and personnel monitoring to ensure compliance and safety.
Health and Safety: Maintain a clean, tidy, and safe work environment, adhering to health and safety policies and procedures.
Training and Mentoring: May require to train and mentor newer or junior members of the lab personnel.
Quality Audits and Regulatory Compliance: Participate in internal quality audits and regulatory audits as required.
Audit Readiness: Maintain a constant state of readiness for audits across all laboratory areas.
Protocol and SOP Development: Author laboratory protocols, SOPs, and workbooks for projects.
Peer Review and Data Management: Conduct peer reviews of raw data records and ensure accurate data management practices on a timely manner.
Deviation/Discrepancies: Raise and progress deviation and Corrective and Preventive Action (CAPA) records promptly.
Continuous Improvement: Proactively identify and implement improvements to laboratory processes and procedures to enhance efficiency and reduce waste.
Site or Global Initiatives: participate in site or global initiatives

Who You Are

Minimum Degree in Biological Sciences or higher qualification in relevant scientific subject
3 plus years of working experience in biologics or biopharmaceutical industry
3 plus years of working experience in a regulated environment (GMP or equivalent)
2 plus years of working experience in specific area of expertise (molecular biology, virology, microbiology/mycoplasma) with demonstrated ability to trouble-shoot
Quality mindset and good understanding of GMP
Demonstratable experience in implementing projects to set-up/improve lab processes/systems
Good oral and written communication skills in English
Capability on problem solving and planning skills
ERP experience is an asset (Oracle / SAP/ LIMS/ Trackwise)
Proficient in Microsoft programs (Word, Excel, PowerPoint, etc)
Adheres to safety SOPs and follows safe work practices
Always ensures a safe and healthy work environment
Team player, proactive and willing to take ownership
Strong Aseptic Technique and cell culture skills (for Virology focus)
Strong molecular biology skills and NGS applications (for NGS focus)
Flexibility to work overtime or shifts to cover Business spikes/ needs when necessary.

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)

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

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.

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！

Head of Global Development Operations (GDO) Japan / Biopharma (Tokyo, Tokyo, JP, 106-0041)

YOUR ROLE:

The Head of Global Development Operations Japan is responsible for providing strategic leadership and operational oversight for all clinical development activities in Japan. This role requires building strong relationships with investigators, sites, and internal stakeholders while ensuring compliance with regulatory requirements and company standards. The ideal candidate will possess extensive experience in clinical research, strong leadership abilities, and the capacity to drive performance excellence in a complex, matrix organization.

WHO YOU ARE:

10+ years of professional experience in Clinical Research in biotech, pharma, or CRO, including experience in Clinical Trial Management and managing Clinical Monitoring/Site Management
At least 5 years of people and resource management in a multifunctional or multinational setting
Graduate degree (Medical or Life Sciences) in a clinical research related discipline or equivalent
Ability to think beyond own function, considering overall business objectives and company strategy while anticipating internal and external business challenges.
Outstanding leadership skills to ensure high-level harmonization and excellence across teams and geographies, with the ability to direct, influence, and motivate people.
Demonstrated excellent organizational skills, including time management, prioritization, and the ability to handle multiple tasks simultaneously.
Approaches change positively, adapting behavior or work methods in response to new information, changing conditions, or unexpected obstacles.
Strong cultural awareness with fluency in English (oral and written)
Japanese language is a must have.

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！

【障害者雇用枠】Farm Worker (Ebina勤務) (Tokyo, Tokyo, JP, 106-0041)

＜業務内容＞

屋内型農園でハーブなどの栽培・加工から製品にするまでの業務全般

栽培・加工業務
種まきから収穫
収穫したハーブの乾燥
ハーブティー、ポプリ等の製品加工、ラッピング
製品の出荷準備

栽培・加工に関わる清掃や日報作成、それに付随する業務

＜応募条件＞

他の障害者社員とチームワークで仕事が出来る方
栽培等の経験不問

その他：

栽培・加工・ラッピングしたハーブティー、ポプリは本社、各事業所にて社員の方に提供されます。
管理者（指導員）が常駐し、丁寧な指導・サポート体制がありますので、安心して就業いただけます。

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！

Medical Director or Clinical Scientist (Oncology experience required) / Biopharma (Tokyo, Tokyo, JP, 106-0041)

MEDICAL DIRECTOR or CLINICAL SCIENTIST (Oncology experience required)

YOUR ROLE

Act as a medical responsible:

Provide medical/scientific input and drive/contribute to the creation of relevant clinical documents or parts thereof to ensure high quality of e.g. study concept sheets, study protocols and reports, Investigator Brochures, publications, etc.
Review and sign off all clinical documents related to the clinical studies (e.g. study protocols and study reports) within area of responsibility
Conduct medical monitoring for responsible project/study, if applicable
Oversees all medical scientific aspects of the trial and provides respective guidance to the trial team Oversee all aspects related to the scientific and medical risks in collaboration with the safety representative
Support the review, analysis and interpretation of study data
Support communication of study results as assigned

Act as a clinical representative in global project/regional team:

Propose clinical development strategies in Japan for assigned indication(s)/product(s) in order to establish its safety and efficacy and support registration in the shortest possible time in Japan for information on local medical environment
Develop Biomarker strategy in collaboration with the global biomarker team
Propose translational studies in collaboration with the global clinical lead and the biomarker team and facilitate the study.
Develop, support and/or prepare integrated development plans, submission/registration documents, publications, etc in collaboration with clinical and project team members for assigned indication(s)/product(s)
Liaise with (principal) investigators, health authorities, IEC/IRB, consultants, opinion/thought leaders and academic institutions within area of responsibility to deliver on key accountabilities.
Participate in cross-functional development project team activities to provide medical/scientific input into e.g. business plan, project strategy, in-/out-licensing activities and Due Diligence as assigned
Support business development activities by providing medical-scientific expertise for evaluation of in/out licensing opportunities as appropriate. Provide medical-scientific input to the biomarker strategy in alignment with respective interface functions

Act as a clinical representative in global project/regional team:

Propose clinical development strategies for assigned indication(s)/product(s) in order to establish its safety and efficacy and support registration in the shortest possible time worldwide
Provide medical input to regulatory development strategy and contribute to clinical sections of the Common Technical Document (CTD)

WHO YOU ARE

Must have at least five years of experience in clinical development in the field of oncology at a pharmaceutical company.
Fluent in English with native Japanese language skills.
A strong scientific background is required, with a bachelor's degree in pharmacology, biology, or a related field at minimum, and preferably a Ph.D. for the Clinical Scientist role. (MD degree is required for the Medical Director position)
Ability to work effectively within a team.
Availability for evening-to-night calls to discuss programs/studies with Europe/US-based colleagues.
Willingness to visit Key Opinion Leaders (KOLs) and investigators when necessary
Effectively drive projects even in uncertain and ambiguous situations

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！

Medical Director or Clinical Scientist (Immunology experience required) / Biopharma (Tokyo, Tokyo, JP, 106-0041)

MEDICAL DIRECTOR or Clinical Scientist (Immunology experience required)

YOUR ROLE

Act as a medical responsible:

Provide medical/scientific input and drive/contribute to the creation of relevant clinical documents or parts thereof to ensure high quality of e.g. study concept sheets, study protocols and reports, Investigator Brochures, publications, etc.
Review and sign off all clinical documents related to the clinical studies (e.g. study protocols and study reports) within area of responsibility
Conduct medical monitoring for responsible project/study, if applicable
Oversees all medical scientific aspects of the trial and provides respective guidance to the trial team Oversee all aspects related to the scientific and medical risks in collaboration with the safety representative
Support the review, analysis and interpretation of study data
Support communication of study results as assigned

Act as a clinical representative in global project/regional team:

Propose clinical development strategies in Japan for assigned indication(s)/product(s) in order to establish its safety and efficacy and support registration in the shortest possible time in Japan for information on local medical environment
Develop Biomarker strategy in collaboration with the global biomarker team
Propose translational studies in collaboration with the global clinical lead and the biomarker team and facilitate the study.
Develop, support and/or prepare integrated development plans, submission/registration documents, publications, etc in collaboration with clinical and project team members for assigned indication(s)/product(s)
Liaise with (principal) investigators, health authorities, IEC/IRB, consultants, opinion/thought leaders and academic institutions within area of responsibility to deliver on key accountabilities.
Participate in cross-functional development project team activities to provide medical/scientific input into e.g. business plan, project strategy, in-/out-licensing activities and Due Diligence as assigned
Support business development activities by providing medical-scientific expertise for evaluation of in/out licensing opportunities as appropriate. Provide medical-scientific input to the biomarker strategy in alignment with respective interface functions

Act as a clinical representative in global project/regional team:

Propose clinical development strategies for assigned indication(s)/product(s) in order to establish its safety and efficacy and support registration in the shortest possible time worldwide
Provide medical input to regulatory development strategy and contribute to clinical sections of the Common Technical Document (CTD)

WHO YOU ARE

Must have at least three years of experience in clinical development in the field of immunology at a pharmaceutical company.
Fluent in English with native Japanese language skills.
A strong scientific background is required, with a bachelor's degree in pharmacology, biology, or a related field at minimum, and preferably a Ph.D. for the Clinical Scientist role. (MD degree is required for the Medical Director position)
Ability to work effectively within a team.
Availability for evening-to-night calls to discuss programs/studies with Europe/US-based colleagues.
Willingness to visit Key Opinion Leaders (KOLs) and investigators when necessary
Effectively drive projects even in uncertain and ambiguous situations

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！

Senior R&D Scientist in Abrasive Technology, Chemical Mechanical Planarization (CMP) / Electronics (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？

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。

Senior Scientist in Abrasive Technology, Chemical Mechanical Planarization (CMP)

Your role:

Who you are:

Minimum Qualifications:

M.S. or Ph.D in Chemistry, Chemical Engineering or Material Science
5+ years’ experience in particle related research, development, application

Preferred Qualifications:

Ph. D degree within abrasive/inorganic nanoparticle research area, is a plus
Proven expertise in nanoparticle synthesis, characterization and development through publication and commercialization
Working experience in abrasive/inorganic nanoparticle RD, metrology and application in an industrial setting, is a strong plus
Previous exposure to the semiconductor industry, particularly in CMP formulation and/or applications, is a strong plus
Excellent leadership and interpersonal skills that support a diverse team environment
Hands-on experience in project management is highly desirable.

Excellent verbal and written communication skills in English.

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！

Regulatory Affairs Senior Manager / Biopharma (Tokyo, Tokyo, JP, 106-0041)

Your Role:

Develop and execute regulatory affairs (RA) activities from the development to the life cycle management, with collaborative with global and Japan stakeholders. Regulatory Affairs Senior Manager focuses on some of the following activities in Regulatory Affairs Group 1 or Group 2:

Lead RA-related Health Authority (HA) interactions. e.g., PMDA or MHLW interaction
Lead New Drug Application (NDA) and supplementary NDA (sNDA) such as indication expansion, new formulation, etc.
- Lead preparation of the Japan NDA activities and HA’s review for approval.
- Prepare the Japan-CTD regulatory parts such as Approval Application Form, Module 1, etc.
Lead Partial Change Application (PCA)/Minor Change Notification (MCN) [Change Control Process/Post-marketing activities] with collaborative with CMC team.
Lead electronic Japanese Package Inserts (J-PI), respond to query, and join artwork activities. Review promotion materials.
Support the Group Head to oversee, manage, mentor, and ensure the Group plans and delivers the regulatory deliverables (as the alternative representative of the Group as needed), while complying with applicable regulations.
Provides coaching to staff.
Manage Outsourcing vendors as needed.

Represent RA for the SOPs/WI updates and improvement tasks.

Who You Are:

Education and Preferable work experiences:

Experiences and knowledge in Regulatory Affairs, especially development or post-marketing activity.
Experiences of Collaborating with cross-functional team and global member.

Competencies and skills:

Language: Japanese- native level. English: Able to communicate with global members as J-RA representative.
Stakeholder management, Communication/coordination, leadership/ownership skills, strategic consideration and project/risk management skills (e.g., To Clarify regulatory risks and plan/execute minimization/mitigation).

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！

Farm Supervisor (Ebina勤務) (Tokyo, Tokyo, JP, 106-0041)

＜業務内容＞

屋内型ハーブ農園で就業する障害者社員の就労サポートと管理業務

就労サポート：

ハーブ栽培、加工業務のサポート
障害者社員との定期面談や体調管理
支援員定着支援との面談

管理業務：

勤怠管理
栽培物、製品関連の備品購入および管理
栽培物、製品の管理
衛生管理
その他本社からの依頼業務等

＜応募条件＞

PCスキル（簡単な書類作成（Word）、メール（Outlook）、インターネット）
障害者と一緒に働くことに興味関心がある方であれば、経験不問

その他：丁寧な研修、相談出来る同僚、サポート体制がありますので、未経験の方も応募歓迎

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！

Therapeutic Area Specialist Thyroids (m/w/d) (Wien, Wien, AT, 1120)

Entfalte das Besondere mit uns!

Zu Ihren Aufgaben zählen die persönliche und virtuelle Betreuung von Meinungsbildnern, Spezialisten, Allgemeinmedizinern und Internisten. Sie informieren hauptsächlich, aber nicht ausschließlich über unser Schilddrüsenportfolio, und betreiben wertvolle Aufklärungsarbeit im Bereich medizinischer Awareness. Zu den Aufgaben zählen auch die Vertretung von Merck bei regionalen und überregionalen Veranstaltungen und Kongressen. Ein Hauptaugenmerk liegt auf innovativer Kundenkommunikation und -Engagement mit digitalen Kommunikationstools sowie Offenheit und proaktiver Nutzung neuer Medien.

Ihre Qualifikation:

Sie haben ein abgeschlossenes Studium im naturwissenschaftlichen Bereich oder gleichwertige Erfahrung in dem Bereich / Pharmaindustrie
Sie haben die Pharmareferentenprüfung abgelegt und bringen mind. 2 Jahre Erfahrung im Außendienst/ Sales-Bereich mit
Sie sind eine dynamische Persönlichkeit mit dem Willen zum Erfolg
Sie sind sehr digital-affin und haben Freude an virtueller Kommunikation mit ihren Kunden. Die Nutzung moderner Devices ist für Sie selbstverständlich
Die Arbeit mit CRM-Tools sowie Segmentation und Targeting sind Ihnen in Ihrer täglichen Arbeit vertraut
Sie verfügen über sehr gute kommunikative und soziale Fähigkeiten
Sie sind ein ausgesprochener Team-Player und erreichen Ihre Ziele am besten durch enge Kooperation mit Medical, Ihrem Sales Manager und den Kollegen aus dem Marketing
Sie sind strategisch, wissen, was Sie langfristig zum Erfolg führt und übernehmen Ownership
Engagement, Ausdauer und Leistungswille zeichnen Sie aus
Sie sprechen fließend deutsch und sind verhandlungssicher auf englisch

Was wir Ihnen bieten:

Die Möglichkeiten, sich in unserem wachsenden Unternehmen weiterzuentwickeln, sind genauso vielfältig wie unser Brand-Portfolio. Es erwartet Sie ein modernes, internationales Arbeitsumfeld, in dem Sie Ihr innovatives Potenzial in bunt gemischten Teams voll ausschöpfen können. Wir übernehmen Verantwortung für unsere Mitarbeiter, Produkte, die Umwelt oder Gesellschaft. Das Jahresbruttogehalt beträgt € 50.000,- und ist abhängig von Ihrer beruflicher Qualifikation und Erfahrung.

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

Internship - Wearable 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, Switzerland

Role Level: Internship

Your role:

The Connected Device Department is seeking an engineering student to help us evaluate the feasibility of running AI models on smartwatches (Wear OS and watchOS). You’ll port existing server-side models to edge devices, design and run experiments to measure prediction performance and battery impact under different usage patterns and deliver practical guidelines to correctly port the model into an edge device. You won’t build new models; our team will provide candidate models and parameters to vary. The main focus is software porting, rigorous measurement, and clear recommendations.

Your Profile:

Must-Haves

You are currently studying Software Engineering, Computer Science, Electrical/Computer Engineering, or a related field.
Basic familiarity with mobile development (Android/Wear OS or iOS/watchOS).
Comfortable writing clean, testable code and documenting findings clearly.
Strong analytical mindset and attention to detail; able to compare configurations and interpret trade-offs.
Interest in edge AI and on-device inference.

Nice-to-haves

Experience with on-device inference frameworks or model conversion (e.g., TensorFlow Lite, Core ML, ONNX).
Understanding of optimization techniques (e.g., quantization,).
Exposure to sensor data pipelines or streaming workloads on mobile/wearables.
Prior projects that involve benchmarking, parameter sweeps, or porting models to constrained devices.

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

Supply Chain Planning Solution Architect (all genders) (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your role:

Join our IT organization as a Supply Chain Planning Solution Architect and play a pivotal role in our upcoming SAP IBP implementation, enhancing and transforming our supply chain planning landscape. You will be responsible for preparing and deploying functionality in our new SAP IBP solution across our ERP and APS landscapes. Your experience in implementing SAP IBP within complex landscapes at a global scale will be invaluable, guiding projects from template definition to deployment and support. Collaborating with Business Process Experts, Key Users, and SMEs, you will ensure the SAP IBP design aligns with business objectives. You will be part of a team of solution experts across core IBP modules, contributing to the overall success of our supply chain strategies. Your expertise in Supply Chain SAP ERP and APS functionality, particularly within the Life Sciences industry, will drive operational excellence. You will identify areas for improvement, develop designs, and implement solutions to deliver high-quality results. If you are passionate about making a significant impact and advancing your career, this is your opportunity.

Who you are:

Bachelor's degree in business or a relevant field; advanced degree preferred
Minimum of 5 years of experience in Advanced Planning System (preferably SAP APO and SAP IBP) implementation
Experience with state-of-the-art SAP ERP (S/4 Hana) and Advanced Planning Systems, preferably in the Life Sciences industry
Proven track record in designing solutions and implementation within multi-systems ERP/APS landscapes
Familiarity with change control methodologies
Strong analytical skills
Effective communication skills to collaborate with various stakeholders globally
Willingness to travel for key project stages and meetings

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

Supply Chain Planning Transformation Manager (all genders) (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your role:

In this role, you will be at the forefront of our supply chain planning transformation, leading the implementation of SAP IBP within our IT organization. You will manage the preparation and deployment of our new SAP IBP solution, significantly enhancing our supply chain planning landscape. Your experience in implementing SAP IBP across complex global environments will be invaluable as you collaborate with Business Process Experts and Key Users to align the design and implementation with business objectives. You will oversee a team of Solution experts, guiding them in the core IBP modules to ensure the functionality meets our target solutions. Your expertise in Supply Chain SAP ERP and APS functionality, particularly in the Life Sciences sector, will drive the identification of improvement areas and the development of effective solutions. You will be responsible for documenting key design decisions and maintaining accurate records of all deployment activities. Your ability to balance multiple projects and priorities will be essential as you engage with various stakeholders to gather requirements and feedback. If you have a passion for operational excellence and a proven track record, this position offers a unique opportunity to make a significant impact on our organization and advance your career.

Who you are:

Bachelor's degree in business or a relevant field; advanced degree preferred
Minimum of 10 years of experience in Advanced Planning System implementation, preferably SAP APO and SAP IBP
Expertise in SAP ERP (S/4 Hana) and Advanced Planning Systems within the Life Sciences industry
Proven track record in managing solutions and implementations across multi-systems ERP/APS landscapes
Strong project management experience using change control methodologies
Excellent analytical skills
Effective communication skills for collaboration with global stakeholders
Willingness to travel for key project stages and meetings

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

Solids Bulk Supervisor (Mollet del Valles, Barcelona, ES, 08100)

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.

Gestión de la producción:

Asegurar que los operarios cumplan con la normativa de calidad (GMP) y EHS
Supervisar los procesos productivos y el cumplimiento de los programas de fabricación.
Adaptar recursos ante incidencias para minimizar pérdidas de capacidad productiva.
Gestiona cualquier desviación o incidencia ocurrido durante el turno con los departamentos implicados siguiendo las instrucciones y protocolos de trabajo definidos. Para incidencias más complejas, escala a técnicos/as o manager del área.
Participa en la investigación de ciertas desviaciones y/o reclamaciones cuando sea requerido para ello.
Supervisa y realiza formación continuada al personal de su cargo en la correcta cumplimentación de toda la documentación relacionada con los procesos productivos y limpiezas del área.

Gestión de personal:

Supervisa el desempeño diario del equipo, asegurando que se sigan las normativas de calidad, seguridad y generales
Evalua también el desempeño del equipo de forma más global, proporcionando retroalimentación constructiva y gestionando cualquier problema de desempeño que pueda surgir.

Mejora Continua:

Participa en proyectos o iniciativas de mejora contínua, ya sea como integrante de un equipo o bién liderándolos
Monitoriza las pérdidas de eficiencia ocurridas durante el turno., en los sistemas diseñados para ello.

Requisitos:

Licenciatura en Ciencias de la Salud o Ingeniería (preferentemente).
Disponibilidad para trabajar en turnos rotativos (mañana, tarde y noche) según las necesidades del área.
Nivel de inglés intermedio.

Competencias clave:

Apasionado/a por la gestión de las personas.
Experiencia demostrada en liderazgo de equipos en entornos productivos.
Habilidad en la gestión de equipos y resolución de conflictos.
Capacidad de influencia y trabajo en equipo.
Comunicación directa, clara y escucha activa.
Aptitud para identificar mejoras en la gestión de personas y en los procesos relacionados.

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!

Working student data architecture (Mollet del Valles, Barcelona, ES, 08100)

Your Role

Ready to shape the future of data in R&D? As a Working Student for Data Architecture you will support the team to design efficient, scalable data architectures and pipelines that enable analytics and AI across Pharmaceutical R&D. Based on communication with R&D stakeholders you will help translate functional requirements into technical concepts and implement components together with data engineers. You will gain hands‑on project experience across the R&D data value chain and work in a global, agile environment.

Key responsibilities

Support design and implementation of data models, data pipelines and ETL/ELT flows that feed reporting, analytics and AI solutions.
Assist in building and operating data repositories (e.g., Snowflake) and cloud-based data processing (AWS services) together with senior architects and engineers.
Collaborate with product owners, data engineers, business analysts and domain users to translate requirements and ensure correct solution delivery.
Help create and maintain architecture blueprints, standards, data dictionaries and best practices for the team.
Support automated CI/CD for data pipelines and integration tests (Azure DevOps / Git / warehouse automation tools).
Assist in data quality checks, basic troubleshooting and third‑level support tasks for R&D data systems.
Contribute to documentation, knowledge sharing and operational run‑books.

Experiences

Familiarity or exposure to Snowflake and AWS data services (Glue, Lambda, DMS) is expected; these are core to our Data & AI ecosystem.
Hands‑on or coursework knowledge of ETL/ELT concepts and tooling such as Informatica (PowerCenter / IICS) and warehouse automation tools (e.g., dbt, Coalesce) is a strong advantage.
Understanding of data modelling patterns, data flows and the end‑to‑end lifecycle from ingestion to consumption; experience with testing data integrations is beneficial.
Good SQL skills; basic Python experience is desirable.
Basic understanding of CI/CD concepts and experience (or interest) with Azure DevOps / Git for pipelines and deployments.
Fluent English and the ability to work in virtual, cross‑functional agile teams.

What we offer

Real project responsibility and mentorship from senior data architects; exposure to Snowflake, AWS and enterprise data tooling.
Opportunity to work across global teams and directly contribute to data solutions that accelerate R&D.

Apply now and become part of a team dedicated to Awakening Discovery and Elevating Humanity!

Energies & Utilities Technician (Mollet del Valles, Barcelona, ES, 08100)

Apply Your Magic with Us

Are you ready to explore, break barriers, and discover much more? We know you have great plans. We do too; innovating with science and technology to enrich people's lives with solutions in Healthcare, Life Science, and Electronics excites our colleagues around the world. Together, we dream big and share the enthusiasm for caring for a great diversity of people, customers, patients, and the planet. That's why we are always looking for curious minds to imagine the unseen with us.

United as one for patients: our goal in Healthcare is to help create, improve, and prolong lives. We create treatments, smart devices, and innovative technologies in therapeutic fields such as oncology, neurology, and fertility. Our teams collaborate across 6 continents with passion and relentless curiosity with the aim of helping patients at every stage of their lives. Joining our Healthcare team means being part of a diverse, inclusive, and flexible work culture that offers fantastic opportunities for personal and professional development around the globe.

Job Title: Energy and Utilities Technician
Location: Mollet Site

Job Description:

The Energy and Utilities Technician is responsible for the maintenance, troubleshooting, and optimization of energy and utility systems. This role ensures the efficient and reliable operation of HVAC sytems, clean and black utilitites and water systems.

Key Responsibilities:

Conduct routine maintenance and repairs on energy and utility systems.
Monitor system performance and identify energy efficiency improvement opportunities.
Perform inspections and diagnostics to troubleshoot equipment issues.
Collaborate with engineering and operations teams on energy management initiatives.
Maintain accurate records of maintenance activities and system performance data.
Ensure compliance with safety regulations and company policies.
Participate in training programs to enhance technical skills and knowledge.

Qualifications:

Technical degree or certification in Energy Management, Mechanical Engineering, Electrical Engineering, or a related field.
Experience in maintenance and troubleshooting of energy and utility systems.
Understanding of energy efficiency practices and technologies.
Strong problem-solving skills and attention to detail.
Ability to work independently and within a team.
Effective communication and interpersonal skills.

Apply Your Magic with Us

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

Work Your Magic with us!

Your Role:

As a Cloud Solutions Architect /Senior Cloud Platform Engineer, you will join the Data & AI Solutions - Engineering team in our Healthcare R&D business. You will leverage your expertise in our D&A Landscape primarily using AWS Cloud Services and Azure AD, supporting our R&D efforts in drug discovery and development.

Your role includes supporting and implementing the technical roadmap, maintaining platform functionalities, engineer data archive process and adapting to emerging technologies. Responsibilities involve implementing new features and building and managing deployments.

Who You Are:

A university degree in Computer Science, Engineering, or a related field.
Exceptional problem-solving skills.
With 5 plus years of relevant experience.
You are a proficient software engineer who knows the fundamentals of computer science and you master the Python programming language.
A proven track record of building and delivering secure, scalable, and resilient cloud-native systems using AWS services at an enterprise level.
Fluency in English with excellent communication skills.
Eager to learn and collaborate in a multinational environment, working with cross-functional teams across the US, Europe (primarily Germany), and India.
A strong business facing skills with a sense of accountability and ownership, with a capacity for rapid learning.

Key Technical Skills and Experience:

Programming Skills: In-depth experience in Python, relational databases, SQL, and a background in object oriented programming languages such as Scala, C#, or Java is advantageous
Services : Knowledge of distributed services, RESTful APIs and microservices built on AWS, with experience in AWS Lambda (using the boto3 library) and serverless design.
Cloud Skills: Experience working with high volume heterogenous data and preferably distributed systems like Spark, building cloud-native systems using AWS services at an enterprise level with a learning mindset.
Best Practices: Knowledge of Object Oriented Programming (OOP) and design patterns and excellent code and technical documentation as well as experience with code review.
CI/CD & Automation: Understanding of CI/CD pipelines, with experience in building and deploying CI/CD pipelines (preferably using Azure DevOps).
Data Governance: Knowledge about data governance, data access and data storage techniques
Testing Framework: Experience in testing framework
Security: Familiarity with AWS security best practices (MFA, encryption, user roles & policies).

Nice to Have:

Containerization: Experience in building and deploying container services (Docker, Kubernetes, AWS Fargate).
Data Tools: Experience with Iceberg and Snowflake.
Familiarity with Terraform, CloudFormation, or CDK for infrastructure automation.
Knowledge of NoSQL databases.

This role can be hired in Portugal and Poland, in addition to Spain.

*Todos los candidatos internos, sin importar si trabajan a tiempo completo o parcial, tendrán la oportunidad de ser considerados para las vacantes disponibles

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

Global Occupational Safety Lead (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your Role: As the Global Occupational Safety and Process Safety Lead, you will be at the forefront of ensuring the safety and well-being of employees and operations across our Global Healthcare Operations. Your strategic vision and operational expertise will be essential in identifying, assessing, and managing safety risks while driving continuous improvement in occupational and process safety on a global scale. You will collaborate closely with the EHS global team to define and implement a comprehensive safety strategy that aligns with corporate goals and regulatory requirements. Serving as a key advisor to senior leadership, you will provide regular updates on safety performance and initiatives, ensuring excellence in hazard analysis and risk assessments. Your leadership will guide the development and standardization of safety procedures and tools across all sites, fostering a robust safety culture. You will also play a critical role in incident investigations, helping to identify root causes and implement lessons learned to prevent recurrence. Your ability to communicate effectively will facilitate the sharing of safety successes and lessons learned throughout the organization. With approximately 30% travel to sites globally, you will enable and oversee the implementation of safety initiatives, making a significant impact on our operations.

Who You Are:

Bachelor’s degree in scientific, engineering, chemical, safety, or other life science field.
At least 10 years of experience in Occupational and Process Safety, preferably in an international environment.
Strong knowledge of occupational and process safety management, hazard analysis, and regulatory compliance.
Proven ability to lead cross-functional teams and influence stakeholders at all levels.
Strong communication, problem-solving, and change management skills.
Fluent in English; additional languages are a plus.
Experience with ISO 14001/45001 management systems is preferred.
Critical requirement to be well-organized and able to manage multiple projects simultaneously.

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

Senior DevOps Engineer (Mollet del Valles, Barcelona, ES, 08100)

Work Your Magic with us!

Your Role: As a Senior DevOps Engineer with a strong background in AWS, you will join the Data & AI Solutions - Engineering team in our Healthcare R&D business. Your expertise will enhance cloud-based platforms in our D&A Landscape using AWS Cloud Services and Azure AD, supporting our R&D efforts in drug discovery and development.

You will bridge software development, quality assurance, and IT operations, ensuring our platform is reliable, scalable, and automated. Your expertise will contribute to accelerate deployment cycles and minimize downtime. Key responsibilities include deploying new releases, maintaining Azure AD for identity management, and collaborating with cross-functional teams to advocate for DevOps best practices and guide architectural decisions.

Join a multicultural team working in agile methodologies with high autonomy. The role requires office presence at our Spain location.

Who You Are:

University degree in Computer Science, Engineering, or a related field 
5+ years of experience applying DevOps in solution development & delivery
Proficiency in Infrastructure as Code (IaC) using Terraform and AWS CloudFormation for automated and repeatable cloud infrastructure deployments.
Mandatory understanding of AWS services and cloud system design
Strong experience in observability practices, including logging, monitoring, and tracing using tools like Prometheus, Grafana, ELK Stack, or AWS-native solutions.
Understanding of Azure active Directory (Azure AD) and handling project configurations, repositories, pipelines, and environments using Azure Devops
Proficiency in Azure AD incl. apps registration, and authentication flows (OBO, Client Credentials)
Experience with configuration management tools such as Ansible for automating service provisioning, configuration and management.
Knowledge of security best practices in AWS DevOps, including secrets management, role-based access control (RBAC), and compliance frameworks
Strong scripting and automation skills using Python for developing of automations and integration workflows
Willingness to work in a multinational environment and cross-functional teams distributed between US, Europe (mostly, Germany) and India 
Sense of accountability and ownership, fast learner 
Fluency in English & excellent communication skills for technical and non-technical stakeholders

If you are curious and ambitious to take up this challenge, apply today and be in the driver seat implementing our Data and Analytics landscape. Your contribution will make a lasting impact on our customers and our organization and elevating Data & Analytics to the next level! 

This role can be hired in Portugal and Poland, in addition to Spain.

Role: Expert 3

*Todos los candidatos internos, sin importar si trabajan a tiempo completo o parcial, tendrán la oportunidad de ser considerados para las vacantes disponibles

Area Business Director, HIV/Endo (Northeast) (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 Area Business Director (ABD) is directly accountable for the management, profitability, and overall performance of the area business, leading Area Business Managers (ABMs) and Senior Area Business Managers (SABMs) through the effective implementation of objectives, strategies, and tactics. In this capacity, the ABD is a key member of a multidisciplinary team—including Marketing, Market Access, Field Operations, Patient Access Solutions, Training, Human Resources, Compliance, Legal, and Communications—working collectively to achieve both individual and team goals.

Location: Field-based. Assigned Territory:

The position requires travel up to >80% and a valid, active driver’s license. Occasional evening or weekend work may be required.

Cross-Functional Collaboration:

The ABD coordinates regular strategy meetings with Marketing and Market Access to align initiatives, resolve challenges, and ensure unified messaging and execution across all commercial channels. Collaboration with Field Operations, Patient Access Solutions, and other internal partners is facilitated through ongoing communication and joint planning sessions, enabling rapid response to market dynamics and optimizing resource allocation.

Team Development:

The ABD is responsible for recruiting, coaching, and developing ABMs and SABMs to reach their highest potential. This includes setting clear performance expectations, providing feedback, and fostering a culture of accountability and continuous improvement that drives achievement of key results.

Strategic and Operational Balance:

The ABD balances long-term strategic planning—such as market analysis and competitive positioning—with day-to-day operational management. Examples include overseeing territory sales activities, monitoring key performance indicators, and implementing tactical adjustments to meet evolving business needs.

Relationship Building:

The ABD cultivates and maintains strong relationships with key physician practices, hospitals and clinics, and patient advocacy organizations, acting as an ambassador for EMD Serono. This engagement provides valuable market insights to the broader organization and enhances the company’s reputation as a leader in science and technology.

Compliance:

The ABD consistently ensures compliance with all company policies, industry regulations, and government guidelines, upholding the highest ethical standards in all business activities.

Who You Are

Minimum Qualifications:

Bachelor’s degree in business, life sciences, or related field (advanced degree preferred).
Minimum of 8 years of progressive experience in pharmaceutical, biotech, and/or healthcare industry with demonstration of successful results.
Minimum of 3-5 years of leadership experience, preferably in specialty sales.

Preferred Qualifications:

Demonstrated leadership and people management skills.
Experience in Cross-functional collaboration required.
Proficient knowledge of Market Access and Solutions.
Understand local market landscape and influences.
Home Office/Headquarter experience is a plus.
Experience in the HIV market, rare disease and/or specialty biologics markets are highly desirable.

Cultivate Talent - Challenge and inspire diverse teams of high-performers
to reach their full potential.
Strategic thinking and business acumen
Excellent communication and interpersonal skills
Ability to foster a culture of collaboration and accountability
Inspire Purpose - Work as a team to communicate a bold, inspiring and collective purpose.

ADA REQUIREMENTS (i.e., normal office duties; must be able to push, lift, pull up to 30 pounds; etc.)

Normal Office duties.
Able to travel up to 80%, may vary based on location.

Pay Range for this position: $213,500 - 320,300
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 prequisites. For more information click here.

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

Medical Science Liaison (MSL), Fertility - South Central region (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 Medical Science Liaison (MSL) is a crucial role within the Medical Affairs team, representing EMD Serono in the education of the healthcare community externally and leading the transfer of insights to drive strategic decision making internally. The Medical Science Liaison (MSL) is responsible for cultivating and maintaining collaborative relationships with influential members of the medical community to promote company, disease state and therapeutic awareness, in addition to serving as an advanced technical, scientific, and medical expert in the specified therapeutic area (Fertility) for the assigned region.

Location: Field-based, Assigned Territory: South Central US

Responsibilities:

Provide in-depth scientific, clinical, and educational support to academic thought leaders and community decision makers through the dissemination of pertinent educational, scientific, and clinical information on the specific disease state and its treatment
Cultivate and maintain relationships with Key Opinion Leaders as peers whose opinions, disease and disease treatment insights and competitive knowledge provide direction to US Medical Affairs and EMD Serono
Disseminate to healthcare professionals state-of-the-art research and medical concepts related to fertility and fertility treatments through one-to-one peer interactions and group learning activities
Lead Medical Affairs activities in your region coordinating with internal departments and external customers
Represent EMD Serono at medical events, programs, meetings, and conventions
Liaise with the US Medical Affairs Fertility Team on the development and implementation of medical initiatives both regionally and nationally
Communicate research and development concepts, key field insights and competitive intelligence to appropriate internal stakeholders
As appropriate, coordinate with Clinical Development and Fertility Medical Affairs in providing field support for clinical research studies
Act as a liaison between investigators and Medical Affairs for the Investigator Sponsored Studies (ISS) program
Maintain HCP and institutional profiling and visitation records for the territory
Administer and monitor appropriate budget expenditures to meet the responsibilities as outlined above
Ensure compliant use of field material and conduct of activities
Act as a respected and highly regarded representative of EMD Serono by demonstrating our values, behaviors, and high impact culture
Extensive (80%) regional travel including overnight travel, national meetings, and may include international conferences

Who you are:

The MSL must command a comprehensive understanding of reproductive medicine focused on fertility and will partner with other members of the US Field Medical, US Medical Fertility and other key stakeholders to contribute to the overall understanding of fertility and the fertility treatment landscape, developing significant and long-term relationships for EMD Serono with KOLs and community clinical leaders

Minimum Qualifications:

PharmD, PhD, MD, DO and 2+ years of relevant experience or NP / PA and 3+ years of relevant experience. Equivalent combination of education and fertility clinical experience may be considered
Advanced scientific knowledge, relationship building and networking skills
Ability to maintain collaborative relationships within a dynamic team environment
Ability to communicate complex scientific and clinical information tailored to a wide-variety of audiences through multiple channels
English language competency
Excellent communication skills
Comfortable with extensive (80%) regional travel including overnight travel, national meetings, and potentially international conferences
Live within the assigned territory or within a reasonable commuting distance

Preferred Qualifications:

3 or more years of clinical and/or pharmaceutical experience in Fertility (required for Sr. MSL role)
Prior experience as a field medical science liaison or equivalent (e.g., nurse clinical liaison) (required for Sr. MSL role)
Live within the assigned territory
Ability to communicate openly and share information to foster trust while encouraging constructive debate, making informed decisions, and ensuring shared commitment to outcomes.
Demonstrated willingness to take risks and stand up for what is right while prioritizing the needs and experiences of customers and patients in all decisions.
Commitment to setting and reaching ambitious goals and setting high standards while acting in the best interest of the company and taking initiative to drive results.
Uphold ethical standards and being honest in all interactions.
Ability to streamlining processes to focus on what matters and creates impact and acting quickly to adapt to changes.
Demonstrated ability to embrace new ideas, challenge the status quo, and seek innovative solutions while valuing diverse perspectives and treating others with respect and dignity.

Pay Range for this position: $157,100-235,700
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 prequisites. For more information click here.

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

Sr. Manager, Analytics Engineering & BI Architecture (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 Sr. Manager, Analytics Engineering & BI Architecture is a hands-on technical leader responsible for architecting analytical data models, designing scalable cloud-based data layers, and delivering high-impact Tableau dashboards that directly support business decision-making. This role requires deep expertise in data modeling and transformation within Redshift and Snowflake, ownership of the semantic and extract layers powering Tableau, and the ability to translate complex stakeholder needs into intuitive, performance-optimized, executive-ready analytics products.

The role partners closely with business stakeholders, data engineering, analytics teams and IT team to ensure data solutions are accurate, trusted, scalable, and aligned to evolving business priorities. Success in this role requires strong architectural judgment, advanced Tableau design skills, and the ability to balance speed, quality, and governance. You will lead, inspire, and engage with passion by modeling EMD Serono behaviors and working with a sense of urgency to achieve organizational goals.

Key Responsibilities

Data Architecture & Modeling

Design, build, and maintain analytical data models in Amazon Redshift and Snowflake to support enterprise-grade BI and advanced analytics use cases.
Define and implement business transformation logic, conformed dimensions, fact tables, and semantic layers optimized for Tableau performance and scalability.
Partner with data engineering and upstream teams to ensure data quality, consistency, and governance across sources.

Advanced Tableau Development & Visualization

Architect and develop high-quality Tableau dashboards and data products that go beyond standard reporting, incorporating best practices in UX, performance optimization, and storytelling.
Build and maintain Tableau extracts and live connections, ensuring reliability, refresh efficiency, and security compliance.
Act as the technical authority for Tableau on prem and cloud development standards, data source design, and visualization best practices.

Stakeholder Partnership & Delivery

Lead requirements discovery sessions with stakeholders to translate business questions into scalable analytical solutions.
Serve as the primary point of contact for complex analytical questions, ad-hoc requests, and interpretation of data.
Balance short-term business needs with long-term architectural integrity and platform strategy.

Platform Ownership & Modernization

Manage and evolve the Redshift and Snowflake BI data layers, ensuring best practices around performance, security, and cost efficiency.
Continuously evaluate and adopt new BI, analytics, and data-warehouse tools as the platform modernizes.
Mentor and guide other BI resources by modeling strong engineering discipline and analytical thinking.

Who You Are

Minimum Qualifications:

Bachelor’s degree in Computer Science, Engineering, Analytics, or a related technical discipline (or equivalent practical experience).
5+ years of experience in data warehousing, BI, or analytics engineering roles.
5+ years of hands-on experience designing and implementing data models in cloud-based data warehouse (such as Redshift, Snowflake, Databrick, etc.) for analytics and BI use cases.
5+ years of advanced Tableau (Tableau Cloud) development experience, including dashboard architecture, performance tuning, and complex data sources.
Strong SQL expertise, including writing and optimizing complex queries for analytical workloads.

Preferred Qualifications:

Experience applying GenAI techniques within BI and Tableau ecosystems to augment reporting, enable natural-language exploration, and enhance user experience.
Basic Python skills for data manipulation, analytics automation, and integration with Tableau workflows.
Experience with Tableau Prep or similar data preparation tools.
Working knowledge of AWS services (e.g., Glue, Redshift, IAM) and modern data platforms.
Exposure to pharmaceutical, life sciences, or regulated data environments.
Experience collaborating with cross-functional and geographically distributed teams, including external vendors.
Tableau Desktop and/or Server certifications (Developer or Administrator).
Strong communication skills with the ability to explain complex technical concepts to non-technical audiences.

Pay Range for this position: $137,800 - 206,600
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 prequisites. For more information click here.

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

Director, Commercial Forecasting & Business Insights (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:

We are seeking a highly experienced and strategic Director, Commercial Forecasting & Business Insights to lead our forecasting and business insights function across multiple therapeutic areas including Oncology, Fertility, HIV and N&I. This role is ideal for a hands-on leader who combines deep forecasting expertise with a passion for leveraging technology, automation, and AI to deliver actionable business insights. You will own the end-to-end forecasting process, run monthly KPI meetings with stakeholders, and drive the modernization of forecasting and reporting practices.

Key Responsibilities:

Lead, mentor, and develop a high-performing forecasting and KPI reporting team across multiple therapeutic areas.
Drive accurate, timely, and actionable brand-level forecasting for Oncology, Fertility, HIV and N&I products.
Develop robust patient-based and trend-based models, incorporating epidemiological data, market share shifts, competitive launches. and secondary data (claims, Rx, EMR) to deliver data-driven insights. Guide calibration, scenario planning, and sensitivity analysis.
Design, implement, and continuously improve forecasting processes using modern tools, automation, and AI to enhance speed, accuracy, and efficiency.
Own monthly KPI meeting and insight sessions with business stakeholders, simplifying complex data into clear, actionable business insights.
Identify opportunities to automate and optimize recurring processes, including dashboards, reports, and presentations for KPI meetings.
Collaborate with cross-functional teams (Commercial, Marketing, Market Access, Finance) to ensure forecasting and KPI reporting aligns with business needs.
Collaborate with Data Science team to utilize AI, machine learning, and predictive analytics to enhance forecasting accuracy and provide forward-looking insights.
Establish best practices, metrics, and governance for forecasting and KPI reporting processes.
Communicate insights and recommendations effectively to senior leadership, highlighting trends, risks, and opportunities.

Who You Are

Minimum Qualifications:

Bachelor’s degree in Business, Finance, Economics, Data Science, or a related field; advanced degree preferred (MBA, MS in Analytics, or equivalent).
10+ years of progressive experience in forecasting, business analytics, or commercial analytics in the pharmaceutical or healthcare industry.
Hands-on experience in forecasting across multiple therapeutic areas, ideally including Oncology, Fertility, HIV, and N&I
Strong expertise in KPI reporting, data visualization, and presenting insights to senior stakeholders.
Proficiency in forecasting and analytics tools (e.g., Tableau, Power BI, Snowflake, Redshift, Excel, Python, R, or similar).

Preferred Qualifications:

Experience implementing automation and AI/machine learning solutions in forecasting and reporting processes.
Strong leadership skills with experience managing and developing high-performing teams.
Excellent communication and collaboration skills, with the ability to translate complex data into actionable business insights.
Experience in modern, AI-driven forecasting methodologies, scenario modeling, and predictive analytics.
Demonstrated success in modernizing business processes and driving digital transformation in forecasting or reporting.
Familiarity with pharma commercial data, including claims, sales, and market research datasets.

Pay Range for this position: $196,000 - 294,000
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 prequisites. For more information click here.

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

Director, Analytics Engineering & BI Architecture / Reporting (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 Director, Analytics Engineering & BI Architecture / Reporting is a pivotal strategic leader who will define and execute the enterprise BI and reporting architecture, enabling data-driven decision-making across the organization. This role encompasses both strategic oversight and hands-on leadership, guiding a team of BI Architects and Analytics Engineers in the design of scalable analytical data models, development of modern cloud-based data layers, and delivery of impactful Tableau dashboards.

The Director will collaborate closely with business stakeholders, data engineering, analytics teams, and IT to ensure that reporting solutions are accurate, scalable, and aligned with the evolving needs of the business. In addition to possessing strong technical expertise in cloud data platforms and Tableau, this role requires exemplary leadership skills, including the ability to manage priorities, influence, coach the team, and represent the reporting function across cross-functional initiatives.

Success in this role necessitates exceptional architectural judgment, robust stakeholder engagement, and the capability to balance immediate delivery with long-term platform strategy.

Key Responsibilities:

Team Leadership

Lead, develop, inspire, and manage a high-performing team of BI Architects and Analytics Engineers responsible for enterprise reporting and analytics solutions.
Provide coaching, mentorship, and technical guidance to uphold superior engineering and visualization standards.
Strategically manage team priorities, performance, reporting requests, and resource allocation across diverse business initiatives.
Define and communicate a clear vision and strategy for the team, aligning team goals with organizational objectives to drive innovation and excellence.
Foster a culture of collaboration, continuous learning, and professional growth by identifying training needs, facilitating skill development, and mentoring team members.
Implement performance management processes, including regular feedback, performance reviews, and development plans, to ensure team members meet their potential and contribute effectively
Guide the team through change initiatives, ensuring smooth transitions and maintaining morale during periods of transformation or adaptation.
Promote a culture of innovation by encouraging team members to explore new technologies, methodologies, and processes that enhance productivity and quality
Build strong relationships with internal and external stakeholders to understand their needs and ensure the technical team delivers effective solutions that meet business requirements.
Provide technical direction and support to the team, ensuring alignment with industry best practices and organizational standards.

Analytics Architecture & Data Modeling

Define and maintain scalable analytical data models within cloud data platforms such as Redshift and Snowflake.
Design business transformation logic, semantic layers, and data structures optimized for BI and Tableau performance.
Collaborate with data engineering teams to ensure data quality, governance, and consistency across the organization.

Tableau Development & Visualization

Oversee the development of high-quality Tableau dashboards and data products that support critical business and executive decision-making.
Establish development standards, performance optimization protocols, and visualization best practices.

Stakeholder Engagement

Lead requirements discussions, translating business needs into scalable reporting solutions.
Serve as the reporting team representative in cross-functional meetings and strategic initiatives.
Manage stakeholder expectations effectively while communicating delivery timelines and priorities.

Platform Ownership

Own the BI architecture across Redshift, Snowflake, and Tableau platforms.
Drive the modernization of reporting capabilities and the adoption of emerging technologies, including AI/ML and GenAI, where appropriate.

Who You Are

Minimum Qualifications

Bachelor’s degree in Computer Science, Engineering, Analytics, or a related field.
10+ years of experience in data warehousing, analytics engineering, or BI architecture.
5+ years of experience with cloud data platforms such as Redshift, Snowflake, or similar.
5+ years of advanced Tableau development experience.
Strong SQL expertise and proven experience in building scalable analytics solutions.
Experience in leading or mentoring BI or analytics teams.

Preferred Qualifications

Experience with GenAI applications in analytics or BI environments.
Proficiency in Python for analytics automation and data workflows.
Familiarity with AWS services and modern data platforms.
Experience in the pharmaceutical, life sciences, or regulated industries.
Tableau certifications and exceptional communication skills.
Ability to communicate openly and share information to foster trust while encouraging constructive debate, making informed decisions, and ensuring shared commitment to outcomes.
Demonstrated willingness to take risks and advocate for ethical practices while prioritizing the needs and experiences of customers and patients in all decisions.
Commitment to setting and achieving ambitious goals while upholding high standards and acting in the best interest of the company.
Uphold ethical standards and demonstrate honesty in all interactions.
Ability to streamline processes to focus on impactful outcomes, adapting quickly to changes.
Proven ability to embrace new ideas, challenge the status quo, and seek innovative solutions while valuing diverse perspectives and treating others with respect and dignity.

Pay Range for this position: $207,600 - 311,400
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 prequisites. For more information click here.

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

Senior Strategic Product Manager - Life Sciences (Bedford, Massachusetts, US, 01730)

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 have an exciting opportunity for you to join as a Senior Strategic Product Manager in a highly visible role within the Single Use and Integrated Systems Business Franchise. You will act as the business owner to set the direction and drive the growth of our product portfolio, focusing on Fill & Finish and Sterile Sampling applications in the GLP-1 market. Your deep knowledge of global market dynamics, customer applications, and business opportunities will be essential in developing and implementing strategies for market leadership in this evolving sector.

What you will do:

Develop a clear vision and strategic plan, including long-range planning, product portfolio positioning, and evolution of the portfolio for modalities/applications that create value for customers, with a focus on the GLP-1 market.
Act as the owner to drive the product development roadmap, including business cases, market sizing, financial analysis, and forecasting, and lead successful product launches from concept through commercialization, particularly for the GLP-1 market.
Work collaboratively and cross-functionally with R&D, commercial, operations, and other key business partners to drive business results in a global high matrix setup.
Actively monitor competitive activity, market trends, and customer feedback related to GLP-1, translating these insights into winning strategies for new and existing products.
Develop and execute Annual Operating Plans (AOP), including go-to-market execution focused on revenue growth, operating margin, innovation, and lifecycle management.
Formulate pricing strategies to maximize top and bottom-line goals, taking into account the competitive landscape.
Frequently present updates and insights to stakeholders, sponsors, and senior management, focusing on the impact of your strategies in the GLP-1 market.

We invite you to bring your expertise and passion for innovation to our team as we strive to lead in the GLP-1 market and beyond. Join us in making a meaningful impact!

Who You Are

Minimum Qualifications:

Bachelor’s Degree in a scientific or engineering discipline.
5+ years of experience in a product management and/or strategic marketing role, preferably within the bioprocessing industry.

Preferred Qualifications:

Experience in the bioprocessing industry and single-use manufacturing, ideally in sampling and Fill & Finish applications.
Comprehensive Understanding of Single-Use Assemblies: Strong understanding of single-use assemblies and their critical role in sampling and Fill & Finish applications within the bioprocessing industry, focusing on their impact on process efficiency, regulatory compliance, and overall enhancement of operational workflows.
Familiarity with the GLP-1 market and its dynamics is highly desirable.
Advanced degree in a quantitative or scientific field (MBA, Master’s, or PhD) is preferred.
Strong problem-solving skills with attention to detail, along with the ability to analyze business impact and make effective decisions.
Excellent analytical and communication skills, including proficiency in written, verbal, and presentation formats.
Proven experience in digital solutions, particularly integrated systems with software and customer-facing design configurator tools.
Self-motivated and energetic, with a strong ability to drive business results and initiatives.
Excellent organizational and interpersonal skills, demonstrating the ability to thrive in a fast-paced, cross-functional environment.
Ability to manage multiple projects simultaneously with a high degree of independence and agility.
Highly collaborative, with a demonstrated ability to influence and navigate within a global matrix organization.

Pay Range for this position: $120,600-181,300

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

Senior Strategic Product Manager - Life Sciences (Bedford, Massachusetts, US, 01730)

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 have an exciting new opportunity for you to join as Senior Strategic Product Manager within the Single Use and Integrated Systems Business Franchise, focusing on our Sterile Sampling and Final Fill portfolio. In this role, you will own and define the strategy that drives the growth of this product portfolio, particularly in relation to the evolving GLP-1 market opportunity. Your expertise will be essential in shaping our approach to this dynamic landscape, ensuring that we effectively address customer needs and manage projects while driving our strategic revenue growth and market share objectives.

What you will do:

Develop a clear vision and strategic plan, including long-range planning, product portfolio positioning, and evolution of the portfolio for modalities/applications that create value for customers, with a focus on the GLP-1 market.
Actively monitor competitive activity, market trends, and customer feedback related to GLP-1, translating these insights into winning strategies for new and existing products.
Act as the owner to drive the product development roadmap, including business cases, market sizing, financial analysis, and forecasting, and lead successful product launches from concept through commercialization, particularly for GLP-1 market.
Develop and execute Annual Operating Plans (AOP), including go-to-market execution focused on revenue growth, operating margin, innovation, and life cycle management
Work collaboratively and cross-functionally with R&D, commercial, operations, and other key business partners to drive business results in a global high matrix setup.
Formulate pricing strategies to maximize top and bottom-line goals, taking into account the competitive landscape.
Frequently present updates and insights to stakeholders, sponsors, and senior management, focusing on the impact of your strategies in the GLP-1 market.

We invite you to bring your expertise and passion for innovation to our team as we strive to lead in the GLP-1 market and beyond. Join us in making a meaningful impact!

Who You Are

Minimum Qualifications:

Bachelor’s Degree in a scientific or engineering discipline.
5+ years of experience in a product management and/or strategic marketing role, preferably within the bioprocessing industry.

Preferred Qualifications:

Experience in the bioprocessing industry and single-use manufacturing, ideally in sampling and final fill applications.
Familiarity with the GLP-1 market and its dynamics is highly desirable.
Advanced degree in a quantitative or scientific field (MBA, Master’s, or PhD) is preferred.
Strong problem-solving skills with attention to detail, along with the ability to analyze business impact and make effective decisions.
Excellent analytical and communication skills, including proficiency in written, verbal, and presentation formats.
Proven experience in digital solutions, particularly integrated systems with software and customer-facing design configurator tools.
Self-motivated and energetic, with a strong ability to drive business results and initiatives.
Excellent organizational and interpersonal skills, demonstrating the ability to thrive in a fast-paced, cross-functional environment.
Ability to manage multiple projects simultaneously with a high degree of independence and agility.
Highly collaborative, with a demonstrated ability to influence and navigate within a global matrix organization.

Pay Range for this position: $120,900-181,300

Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses.

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

Integration Engineers (Bedford, Massachusetts, US, 01730)

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

Job Title: Integration Engineers

Employer: EMD Millipore Corporation, 400 Summit Drive, Burlington, MA 01803

Job Location: EMD Millipore Corporation, 80 Ashby Rd., Bedford, MA 01730

This position is eligible for the EMD Millipore Corporation Employee Referral Program.

Job Responsibilities:

The Integration Engineer will leverage electrical engineering principles to carry out the networking and security implementation for our organization. Job duties include the following:

Coordinate and perform the system integration functions for the Infrastructure and Release team;
Provide support to the digital Bioprocessing platforms team; and
Assist in the development of Bioprocessing systems and applications using industrial PLCs, SCADA, .NET technologies, and Java based microservices with React/JavaScript front-end.

Telecommuting is available. The employee must work from the office at least three (3) days per week.

Job Requirements:

Employer requires a candidate to have at least a master's degree in Electrical Engineering, or a closely related engineering field, and at least three (3) years of work experience as an

Electrical Engineer involved in the design, development, and integration of complex IT and OT systems.

Additionally, employer requires the following:

Demonstrated ability handling Industrial field buses and communication protocols like OPC UA and Ethernet/IP gained through three (3) years of work experience;
Demonstrated knowledge of virtualization technology, including VMware and Hyper-V, gained through three (3) years of work experience;
Demonstrated ability supporting and securing the deployment of life sciences applications and data pipelines in AWS or Azure cloud gained through three (3) years of work experience;
Demonstrated ability configuring cloud-native networking (VPCs, subnets, security groups) to securely connect lab sites and cloud environments gained through three (3) years of work experience; and
Demonstrated technical ability handling automated systems including PLC (ex: Wago / Allen Bradley /Siemens) and SCADA (ex: Wonderware) gained through three (3) years of work experience.

All years of experience may be gained concurrently.

Salary Range: $134,597 to $154,597 per year

Applicants can mail resumes to EMD Millipore Corporation., 400 Summit Drive, Burlington, Massachusetts 01803 (Attn: req# 297372 or apply online at https://www.emdgroup.com/en/careers/job-search.html)

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

Head of Commercial Excellence (Burlington, Massachusetts, US, 01803)

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

Your Role:

You will be responsible for driving the transformation of commercial capabilities to achieve sustainable growth and operational effectiveness. This role will define and execute a cohesive commercial strategy, aligning cross-functional teams and optimizing tools, processes, and programs to enhance sales effectiveness, customer engagement, and marketing impact. The role will drive impact through functional excellence by building high-performing teams and processes, tool excellence by implementing scalable and innovative solutions, and governance excellence by establishing clear frameworks for performance management and accountability. This role encompasses key areas such as CRM, commercial learning, territory management, sales incentives, X-Franchise growth initiatives.

Key Responsibilities:

Drive CRM excellence across the life sciences division by establishing and continuously enhancing a best-in-class customer relationship management system, aiming at optimizing customer engagement and supporting sales efforts.
Oversee education and capability planning initiatives across the life sciences division, ensuring that teams are equipped with the necessary skills and knowledge to excel.
Develop and implement pricing strategies that align with market conditions and business objectives, ensuring competitive positioning and profitability.
Define, monitor, and analyze commercial performance metrics to assess effectiveness and identify areas for improvement. Develop and implement best-in-class sales incentive systems.
Establish robust commercial KPI frameworks and governance structures to enable data-driven decision-making and resource allocation.
Drive the optimization, simplification, and streamlining of commercial processes to enhance efficiency, reduce complexity, and support sustainable business growth.
Establish and champion customer experience initiatives by leveraging NPS and CSAT KPIs to ensure all customer interactions drive satisfaction, foster loyalty, and contribute to revenue growth.

Develop and deliver impactful presentations and insights that inform business unit decision-making and enhance execution.
Lead cross-functional workshops and initiatives to align sales, marketing, and operations around customer-centric execution.
Collaborate with diverse business units and regions to co-develop and implement sales plans, manage conflicting priorities, and enable sales effectiveness through robust support functions.
Provide coaching and performance management to enhance team capabilities and foster a high-performance culture.
Foster collaboration across Sales, Marketing, and Digital teams to deliver integrated solutions that meet customer needs.
Embody High Impact Culture values, including customer obsession, ownership, curiosity, urgency, raising the bar, and the 3Ds: Disagree, Decide, Deliver.

Who you are:

Minimum qualifications:

Bachelor’s degree in Business Administration, Marketing, or a related field.

Proven track record as a hands-on commercial leader, with direct experience in driving sales performance and successfully implementing strategies that deliver measurable growth and revenue impact within the life sciences products or services industry.

Proven experience in commercial strategy, sales enablement, and marketing within a global organization.

Demonstrated experience in leading and managing global, cross-functional teams with a focus on collaboration, alignment, and achieving strategic objectives.

Strong analytical skills with the ability to interpret complex data and market trends.
Excellent presentation and communication skills, with a track record of influencing senior leadership.
Strong problem-solving skills with a result-driven approach.
Experience in coaching and developing team members.

Preferred qualification:

MBA preferred

Pay Range for this position: $231,200 – $357,700.

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

Global Life Science Communications Business 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:

You will be responsible for supporting the Chief Technology Officer (CTO) of Merck KGaA, Darmstadt, Germany and the associated responsibilities aligned within the group, as well as the CTO's representation as the country speaker. You will also support our Quality and Regulatory business. The role will focus on developing integrated strategies to increase employee awareness of key topics and initiatives, while driving owned and earned media activities to maintain a strong external image and reputation. Key activities include stakeholder management, messaging development, content creation, content curation and program management to ensure high quality, consistent communication to our target audiences. This role requires creative problem solving, and an innovative, data-driven mindset to successfully contribute to the team’s objectives of mobilizing employees and lifting our reputation.

Who You Are

Minimum Qualifications:

8-10+ years working in a Communications, or related role
Previous experience in the Life Sciences, Biotech, Bio-pharma or related scientific industry
Very strong written and verbal communications skills
Proven ability to multi-task with strong organizational skills
Ability to prioritize complex topics and manage high-impact deliverables

Preferred Qualifications:

Experience leading the development and execution of internal and external communication strategies across channels

Role will be based in MA office

Pay Range for this position: $151,00- $226,600. 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 Performance Marketing (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:

Digital & eCommerce is a global team with colleagues across North America, EMEA and APAC. This is an exciting opportunity to work in one of the leading eCommerce businesses in the Life Science industry. The primary focus of the Digital & eCommerce team is to drive profitable growth for the multi-billion-dollar global eCommerce business, operating at significant scale across markets and regions.

**This role can be based out of either St Louis, MO or Burlington, MA/Greater Boston Area**

This is a high visibility role with opportunities to present and interact regularly with senior and executive leadership teams. The person in this role will be responsible for developing short and long-term performance marketing strategies across channels including (but not limited to) Paid Search, Display, Video, Social, Programmatic and more. This includes owning a full-funnel strategy that balances demand capture with demand creation and brand-building initiatives to drive both short-term revenue and long-term customer loyalty. They will also have a forward-looking vision for how our channels should evolve, ensuring we are positioned to win in a rapidly changing landscape, including agentic AI, search transformation, and emerging media technologies. They will collaborate cross-functionally within eCommerce, Commercial/Sales, Product, Supply Chain, Finance/Controlling, and regional teams to build paid media plans that clearly outline impact to sales, underpinned by industry trends, competitor threats and market opportunities on a global scale. They will also be responsible for further strengthening channels that are strong revenue contributors while exploring new channels for growth and revenue contribution.

Who You Are:

The authority on performance marketing strategy and investment across the global eCommerce organization
Anticipates and plans for the future of performance marketing, including the evolution of channels, agentic AI, and search transformation, ensuring the organization is set up to maintain a competitive advantage
Develops annual and long-term performance marketing strategies
Responsible for strategy, planning and execution of paid media programs to meet/exceed financial targets
Determine the optimal media mix across all channels, including pivoting when opportunities arise to diversify
Identifies and incubates emerging paid media channels and tactics, building business cases and scaling those that demonstrate incremental value
Translates business growth priorities into actionable media investment strategies
Oversees all performance marketing channels (paid search, Shopping, display, social, programmatic, etc.)
Key contributor to developing the vision and implementation of MarTech roadmap that will enable customer-centric marketing and personalization at scale
Fluent in advanced measurement solutions to quantify the incremental revenue impact from paid media, including marketing mix modeling (MMM), multi-touch attribution (MTA), incrementality testing, and experimental design methodologies
Builds and develops a high-performing team by attracting and retaining top talent
Drives strategic initiatives forward with agility while collaborating in a highly matrixed global environment, effectively communicating and influencing at various levels of management
Understands the roles of brand and creative in the financial outcomes of performance marketing
Articulate storyteller capable of elevating and simplifying your message for all levels of audience
Unafraid of challenging the status quo and embracing change to test new ideas, experiment with emerging tactics, and lead in next-generation digital and AI-driven marketing approaches

Minimum Qualifications:

Bachelor’s Degree or direct experience in performance / digital marketing
10 or more years of relevant experience with minimum 6 years working hands on developing media plans and directly executing performance marketing campaigns
Experience working in marketing roles involving direct impact on revenue / sales
Experience managing an 8-figure advertising budget
Experience managing multiple layers of direct reports and managing external agencies

Preferred Qualifications:

Experience building emerging channels from pilot stage into scalable revenue contributors
Mastery in full funnel heavy up campaigns targeting customers across their purchase journey
Experience across MarTech and Data & Analytics platforms
Statistical Techniques: experimental design, analyses with probabilities and confidence intervals
Demonstrated experience building and leading high-performing teams
Ability to present complex analytical information in clear, concise, and compelling manner to executive leadership to inspire action
Enthusiastic and self-motivated, with the ability to lead projects proactively
Meticulous attention to detail, with an overall passion for continual improvement
Innovative and creative, with a logical and methodical approach to problem solving
Credible and articulate, with excellent communication, presentation, and interpersonal skills
Ability to communicate effectively with others using the spoken word and in writing clearly and concisely
Ability to think in such a way as to produce a new concept or idea and to make decisions or take actions to solve a problem or reach a goal
Ability to be internally inspired to perform a task to the best of one’s ability using his or her own drive or initiative and to utilize the available time to organize and complete work within given deadlines

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

Quality Operational Excellence 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:

We believe that effective processes are the backbone of our success, and we are looking for a talented Operational Excellence Quality Lead to join our team. In this role, you will be responsible for analyzing, and optimizing GLP, GCP, and GVP related processes across the organization in close collaboration with Business Process Owners and cross-functional stakeholders.

Evaluating current processes to identify inefficiencies and eliminate complexity will be a critical part of your responsibilities, along with creating detailed process maps and documentation to provide clarity for all involved parties. Collaboration will be essential as you engage with various teams to incorporate diverse perspectives into your designs.

Additionally, you will establish process metrics to monitor process performance and drive continuous improvement in partnership with Business Process Owners and stakeholders.

You will report to the Head of Central Quality Systems at R&D Quality and Risk Management (RDQRM).

Who You Are:

Minimum Qualifications:

B.S. in a Life Science-related with 5+ years professional experience and expertise.
A minimum of 3 years of working knowledge of Good Clinical Practice (GCP), Good Vigilance Practice (GVP), and Good Laboratory Practice (GLP).
A comprehensive understanding of the drug development process and the regulatory environment, particularly in areas relevant to our Healthcare business.
Strong expertise in process design and optimization methodologies.

Preferred Qualifications:

Excellent analytical skills with the ability to identify inefficiencies and propose effective improvements.
Proficiency in creating process maps and flow charts.
Strong collaboration and communication skills to work effectively with Business Process Owners and cross-functional teams.
Experience in training and change management during process implementation.
Familiarity with establishing process metrics for performance monitoring.
Professional experience in multiple international pharmaceutical organizations is a plus.

Pay Range for this position: $144,500 - 216,800
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!

COCO-0, Director Clinical Operations (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.

Location:

The COCO-0, Director Clinical Operations is a hybrid position located in the Boston area (Billerica).  There will be minimal travel, possibly domestic and international, to meet business needs.

Your Role:

The Compound Operation Lead (COL) is a global role within Global Development Operations (GDO), which is accountable for the operational leadership and delivery of one or more clinical program(s) from First-in-Human (FiH) through to launch. The COL serves as the GDO representative on the Global Program Team (GPT) and is the single point of operational accountability for translating asset strategy into executable clinical programs. Partnering with Global Program Teams, Clinical Trial Leads (CTLs), and cross-functional R&D functions, the COL drives patient-centric trial delivery within budget, timelines, and quality standards aligned to industry benchmarks.

Why This Role Matters?

Enables faster patient access by reducing clinical program cycle times through operational excellence
Ensures audit-ready governance and compliance with GCP and ICH standards
Drives cost efficiency and delivery performance vs. industry benchmarks
Builds organizational capability in clinical operations leadership across global programs

Key Accountabilities:

Operational Strategy & Program Leadership

Develops and executes operational strategy for assigned clinical program(s), translating asset strategy into executable plans that connect science, operations, and patient outcomes
Leads program-level operational execution using disciplined project management principles, ensuring delivery within budget, timelines, and quality standards across multiple trials and indications
Serves as GDO representative on the GPT; provides operational input into asset strategy, governance decisions, and lifecycle planning
Accountable for preparation and presentation of operational content at key governance forums

Risk Management & Delivery

Identifies and evaluates program-level operational risks; develops and implements mitigation strategies and contingency plans to ensure delivery of asset strategy and governance milestones
Ensures strong oversight, quality delivery, and resolution of program-level CAPAs and audit findings
Monitors program-level KPIs and operational metrics; drives corrective action where performance deviates from plan

Stakeholder & Cross-Functional Leadership

Influences cross-functional leaders and senior management to align on operational priorities; negotiates resource allocation, timelines, and trade-offs to achieve program objectives
Partners with Finance, DU, and GDO leadership to develop, track, and optimize program budgets across the full portfolio of trials within assigned program(s)
Builds and maintains effective working relationships with internal and external stakeholders including CROs, vendors, and regulatory partners

Matrix Leadership & Talent Development

Provides matrix leadership of Global CTLs within assigned program(s); accountable for team performance, resource allocation, objective-setting, and coaching within matrix structure
Builds and develops a pipeline of clinical operations talent through mentoring, coaching, and performance management
Identifies high-potential team members and creates development opportunities aligned to organizational capability needs

Core Competencies:

Program Management: Leads global, multi-trial programs with complex operational and strategic dimensions; expert in risk management, budgeting, and scenario planning
Operational Leadership: Drives execution excellence across cross-functional, matrixed teams; holds self and others accountable to high performance standards
Stakeholder Influence: Communicates and influences effectively at all levels of the organization; builds alignment and drives decisions in ambiguous, fast-moving environments
Patient & Science Focus: Maintains unwavering focus on patient centricity and scientific integrity as the foundation of all operational decisions
Talent Development: Inspires and develops clinical operations talent; fosters a culture of continuous learning, accountability, and growth

Who You Are

Minimum Qualifications:

Advanced degree in life sciences, pharmacy, medicine, or related field (PhD, PharmD, or MD preferred)
10+ years of progressive experience in clinical drug development within the pharmaceutical or biotech industry
Proven track record of leading complex, global clinical programs across multiple phases and therapeutic areas
Demonstrated experience representing clinical operations at senior governance forums (e.g., Program Review Committees, R&D leadership meetings)

Preferred Qualifications:

Deep knowledge of GCP, ICH guidelines, and global regulatory requirements
Strong financial acumen; experience managing program-level budgets of significant scale
Proficiency in clinical operations tools, systems, and performance metrics frameworks

Pay range for this position: $173,000 - $259,000

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

Director Real World Evidence (N&I) (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.

Location: The Director Real World Evidence (N&I) is an onsite position located in Billerica, MA with minimal travel required to meet business needs.

Your Role:

Who You Are

Minimum Qualifications:

Experience in health and life sciences (MD, pharmacist epidemiology, public health), or quantitative data sciences, biostatistics
Bachelor's degree and/or master’s degree in Epidemiology, Public Health or related field
8+ years experience in RWE/D within the pharmaceutical industry, particularly in the application of RWE

Preferred Qualifications:

Demonstrable experience in leading RWE generation plans and studies end-to end, including application of innovative designs and methods
Excellent oral and written communication skills and demonstrated ability to engage and communicate scientific evidence to peers and at scientific meetings
Collaborative, proactive working style, with ability to work independently

Pay range for this position: $172,200 - $258,000

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

QA Specialist (18개월 계약직, QA/QC, 약사, 서울근무) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your Role:

Support the Quality Manager in ensuring compliance with GMP and GDP requirements in South Korea, including Medical Device guidelines
Support the Quality Manager in implementing the defined Global Healthcare Operations strategy and monitoring the Quality Management System for continuous improvement
Manage product release, documentation, metrics/trend reports for complaints and deviations, and provide assistance to field force with product complaint management
As the registered pharmacist, managing the overall import of pharmaceutical drugs/products, including reviewing shipping documents and batch records
Handle the customer complaints process, including investigation, documentation, and recording of complaints via the complaint database TrackWise, and assist with adverse event and safety information reporting
Assist with creating and maintaining Quality Standard Operating Procedures and Work Instructions, and preparing training presentations as needed
Support audit and inspection management/preparation carried out by Health Authorities and corporate internal audits, and assist with risk management activities
Work within company Standard Operating Procedures, industry guidelines, and apply company values and code of conduct in daily duties and activities
Perform other functions and duties as assigned by the Quality Manager or your superior
Support to simplify internal operation process via digitalization

Who You Are:

Pharmacist license is a must
Bachelor’s degree or above
Minimum 1 year of Quality/Manufacturing experience in pharmaceutical industry preferable but not mandatory
Understanding/Knowledge of GMP/GIP guidelines is highly preferred
IT skill experience (ex. Excel, VBA, macros, automation program) preferrable
Business Proficient in English

<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.

Senior R&D Scientist (대만/한국, Particle, CMP, 5년 이상의 유관경력) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Senior Scientist in Abrasive Technology, Chemical Mechanical Planarization (CMP)

Your role:

Who you are:

M.S. or Ph.D in Chemistry, Chemical Engineering or Material Science
5+ years’ experience in particle related research, development, application

Preferred Qualifications:

Ph. D degree within abrasive/inorganic nanoparticle research area, is a plus
Proven expertise in nanoparticle synthesis, characterization and development through publication and commercialization
Working experience in abrasive/inorganic nanoparticle RD, metrology and application in an industrial setting, is a strong plus
Previous exposure to the semiconductor industry, particularly in CMP formulation and/or applications, is a strong plus
Excellent leadership and interpersonal skills that support a diverse team environment
Hands-on experience in project management is highly desirable
Excellent verbal and written communication skills in English

지금 지원하여 발견을 이끌고 인류를 발전시키는 팀의 일원이 되어 보세요.

Field Service Expert (제약/바이오 산업군, 5년 이상 경력, 대전/충청/전라도 지역 담당) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your Role:

Install, operate, repair, validate, and modify complex technical equipment with minimal supervision.
Handle spare parts, ordering, visit scheduling, and control the entire service process using CRM (SVMAX).
Develop and maintain strong interpersonal relationships regarding technology service with distributor channels, support, and customer representatives to ensure customer satisfaction.
Establish and maintain highly responsive relationships and effective communication with customers, the sales department, and other departments to ensure customer satisfaction.
Drive business results by creating service contracts and conducting frequent preventative maintenance visits to boost consumable sales.
Maintain a commercial mindset and work closely with the sales organization and distributors.
Perform total system-level troubleshooting on complex, multi-symptom problems.

Who You Are:

Bachelor's degree in a relevant field (Life Science, Engineering, etc.).
5~10 years of working experience in the relevant field (lab instruments or medical devices preferred).
Experience in other instruments, electronics, equipment, or related fields will also be considered.
Demonstrate a strong sense of responsibility and accountability in work.
Business proficiency in English.
Valid driving license.

<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.

IT/OT Service Manager - Electronics (5년 이상 경력, IT/OT 서비스 관리 경험) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your Role

An exciting new opportunity has arisen to join the IT/OT team as a Sector IT/OT Service Manager. Your key responsibilities will include:

Overseeing Electronics IT/OT Applications:
- Ensure compliance with internal processes such as Data Privacy, Data Retention, Cybersecurity, and Disaster Recovery.
IT/OT Service Management Ownership:
- Act as the link between stakeholder feedback and global projects aimed at enhancing IT/OT service delivery.
- Maximize value through integration with the IT service management framework (ServiceNow).
Collaboration Across Teams:
- Work closely with site IT/OT teams and peers from other sectors.
- Collaborate with core IT/OT pillars, including Portfolio Management, Architecture, and Cybersecurity.
- Partner with corporate IT infrastructure and application teams.
Framework Development & Implementation:
- Develop and implement an IT service management framework tailored to IT/OT needs.
- Align frameworks with business priorities, budgets, and risk considerations.
Program Leadership:
- Lead IT/OT inventory and CMDB programs.
- Design a cross-sector training strategy for IT/OT teams on IT Service Management and ServiceNow.
Participation in Centers of Excellence & Audits:
- Contribute to cross-sector IT/OT Service Management Centers of Excellence.
- Participate in audits to ensure compliance and continuous improvement.
Stakeholder & Partnership Management:
- Ensure transparency in IT/OT service decisions through effective stakeholder management.
- Manage external partnerships with key IT/OT service providers.

Who You Are

Graduate degree in IT/computer science, engineering, business/economics, or a related field.
At least 5 years of experience in IT/OT.
Proficient in implementing IT Service Management practices leveraging the ServiceNow platform.
Knowledge of leading IT Service Management frameworks such as ITIL 3 or 4.
Domain knowledge in manufacturing processes, machinery, and control systems.
Expertise in integrating IT/OT systems into broader IT infrastructure.
Strong communication skills to collaborate effectively with cross-functional teams and stakeholders.
Multicultural experience; fluent in English and at least one additional language.

* 근무지의 경우, 상황에 따라 서울 혹은 배곧으로 진행될 예정입니다.

* 머크 IT/OT 전문가의 커리어 스토리 : Click

<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.

Apprenti-e logisticien-ne CFC (h/f/d) (Aubonne, Vaud, CH, 1170)

Exprimez votre talent avec nous !

Date de début: 1er août 2026
Durée: 3 ans
Lieu: Aubonne, Suisse

Ton rôle:
En tant qu’apprenti(e) logisticien(ne), tu joueras un rôle clé dans la gestion des flux de marchandises, depuis la réception des produits jusqu’à leur expédition. Sous la supervision de professionnels qualifiés, tes tâches principales seront :

Réceptionner, contrôler et stocker les marchandises
Préparer les commandes
Assurer les expéditions des commandes
Gérer les stocks et optimiser leur organisation
Conduire et entretenir les équipements de manutention
Participer à l’amélioration continue des processus logistiques

Tu auras l’opportunité d’acquérir des compétences solides dans le domaine de la logistique et de contribuer au bon fonctionnement de l’entrepôt.

Ton profil:

Avoir 15 ans révolus
Intérêt pour les activités physiques et pratiques
Sens de l’organisation
Esprit méthodique
Capacité à travailler en équipe et à gérer des responsabilités
Fiabilité, rigueur
Aisance avec les outils informatiques, un plus

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

Sales and Marketing Manager - Oncology (Bangkok, Klongtoey, TH, 10110)

Work Your Magic with us!

What You Do

To be responsible for develop and implement marketing strategies, activities, and also oversee medical representative for Special portfolio. You will go out in field with team every month together with your field visit as a PM (it can be combined). Your responsibility for sales team will be coaching and provide guidance on MR initiative. 70% of field time will be in Bangkok.

Marketing Responsibilities:

Develop and implement marketing objectives, strategies, develop marketing activities, advertising, promotions and initiatives in line with global positioning and messaging for assigned product, and tracking plan to achieve sales targets.
Implement marketing plan approved through educational and promotional marketing activities, including competitive tactics and selling message to increase market share and profits.
Create initiatives and road map to new product launches in accordance with regulatory and target audience.
Work closely with advertising agency / medical journals on advertising campaign or other production or relevant promotional pieces. Responsible for promoting product to target markets in hospital channel.
Analyze market and competitive activities. Evaluate the implementation of marketing plan of respective product.
Constantly seek new business opportunities with existing or new products. Regularly reaching agreed targets to ensure business growth.
Work closely with Medical and Commercial team to ensure that marketing activities planned are implemented effectively and in-line with product objectives.
Builds up and enhance relationships with target doctors, especially with KOLs, hospitals, and institutions of assigned product.
Train product knowledge to sales team and able to work collaboratively with cross functional team to gain market share.
Facilitates inventory turnover and product availability by review and adjust demand forecast.
Determines customers' needs and desires by specifying the research needed to obtain market information.
To recognize a reportable Adverse Event (AE), special situations or other pharmacovigilance information and ensuring the necessary information is forwarded according to the company procedures.
To obtain and compile the information regarding the receiving complaint and transfer to quality manager.

Responsibility for a growing Oncology portfolio (established product, product launches and portfolio under development).
Support market access / reimbursement activities, in particular CSMBS.
Support development and implementation of Patient Access Programs.

Sales Responsibilities:

Develop Medical Representatives to enhance their skills and advance their careers through training, development, and evaluation.

Support, motivate, and collaborate closely with the sales team to deliver innovative and exceptional customer care.
Proactively anticipate and address obstacles that may hinder results.
Ensure commercial excellence through sales analysis and management of assigned projects.

Who You Are

Bachelor’s degree in Pharmacy, Biology, Sciences, medical related field or equivalent
MBA degree is a plus
Good command of English

Experience as Medical Representative

Minimum 3 years of experience in Product Management / Marketing in Pharmaceutical or Healthcare industry, Oncology field is preferred
Established relationship with relevant KOLs is an advantage
Excellent project management skill, with communications and stakeholder management ability
Strategic thinking ability with commercial acumen and long-term vision
Excellent communication and coaching skill
People manager experience

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

Sales Specialist (Lab Water) (Bangkok, Klongtoey, TH, 10110)

Work Your Magic with us!

What You Do

Responsible for selling, increasing market shares, achieving sales goal and profit growth.
Maintaining loyalty of existing customers & dealers, also acquiring the new markets through the understanding of customers, business needs and consulting skills.
Developing overall strategies to approach existing and new customers in potential industries.
Identifying marketing opportunities by identifying consumer requirements, conducting competitor analysis, and establishing targeted market share.
Extracting customer’s data to analyzing Customers to understand, identifying Customer’s Segmentation, building customer needs and opportunities.
Looking for new markets and opportunities to further grow business.
Developing and implementing appropriate sales & marketing activities with customers.
Develop new markets by collaboration with dealers, distributors, and partnership to expand products into their markets.
Managing the sale tender process together with customers.
Creating and initiating the new projects with key customers.
Providing the excellent services in to exceed sales targets.
Acting as an information channel between company and existing/potential partners
Coordinating with both internal and external relevant parties to ensure smooth & effective cooperation.

Who You Are

Bachelor’s degree or higher in Chemistry, Chemical Engineer, Petrochemical or Engineering/Science, other related or equivalent work experience.
Experience in Sales for at least 2 years in field sales and marketing. Also having experience in life science business or equivalent work experience in laboratory equipment products and project management.
Strong interpersonal skills, ability to interact positively and constructively with all functions in matrix organization environment.
Able to work under pressure, be positive, having growth mindset and high flexibility of working hours.
80% working in field.
Able to communicate English on business level; both writing and speaking.

医药代表-心血管代谢及内分泌-舟山 (Beijing, Beijing, CN, 100016)

与我们携手施展你的超能力！

职位描述：

1. 制订有挑战性的和可行性的区域计划，并能成功地实施。

1）根据自己对所辖市场的了解, 制订区域计划和医院销售目标,活动计划和费用预算。

2）在工作中定期的回顾和修正行动计划, 以更高的达到销售目标。

3）计划和执行每天的拜访活动, 确保有效拜访时间符合公司的要求

4）建立和维护与临床医生和学术带头人的关系

5）定期拜访药剂科以保证良好的供货

6）组织GSA和其他销售和市场活动

7）如果有需要，应当协助销售经理处理经销商供货和医疗保险目录的申报

2. 发展和拓宽市场, 了解市场潜力和维护销售的持续稳定的增长

1）执行销售和市场策略并对执行后情况进行反馈

2）提供竞争对手,医疗保险目录和商业供货等信息

3. 工作态度端正，执行公司的行为要求，树立自身良好形象，维护公司品牌形象

1）体现公司的学术形象，掌握产品及相关知识并在每天的工作中运用。

2）掌握销售技巧和演讲技巧并运用到工作中。

3）工作积极努力,有责任感，保持衣冠整洁，对待客户礼貌周到

4. 报告和培训

1）按时和准确的提交各种报告和报表。

2）认真参加公司组织的各项培训和会议。

任职要求：

1. 医药及相关专业本科以上学历。

2. 熟练掌握产品知识，了解相关医学知识

3. 具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

4. 有相关领域经验为佳

5. 具备RDPAC认证资格优先考虑

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！

医药代表-心血管代谢及内分泌-北京 (Beijing, Beijing, CN, 100016)

与我们携手施展你的超能力！

职位描述：

1. 制订有挑战性的和可行性的区域计划，并能成功地实施。

1）根据自己对所辖市场的了解, 制订区域计划和医院销售目标,活动计划和费用预算。

2）在工作中定期的回顾和修正行动计划, 以更高的达到销售目标。

3）计划和执行每天的拜访活动, 确保有效拜访时间符合公司的要求

4）建立和维护与临床医生和学术带头人的关系

5）定期拜访药剂科以保证良好的供货

6）组织GSA和其他销售和市场活动

7）如果有需要，应当协助销售经理处理经销商供货和医疗保险目录的申报

2. 发展和拓宽市场, 了解市场潜力和维护销售的持续稳定的增长

1）执行销售和市场策略并对执行后情况进行反馈

2）提供竞争对手,医疗保险目录和商业供货等信息

3. 工作态度端正，执行公司的行为要求，树立自身良好形象，维护公司品牌形象

1）体现公司的学术形象，掌握产品及相关知识并在每天的工作中运用。

2）掌握销售技巧和演讲技巧并运用到工作中。

3）工作积极努力,有责任感，保持衣冠整洁，对待客户礼貌周到

4. 报告和培训

1）按时和准确的提交各种报告和报表。

2）认真参加公司组织的各项培训和会议。

任职要求：

1. 医药及相关专业本科以上学历。

2. 熟练掌握产品知识，了解相关医学知识

3. 具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

4. 有相关领域经验为佳

5. 具备RDPAC认证资格优先考虑

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！

客户主任-甲状腺-南京 (Beijing, Beijing, CN, 100016)

与我们携手施展你的超能力！

职位描述：

1. 制订有挑战性的和可行性的区域计划，并能成功地实施。

1）根据自己对所辖市场的了解, 制订区域计划和医院销售目标,活动计划和费用预算。

2）在工作中定期的回顾和修正行动计划, 以更高的达到销售目标。

3）计划和执行每天的拜访活动, 确保有效拜访时间符合公司的要求

4）建立和维护与临床医生和学术带头人的关系

5）定期拜访药剂科以保证良好的供货

6）组织GSA和其他销售和市场活动

7）如果有需要，应当协助销售经理处理经销商供货和医疗保险目录的申报

2. 发展和拓宽市场, 了解市场潜力和维护销售的持续稳定的增长

1）执行销售和市场策略并对执行后情况进行反馈

2）提供竞争对手,医疗保险目录和商业供货等信息

3. 工作态度端正，执行公司的行为要求，树立自身良好形象，维护公司品牌形象

1）体现公司的学术形象，掌握产品及相关知识并在每天的工作中运用。

2）掌握销售技巧和演讲技巧并运用到工作中。

3）工作积极努力,有责任感，保持衣冠整洁，对待客户礼貌周到

4. 报告和培训

1）按时和准确的提交各种报告和报表。

2）认真参加公司组织的各项培训和会议。

任职要求：

1. 医药及相关专业本科以上学历。

2. 熟练掌握产品知识，了解相关医学知识

3. 具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

4. 有相关领域经验为佳

5. 具备RDPAC认证资格优先考虑

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！

区域医学顾问经理 (Beijing, Beijing, CN, 100016)

Work Your Magic with us!

Your Role

Strategy & Leadership

Partner with the TA Medical Director to shape and execute China Medical Affairs strategy
Maintain current, in-depth knowledge of assigned therapeutic areas to guide team direction and support medical and brand objectives
Integrate cross-functional strategies and provide regular reporting on MSL performance, KOL engagement, and competitive intelligence

People Management

Lead all aspects of team management: hiring, goal setting, performance reviews, coaching, and career development
Review and approve regional medical plans and KOL evaluation reports
Monitor query response records and report findings to the central medical team

Compliance & Operations

Ensure all medical activities comply with company SOPs, GCP standards, and local regulations
Drive completion of required compliance training across the team

External Engagement

Build and maintain science-driven relationships with KOLs and HCPs
Guide the team in executing targeted educational strategies to address scientific gaps and support safe, appropriate product use

Who You Are

Master's degree or above in Clinical Medicine, Pharmaceutical Sciences, or related field
5+ years in pharmaceutical Medical Affairs, Sales & Marketing, or as a hospital physician with oncology area experience.
Strong knowledge of the assigned therapeutic area (disease mechanisms, clinical endpoints, treatment guidelines)
Proven people leadership and team development skills
Strategic thinker with solid operational and cross-functional collaboration abilities
Good understanding of drug development, commercialization, and marketing
Excellent communication and presentation skills; effective in scientific discussions
Fluent in English (written and spoken); proficient in standard office tools

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

客户经理-Pimi-北京2 (Beijing, Beijing, CN, 100016)

与我们携手施展你的超能力！

职位描述：

一、区域规划与目标达成

根据对所辖市场及罕见病疾病领域的深入了解，制定具有挑战性且可行的区域业务计划，包括目标医院及科室覆盖策略。
合理规划和执行每日拜访计划，确保有效拜访时间和拜访质量符合公司要求。保障产品在重点医院、重点科室的规范使用和持续增长，实现长期业务发展。

二、客户关系维护与学术推广

体现公司的专业学术形象，熟练掌握产品知识、疾病知识及相关指南，确保在学术拜访和活动中进行准确、规范的学术沟通。
与市场部、医学部及公司其他相关部门保持良好沟通与协作，共同推进公司在罕见病领域的整体策略落地。

三、报告与内部协同

按时、准确地提交各类工作报告和数据报表，包括拜访记录、活动总结、销售数据等。
积极参与公司组织的各类培训、会议和项目，持续提升专业知识和业务能力。
严格遵守公司合规及行为准则，在对外沟通中维护公司的品牌形象和学术声誉。

任职要求

教育背景：本科及以上学历，医学、药学、生物学或相关专业优先。
经验需求：具有5年以上医药推广经验，具有外企经验优先
治疗领域：具有罕见病领域、骨科领域、肿瘤罕见靶点推广经验
熟练掌握产品知识，了解相关医学知识
具备一定的市场分析和业务规划能力，具备较强的业务实施能力

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！

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!

客户经理-Pimi-济南 (Beijing, Beijing, CN, 100016)

与我们携手施展你的超能力！

职位描述：

一、区域规划与目标达成

根据对所辖市场及罕见病疾病领域的深入了解，制定具有挑战性且可行的区域业务计划，包括目标医院及科室覆盖策略。
合理规划和执行每日拜访计划，确保有效拜访时间和拜访质量符合公司要求。保障产品在重点医院、重点科室的规范使用和持续增长，实现长期业务发展。

二、客户关系维护与学术推广

体现公司的专业学术形象，熟练掌握产品知识、疾病知识及相关指南，确保在学术拜访和活动中进行准确、规范的学术沟通。
与市场部、医学部及公司其他相关部门保持良好沟通与协作，共同推进公司在罕见病领域的整体策略落地。

三、报告与内部协同

按时、准确地提交各类工作报告和数据报表，包括拜访记录、活动总结、销售数据等。
积极参与公司组织的各类培训、会议和项目，持续提升专业知识和业务能力。
严格遵守公司合规及行为准则，在对外沟通中维护公司的品牌形象和学术声誉。

任职要求

教育背景：本科及以上学历，医学、药学、生物学或相关专业优先。
经验需求：具有5年以上医药推广经验，具有外企经验优先
治疗领域：具有罕见病领域、骨科领域、肿瘤罕见靶点推广经验
熟练掌握产品知识，了解相关医学知识
具备一定的市场分析和业务规划能力，具备较强的业务实施能力

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！

医药代表-心血管代谢及内分泌-天津 (Beijing, Beijing, CN, 100016)

与我们携手施展你的超能力！

职位描述：

1. 制订有挑战性的和可行性的区域计划，并能成功地实施。

1）根据自己对所辖市场的了解, 制订区域计划和医院销售目标,活动计划和费用预算。

2）在工作中定期的回顾和修正行动计划, 以更高的达到销售目标。

3）计划和执行每天的拜访活动, 确保有效拜访时间符合公司的要求

4）建立和维护与临床医生和学术带头人的关系

5）定期拜访药剂科以保证良好的供货

6）组织GSA和其他销售和市场活动

7）如果有需要，应当协助销售经理处理经销商供货和医疗保险目录的申报

2. 发展和拓宽市场, 了解市场潜力和维护销售的持续稳定的增长

1）执行销售和市场策略并对执行后情况进行反馈

2）提供竞争对手,医疗保险目录和商业供货等信息

3. 工作态度端正，执行公司的行为要求，树立自身良好形象，维护公司品牌形象

1）体现公司的学术形象，掌握产品及相关知识并在每天的工作中运用。

2）掌握销售技巧和演讲技巧并运用到工作中。

3）工作积极努力,有责任感，保持衣冠整洁，对待客户礼貌周到

4. 报告和培训

1）按时和准确的提交各种报告和报表。

2）认真参加公司组织的各项培训和会议。

任职要求：

1. 医药及相关专业本科以上学历。

2. 熟练掌握产品知识，了解相关医学知识

3. 具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

4. 有相关领域经验为佳

5. 具备RDPAC认证资格优先考虑

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！

(高级)产品经理 (Beijing, Beijing, CN, 100016)

Work Your Magic with us!

Reports to: Associated Marketing Director
Location: Beijing/Shanghai

Your role:

Responsible for strategic development that fits the overall thyroid business cross brands and cross indication in thyroid therapeutic area.
Endocrinology area management to make sure Hypothyroidism and Hyperthyroid-ism strategy and key tactics including sales and marketing promotion implemented effectively to enhance Euthyrox and Thyrozol diagnosis and treatment capacity.
Cooperate with sales team and KOLs to gain thorough understanding of the oppor-tunities and issues for Euthyrox and Thyrozol through in-depth analysis including market data analysis, medical literature review, expert opinion collection, and in-ternal feedback.
Assist in budgets management and control the expenses of market activities in brand management.
Strategic planning and brand management in thyroid business

Who you are：

At least Bachelor's degree in medical and pharmaceutical related disciplines
Experience in product management and cross department/indications is preferred
Solid background of at least 8 years in sales and marketing experience
Multi- national working experience is preferred
Ability to effectively influence others with excellent interpersonal and communication skills.
Good English communication skills.

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

Marketing Communications Manager (Glasgow, Glasgow, GB, G20 0SP)

Work Your Magic with us!

Your Role: We are looking for a dynamic and results-driven Marketing Communications Manager to spearhead strategic initiatives for our Testing Services business. In this pivotal role, you will position our brand as a trusted partner in the biopharma and pharmaceutical industries. You will drive awareness, engagement, and lead generation through innovative marketing strategies that make a measurable impact.

Your responsibilities will include developing and implementing a comprehensive, omnichannel marketing and communications plan that aligns with our business objectives and delivers a consistent brand experience across all touchpoints. You will collaborate with cross-functional teams to ensure marketing initiatives support our commercial goals. Additionally, you will conduct competitive reviews and market analyses to refine our messaging and enhance our market positioning.

As you plan and execute omnichannel marketing campaigns, you will create high-quality marketing assets that showcase our expertise. Your leadership in digital marketing efforts will be crucial for driving traffic and conversions. Lastly, you will monitor and analyze campaign performance, using data-driven insights to optimize our strategies continuously.

Who You Are:
· You have a strong background in marketing communications, preferably in the Testing Services or life sciences industry.
· You possess proven experience in developing and executing omnichannel marketing and communication plans that deliver measurable business impact.
· You are skilled in digital marketing, including SEO/SEM strategies and social media engagement.
· You have a track record of developing high-quality marketing assets such as brochures, whitepapers, and videos.
· You are adept at conducting competitive reviews and market analyses to inform strategic decisions.
· You have excellent analytical skills, with the ability to monitor and report on campaign effectiveness using KPIs.
· You are a creative thinker, continuously exploring innovative marketing strategies and tools.
· You have strong communication skills and can foster relationships with internal and external stakeholders.

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

Customer Applications Expert (Semi - Spec Gas, Business Development, 5 years+) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your Role

Drive New Product Success

Identify and champion new Process of Record (POR) opportunities across current and next-generation technology nodes, focusing on innovative materials for semiconductor manufacturing
Lead key customer-facing aspects of the complete product lifecycle from initial opportunity identification through successful high-volume manufacturing (HVM) ramp
Build and manage a robust pipeline of POR opportunities to achieve yearly revenue targets as well as the 5-year strategic growth ambitions of Specialty Gases

Lead Technical Customer Engagement

Conduct quarterly Technical Review meetings and annual Technology Roadmap sessions as applicable with customers
Translate complex customer requirements into actionable development priorities for our R&D and marketing teams
Deliver technical presentations and strategic proposals that advance customer objectives and strengthen partnerships

Collaborate Across the Organization

Partner with Market Managers, R&D teams, and account managers to prioritize development efforts based on commercial potential and customer timing
Coordinate with our MBER team for sample planning and fulfillment of developmental products
Leverage Salesforce (SFDC) and data analytics tools to drive informed decisions and maintain pipeline visibility

Resolve Technical Challenges

Act as the primary escalation point for customer quality issues and technical concerns related to Specialty Gas products
Guide cross-functional teams to deliver rapid, effective solutions that resolve customer issues and maintain high customer satisfaction
Assess competitive landscape and provide strategic intelligence on materials technology trends

Who You Are

Master's degree in Chemistry, Materials Science, Chemical Engineering, or a related field.
At least 5 years of experience in the semiconductor industry, specifically in customer-facing technical or commercial roles.
Strong understanding of semiconductor manufacturing processes, material science, and integrated circuit (IC) fabrication.
Fluent in both spoken and written English, as well as the primary language of the local market.
Willingness to travel domestically and internationally as required.
Proven ability to develop productive relationships with customers at multiple organizational levels, including engineering, procurement, and executive.
Exceptional communication and influencing skills, with the ability to translate technical concepts for diverse audiences.
Self-motivated with a demonstrated ability to deliver on commitments under tight timelines.
A collaborative team player with the ability to work effectively across global, matrixed organizations.
Strong analytical capabilities, including data analytics, pipeline management, and forecasting.
Experience with CRM systems (Salesforce preferred) and business intelligence tools.

Preferred Experience

Advanced degree (PhD) in science, engineering.
Background in fabrication operations or Original Equipment Manufacturer (OEM) environments.
Experience in technical marketing, commercial negotiations, and project management.
Proven track record of successful new product introductions (NPI) and product offering wins (POR).

<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.

Ausbilder Technische Produktion (all genders) (Buchs, St. Gallen, CH, 9476)

Entfalte das Besondere mit uns!

Für den Bereich Manufacturing am Standort Buchs suchen wir einen

Ausbilder Technische Produktion (all genders)

In einem dynamischen Team stellen wir zahlreiche Produkte für unser Verkaufssortiment oder im Kundenauftrag her. Die anspruchsvollen, teils mehrstufigen chemischen Synthesen werden im Massstab von 20 L bis 1600 L Reaktionsvolumen durchgeführt.

In der Position des Berufsbildners verantworten Sie alle Aspekte der Ausbildung der Lernenden, die Weiterbildung der Mitarbeitenden sowie die Einarbeitung neuer Mitarbeiter in den Abteilungen der technischen Produktion.

Ihre Aufgaben:

Koordination und Durchführung der Ausbildungsaktivitäten für Lernende und neu eingestellte Mitarbeitende sowie der Weiterbildungsprogramme für Produktionsmitarbeitende
Weiterentwicklung der Ausbildungskonzepte in Zusammenarbeit mit den Betriebsveranwortlichen und Abteilungsleitungen
Durchführung der Qualifikationsverfahren im Betrieb in Zusammenarbeit mit den beteiligten Behörden und Bildungseinrichtungen
Planung und Durchführung von internen und externen Veranstaltungen in enger Zusammenarbeit mit der Ausbildungsabteilung
Auswahl geeigneter Personen für die Ausbildungsplätze in Zusammenarbeit mit der Ausbildungsabteilung und den Betriebsverantwortlichen
Erstellung von Bildungsberichten

Ihr Profil:

Abgeschlossene Ausbildung als Chemie- und Pharmatechnologe/in oder vergleichbare Ausbildung
Zertifizierung als Berufsbildner/-in oder Ausbilder/in mit eidg. Fähigkeitsausweis oder vergleichbare Qualifikation
Strukturierte Arbeitsweise, gutes Networking, hohe digitale Affinität
Gute Kenntnisse im Umgang mit Windows Office 365
Berufserfahrung im Produktions- oder Technikbetrieb sowie in der Herstellung von Produkten unter ISO 9001/(c)GMP

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Account Manager (Sydney, New South Wales, AU, NSW 2113)

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The Strategic Account Manager (SAM) territory is comprised of majority Strategic customers as per the PS Customer Stratification model. In-field presence and interstate business travel is a strong expectation of the role.

Your Role:
As a Bioprocessing SAM, you will be responsible for driving growth and protecting revenue across a strategic portfolio of biotechnology and pharmaceutical accounts in the ANZ region. You will develop deep relationships with key stakeholders, understand customer needs, and deliver high-value solutions that advance customer success and the company's market leadership.

Key Responsibilities:

Sales Growth & Strategic Execution
- Achieve sales targets within the assigned territory through proactive execution of sales strategies and value-based selling.
- Defend and grow account sales across customer segments using solution selling and a strong understanding of the bioprocessing industry.
- Submit accurate sales forecasts and pipeline updates in a timely manner.

Customer Engagement & Account Development
- Build and maintain strong relationships with key decision makers, influencers, and opinion leaders in biotechnology and pharmaceutical accounts.
- Develop and manage account profiles to identify growth opportunities and align with global account strategies.
- Actively manage the customer journey using digital and in-person touchpoints to enhance engagement and deliver solutions that meet evolving needs.

Cross-Functional Collaboration & Operational Excellence
- Collaborate closely with internal teams including Marketing, Technical Specialists, Customer Service, Distribution, and Supply Chain to ensure seamless service and solution delivery.
- Prepare and coordinate commercial proposals, quotations, and technical documents tailored to customer requirements.
- Support inventory planning and product delivery schedules for key customers.

Market Presence & Thought Leadership
- Participate in industry trade shows, seminars, and conferences to promote our company's capabilities and stay abreast of market trends.
- Leverage digital tools, CRM platforms, and market intelligence to drive informed decision-making and customer engagement.

Who You Are:

You are a driven and adaptable sales professional with strong scientific foundations and a passion for delivering value in the bioprocessing, life science, or pharmaceutical industry. You thrive in a dynamic, customer-facing role and bring a blend of technical acumen, commercial savvy, and collaborative spirit to everything you do.

A self-starter with 1–3 years of relevant experience in sales or technical sales, ideally in biomanufacturing, pharmaceuticals, or life sciences.
Hold a degree in Science or Engineering, specialising in Biotech, Life Sciences, or Chemistry.
Demonstrated success in complex solution-based selling, project management, and account development within a business-to-business setting.
Skilled in influencing and building relationships across internal and external stakeholders, including cross-functional and global teams.
Strong communicator with excellent interpersonal, negotiation, and presentation skills.
Tech-savvy and comfortable using CRM systems, digital tools, and data analytics to drive performance and insights.
Organized and efficient, with strong time management and business acumen.
Highly collaborative, agile, and growth-oriented, with the ability to adapt and thrive in a fast-paced, matrixed environment.
Possess or willing to obtain a valid driver’s license and have access to a personal vehicle for customer visits.

At Merck KGaA, Darmstadt Germany, we are committed to advancing reconciliation through meaningful action, collaboration, and cultural respect. Our Innovate Action Plan (RAP) represents the next phase of our journey to strengthen relationships with First Nations people and communities. We are focusing on tangible actions including increasing employment pathways for First Nations peoples and enhancing capabilities within our workforce

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

Production Supervisor (Carrigtwohill, 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 Supervisor will be responsible for supporting the initial Operation Readiness of the Blarney facility.
In addition, the Supervisor will be accountable for the achievement of Production targets, Department metrics and key Department/Site objectives using Life Science Production System (LSPS).

The Production Supervisor directs all aspects of production activity at the assigned area to ensure that the desired quantities and quality of products are manufactured on schedule in a safe manner at minimum cost. Is responsible for human resources and may be responsible for accounting and other staff functions.

The Production Supervisor is initially a days based position. However, as production ramps up, the position will become a shift based position.

The role may require travel to the United States for training purposes.

Duties:

• Supervision of employees, allocating work, co-ordinate training and dealing with issues as arise up to counselling stage of disciplinary process.

• Ensure Attendance Management policy is adhered to.

• Supporting the Training & Production coordinator with pre-interview, on-boarding and training activities to ensure F2.0 project and manufacturing commitments are met.

• Performance Management – prepare, assess and conduct all MyImpact conversations. Assist operators with developing their commitments.

• CORE Time & Attendance – Sign off T&A on a weekly basis in a correct and accurate manner.

• Responsible for on the job training and specific training as required.
• Responsible for assigning tasks to operator team(s) and for the material flow / work within department. Co-ordination of operator tasks to meet weekly plan.

• Partner with the planning department to deliver on the manufacturing plan.
• Accountable for physical movement and information flow of materials from order opening to order closing.
• Responsible for Kitting & Closing of SAP Process Orders.
• Responsible for adherence to Cycle Count Procedure and meeting cycle count accuracy metrics.

• Partner with the Quality department to ensure compliance with Quality Standards.
• Foster culture of right first time ensuring product quality.

• Ensures documentation is maintained in accordance with quality requirements & completes necessary updates as appropriate.
• Supporting the investigation & follow-up in relation to complaints and implements corrective & Preventative actions.
• Ensures Audit readiness – drives this culture and aligns this through 6S Audit approach.
• Supports the validation activities.

• Providing a safe workplace for all employees.
• Ensures compliance with all applicable Environmental, Health and Safety legislation & adherence to Safety procedures & requirements.

• Ensures that timely communication and measurement systems are in place, and active, for department metrics including, but not solely:
EHS proactive reporting & appropriate, timely EHS Action close out
FPQ tracking & reporting
MyLearning tracking & reporting
Daily OEE tracking & reporting
Financial (including Absorption, Material Variance, Overtime & Disc Spend).
• Communicate Scorecard(s) weekly and ensure targets are met/exceeded.

• Foster a Culture of continuous improvement using Life Science Production System (LSPS). Using processes and daily management systems (DMS) and Leaders Standard Work.

Who You Are

• Minimum 3 years Supervisor experience within a Manufacturing operation.
• Excellent computer skills (Word,Excel,Powerpoint,etc..)
• Excellent Operation systems knowledge (MES, SAP, LIMs, etc.)
• Strong knowledge of EHS, Quality, GMP standards and regulations.
• Strong leadership & people skills, with excellent interpersonal and communication skills and ability to liaise effectively with various support groups
• Strong, capable decision maker who provides clear direction to all team members including all support functions.
• Qualification in Supervisory / Management training desirable.
• Diploma/FETAC Level 7 qualification desirable.
• Knowledgeable in Lean Manufacturing, Six sigma (Greenbelt or Bluebelt) desired.

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!

E&I Technician (Cork, Cork, IE, T23 A5NR)

The Role

The E&I maintenance technician will be responsible for adhering to site procedure in relation to the calibration of key manufacturing instrumentation. Release calibration work orders on CMMS, perform calibration, complete calibration work orders, enter obtained results on CMMS and verify other technician calibration work orders. Other responsibilities would be to organize and oversee external contractors to carry out specific calibration work on site.

Duties

• Responsible for carrying out calibrations at the required intervals according to the device listing and completing the relevant documentation.
• Adhere to site procedure in relation to raising Deviation/Change control on Trackwise system
• Complete troubleshooting for key manufacturing instrumentation.
• Perform Preventive Maintenance tasks
• Represent the maintenance team with regards to safety initiatives and practices to develop and maintain an injury free workplace.
• Work within a larger engineering team of mechanical and electrical resources including automation, facilities, project and system engineers, with emphasis on performance, involvement, teamwork and personal development.
• Utilize SAP Next to ensure all maintenance activities through consistent application of a work order system.
• Identify areas in which calibration capability should be improved in relation to calibration system. (areas of focus to include latest technology \ instrumentation)
• Reduce the dependence on external calibration providers for critical calibrations.
• Ensure that all maintenance activities meet all the regulatory standards (e.g. FDA, IMB, HSA, EPA...)
• Identify, develop and implement projects in the areas of efficiency improvement.
• Develop scientific risk-based approach to identifying key critical spares for plant and equipment and ensure that critical spares are in stock or are always readily available. Ensure that an effective program is then maintained.
• Perform all tasks with due recognition of safety, environment, GxP & plant procedures.
• Assists with resolutions of major technical issues with onsite equipment.
• May be required to assistance to other shift technicians if technical resources are low.
• Administration work related to duties such as placing POs, control/filing of calibration certificates.

Who You Are

• Candidate must have successfully completed an Instrumentation, Electrical or E&I apprenticeship
• Extensive calibration experience (If electrical qualified further calibration certification preferable)

• Minimum of 3-5 years working in a Med Device or Pharma manufacturing environment
• Working knowledge of electrical, pneumatic and control systems in a production environment
• Previous experience within an ATEX environment an advantage
• Demonstrated high performance history, proven ability to execute and get results
• Ability to work with employees at all levels of the organisation.
• Preferable experience with CMMS System;
• Be familiar with planned preventative maintenance approaches
• Excellent awareness and experience in relation to Quality and Environmental Health and Safety

• Familiar with GMP requirements within a regulated industry.
• Effective verbal, written & interpersonal communication skills.
• The ability to work effectively within a team environment
• High level of energy and enthusiasm and the ability to energize others
• Self-motivated.
• Keen to learn & take responsibility.
• Strong organisational, time management and planning ability.
• Computer Literate Excel, Word etc.
• Methodical Work Approach
• Willingness to work shift if required
• Willingness to work a reasonable amount of Overtime

Process Safety Expert 1 (Carrigtwohill, Cork, IE, T45 HE47)

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The Role

The Process Safety Expert will support the Cork and Arklow Manufacturing Sites in the day-to-day implementation of the Process Safety program. This role involves participation in the Life Science Process Safety Center of Excellence, which is responsible for the business-level implementation of corporate governance programs related to process safety.

Key Responsibilities:

Develop compliance programs and site Operating Plans to implement process safety requirements
Maintain a comprehensive list of process safety-related actions.
Prepare process safety deliverables for CapEx projects as outlined in the corporate program, including conducting Process Hazard Reviews using HAZOP methodology and facilitating Pre-Startup Safety Reviews.
Facilitate Process Hazard Analysis.
Conduct or request consequence modeling.
Provide technical expertise in one or more of the following areas:
- Risk Assessment
- Chemical Reactivity
- Fire Protection System
- Mechanical Integrity

Liaise with the Life Science Process Safety Center of Excellence by:
- Participating in CoE meetings
- Actively contributing to the development of the Business Process Safety program (standards, tools)
- Attending and leading training sessions
- Leading site process safety initiatives developed by the CoE

Who you are:

Bachelor’s Degree (Level 8) in Health and Safety, Science, Engineering, or a related field
Over 8 years in a regulated manufacturing environment, particularly within the chemical or pharmaceutical industry, with experience in implementing process safety programs and leading HAZOP studies and other process hazard analyses.
Experience of working with Irish and EU process safety legislation and standards, including the Seveso-III Directive, COMAH Regulations and ATEX Directives.
Strong leadership and organizational skills, with the ability to influence and motivate colleagues.
Excellent initiative and adaptability to changing priorities.
Effective presentation and communication skills, both written and verbal.

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

Head of Environmental Health and Safety, Cork (Carrigtwohill, Cork, IE, T45 KD29)

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The Role:

As the Head of EHS, you will be responsible for developing and executing our company's comprehensive environmental, health, and safety strategy. This pivotal role ensures alignment with our business objectives while maintaining compliance across all operations. You will lead efforts in EHS risk identification and mitigation, utilize data analytics to monitor trends, and manage emergency response plans for critical incidents. Additionally, you will cultivate a safety-driven culture by establishing performance metrics and ensuring the effective integration of safety protocols and training throughout the organization. This position also includes oversight of the EHS function budget.

Key Responsibilities:

Act as a role model in coaching and mentoring to enhance both team and individual performance.
Expertly identify issues and foster problem-solving capabilities within the organization.
Promote autonomous teams, encouraging cross-functional collaboration and local decision-making.
Ensure compliance with safety and quality standards, leveraging data for proactive risk management.
Use data analytics to identify and mitigate potential hazards, fostering a comprehensive safety culture.
Swiftly address unforeseen safety, health, or environmental incidents with real-time monitoring and response strategies.
Maintain a strong knowledge of local and global sustainability and environmental compliance requirements.
Encourage the adoption of emerging technologies and best practices for continuous improvement in EHS.
Define and communicate a visionary safety strategy that aligns with organizational goals.
Develop key performance indicators (KPIs) to assess the effectiveness of the EHS program and ensure compliance with regulations.

Who You Are:

Hold an honors degree in an Engineering or Science discipline; a postgraduate qualification in Environmental, Health & Safety is advantageous.
Possess at least 10 years of experience in an EHS role or equivalent.
Have relevant leadership experience in a health and safety manufacturing environment, with direct process safety and/or machine safety experience being a distinct advantage.
Demonstrate a strong understanding and in-depth knowledge of health and safety regulatory requirements and technical codes of practice.
Have a proven track record of successful interactions with regulatory agencies.
Exhibit strong verbal, written, and interpersonal communication skills.
Possess the ability to work effectively within a team environment.
Show a demonstrated commitment to safety and continuous improvement.

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

China Clinical Physician, Associate Director/Senior Manager (Beijing, Beijing, CN, 100016)

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Your role:

Strategy related responsibilities and tasks:

•    Contribute to the clinical development strategy by providing medical-scientific input for portfolio management, development projects, research projects and licensing in opportunities.
•    Provide scientific and clinical leadership in clinical development projects, and design and implement Clinical Development Plans in China R&D Center.
•    Attend Project Review Meeting in China as an ad-hoc member for expertise contribution. •    Support business development function to develop business case.
•    Provide required medical knowledge about the new products and related therapeutic areas.
•    Take initiatives to foster high-performing culture and to enhance company's scientific reputation with impact beyond GCDC function.

Operational responsibilities and tasks:
•    Take overall responsibility of medical responsible role of trials initiated by China R&D Center in assigned therapeutic areas as per the portfolio in China.
•    Work with global clinical lead on global clinical trials execution including protocol development, start-up, medical monitoring and CSR etc, focus on China population. •    Manage and support junior medical physicians in clinical development function for relevant activities and documents by providing medical-scientific input, advice and guidance.
•    Responsible for the document quality control issued from clinical development function in China R&D Center from concept to final trial report, including concept sheet, protocol, amendment, CSR and so on.
•    Ensure optimal interfaces with the other functions contributing to each clinical trial, within and outside of China R&D Center.
•    Responsible for presentation of the medical scientific position and clinical development function in internal meetings and committees and towards external organizations and experts.
•    Plan and budget function activities.
•    Create and maintain a competent group of external KTLs to support the clinical trial, including synopsis and protocol development, trial result interpretation and so on.
•    Support business development by coordinating the scientific input to in-licensing and global product opportunities.
•    Other related task as necessary or as required by line manager.

Managerial Tasks
•    Mentor junior medical physicians to increase their medical knowledge and capability.
•    Foster a performance-related culture and provide training in the technical skills needed. •    KTLs management.
•    External vendor management.

Who you are:
Education/Language:
•    Master degree of clinical medicine. M.D. or MBA degree will be an advantage.   •    Fluent English is a must.
Professisonal & Technical Skills
•    Experience in GCP clinical trials as an investigator or sponsor role.
•    At least 5-8 years working experience in clinical practice, international pharmaceutical industry, biotechnology sector or Contract Research Organization, and experience in Corporate R&D.

Oncology experience/background is preferred.

•    Recognized expertise in clinical drug development through all phases (phase I to IV) in China.
•    General knowledge of clinical research methodology.
•    Understanding of the concepts of statistical analysis. •    Hands-on experience of clinical trial management.
•    Ability to adjust clinical trial designs for safety reasons and/or to optimize opportunities.
•    Ability to analyse, interpret, present and publish clinical study results.
•    Thinking logically and strategically
•    Leadership competencies and people management skills to support and educate staffs and improve functional capability is preferred.

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

Utility Engineer (Kaohsiung, Kaohsiung, TW, 82151)

與我們攜手施展你的超能力！

Your Role
1. Operate and maintain facility systems (including HVAC, air compressors, liquid nitrogen systems, cooling towers and chillers, water supply, drainage, and wastewater treatment) to ensure stable operation, continuous utility supply, and compliance with regulatory requirements.
廠務系統操作維護 (包括空調、空壓機、液氮系統、冷卻水塔與冰機、供水、排水、廢水等相關設備)，確保系統穩定操作並持續供應公用流體且符合法規要求。

2. Perform routine meter readings, inspections, and handle abnormalities in facility systems.
廠務系統抄表巡檢及異常處理。

3. Conduct risk assessments of facility equipment operations and drive continuous improvement.
廠務設備運轉風險評估與持續改善。

4. Collaborate with customer requirements and support project execution.
持續配合客戶要求並推動專案執行。

5. Promote and implement energy-saving and carbon-reduction initiatives to
achieve sustainable operations.
推動與執行廠區節能減碳，達到永續操作。

6. Maintain and operate fire protection systems.
消防系統維護與操作。

7. Execute facility budgets and control operating expenses.
廠務預算執行及費用管控。

8. Carry out other assigned tasks.
其它交辦事項。

Who You Are

1. Education: Associate degree or higher in Chemical Engineering, Environmental Engineering, or a related engineering discipline.
學歷: 專科或大學以上化工、環工等工程相關科系

2. Experience: Minimum of 3 years of relevant facility operations experience in the optoelectronics, semiconductor, or chemical manufacturing sectors, with a strong understanding of wastewater treatment systems and fire protection systems.
資歷: 光電、半導體或化工廠相關廠務工作經驗3年以上，熟悉廢水處理及消防系統操作。

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！

IT Project Manager (Kaohsiung, Kaohsiung, TW, 82151)

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Job Title: IT Project Manager
Work Location: Flexible within Taiwan.Located in Kaohsiung or Tainan are preferred.

We are seeking a highly skilled IT Project Manager to join our team at Electronics DDIT. The Project Manager is responsible for planning, executing, and closing of medium-to-large IT projects, ensuring they are delivered on time, within scope, and within budget. Depending on the target architecture, projects are executed in close collaboration with international teams from various areas including IT Business Partnering, IT/OT, IT infrastructure and IT application. The IT Project Manager is overseeing the full project lifecycle (i.e., design, development/configuration, testing, cutover/go-live etc.) and ensures security and quality of delivered solutions, including handover to operations and support. This role requires strong leadership skills, excellent communication abilities, and a solid understanding of project management methodologies.

Your Role

Lead and manage IT projects from initiation to closure, ensuring alignment with business objectives.
Develop project plans, including scope, timelines, resources, and budgets.
Coordinate cross-functional teams and manage stakeholder communications.
Identify project risks and develop mitigation strategies.
Monitor project progress and provide regular updates to senior management.
Ensure adherence to project management best practices and methodologies.
Ensure overall solutions fulfills business requirements and expectations.
Facilitate project meetings and document meeting notes and action items.
Manage project documentation, including project charters, status reports, and post-project evaluations.
Escalate major issues or showstoppers to senior management throughout project life cycle.

Who You Are

Bachelor’s degree in information technology, Computer Science, or a related field. Master preferred.
PMP, PRINCE2, or equivalent project management certification is preferred.
Minimum of 5 years of experience in IT project management. Proven track record of successfully delivering IT projects in a complex, global matrix organization.
Strong knowledge of project management tools and software.
Domain experience in logistics, digital supply chains, manufacturing and IT/OT convergence of strong advantage.
Excellent organizational and multitasking skills.
Strong leadership and team management abilities.
Exceptional verbal and written communication skills in English. Local language skills are a benefit.
Ability to work collaboratively in a fast-paced environment.

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！

Associate Fellow (Temecula, California, US, 92590)

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

Your Role:

As an Associate Fellow for Biology, you will be instrumental in shaping the strategic direction and growth of the Next Gen Biology R&D projects, directly influencing success in the competitive life sciences market.

Key responsibilities:

Lead cross-functional core teams for next-generation biology programs, establishing objectives, milestones, governance, and decision-making processes.
Develop and maintain program strategies and roadmaps, translating scientific opportunities into hypotheses, success criteria, stage gates, resourcing, and risk mitigation aligned with portfolio priorities.
Provide guidance on lyophilization strategies for reagents and consumables.
Offer deep technical leadership in next-gen biology areas (e.g., functional genomics, synthetic biology, cell engineering, multi-omics/spatial), linking emerging science to innovative product concepts.
Ensure rigorous experimental planning, reproducible execution, high-quality documentation, and data-driven decision-making.
Align stakeholders across R&D, operations, quality, marketing, and global partners; resolve conflicts and remove obstacles.
Identify, evaluate, and integrate external technologies and partnerships to accelerate program progress.

Who You Are:

Minimum Qualifications

B.S. in Biology, Bioengineering, Biochemistry, or related discipline plus 5+ years of proven experience in Biotechnology or related fields
5+ years as team lead or similar roles
Thought leader in a scientific discipline; connects ideas across domains and drives project formation.
Capable of generating plans and mitigation actions within complex stakeholder environments; strong governance/influencing skills.
Able to generate communication plans and succinctly distill complex information for senior stakeholders.
Ability to drive high quality standards; models ethical behavior and strong data integrity practices.

Preferred Qualifications

M.S. plus 10+ years of experience; or PhD plus 5+ years of experience in Biology, Bioengineering, Biochemistry, or related discipline.
Experience in lyophilization and leading R&D roadmapping initiatives is preferred

Pay Range for this position: $120,900 - $181,300

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!

Semiconductor Materials Site Quality Manager, Thin Films (Carlsbad, California, US, 92011-1321)

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 Semiconductor Materials Site Quality Manager, Thin Films is an on-site position located in Carlsbad, CA with 5% domestic and international to meet business needs.

Your Role:

You will be leading the next generation precursor Thin Films materials to enable the innovation to the digital age. This position is located in Carlsbad, California USA and will be responsible for a team of quality professionals that engage in R&D, SVM, and HVM activities to our customers worldwide.

Key Responsibilities:

Manage a team of Quality engineers in the execution and quality of thin films materials at the Carlsbad facility to major semiconductor customers globally
Lead cross-functional teams in resolving technology issues
Lead investigations to root cause and manage cross-functional teams in implementation of preventative/corrective or mitigation actions to ensure best in class quality.
Be the persistent voice of the customer to the site
Be accountable to the business in maintaining Thin Films quality performance and drive continuous improvement at the sites by driving collaboration with Site and global functional groups.
Ensure discipline to process controls tools to ensure (e.g. SPC reviews) quality, identify continuous improvement opportunities, and variation reduction.
Identify and enable automation activities to make decisions faster, improve quality controls, and streamline operations/manufacturing processes.
Be key voting member to disposition discrepant material, identifying gaps in the process, and managing cross-functional teams to implement controls to prevent/reduce variation
Lead and/or delegate Quality related Audits at the sites
Contribute and support to the advancement of global quality related projects, process improvements with Lean and/or Six Sigma, and internal/customer related data-driven process optimization projects.
Lead Site quality culture, quality structure, process transfer, and activities from NPI to SVM (small volume manufacturing) to HVM (high volume manufacturing)

Who You Are

Minimum Qualifications:

Bachelors degree in Engineering, Chemistry, Physics, Material Science, or other Technical discipline
5+ years of experience in chemical manufacturing, process engineering, control engineering, analytical chemist, or semiconductor fabrication experience
Leadership, coaching and team building skills

Preferred Qualifications:

Demonstrated ability to motivate others and work collaboratively with multiple internal stakeholders
Demonstrated ability to identify abnormal variation, assess risk and hold stakeholders accountable for risk mitigation, corrective/preventative action.
Demonstrated experience with Lean and/or Six Sigma projects or in data-driven process optimization projects
Excellent time management and organizational skills with the ability to handle multiple activities and projects.
Moderate to Advanced Statistical knowledge (SPC, t-test, ANOVA, single and multivariate statistical modelling)
Experience in quality tools for problem solving (5Whys, segmentation, Model Based Problem Solving), FMEAs, continuous improvement (CI) activities, management of change, and document control systems.
Proficient with data science/statistical software including JMP, Palantir Foundry, Python, and/or visualization tools such as Tableau
Experience with process improvement, data automation, and data digitization.
Excellent communication skills–oral and written
Ability to work with people from various backgrounds/cultures
Experience within the semiconductor industry, highly automated factory controls environment, and/or in-depth Thin Films application in the semiconductor industry
Experience with ISO9001 Quality Management Systems
ISO9001 or IATF 16949 Internal Auditor Certification
Six Sigma Green Belt or Black Belt certification
SAP experience

Pay Range for this position: $124,400 - $186,700

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

Head of Application Technology Japan / Susonity (Onahama) (Onahama, Fukushima, JP, 971-8189)

Title: Head of Application Technology Japan

Location: Onahama, Fukushima

Report to: Head of Innovation and Application (Japan)

Team: The position is a people manager position and will manage a team of approx. 5 members

Role Scope:

We are currently seeking a Head of Application Technology Japan for the Surface Solutions business.

You will be heading an application group of about 5 team members in the field of inorganic pearlescent pigments and related functional materials. The team consists of a dedicated expert engineers for coating, printing and plastic applications. You will be reporting directly to the Head of Innovation and Application Japan. The job is based in Onahama, Fukushima prefecture, Japan.

Your responsibilities as Head of Application Technologies Japan will include:

Execution and accountability for the planning and successful execution of the team's new business programs in collaboration with the assigned sales and marketing department to expand our business and increase our market presence.

Responsibility and accountability for the technical customer support in Japan and Korea by close cooperation with our sales and marketing department

Technical support for a successful R&D program and the technical activity responsibilities required to make it a success.

Driving scouting activities with commercial and academic partners adding of new technologies to our competencies and licensing new products and technologies

Continuously improving scientific expertise of the responsible team by capturing external technical and industrial trends and developing internal capabilities accordingly

Driving process improvement initiatives in our Onahama production works including continuous improvement

Closely interact in a global team with peers by adopting and developing best practice sharing

Fostering a safe, collaborative, inclusive and efficient team environment and working culture. Fostering of future oriented team capabilities in areas like digitalization and sustainability

Candidate Profile:

M.Sc. in material science related fields, e.g. Chemistry, Chemical Engineering, Physical Chemistry etc., MBA and or PhD is a plus, but not essential

5~10+ years’ industry experience in technical raw materials at least one of the fields coatings, plastics and/or printing, preferable for pigments and particle materials

Proven experience in leading team, project management and working in an international, cross-functional environment. (People Management experience is as MUST to have.)

Strong leadership skills to effectively execute projects for business expansion

Effective project management, planning and organizational skills

Strong communication skills (written and verbal in both Japanese and English), effective in scientific presentations and communication to customers

Recruiting contact: Maiko Yamasue

Consequence Analysis Leader (Life Science Process Safety Center of Excellence) (Haverhill - all, Suffolk, GB, CBP 8QP)

Work Your Magic with us!

Your Role:

The LS Global EHS team is comprised of regional EHS leaders dedicated to the business-level implementation of corporate EHS governance programs. As part of this extended team, you will support the Life Science Process Safety Center of Excellence by developing our business’s expertise in process safety hazard assessment and consequence analysis.

As the Hazard Assessment and Consequence Analysis Leader, you will be responsible for developing a global program and providing guidance and direction to both business leadership and operational sites.

Key tasks include developing and delivering internal business-level training programs for the following based on corporate standards:

PHA Facilitation
Facility Siting Facilitation
LOPA completion
SIL Calculation
Quantitative Consequence Analysis for hazardous releases (Fire, Explosion, Toxic releases)
Hazardous Enclosure Assessment (Asphyxiants, toxics, oxidants, flammables, etc.)

Serving as a subject matter expert and individual contributor to:

Participate in incident investigations as requested
Complete LOPA, SIL, and other QCA
Develop relationships with third-party consultants capable of supporting such tasks when they cannot be completed internally
Develop Life Science best practices for performing these evaluations, including documentation of basis and assumptions used

This position offers flexible work arrangements within the UK, allowing for hybrid or onsite options. Preferred locations include Haverhill, Gillingham or Irvine.

Who You Are:

We are seeking a leader in hazard assessment and consequence analysis to develop business-level process safety consequence analysis implementation programs. An ideal candidate will bring both technical expertise and demonstrated leadership in conducting consequence analyses through past career roles. The candidate should be stakeholder and safety-focused, with a desire to engage existing teams, promote best practices, and increase overall knowledge of consequence analysis principles within the Life Science business.

Minimum Qualifications:

B.S. in Engineering or related field or no degree with 8+ years of relevant work experience.
5+ years of experience with responsibility for implementing process safety programs at a site or business level, with working knowledge of global Process Safety regulatory programs (e.g., OSHA PSM, Seveso III, COMAH, AQ/T 3034-2022).
Experience facilitating PHAs using HAZOP methodology (preference for experience using PHAWorks).
Experience completing quantitative consequence analysis models with the ability to generally describe programs or tools previously used (e.g., PHAST, ALOHA, HYSYS).
Demonstrated history of delivering technical and awareness training on consequence analysis-related topics.
Ability to travel domestically and internationally to support site programs as needed.  (Anticipated <15% annually)

Preferred Qualifications:

Experience managing process safety programs, with a preference for those with experience building and implementing programs.
Experience performing LOPA and SIL calculations based on industry RAGAGEPs.
Experience facilitating DHAs per industry RAGAGEPs.
Experience building consequence analysis modeling tools based on standards and engineering principles.
Ability to build professional relationships with various levels of leadership and site management through digital and in-person platforms.
Proven track record of working in large matrix organizational environments with various stakeholders.
Excellent oral and written communication skills, including presentation and meeting management skills.
Experience in one or more of the following chemical manufacturing disciplines: solvents, organic chemistry, inorganic chemistry, biologics.
Ability to don standard plant PPE, including but not limited to head, eye, hand, body, and foot protection for an 8-hour shift.
Ability to work in electrically classified areas if/when necessary.

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

Working Student (Santa Fe de Bogota, Bogota, CO, 9896)

Work Your Magic with us!

Tu Rol: Brindarás apoyo al equipo de Operaciones de Marketing en el análisis de datos relacionados con el consumo de productos y tendencias en diversos países y segmentos del negocio de Life Science: Discovery Solutions. El objetivo principal es identificar hallazgos (insights) y conclusiones que ayuden a evaluar acciones destinadas a mejorar el nivel de servicio del portafolio. Utilizarás herramientas como Palantir, Excel, Power BI y tecnologías de inteligencia artificial para contribuir a la generación de información clave que conduzca a mejoras en los procesos internos y al logro de los objetivos estratégicos. Brindarás soporte a diferentes áreas en América Latina para alinear esfuerzos, entregar informes con conclusiones accionables y asistir en la actualización de los pronósticos de consumo. Colaborarás con áreas relacionadas para generar documentos técnicos o materiales colaterales para requisitos regulatorios o promocionales (por ejemplo, fichas técnicas de uso, volantes de campañas). Esta posición combina el aprendizaje y la implementación de análisis técnico, pensamiento estratégico y comunicación constante con diferentes equipos en un entorno multicultural, ofreciendo oportunidades reales de desarrollo.

Quién Eres:

Estudiante universitario de Ingeniería Industrial, Ingeniería de Negocios, Negocios Internacionales, Marketing, Ciencia de Datos, Tecnologías de la Información o un campo relacionado enfocado en el análisis de datos y la tecnología. También se aceptan técnicos en cualquiera de las áreas mencionadas.
Conocimientos básicos en análisis de datos y herramientas analíticas.
Familiaridad con tecnologías de inteligencia artificial aplicadas al análisis de información.
Inglés técnico intermedio o avanzado, suficiente para interpretar fuentes de datos y generar informes.
Capacidad para comunicar hallazgos con claridad y trabajar en equipo.
Proactivo, capaz de trabajar de forma autónoma y con capacidad de aprender rápidamente en un entorno dinámico y multicultural.

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

Team Leader Warehouse (all genders) (Schaffhausen, Schaffhausen, CH, 8200)

Entfalte das Besondere mit uns!

Ihre Aufgaben:
In dieser verantwortungsvollen Position führen Sie ein Team von drei Mitarbeitenden und stellen die effiziente und termingerechte Belieferung interner sowie externer Kunden und Partner sicher. Sie steuern sämtliche Warenbewegungen im Lager unter Einhaltung der cGMP-Richtlinien und dokumentieren diese im ERP-System (z. B. SAP). Dabei planen, disponieren und bemustern Sie Rohstoffe und Zwischenprodukte und verantworten den Versand unserer Fertigprodukte.

Sie optimieren kontinuierlich die Prozessabläufe und treiben Projekte in den Bereichen EHS, OPEX und CAPEX aktiv voran. Die Einhaltung gesetzlicher Vorgaben und interner Standards in der Lagerhaltung liegt in Ihrer Verantwortung. Als Führungskraft fördern und entwickeln Sie Ihr Team individuell weiter und sorgen für ein sicheres, effizientes und modernes Arbeitsumfeld.

Ihr Profil:

Abgeschlossene Ausbildung mit chemischem Hintergrund und Weiterbildung im Bereich Logistik/Supply Chain
oder
Abgeschlossene Ausbildung zum Logistiker EFZ mit Zusatzqualifikation im chemischen Bereich
Mehrjährige Führungs- und Berufserfahrung im Logistik- oder Supply-Chain-Umfeld
Betriebswirtschaftliche Kenntnisse sowie Erfahrung in der Leitung von Projekten
Ausgeprägte konzeptionelle und analytische Fähigkeiten
Hohe Sozialkompetenz, Teamfähigkeit sowie Dienstleistungs- und Lösungsorientierung
Erfahrung im Umgang mit Arbeitshygiene, idealerweise aus dem cGxP- oder Lebensmittelumfeld
Sehr gute Kenntnisse in Microsoft Office und SAP (Modul MM/IM, weitere Module von Vorteil)
Sehr gute Deutsch- und Englischkenntnisse

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

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.

(Sr.) Medical Science Liaison Mid Germany Rare Disease / Tumour (all genders) (Munich, Bavaria, DE, 81671)

Work Your Magic with us!

We’re looking for a passionate and highly skilled (Senior) Medical Science Liaison (MSL) to join our Medical Affairs team. In this field based role, you will drive scientific engagement, support clinical development, and shape our medical strategy within your assigned region. You will serve as a trusted scientific expert, build impactful relationships with KOLs, and play a key role in bringing innovative therapies to patients.

The focus area within Germany for this position in Mid Germany is Rhein/Ruhr, Köln, Gießen/Mainz/Frankfurt, Göttingen/Erfurt, Leipzig, Dresden .
Ideally the future position holder lives in that area.

Key responsibilities will include:
• Serve as a scientific expert to the medical community and facilitate the appropriate exchange of scientific information
• Build and maintain strong scientific relationships with national, regional, and local KOLs
• Gather and communicate medical insights to inform strategy and improve patient outcomes
• Support investigator initiated research as primary liaison
• Provide scientific support at national and European congresses, advisory boards, and medical programs
• Lead selected national medical projects and initiatives
• Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, non-academic, and healthcare provider settings
• Collaborate with Clinical Operations to support trial site identification and patient enrollment
• Develop and execute territory plans aligned with national and regional medical strategy
• Partner with HEOR/Market Access to support health economic and outcomes data generation
• Support Medical Information requests
• Assist the Country Medical Director in shaping national KOL engagement and medical plans
• Mentor new or less experienced MSLs
• Support onboarding and training of field medical and commercial colleagues
• Contribute to national and regional medical strategy as a senior team member

Who you are:
• Advanced scientific degree (MD, PhD, PharmD or equivalent)
• Minimum 5 years of MSL experience
• Experience in rare diseases preferred; oncology or neuroscience a plus
• Strong ability to communicate and present complex scientific information
• Self driven, collaborative, and comfortable working independently

• Valid driver license

• German native level, English fluent

#swjob2026

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

SSO & Keycloak Expert (all genders) (Bratislava, Bratislava, SK, 81006)

Work Your Magic with us!

REMOTE ROLE WITHIN CZECH REPUBLIC OR SLOVAKIA

Your role: Build and evolve components in our self-developed identity and security platform used across 150+ global sites. As a Lead Developer, you’ll own the technical direction of key services (from design to production), lead by example in implementation, and work closely with a dedicated SRE team that runs and operates the solutions—so you can focus on building robust software.

What you’ll do:

Lead the design and development of cloud-native services and platform components (security, IAM/SSO, data/observability).
Translate product and security requirements into robust architectures and high-quality implementations.
Drive engineering best practices (code quality, testing, reviews, CI/CD, secure-by-design).
Collaborate with SREs to ensure reliability, scalability, and operational excellence (SLIs/SLOs, incident learnings, hardening).
Mentor engineers and enable the team to deliver sustainably and confidently.

Who you are:

Professional software engineering experience with ownership of production systems.
Strong hands-on development skills (ideally Java ; TypeScript and Go is a plus).
Solid understanding of microservices and Kubernetes-based delivery.
Good grasp of security fundamentals (authentication/authorization, secure coding; familiarity with SSO protocols like OIDC/OAuth/SAML is a plus).
Experience working with modern platform components such as streaming, analytics, and observability stacks is beneficial.Interest or experience in IT security (e.g., threat modeling, secure architecture, vulnerability management, or security testing) is beneficial.
Fluent in English (German is a plus).

Our environment aka you’ll work with:

Kubernetes, IaC, GitOps, and a self-hosted, cloud-native ecosystem
Other common technologies across the team: Kafka, Flink, Postgres, Neo4J, Grafana, Elasticsearch, plus Java, TypeScript, Go
Strong partnership with an experienced SRE team for operations and reliability

Salary starts at 3.000 EUR and is dependent upon relevant experience.

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

SAP ERP Security Specialist APAC (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

The SAP ERP Security Specialist is responsible for safeguarding the security architecture across SAP S/4HANA and SAP ECC landscapes, ensuring alignment with enterprise security frameworks. This role involves managing user access governance, compliance management, and integrating security controls into critical business processes. Additionally, the specialist will monitor SAP systems for vulnerabilities, conduct risk assessments, and drive continuous improvement in security processes. Collaboration with cross-functional teams and strategic leadership in security governance are key aspects of this position, ensuring effective communication of security risks to stakeholders and counterparts.

Key Accountabilities

Process and System Responsibility

Enterprise SAP Security Strategy & Architecture Ownership- Ensure architecture and security level meet the IT/OT Cyberscurity SOP.
Support the end-to-end security architecture across SAP S/4HANA and SAP ECC landscapes.
Define and govern role design standards, authorization concepts, Fiori security architecture, and cross-system integration controls.
Ensure alignment with enterprise security frameworks and business process requirements.
Implement and enforce Zero Trust – enable security principles within SAP ERP landscapes, ensuring strict identity verification, least-privilege access, and continuous authentication across SAP applications, users, and integrated systems.
Learn the new trend, threat, and new challenges in cybersecurity area. Like Zero Trust, Double ZeroAccess Governance & Compliance Management- Manage user access provisioning, modifications, and de-provisioning in line with internal policies and regulatory standards (e.g., SOX, GDPR where applicable).
Perform regular access reviews, SoD analysis, and audit support to ensure ongoing compliance.
System Monitoring & Risk Management- Monitor SAP systems for security risks, vulnerabilities, and unauthorized activities.
Conduct risk assessments, support remediation plans, and ensure timely resolution of security incidents related to SAP ERP platforms.
Process Ownership & Security Integration- Act as the security process owner for SAP ERP environments, embedding security controls into business processes such as Finance, Procurement, Supply Chain, and HR.
Collaborate with functional teams to ensure secure configuration and change management practices.
Continuous Improvement & Stakeholder Collaboration- Drive continuous improvement of SAP security processes, including automation, Cybesecurity tool optimization, and documentation updates.
Provide guidance and training to business users, IT teams, and management on SAP security best practices and governance standards.

Collaboration

Security & Governance Stewardship- Provide the SAP security governance across S/4HANA and ECC platforms.
Support security review boards, define policy standards, and ensure consistent enforcement of global SAP access and control frameworks.
Support to resoluve the daily incidnets and tasks related to security topics.
Cross-Functional & Executive Collaboration- Partner closely with Business Process Owners, IT leadership, Internal Audit, Risk & Compliance, and external auditors to align SAP security with enterprise risk strategy.
Translate technical security risks into business-impact language for executive stakeholders and steering committees.
Transformation & Change- Lead security workstreams during SAP implementations, upgrades, rollouts, and S/4HANA and ECC transformation programs.
Drive organizational change by promoting secure-by-design principles, influencing stakeholders, and ensuring security requirements are embedded early in project lifecycles

Impact and Performance Management

Supportive for the liaison & enablement team’s results, impacting performance of related Cybersecurity Operation teams through effective demand, capacity and change management.
Meet key KPIs (e.g., demand throughput, lead times, change success rate, capacity utilization, compliance) and drives performance improvements.
Develops and applies policies and guidelines to enhance cybersecurity operational efficiency and process consistency in Cybersecurity Operation liaison and enablement.
Efficent and Effevively support the cybersecurity tasks to meet the SOP and KPI.

Complex Problem-Solving

Analyzing skills-Analyzes complex information (e.g., audit findings, security advisories, demand/capacity data, vendor input) to support sound decision-making.
Sustainable and Reslience solution- Addresses operational challenges across demand, security, testing, release and lifecycle processes with sustainable solutions.

Technology Skills

Minimum 2 years of experience in SAP solution consulting, with a strong track record in solution design, and full-cycle product implementations.
Good knowledge on SAP system components, architecture, technical integration concept, ABAP and API.
Experience on SAP BASIS, Unix system administrator.
Deep understanding of SAP security and authorization concepts, including access control, authentication and data protection.
Hands-on experience with SAP security administration and risk management (roles/profiles, provisioning, policy maintenance, risk assessment) and relevant security/compliance standards (e.g., NIS, KRITIS, GDPR, SOX).
Proficiency with test and release management tools, ticketing systems, SAP security tools/transaction codes and ABAP for security-related custom solutions and troubleshooting
Need the cybersecrutiy knowledge or skills related to SAP framework-OS security, DB security, Firewall concept, SAP Netowrk zone design, Network infra knowledge, Vulnerability, SAP application design security, encryption, Cloud cybersecurity architecture. Data privace and Integrity, Data protection.
Advanced certifications in SAP Security, SAP Architecture, or Service Management technologies (e.g., SAP Certified Technology Associate)
Knowledge on SAP DevSecOps- Deep SAP Security & Architecture Expertise, strong knowledge of SAP platforms and security architecture, including: SAP S/4HANA, SAP NetWeaver, SAP BTP, and SAP Fiori, SAP transport management and secure configuration, SAP-specific vulnerabilities and patch management.
Integration of Security into DevSecOps Pipelines - Automating SAP code security scans (ABAP, UI5, integrations)
Implementing security gates in pipelines.
Supporting secure transport and release management.
Implement continuous monitoring and compliance controls.
SAP security monitoring and logging (SIEM integration).
Compliance with standards such as ISO 27001, NIST, KRITS and GDPR.
Managing identity governance and access risk analysis.

Education, Skills & Experience

Bachelor's degree in Business Informatics, IT technology, or a comparable field.
Graduate degree in a relevant discipline (IT Technolocy or Computer Science)
Several years of experience in SAP-based Authorization, BASIS, Cyberscurity, Techical integration and Cyberscurity areas.
Understanding about SAP system profiles, Authentication, Patching, Secure Network Communication, Encryption, Database security, Infra security.
Good knowledge on information security policy, cybersecurity issue response, disaster recovery, industrial policy and compliance, physical security, OS security,
MFA, Netowrk architecture, vulnerability management, log and monitoring, OWASP Top 10, Secure configuration.
Experience on DevOps to DevSecOps-understood secure development lifecycle(SLDC), Cybersecurity framework-27001, NIST. Testing and Automation.
Understood different cybersecurity related concepts: cyber defence model, ISC, Cloud security concept.
Proven experience in managing teams and driving operational performance in a technology-driven environment.
Any certifications-CISSP, CCSP, SSCP and Secruity+ is plus.
Strong analytical and problem-solving skills, capable of navigating complex issues.
Excellent communication and interpersonal skills, with the ability to influence stakeholders at all levels.
Proven ability to develop and implement effective strategies and policies, supported by an in-depth understanding of industry trends, market dynamics, and the competitive landscape.

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

SAP ERP Security Specialist APAC (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Key Accountabilities

Process and System Responsibility

Enterprise SAP Security Strategy & Architecture Ownership- Ensure architecture and security level meet the IT/OT Cyberscurity SOP. Support the end-to-end security architecture across SAP S/4HANA and SAP ECC landscapes. Define and govern role design standards, authorization concepts, Fiori security architecture, and cross-system integration controls. Ensure alignment with enterprise security frameworks and business process requirements.
Implement and enforce Zero Trust – enable security principles within SAP ERP landscapes, ensuring strict identity verification, least-privilege access, and continuous authentication across SAP applications, users, and integrated systems. Learn the new trend, threat, and new challenges in cybersecurity area. Like Zero Trust, Double Zero
Access Governance & Compliance Management- Manage user access provisioning, modifications, and de-provisioning in line with internal policies and regulatory standards (e.g., SOX, GDPR where applicable). Perform regular access reviews, SoD analysis, and audit support to ensure ongoing compliance.
System Monitoring & Risk Management- Monitor SAP systems for security risks, vulnerabilities, and unauthorized activities. Conduct risk assessments, support remediation plans, and ensure timely resolution of security incidents related to SAP ERP platforms.
Process Ownership & Security Integration- Act as the security process owner for SAP ERP environments, embedding security controls into business processes such as Finance, Procurement, Supply Chain, and HR. Collaborate with functional teams to ensure secure configuration and change management practices.
Continuous Improvement & Stakeholder Collaboration- Drive continuous improvement of SAP security processes, including automation, Cybesecurity tool optimization, and documentation updates. Provide guidance and training to business users, IT teams, and management on SAP security best practices and governance standards.

Collaboration

Security & Governance Stewardship- Provide the SAP security governance across S/4HANA and ECC platforms. Support security review boards, define policy standards, and ensure consistent enforcement of global SAP access and control frameworks. Support to resoluve the daily incidnets and tasks related to security topics.
Cross-Functional & Executive Collaboration- Partner closely with Business Process Owners, IT leadership, Internal Audit, Risk & Compliance, and external auditors to align SAP security with enterprise risk strategy. Translate technical security risks into business-impact language for executive stakeholders and steering committees.
Transformation & Change- Lead security workstreams during SAP implementations, upgrades, rollouts, and S/4HANA and ECC transformation programs. Drive organizational change by promoting secure-by-design principles, influencing stakeholders, and ensuring security requirements are embedded early in project lifecycles

Impact and Performance Management

Supportive for the liaison & enablement team’s results, impacting performance of related Cybersecurity Operation teams through effective demand, capacity and change management.
Meet key KPIs (e.g., demand throughput, lead times, change success rate, capacity utilization, compliance) and drives performance improvements.
Develops and applies policies and guidelines to enhance cybersecurity operational efficiency and process consistency in Cybersecurity Operation liaison and enablement.
Efficent and Effevively support the cybersecurity tasks to meet the SOP and KPI.

Complex Problem-Solving

Analyzing skills-Analyzes complex information (e.g., audit findings, security advisories, demand/capacity data, vendor input) to support sound decision-making.
Sustanable and Reslience solution- Addresses operational challenges across demand, security, testing, release and lifecycle processes with sustainable solutions.

Technology Skills

Minimum 2 years of experience in SAP solution consulting, with a strong track record in solution design, and full-cycle product implementations.
Good knowledge on SAP system components, architecture, technical integration concept, ABAP and API.
Experience on SAP BASIS, Unix system administrator.
Deep understanding of SAP security and authorization concepts, including access control, authentication and data protection.
Hands-on experience with SAP security administration and risk management (roles/profiles, provisioning, policy maintenance, risk assessment) and relevant security/compliance standards (e.g., NIS, KRITIS, GDPR, SOX).
Proficiency with test and release management tools, ticketing systems, SAP security tools/transaction codes and ABAP for security-related custom solutions and troubleshooting
Need the cybersecrutiy knowledge or skills related to SAP framework-OS security, DB security, Firewall concept, SAP Netowrk zone design, Network infra knowledge, Vulnerability, SAP application design security, encryption, Cloud cybersecurity architecture. Data privace and Integrity, Data protection.
Advanced certifications in SAP Security, SAP Architecture, or Service Management technologies (e.g., SAP Certified Technology Associate)
Knowledge on SAP DevSecOps- Deep SAP Security & Architecture Expertise, strong knowledge of SAP platforms and security architecture, including: SAP S/4HANA, SAP NetWeaver, SAP BTP, and SAP Fiori, SAP transport management and secure configuration, SAP-specific vulnerabilities and patch management.
Integration of Security into DevSecOps Pipelines - Automating SAP code security scans (ABAP, UI5, integrations), Implementing security gates in pipelines,
Supporting secure transport and release management, Implement continuous monitoring and compliance controls, SAP security monitoring and logging (SIEM integration)
Compliance with standards such as ISO 27001, NIST, KRITS and GDPR, Managing identity governance and access risk analysis.

Education, Skills & Experience

Bachelor's degree in Business Informatics, IT technology, or a comparable field.
Graduate degree in a relevant discipline (IT Technolocy or Computer Science)
Several years of experience in SAP-based Authorization, BASIS, Cyberscurity, Techical integration and Cyberscurity areas.
Understanding about SAP system profiles, Authentication, Patching, Secure Network Communication, Encryption, Database security, Infra security.
Good knowledge on information security policy, cybersecurity issue response, disaster recovery, industrial policy and compliance, physical security, OS security, MFA, Netowrk architecture, vulnerability management, log and monitoring, OWASP Top 10, Secure configuration.
Experience on DevOps to DevSecOps-understood secure development lifecycle(SLDC), Cybersecurity framework-27001, NIST. Testing and Automation.
Understood different cybersecurity related concepts: cyber defence model, ISC, Cloud security concept.
Proven experience in managing teams and driving operational performance in a technology-driven environment.
Any certifications-CISSP, CCSP, SSCP and Secruity+ is plus.
Strong analytical and problem-solving skills, capable of navigating complex issues.
Excellent communication and interpersonal skills, with the ability to influence stakeholders at all levels.
Proven ability to develop and implement effective strategies and policies, supported by an in-depth understanding of industry trends, market dynamics, and the competitive landscape.

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

Internship as Digital Automation Specialist - All Genders (Corsier-sur-Vevey, Vaud, CH, 1804)

Work Your Magic with us!

Date de début:ASAP
Durée: 6 month
Lieu: Corsier-sur-Vevey, Suisse
Position: Internship

Key Responsibilities:

Develop, implement, and manage RPA solutions to automate supply chain and logistics processes, such as order processing, inventory management, and shipment tracking.
Collaborate with supply chain stakeholders to identify automation opportunities and gather project requirements.
Analyze existing supply chain processes to determine automation feasibility and create detailed documentation for automated workflows.
Support and maintain RPA solutions, troubleshooting issues and ensuring optimal performance.
Work with cross-functional teams, including IT, procurement, and logistics, to ensure seamless integration of automation solutions.
Monitor key performance indicators (KPIs) related to automation effectiveness and provide insights for continuous improvement.

Qualifications:

Proven experience in RPA development using tools such as UiPath, Automation Anywhere, or Blue Prism, particularly in supply chain environments.
Strong understanding of supply chain processes, logistics operations, and workflow automation.
Excellent analytical and problem-solving skills, with a focus on process optimization.
Strong communication and interpersonal skills, able to collaborate effectively with various stakeholders.
Experience with Agile methodologies and project management is a plus.
French and English fluent

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

Account Manager (Digital Sales, 5년 이상 경력, 화학/바이오) (Seoul, Seoul, KR, 06178)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

The Account Manager (Digital Sales) role involves working in a fast-paced and rewarding team environment to develop sales of Diagnostics & Regulated Materials across various industrial accounts, aiming to achieve quarterly and annual targets. You will be responsible for executing a yearly plan to optimize sales and introduce new products in growth segments. There will be opportunities to learn how to drive sales through key account management, digitalization, and account-based marketing. You will need to build deeper customer relationships by gaining a better understanding of their application needs and performing proactive outbound activities to secure business deals.

Your Role

Consistently achieve quarterly and annual sales targets established by the leadership team.
Develop and maintain relationships with major accounts in the assigned field.
Execute a sales plan aligned with the overall sales strategy.
Manage stakeholders effectively to develop customer relationships and build a sustainable business.
Respond promptly to all customer requests, quotes, and tenders.
Expand the utilization of digital tools to nurture customer buying behaviors.
Maintain a high level of technical and application competence to add value for customers.
Plan and execute customer site visits to grow your network and influence within the scientific community.
Submit accurate monthly and quarterly forecasts as requested.
Assist in optimizing the sales process.
Collaborate across functions to ensure effective campaign implementation.
Actively follow up on marketing campaigns with growth accounts to influence the adoption of the targeted product portfolio.
Provide the voice of the customer internally to strategize and develop effective programs for customer retention.
Collaborate with other team members to enhance business growth across all segments.

Who You Are

Bachelor’s degree in Biology, Chemistry, or Material Science.
At least 5 years of relevant sales or technical sales experience, or equivalent.
Digital & Inside sales experiences are preferred.
Solid experience with CRM software (SFDC) and MS Office.
Resilient, with the ability to work under pressure and collaborate effectively with colleagues.
Experienced in building sustainable relationships.
Proven ability to influence and sell to all levels of an organization.
Excellent presentation skills to communicate effectively at all levels.
Strong knowledge of customers, competitive landscape, and market trends.
Open-minded to new ideas with high aspirations for career development.
Able to utilize AI effectively
Business level in English

<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.

Regional Marketing Coating (Mumbai, Maharashtra, IN, 400084)

Work Your Magic with us!

Overview

The Regional Coatings Marketing role for APAC incorporates voice of customer and market trends to the Coating segment management process and translates segment strategy into an execution plan for sales.
With the responsibility of Coating product portfolio focusing on Auto OEM COAs, Refinish COAs, Plastic COAs, Powder COAs, Coil COAs, 2-Wheeler COAs, ete as well as Functional applications.
This position is expected to contribute to the development of new out of box concepts, techniques, and standards in regard to the Regional Marketing function.
As an expert in his/her particular technical aspects, this person develops solutions to complex problems which require the regular use of innovation ensuring solutions are consistent with organization objectives.
As needed, this role has to also function in a project leadership role with entire project management in APAC.

Responsibilities include

Develop and implement the regional marketing strategy aligned with global and commercial objectives.
Collaborate with product management to support go-to-market strategies for new raw materials innovations
Initiate customer project and trace a progress of projects of sub-regions in APAC
Drive demand generation through targeted campaigns, events, webinars, digital channels and trade shows.
Create sales tools and training materials tailored to targeted campaigns / activities.
Design, develop, execute, track, analyze, report the performance of marketing campaigns, including social media reach out, managing the marketing budget
Take and drive accountability for activities, develop priorities and sales develop plans, own product launches and tech. training supported by InA, etc.,
Defend and grow market share thru marketing plans and programs for each product with strong collaboration with Sales, Technical, Product Management, Global Marketing, etc., take direct ownership of NPIs & Focus products sales.
Conduct market analysis to identify trends, customer needs, and competitive positioning.
Tailored & customized marketing support to key accounts to strengthen customer relationships
Collaborate closely with leadership to ensure marketing continuity and communication clarity of SUSONITY.
Maintain brand consistency across regional channels
Ensure proactive communication with stakeholders (customers, partners, and internal teams) throughout the transition.

Professional Experience:

5-8 years of marketing and/or sales experience in B2B Coating sectors such as specialty chemicals, raw materials, or manufacturing (i.e. Paint supplier). Technical background about understanding “Paint formulation” is strongly preferred.
Strong experience in go-to-market (GTM) strategy, particularly for new product introductions (NPIs incl. Pre-launch activity).
Demonstrated ability to lead integrated demand generation campaigns (events, digital, trade shows, etc.) with measurable ROI.
Familiarity with cross-functional collaboration (Sales, Technical, Product Management, Global Marketing) and ownership of product launch planning.

Education:

Bachelor degree or above in chemistry related major.

Key Skills:

Strategic planning, regional execution
Strong understanding capabilities on color trend and paint formulations
Strong communication and presentation skill
Excellent communicator, able to work effectively across cultures and departments
Representative of MarCom in Coatings for the region
Responsible for customer training program (e.g. Pigments Academy program)
Market & Competition intelligence

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

Principal Quality Engineer (Cork, IE)

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Principal Quality Engineer

Reporting to the Quality Manager - Blarney Operations, the Principal Quality Engineer will be responsible for overseeing and delivering on all aspects of the Quality Functions related to Filtration Site 2, Blarney.

Duties & Responsibilities

Supervision and talent development of Quality Engineers and Technicians with focus on compliance, issue prevention, problem solving, and team working ethic as required.
Support colleague engagement model to foster a positive team environment through open communication and feedback.
Manage performance expectations for Quality Engineers and Technicians and drive accountability as required.
Manage the technical quality aspects for area of responsibility and work closely with the operations team to achieve all key department metrics.
Ensure key quality metrics such as CAPA management, Right First Time, Complaints etc are consistently achieved.
Ensure effective and efficient closure of deviations, CAPAs, change controls, audit observations and customer complaints.
Ensure thorough investigation of Quality issues using Root Cause Analysis methodology and implementation of robust corrective and preventative actions to prevent recurrence.
Oversee the Quality Management System in the area to align with site QMS and to ensure effective use, compliance with relevant corporate procedures and quality standards.
Participate in the review of quality trends, identify opportunities for continuous improvement and complete improvement projects using OpEx tools.
Participate in and support the internal and external audit programmes.
Support the successful validation and qualification of process and raw material changes.
Support introduction of new products into the site as per the required standards.
Maintain strong communication with internal and external stakeholders.
Liaise with vendors and customers on quality related issues, internal and external.
Adhere to all company EHS guidelines and Quality procedures.
Additional duties as required.

Education & Experience

BSc qualified in appropriate scientific discipline
Minimum 5 years relevant experience in a similar QA role (ideally Pharma/Biopharma)
Excellent communication, collaboration and leadership skills
Results oriented
Good decision making and problem-solving skills

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

机械技术员 (Nantong, Jiangsu, CN, 226010)

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岗位描述：

职位目标：
在项目阶段，机械维修技术员将协助管理机电安装的质量和进度，并支持系统调试、启动。
机械维修技术员将主要负责日常机械设备维护工作。
主要职责：
项目阶段
监控机电安装过程。
参与项目最终验收。
支持系统调试、启动和验证。
协助准备现场维护工具、文件等。
协助维护主管制定机械设备预防性维护计划。
项目完成后
根据工单完成日常维护工作。
及时完成设备维护记录，并确保所有维护工作都记录在系统或日志中。
协助维护主管改进PM和PDM。
协助维护主管及时更新资产信息。
每天进行机械设备巡视，及时发现设备问题或潜在设备问题。
参与故障分析，持续减少电气设备故障。
协助维修主管控制机械备件库存。
确保行为符合合规和 EHS。
根据要求安排其他工作。
积极参与工厂的质量文化建设和质量相关活动。
主动汇报质量相关事件，积极参与工厂的质量持续改进的活动。

岗位要求：

大专以上学历，机械类或机电一体化教育背景。
8年以上精细化工机械维修工作经验，熟悉包装线、化工设备如泵、带搅拌器容器、机械密封等等设备的维修。
精通机械三视图，熟练电脑Auto CAD者优先。
初级电气知识，低压电气许可证会更好。
在机械维修方面具有出色的动手能力。
具有拆装机械机构的能力。
机械维修知识和解决设备常见问题的技巧。
具有成套设备装置和化工设备的运维经验
基础英语阅读。
如有需要，接受轮班工作。

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

OpEx Engineer (Nantong, Jiangsu, CN, 226010)

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Your role：

Overall Objectives of the Position：

Drive 6S Management: Lead 6S initiatives effectively, keep a well-organized workplace, using the physical environment to drive safety, quality and cost. With a clean, organized workplace, abnormal conditions are quickly recognized and corrected.
Drive Kaizen Management: Keep successfully implement the Kaizen philosophy. Supervising Kaizen system, managing system operation problems, and promoting the achievement of goals.
Keeping tracking CIP projects, summarize report monthly.
As LSPS site deployment team member: Functional experts who are dedicated on the deployment of LSPS in certain area (e.g., production, QC/QA, maintenance, SC) Manage deployment plan for area ensuring all is executed on time and escalate issues as needed to leaders.

Main Tasks：

Fostering the development of a lean culture within the company.
Serving as a leader and facilitator of change, assisting teams in accepting and adapting to improvement measures.
Managing cross-departmental teams to implement lean projects and improvement plans. Monitoring project progress to ensure the achievement of objectives.
Training colleagues and team members on the use of lean principles and tools. Identifying non-value-added activities in production and business processes.
Utilizing lean tools such as 6S, continuous improvement, Value Stream Mapping, etc.
Promoting a zero-defect culture and mistake-proofing (Poka-Yoke) measures.
Other duties required by the superior.

Who are you：

Education and Qualification Required：

University or college graduate in chemistry, pharmaceutic, biology
Extensive professional experience 3+ years in pharmaceutic, biology industry
Lean & Six Sigma 2+ years
Good experience and knowledge of typical secondary pharmaceutical process equipment e.g. filling line, autoclave, packaging line, IBC handling, dispensary, and media preparation system.
Have good knowledge of GMP and ISO9001:2015.
Ability to work effectively across the matrix organization interacting in particular with Supply Chain, and Quality functions.
Good command in English and Chinese in writing and speaking.
Good teamwork attitude, initiative and hardworking, good communication skills.
Green Belt above certification.

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

Senior QMS Expert (Nantong, Jiangsu, CN, 226010)

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Your role:

Overall job purpose：

Reporting to QMS Manager, As QMS Expert, provide expert for quality management system implementation and continuous leading improvement across the Quality and Site cross-functions.
To responsible of GMP compliance monitoring and management, Leading site Quality management system continuous improvement, including change control management, quality risk management, document management and global regulation implementation etc., to ensure the systems compliance with all Domestic and Global regulatory and corporate requirements.
Responsible for leading the continuous improvement projects of the Quality Management System (QMS) team, including proactively identifying discrepancies and risk points within the quality system, and actively and effectively promoting the ongoing optimization and improvement of the factory's quality management system to ensure the efficient and effective operation of the factory system.

Responsibilities：

Compliance (EHS/GMP/CUSTOMS):
Strictly follow regulation\SOP requirements, execute the operations with GMP common sense, fulfil Data Integrity requirements every time, all the time.
Point out the activities or issues which is not compliance, report to manager in timely manner.
Routine Operations R&R：
Leading quality system operation and continual improvement, including quality risk management, change control management, document management and etc., proactively identifying discrepancies and risk points within the quality system, and actively and effectively promoting the ongoing optimization and improvement of the factory's quality management system to ensure the efficient and effective operation of the factory system.
Lead, drive, and enhance the quality management system while supporting site regulatory compliance initiatives. You leverage resources from the QMS group to ensure timely deliverables and adherence to established targets. Additionally, you lead and drive quality initiatives that have a direct impact on site operations.
Lead on site quality index and performance monitoring and Quality Council organization to maintain the process of management review and report the quality index information to global team.
Lead and manage appropriate performance Site Quality Index and works with Site and Global stakeholders to successfully deliver the site deliverables, support to manage Site Quality Councils and the connection to Site quality performance for Global Quality Council while promoting suggestion and proposal for quality system enhancement and lead the improvement events.
Assist with regulatory compliance-related activities, including CMC dossier/variation preparation, compliance checks for submissions, and regulatory assessments to ensure product quality, safety, and compliance.
In charge of participation and implementation of self-inspection, internal audit and HA inspection activities. Ensures that audits are performed per developed schedule. Review findings and makes recommendations for findings. Ensures timely response and closure of all action items / commitments.
Strategy & Operational Improvement
In charge of continuously improve 6 GMP systems within site operation, to develop and certify the capability of system owner and sub-system owner, to cultivate and train SME， enhance quality culture maturity at site level.
People Development
Ensure individual development plan and implementation are in-place and meet the needs of increasing business.
Continuously improve GMP relevant process within site operation, develop individual continuous improvement awareness and capability.

Who you are:
BS in Pharmaceutical or equivalent.
At least 5 years’ experience in similar position areas of pharmaceutical plant.
Familiar with China GMP and regulatory requirements.
Fluent in English, both of written and oral
Result orientation, accuracy and reliability
Excellent communication, problem-solving, planning and organization skills
Project management experience is plus

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

Manufacturing Engineer (5년 이상, 공정 최적화) (Ansan-Si, Gyeonggi-do, KR, 15420)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

We are seeking a results-driven Manufacturing Engineer to lead manufacturing process optimization, continuous improvement initiatives, and operational excellence programs. This role will drive data-based decision making, Lean transformation, and cross-functional collaboration to enhance productivity, quality, and cost efficiency across the site.

The position reports to Manufacturing Manager and plays a key role in strengthening process capability, KPI governance, and sustainable performance improvement.

Your Role

Manufacturing & Process Optimization

- Ensure safe, efficient, and high-quality manufacturing operations
- Analyze and optimize production workflow (cycle time, takt time, throughput)
- Drive process standardization and automation initiatives
- Conduct root cause analysis and implement corrective actions
- Support equipment layout planning and space optimization

Continuous Improvement & Lean Implementation

- Lead Lean / Six Sigma initiatives (5S, Kaizen, DMAIC, VSM, etc.)
- Identify and execute productivity improvement opportunities
- Reduce waste and improve operational efficiency
- Support quality control process enhancements
- Promote continuous improvement mindset across teams

Data-Driven Performance Management

- Develop and monitor KPIs aligned with site objectives
- Analyze production data, schedules, and cost metrics
- Utilize data tools (Excel, Power BI, Minitab, Python, Foundry etc.) for performance insights
- Provide management with actionable performance reports
- Support budget planning and capital investment proposals

Cross-Functional Collaboration & Leadership

- Collaborate with Production, Quality, Maintenance, Supply Chain, and Engineering teams
- Engage stakeholders to drive change and manage resistance
- Support cross-site or global initiatives when required
- Ensure alignment with customer and product specifications

Who you are

Bachelor’s degree or higher in Engineering (Industrial, Manufacturing, Mechanical, Chemical, Electrical, or related field)
5+ years of experience in manufacturing or process engineering
2+ years of Project Management experience
1+ years of experience with Six Sigma, Lean Manufacturing, 5S, VSM, etc.
English communication capability (written & verbal)

Preferred Qualification)

Experience with process controls, high purity piping, and UPW systems.
Previous semiconductor cleanroom experience
Experience with Microsoft Project
Strong communication skills – both oral and written
Ability to effectively work with all levels of the organization
Demonstrated safety focus
Excellent analytical and problem-solving skills
Excellent decision-making skills
Proven track record working with and prioritize multiple tasks within a changing environment
Self-starter and able to work with minimal guidance.
Able to work well within a team-oriented environment.

<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 - Management de l'énergie (m/f/d) (Corsier-sur-Vevey, Vaud, CH, 1804)

Work Your Magic with us!

Date de début : Août 2027

Durée : 2 x 6 semaines puis 1 année sur 4 ans d'étude

Localisation : Corsier-sur-Vevey

Position: Stage Pibs HEIG-VD

Dans le cadre de notre engagement envers la durabilité et l'efficacité énergétique, nous recherchons un stagiaire pour rejoindre notre équipe de gestion de l'énergie. Ce stage offre une opportunité unique d'acquérir une expérience pratique dans le domaine de la gestion de l'énergie au sein d'une entreprise innovante. Ce stage est destiné aux étudiants PiBS pour l'école de la HEIG-VD.

Ton rôle:

Analyse des Consommations Énergétiques: collecter et analyser les données de consommation d'énergie des différents sites (électricité, gaz naturel, eau).
Participer à la mise en place d'outils de suivi et de reporting des consommations énergétiques.
Soutien aux Projets d'Amélioration: contribuer à l'identification et à la mise en œuvre de projets visant à réduire la consommation d'énergie et les émissions de CO2.
Aider à l'élaboration de plans d'action pour atteindre les objectifs de performance énergétique.
Collaboration Interdépartementale: travailler en étroite collaboration avec les équipes de maintenance, d'ingénierie pour intégrer les meilleures pratiques en matière d'énergie dans les opérations quotidiennes.
Participer aux réunions de suivi des projets et des initiatives énergétiques.
Sensibilisation et Communication: aider à la création de supports de communication pour sensibiliser les employés aux enjeux de l'énergie et aux initiatives mises en place.

Ton profil :

Étudiant(e) en école d'ingénieur, en gestion de l'énergie, en environnement ou dans un domaine connexe dans le cursus PiBS
Intérêt pour les enjeux énergétiques et environnementaux
Compétences analytiques
Capacité à travailler avec des données
Bonnes compétences en communication
Capacité à travailler en équipe

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

Internship: Optimization of Cell Line Development (m/f/d) (Corsier-sur-Vevey, Vaud, CH, 1804)

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Start date: August/September

Duration 6-12 months

Location: Corsier-sur-Vevey

Role level: Internship

Recombinant therapeutic proteins such as monoclonal antibodies (mAbs) are an important class of medicines serving patients most in need of novel therapies. The dominating production system for mAbs is a recombinant expression in mammalian cellular systems, mostly Chinese Hamster Ovary (CHO) cells, consisting of introducing a piece of DNA, coding for a mAb, into the genome of a host cell and an intensive selection process to obtain a drug-producing cell line. Cell line development (CLD) is one of the most critical steps in the production of biological medical products. As a team dedicated to CLD innovation, we support the CLD activities by finding ways to identify better cell lines, with increased yield in a reduced timeframe.
We offer an internship opportunity for a motivated individual to join our Technology Innovation team. As an intern, you will focus on investigating the possibility of implementing protein expression system that allows to uncouple the expression of mAb molecule from the protein expression pathways of CHO cells. You will be responsible for leading the generation of cell line stably expressing the exogenous RNA polymerase enzyme and evaluating its impact on the mAb yield. Practically, you will generate and characterize pools of modified cells and perform productivity assay to measure mAb titer. You will perform single cell cloning of best pools to obtain clonal cell lines. You will screen clonal cell lines for expression of the enzyme using ddPCR. You will carry on a comparison between enzyme-expressing and control cell lines at different scales. The productivity assessment will involve the extensive use of the top-tier opto-microfluidic Beacon technology (Berkeley Lights), automate robotic platform and Ambr15. Data analysis of the experimental results will be performed with the programming language of your choice.

Your role:

You will work closely with our team of experienced researchers to design and execute experiments
Analyze data, and present findings to the wider team.
A strong interest in molecular/cellular biology and biotechnologies,
Excellent communication
Excellent organizational skills
A passion for learning

Your profil:

Master/Engineer student in biology, molecular or cellular biology, biotechnology or related subject
Experience in sterile culture handling
Programming Level: R or Python
Language: French and/or English
Ongoing study

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

Internship - QC Chemistry (m/f/d) (Corsier-sur-Vevey, Vaud, CH, 1804)

Work Your Magic with us!

Start date : 01.08.2026

Durée : 12 mois

Role level : stage

Lieu : Corsier-sur-Vevey, Suisse

Au sein de l’équipe QC Chimie, votre rôle sera de contribuer activement aux activités de contrôle qualité dans un environnement dynamique et stimulant. En tant que Stagiaire au sein du QC Chimie, vous aurez à lead des projets mais aussi une immersion dans le fonctionnement d’un laboratoire en réalisant des analyses. Vos principales missions seront les suivantes :

Innover et amener le QC Chimie à être plus performant
Alimenter le parc analytique du QC Chimie avec la sélection de nouveaux équipements
Mener à bien les qualifications des nouveaux équipements
Validation des nouvelles méthodes analytiques
Qualification des nouvelles matières premières pour les besoins en productions
Gestion des échantillons physiques et via notre système de gestion des échantillons GLIMS
Implication dans l'EHS et Normalisation des méthodes
Participation aux projets du QC Chimie et Alignement à la Conformité (Déviation, Investigation, CAPA, Action de changement, mise à jour de procédure qualité)

En tant que membre de l’équipe, vous participerez activement aux discussions et à l’amélioration continue des processus. Vous contribuerez également à l’élaboration et à la mise à jour des procédures et des documents contrôlés pour répondre aux exigences des tests.

TON PROFIL

Connaissance des méthodes Analytiques du laboratoire de chimie
Connaissance des équipements du laboratoire de Chimie
Expérience dans la Gestion de Projets
Connaissance des pharmacopées
Notion des systèmes qualités GMP / ISO
Une forte capacité à communiquer et des compétences diplomatiques
Français courant, bonnes connaissances en Anglais (oral et écrit)

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 EMD Electronics.

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!

Senior Manager Sourcing - Semiconductor Materials (Hybrid) (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.

Location: The Senior Manager Sourcing - Semiconductor Materials is a hybrid position located in either Allentown, PA or Tempe/Chandler, AZ with 20% travel required to meet business needs.

Your Role:

The Sr. Sourcing Manager, Specialty Gases is responsible for developing, negotiating, and maintaining competitively advantageous supply arrangements as the functional expert with a key focus on cost savings and security of supply. You are responsible for identifying new sources of supply from non-traditional suppliers for supply globally. In this position, you are expected to:

Assess and lead global/regional category strategies by negotiating contracts and best source solutions
Develop in-depth commercial and technical knowledge of the materials and categories supported
Monitor, communicate, and respond to changing market conditions and business drivers on a global basis to maximize leverage and minimize risk
Challenge the status quo to create unique and lower “total cost of supply” sourcing options and processes, creating a competitive advantage
Bring innovative supplier solutions (i.e., reclaim/recycling programs, utilization of by-product streams, etc.) to maximize value and minimize the total cost of supply
Apply AI-enabled market intelligence and predictive analytics to track price, capacity, energy, and geopolitical shifts; drive proactive risk mitigation and scenario planning
As the functional expert, guide and influence regional & global supply strategies within strong multi-functional business teams
Challenge technical specifications and business inputs when purchasing capability is severely confined
Develop and manage key supplier relationships with both EMD and supplier organizations within the chemical industry to ensure alignment with business strategies
Identify new source opportunities to support R&D efforts to support the business platform
Build, govern, and improve supplier relationships; set KPIs/SLAs, monitor performance via digital dashboards, and lead QBRs
Supply Contracts Size Range: Up to $80MM

Who you Are: You have a strong teamwork spirit, inter-personal communication, and influencing without direct authority. You are self-motivated with the ability to prioritize and take initiative. You have strong organizational and time management skills with attention to detail. You are skilled in negotiations and able to diffuse conflict.

Minimum Qualifications:

Bachelors degree with 8+ years’ experience or MS degree with 3+ years’ experience
8+ years of sales, purchasing and/or commercially oriented business experience dealing with complex negotiations
Knowledge and experience in electronics grade semiconductor materials

Preferred Qualifications:

Hands-on experience in commercial negotiations, global business planning, supply resilience, global strategy development and execution
Knowledge of the chemical industry
Exposure to semiconductor market
Proven ability to develop and maintain strong relationships; build credibility and trust with internal partners and suppliers
Proven track record in previous procurement and/or sales roles

Pay range for this position: $110,500 - $160,000

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

数字化工厂工程师 (Suzhou, Jiangsu, CN, 215600)

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The Thin Films business unit of Electronics has the ambition to drive information access, interpretation of insights, and action of our operations based on a digital landscape of our processes and systems. As Digital Transformation Engineer, you will play a pivotal role in advancing our digital transformation vision at the Thin Films China site by, transforming digital workflows into daily operation, enabling data access across our processes or sites, driving innovative and standardized digital solutions, improving processes through data and data analytics. The role is to bridge the gap between traditional manufacturing and digital/IT solutions, using advanced digital tools and techniques to enable connected plant and realize the paperless operations and develop the technology roadmap towards smart manufacturing.

Your Role:

Focus on integrating digital workflows into daily operations

Collaborate with operational teams to understand and prioritize user requirements, formulate clear development roadmaps aimed at improving quality, increasing labor efficiency, and/or maximizing production capacity in a standardized way.

Leverage advanced technologies and analytics to level up site digital maturity

Support digital tool adoption within the business through upskilling, training, and engagement initiatives.

Collaborate with global team and bring good practice

Oversee and map out digital plant target data flow from shop floor devices to back-end systems, and design a general data flow in terms of overall production process value chain to ensure data interoperability and achieve paperless factory operations.

Oversee the deployment of digital/IT solutions like MES, EBR, Data Historian, etc., ensuring they meet performance, cost, and timeline requirements.

Coordinate with internal and external stakeholders, including plant managers, engineers, software vendors, and contractors, to ensure project goals are met.

Present digital plant concepts, progress, and results to non - technical stakeholders, translating complex technical information into understandable terms.

Who you are:

A bachelor's or master's degree in engineering (mechanical, electrical, chemical, or industrial), computer science, or a related field.

5+ years of experience in digital plant solutions design and implementation.

Proven experiences with MES, EBR, Data Historian, and digital workers technology.

Familiarity with IoT technologies, data analytics, and machine learning concepts.

Excellent communication and interpersonal skills of communications, coordination, and facilitations to work closely with cross-functional teams like production, engineering, automation, OT and IT teams.

Strong analytical and problem - solving skills compared with Good skills of project management.

Proficiency in programming languages such as Python, Java, or C# for data process (data engineering, statistical modeling, and data visualization ) and system integration.

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

客户主任-甲状腺-苏州 (Suzhou, Jiangsu, CN, 215021)

与我们携手施展你的超能力！

职位描述：

1. 制订有挑战性的和可行性的区域计划，并能成功地实施。

1）根据自己对所辖市场的了解, 制订区域计划和医院销售目标,活动计划和费用预算。

2）在工作中定期的回顾和修正行动计划, 以更高的达到销售目标。

3）计划和执行每天的拜访活动, 确保有效拜访时间符合公司的要求

4）建立和维护与临床医生和学术带头人的关系

5）定期拜访药剂科以保证良好的供货

6）组织GSA和其他销售和市场活动

7）如果有需要，应当协助销售经理处理经销商供货和医疗保险目录的申报

2. 发展和拓宽市场, 了解市场潜力和维护销售的持续稳定的增长

1）执行销售和市场策略并对执行后情况进行反馈

2）提供竞争对手,医疗保险目录和商业供货等信息

3. 工作态度端正，执行公司的行为要求，树立自身良好形象，维护公司品牌形象

1）体现公司的学术形象，掌握产品及相关知识并在每天的工作中运用。

2）掌握销售技巧和演讲技巧并运用到工作中。

3）工作积极努力,有责任感，保持衣冠整洁，对待客户礼貌周到

4. 报告和培训

1）按时和准确的提交各种报告和报表。

2）认真参加公司组织的各项培训和会议。

任职要求：

1. 医药及相关专业本科以上学历。

2. 熟练掌握产品知识，了解相关医学知识

3. 具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

4. 有相关领域经验为佳

5. 具备RDPAC认证资格优先考虑

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！

Legal, Compliance and Data Privacy Lead South Africa (Modderfontein, Gauteng, ZA, 1609)

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Your Role
You will provide expert legal, compliance, and data privacy support primarily to the Healthcare business in South Africa and to the Life Science business across South Western and Eastern Africa (including markets such as Angola, Botswana, Kenya, Nigeria, Tanzania, and others). Reporting to the regional manager, you will serve as a strategic counselor and key contact for leadership teams, facilitating simplified and effective legal, compliance, and data privacy services. Your responsibilities include supporting contractual, commercial, medical, research and digital initiatives, ensuring the application of global compliance and data privacy frameworks, managing risks, conducting training, and leading various projects. You will collaborate closely with regional and global teams, legal entities, and external partners to promote compliance culture and support ethical business practices. You will also oversee due diligence processes and support investigations, audits, and corrective actions to maintain regulatory standards.

Who You Are

Hold a legal degree and admission to practice law in a South African jurisdiction
Minimum 5 years post-qualification experience in healthcare and/or life sciences, preferably within a large law firm or international healthcare/life sciences company
Familiar with multinational corporate compliance, including anti-bribery, anti-corruption, and data privacy regulations
Skilled in managing relationships and interacting effectively with senior management levels across cultures
Strong organizational, communication, and influencing skills
Proactive, pragmatic self-starter comfortable working under pressure
Experienced in change and process management
Fluent in written and spoken English
Able to work effectively in an international and diverse cultural environment

This role is an employment equity position and the company prioritizes such applications. As per the Company’s Employment Equity Plan, the Company encourages previously disadvantaged employees to apply.

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)

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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!

Change & Communication Specialist (Bonifacio Global City, Metro Manila, PH, 1630)

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Your Role:

We are seeking a dynamic and experienced Change & Communication Specialist to support the roll-out of new features and tools within our brand management landscape. This role will be pivotal in designing effective change strategies, roadmaps, and implementation plans, ensuring smooth transitions and successful execution of change initiatives.

Key Responsibilities:

Change Management Leadership: Lead initiatives to oversee, steer, and execute change management measures, ensuring alignment with the overall change concept and other initiatives.
Communication & Enablement: Develop and execute communication strategies to support change initiatives, including writing newsletters, creating stakeholder presentations, and FAQs. Plan, create, and execute communication and enablement activities to ensure stakeholders understand the initiative's vision and its impact.
Training/Development: Develop and execute brand trainings and other educational formats to upskill our organization regarding corporate standards and guidelines in an engaging manner. Execute training activities in line with the central training concept and plan, as availability permits.
Stakeholder Engagement: Develop, own, and drive an engagement plan to ensure stakeholder support and commitment, while keeping teams energized throughout the change process. Actively propose improvements to foster a culture of continuous improvement.
Operational Oversight: Take charge of day-to-day operational activities, ensuring smooth execution and adherence to timelines for various initiatives. Define change KPIs and success metrics, tracking transformation progress and adjusting measures as necessary.
Post-Implementation Reviews: Undertake post-implementation reviews to evaluate the success of communications and identify opportunities for continuous improvement. Conduct regular feedback sessions with initiative leads and impacted stakeholders to tailor change plans as needed.
Cultural Change Advocate: Act as an active partner to management in creating a culture of change, promoting an open mindset towards change, encouraging collaboration, and fostering a sense of ownership and shared responsibility.

Who You Are:

Required Qualifications:

Minimum of 5 years of professional experience in Change & Transformation roles within corporate organizations, with a proven track record of driving change initiatives and transformation projects on a global scale.
Proven experience in change and communication management for complex tasks and multi-functional stakeholder groups.
Exceptional storytelling and communication skills (both written and verbal) in fluent English, with the ability to engage and influence stakeholders at all levels across diverse and multinational environments.
Strong expertise in project management and the ability to work in a fast-paced, collaborative environment.
Proven track record in stakeholder management, being a relationship builder, and effectively managing change resistance.

Preferred Qualifications:

Cultural awareness to foster effective communication and collaboration in diverse environments.
Strong problem-solving and adaptability skills to navigate uncertainty and drive solutions efficiently.
Empathy and passion combined with a strong team spirit, along with a client-focused approach to understand the requirements of VIP clients.

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

Web Analyst (Bonifacio Global City, Metro Manila, PH, 1630)

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The Communications Analytics Service is responsible for managing inquiries related to analytics dashboards, data access, and reporting. This role involves supporting users with Google Analytics, Looker Studio, and Talk walker Social Media Analytics, as well as maintaining a secure database of authorized users. The position also includes global website support, focusing on content management, design, and content creation.

Your Role:

Monitor the service email inbox and assess requests for complexity, addressing level 1 inquiries and forwarding level 2 requests as needed.
Manage a database of authorized users, ensuring secure access by setting expiration dates and sending reminders for renewals.
Create regular reports based on detailed instructions and provide assistance with existing dashboards.
Support global website initiatives, including content management using Adobe Experience Manager (AEM), writing and content creation for the web, and implementing SEO and UX best practices.
Utilize basic HTML and CSS knowledge to enhance web content and support lead generation or eCommerce strategies

Who You Are:

2+ years in analytics, content management, or a related field.
Bachelor’s degree in marketing, Communications, Data Analytics, or a related field.
Knowledgeable in Google Analytics and Looker Studio, with a basic understanding of tagging technologies (e.g., GTM) and social analytics tools like Talk walker.
Familiarity with Looker Studio functions (e.g., calculated fields, Boolean expressions) and basic JavaScript is a plus.
Strong organizational abilities with diligence in maintaining processes and managing access rights securely.
Excellent social skills, capable of conversing with colleagues in a friendly and competent manner.
Able to handle internal and potentially sensitive data with integrity.

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

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

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Your Role:

Handle and perform GL operations tasks for the assigned entity daily, including month-end close (MEC) activities.
Ensure realization of service objectives within set guidelines/policies.
Manage processes and tasks to provide internal customers with financial data/reports.
Manage accounting processes, post to the general ledger, and handle payroll and benefits (when applicable).
Maintain master data and reconcile/maintain accounts.
Prepare reports as required by local finance and Group Accounting.
Perform financial analysis and (pre-)audit tasks.
Handle escalations and perform advanced processing for specific GL activities of a more complex/sensitive nature.
Provide support on user testing for ERP/GL-related tasks.
Seek out better ways of performing processes to contribute to process excellence initiatives.
Support operational performance reporting activities.
Work and collaborate with local entity finance to resolve process-related issues.

Who You Are:

Bachelor’s degree holder in finance, accounting, or any related field required.
Master’s Degree in Finance/Accounting or CPA accreditation preferred.
At least 5-8 years of experience in General Ledger Accounting Operations.
Profound accounting knowledge required (IFRS, GAAP, Tax).
Experience within a Shared Services Center preferred.
Experience with SAP or other ERP systems required.
Fluent English language skills required.
Willing to be based in BGC, Taguig.
Amenable to work on a mid-shift/night shift schedule (Regular Schedule: 1 PM to 10 PM, 3 PM to 12 AM; month end: 9 PM to 6 AM).

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

Medical Representative (Greater Manila Area) (Bonifacio Global City, Metro Manila, PH, 1630)

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The Medical Representative operates within closely defined parameters and under close supervision. S/he contributes to the attainment of the Company’s growth targets by selling a defined range or type of products to specified customers. S/he applies a broad knowledge of the Company’s products and marketing techniques in order to close sales.

Your Role:

·         Generates sales of the Company’s products through close and regular interaction with established customers and by developing new projects.
·         Implements sales and planned marketing programs.
·         Ensures sales objectives are achieved.
·         Makes calls on existing or potential customers and serves as front-line liaison between them and the Company in all matters concerning product and service delivery.
·         Keeps abreast of new products / services and other general information of interest to customers.
·         Continuously upgrades product knowledge and selling techniques.
·         Provides information for forecasting market sales.
·         To recognize a reportable Adverse Event (AE) or safety information and ensure that the necessary information is forwarded to the Local Pharmacovigilance Responsible Person (LPVR) in Company within 24 hours.
·         On handling customer complaint, the employee must obtain and compile the information regarding a received complaint and to transfer the information to the local complaint manager
·         Performs other functions that may be assigned/required from time to time.

MAIN INTERFACES

INTERNALLY:
·         Business Unit Head, Cardio Metabolic Care & General Medicine
·         District Manager
·         Product Managers
·         Key Accounts Associates, trade Sales Manager, Key Accounts Manager
·         Senior Medical Representatives

EXTERNALLY:
·         Doctors
·         Pharmacists, Drugstore Personnel

Who You Are:

·         Graduate of any Bachelor’s degree
·         With Field Sales work experience (Must be flexible to cover GREATER MANILA AREA)
·         Can interpret documents, write routine reports and correspondence
·         Speak effectively
·         Calculate figures and amounts such as discounts, interest, commissions, percentages
·         Interpret a variety of instructions furnished in written, oral form
·         At least three years related experience and/or training
·         Must have above-average know-how in computers, particularly MS Office - Excel, Word, PowerPoint and MS Outlook

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

Operations Manager - NALA & APAC_ Invoice Processing and Inquiry Management (Bonifacio Global City, Metro Manila, PH, 1630)

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Your Role:

As a vibrant science and technology company, we believe in science as a force for good. We make a positive difference in millions of people´s lives every day.

Our passion for science and technology is what drives our more than 64,000 employees across 66 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live.

Job Summary:

We are seeking a detail-oriented and results-driven Invoice Processing Operations Manager to oversee and optimize the end-to-end invoice processing function. This role involves managing a team responsible for timely and accurate processing of invoices, resolving discrepancies, and maintaining compliance with company policies and regulations. The ideal candidate will have strong leadership skills, deep knowledge of accounts payable processes, and experience working with ERP systems to drive efficiency and accuracy in invoice processing operations..

Key Responsibilities:

Team Leadership & Development

Manage and lead the invoice processing team, ensuring high levels of accuracy, timeliness, and productivity.
Provide coaching, performance evaluations, and professional development opportunities for team members.
Foster a collaborative and results-oriented team culture.

Operational Oversight

Oversee the day-to-day operations of invoice processing, including invoice matching, coding, approvals, and payment processing.
Monitor and ensure compliance with internal controls, company policies, and regulatory requirements.
Develop and maintain key performance indicators (KPIs) to track and improve operational efficiency and accuracy.
Handle escalated issues related to invoice discrepancies, vendor communication, and payment processing.

Process Optimization

Identify opportunities to improve processes, reduce errors, and enhance the efficiency of invoice processing workflows.
Partner with cross-functional teams, including procurement and finance, to resolve root causes of recurring issues.
Implement automation and technology solutions where applicable to streamline operations.

Stakeholder Collaboration

Serve as the primary point of contact for internal and external stakeholders regarding invoice processing inquiries.
Collaborate with vendors to resolve invoice-related issues and ensure smooth processing.
Work closely with the accounts payable, procurement, and finance teams to ensure alignment and timely payments.

System Management & Reporting

Maintain deep expertise in ERP systems, ensuring the team leverages system functionality effectively for invoice processing.
Provide regular reports on processing metrics, issues, and resolutions to senior management.
Ensure data accuracy and integrity in all invoice-related transactions and records.

Who Your Are:

Education: Bachelor’s degree in Operations, Business Administration, Finance, or a related field

Qualifications and Experience:

Bachelor’s degree in Finance, Accounting, Business Administration, or a related field.
10+ years of experience in accounts payable or invoice processing, with at least >5 years in a managerial role.
Strong knowledge of accounts payable processes, invoice matching (2-way/3-way matching), and ERP systems (e.g., SAP, Oracle).
Experience with process optimization and implementing automation tools.
Excellent problem-solving, organizational, and analytical skills.
Strong communication and interpersonal skills to effectively interact with team members, vendors, and stakeholders.

Key Competencies:

Leadership & Team Management: Ability to inspire and guide teams toward achieving goals.
Analytical Thinking: Ability to analyze data, identify trends, and implement solutions.
Problem Solving: Expertise in resolving operational and technical issues across Accounts Payable, Purchase Orders, Vendor Master Data, and Travel & Expense processes within ERP systems.
Stakeholder Engagement: Ability to build and maintain strong relationships with internal and external partners.
Process Improvement: A continuous improvement mindset with experience streamlining processes in finance and technical operations.

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

Business Process Expert I2P (Bonifacio Global City, Metro Manila, PH, 1630)

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As the Invoice to Pay (I2P) Global Business Process Expert you will work within the Global Business Services (GBS) Procurement FS organization, as part of the I2P Global Process Owner (GPO) department, enabling an effortless I2P experience for our employees and external suppliers.

You will be involved in implementation of new AP Workflow from requirements gathering throughout validation and testing. Gatekeeper to I2P Process taxonomy, policies, standards and roles authorizations for Procurement I2P. Highly focused on continuous improvement and automations from the invoice ingestion until invoice posting using configuration of conditions and business rules in the latest technology as well ideas for internal team sset upand alignment with supplier for most standard invoice structure and layout.

You will oversee reviewing and approving Knowledge Materials, Test Scripts, Global Work Instructions, and Training materials related to AP Workflow – Invoicetrack by Springtime. You are additionally conducting end-user training for your respective area with the mentioned systems involved.

Main Tasks:

• Project Key user, during AP Workflow implementation

• Gathering requirements incl. local legal exceptions during design & build phase for new AP Workflow

• Consultancy: Assess the need for deviations, change Requests regarding I2P process in newly implementation AP workflow

• Testing: Review & modify test scripts & scenarios for AP workflow implementation, test solution

• Process improvement and system enhancements: seeking for efficiency potential in system usage and functionalities. Analyze ERP and Worfkflow processes to reduce deviations. Support digitalization through technology deployments.

• Process standardization: you will support the standardization of the I2P processes across systems and propose streamlining solutions

Training: Review training materials, and work instructions for AP Workflow solution and onboard new Key Users; act as the content owner for Procure4You(Knowledge materials) articles

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

Who you are:

University degree (business related) – master’s degree strongly preferred.
5+ years of experience in Finance/Accounting/Purchasing/Procurement area in an international environment
Strong P2P process knowledge with focus on Accounts Payable Workflow in SAP FI preferably Invoicetrack by Sprigtime
Experience in AP auto-postings /OCR/ EDI / e-invoicing implementation would be an advantage
Experience in proactively driving ERP improvement initiatives and finding best-practice solutions
Very good communication skills with acting in a way that makes a positive impact
Customer oriented and very good understanding of business requirements
Strong determination and self-motivation
Continuous improvement mindset
Fluent in English with ability to work in an international team.

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

North America Payroll Team Lead (Bonifacio Global City, Metro Manila, PH, 1630)

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Manila based Payroll Team Lead overseeing US & Canada payroll (15k employees) leads daily operations, manages a team, ensures timely and accurate processing, handles escalations for complex issues, maintains compliance with US/CA tax laws, reconciles payroll, drives process improvements, collaborates with HR/Finance, and manages vendor relationships, requiring strong US/CA payroll knowledge, leadership, attention to detail, problem-solving, and system skills (UKG, SAP Success Factors/Employee Central).

Your Role:

Team Leadership: Supervise, mentor, train, and manage daily activities of payroll specialists, ensuring workload balance and high morale. Conduct performance appraisals.
Payroll Operations: Oversee end-to-end processing (bi-weekly/monthly cycles), verify data, calculate wages, deductions, taxes, and ensure accurate direct deposits.
Compliance & Accuracy: Guarantee adherence to all US federal/state (IRS) and Canadian federal/provincial laws (CRA, Revenue Québec), and local payroll regulations, tax laws, and internal policies.
Issue Resolution: Serve as point of contact for escalations, resolving complex payroll inquiries, discrepancies, and employee concerns with urgency and professionalism
Reporting & Reconciliation: Perform Gross-to-Net reconciliations and generate various pay-related reports.
Process Improvement: Develop, implement, and evaluate strategies, processes, and technology solutions to enhance payroll efficiency and accuracy.
Accuracy Rate: Percentage of error-free paychecks.
Issue Resolution Time: Average time taken to resolve payroll tickets or employee disputes.
Process Efficiency: Implementation of automation tools to reduce manual variance and processing time

Who You Are:

Minimum of 5–7 years in payroll processing supporting US and Canada, with at least 2–3 years in a leadership role within a Global Shared Services (GSS) or BPO environment.
Specialized credentials such as Certified Payroll Professional (CPP) for US payroll or Payroll Compliance Professional (PCP) for Canada are highly preferred.
Advanced knowledge of global HCM & Payroll platforms (e.g., SAP SuccessFactors/Employee Central, UKG) and advanced Excel for data analysis.
Exceptional English communication skills to interact with North American stakeholders and explain complex legislative concepts

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

SME Vendor Master Data & Travel Expense (Bonifacio Global City, Metro Manila, PH, 1630)

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The Role:

Develop and maintain expert-level knowledge of the organization's T&E managementsystem and vendor master data system.
Design, develop, and deliver training programs and materials for end-users, ensuringcomprehensive understanding of T&E and VMD system functionalities.
Provide ongoing support, guidance, and troubleshooting assistance to end-users,addressing T&E and VMD system-related queries and issues.
Act as an advocate for end-users, gathering feedback and requirements to enhance theT&E and VMD systems' usability and effectiveness.
Identify opportunities for process improvement within the T&E and VMD systems,working collaboratively with stakeholders to implement enhancements.
Create and update user guides and documentation to ensure clarity and accessibility ofT&E and VMD system-related resources.

Who you are:

Bachelor's degree in a relevant field or equivalent work experience.
Proven experience in a similar role, with a focus on T&E management systems andVendor Master data systems.
Analytical mindset with the ability to troubleshoot and resolve T&E and VMD systemissues.
Detail-oriented with a commitment to delivering high-quality training and support.
Excellent analytical and problem-solving skills, with a keen attention to detail andaccuracy.
Effective communication and interpersonal skills, with the ability to build relationshipsand collaborate across functional areas.
Proficiency in Microsoft Office suite and experience with ERP systems (e.g., SAP,Oracle, Concur) preferred.
Experience with process improvement methodologies such as Lean or Six Sigma isadvantageous for identifying opportunities to enhance T&E and VMD systems' usabilityand effectiveness.

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

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As a vibrant science and technology company, we believe in science as a force for good. We make a positive difference in millions of people´s lives every day. Our passion for science and technology is what drives our more than 64,000 employees across 66 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live.

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!

Operations Manager - Accounting, Controls and Analysis 1 (Bonifacio Global City, Metro Manila, PH, 1630)

Work Your Magic with us!

Work Your Magic with us!

Job Summary:

We are seeking an experienced and results-driven Operations Manager for Accounting, Controls, and Analysis Team (AP). We require a strategic candidate who can address the current backlog and lead the clean-up effort to achieve streamlined operations and longterm efficiency.

Candidate will have in-depth knowledge of Accounts Payable, Purchase Order systems, Vendor Master Data management, T&E processes, and ERP functionalities.

This role requires exceptional leadership skills, operational expertise, and a problem solving mindset to ensure seamless coordination and issue resolution across financial and technical processes.

Key Responsibilities:

Key Responsibilities:

People:

• Build, lead, and sustain high-performing teams through coaching, succession planning, performance management, and capability development.
• Establish a strong accountability and performance culture by setting clear goals, conducting regular performance reviews, and enabling continuous learning and development.
• Foster a collaborative, inclusive environment that encourages cross-functional partnership and effective stakeholder engagement.
• Act as a senior escalation point for people and performance-related matters, ensuring timely resolution and consistent leadership decision-making.

Process:

• Ensure robust governance and control over third-party and balance sheet account reconciliations, including GR/IR, Direct Debit, Debit Balance, and SL/GL, with clear ownership and timely resolution of discrepancies.
• Accountable for the timely and accurate delivery of month-end, quarter-end, and year-end close activities, in alignment with accounting policies, internal controls, and corporate close calendars.
• Define and oversee the strategy for resolving complex invoice and transaction issues, including parked and blocked invoices, unclear 3P accounts, vendor master discrepancies, and T&E exceptions.
• Partner closely with Finance and Accounting leadership to ensure operational processes fully support financial reporting accuracy, balance sheet integrity, and close efficiency.
• Ensure operational readiness for internal and external audits by overseeing the timely and accurate submission of audit requests, schedules, and supporting documentation, and by proactively addressing audit findings.
• Identify operational risks, control gaps, and recurring issues through root cause analysis, implementing sustainable corrective and preventive actions.
• Define, monitor, and govern KPIs, SLAs, and operational metrics to drive continuous improvement and service excellence.

Technology

• Provide strategic oversight of systems and tools supporting P2P operations, ensuring technology enables efficient and compliant processes.
• Partner with IT and system owners to prioritize enhancements, automation opportunities, and system improvements that reduce manual effort and improve accuracy.
• Leverage data, reporting, and analytics to identify trends, improve operational visibility, and support informed decision-making.
• Ensure consistent and effective use of enterprise systems across teams through governance, standardization, and user enablement.
• Support system-related initiatives that enhance scalability, control, and operational resilience.

Who You Are:

Bachelor’s degree in Accounting, Finance, Business Administration, or a related field. CPA or CMA is preferred
Minimum of ~10 years of experience in accounting operations, with at least >5 years in a managerial role.
Strong knowledge of reconciliation processes, accounts payable, and financial controls.
Proven experience in managing and leading a team.
Excellent analytical and problem-solving skills.
Strong communication and interpersonal skills.
Proficiency in accounting software and Microsoft Office Suite.
High attention to detail and a commitment to accuracy.
Ability to work under pressure and meet tight deadlines.
Experience with ERP systems such as SAP or Oracle.
Knowledge of process improvement methodologies such as Lean or Six Sigma.
Familiarity with regulatory requirements and compliance in the accounting field.

Additional Information:

This position may require occasional travel.
Work is primarily performed in a hybrid setup.
Flexible working hours may be necessary to accommodate global operations and time zone differences.

Management Accountant (Bonifacio Global City, Metro Manila, PH, 1630)

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Your Role:

Support in cost accounting and profitability analysis for assigned entities.
Assist local finance and controlling units in cost accounting and profitability.
Manage maintenance and posting processes in cost accounting for accurate overhead cost reporting.
Support the maintenance of cost accounting master data, adhering to global guidelines and integrity constraints.
Establish valid cost centers, internal orders, and projects.
Manage master data-related requests via mailbox and MDG-F tool.
Handle system transfer price updates, reports, and troubleshooting.
Support period-end closing procedures (monthly, quarterly, yearly) and reports in line with international standards and guidelines.

Who You Are:

Bachelor's degree required.
Degree in a business-related discipline strongly preferred.
Initial experience in accounting/finance with direct experience in full-cycle cost accounting and profitability analysis.
Experience within a Shared Services Center preferred.
Familiarity with Cost Accounting and Profitability Accounting.
Experience with SAP CO-OM and SAP CO-PA.
Fluent in English.
Willing to be based in Manila.
Willing to work on night shift.

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

Employee Care Advisor (Bonifacio Global City, Metro Manila, PH, 1630)

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As part of the overall strategy to drive quality-based, cost-efficient and timely service delivery, this role will be part of the HR organization under the Global Support Center. The successful candidate will be responsible for providing tactical and operational HR support for specific country stakeholders from the APAC region. This role will report to a Team Lead overseeing Tier 1.5 HR functions such as onboarding, data management, organizational management, data reporting, customer handling, and inquiry management.

Your role:

• Provide administrative and operational support on defined HR functionalities anchored on KPIs and SLAs focused on quality, timeliness, and responsiveness.

• Proactively collaborate with the country and regional stakeholders in the execution of HR services.

• Work with the local HR Operations team based in Taiwan and Singapore in the sustained and smooth delivery of HR services (in particular onboarding, document management, and reporting).

• Work with HR Business Partners, Centers of Excellence stakeholders for Total Rewards, Talent Development and Talent Acquisition to realize country-specific people priorities and align on program implementation as needed.

• Maintain and administer employee information on HR systems such as SuccessFactors - Employee Central (as needed) and country-specific local systems.

• Actively partner and work with the Team Lead to achieve the agreed-upon performance and developmental objectives.

• Seek opportunities for continuous improvement and work on constructive feedback

• Identify any knowledge gaps and escalate concerns to the Team Lead and the Operations Head.

• Ensure those customer expectations are addressed professionally, effectively and efficiently.

• Demonstrate flexibility and adaptability to work schedule requirements and operation hours in-order to fulfil real time business requirements

• Understanding and compliance of confidentiality requirements to perform HR activities due to the sensitive nature of the work such as personnel data and sensitive information.

Who you are:

Candidate must possess at least a Bachelor's/College Degree in Human Resource Management, Psychology, Behavioral Science, Social Sciences, Business Administration, or any equivalent degree.
Preferably 3 Years minimum professional experience specializing in an HR Operations or HR Generalist function from a Shared Services or BPO organization.
Understanding and experience in the use of HR systems and tools (i.e., MyLearning, SAP P40, PeopleSoft, Workday, Success Factors, Taleo, etc.).
Understanding and experience in the use of Case Management systems and tools (i.e., BMC Remedy, Service Now, Neocase, etc.).
Adequate experience in using MS Office applications. Desired knowledge and expertise on Macros.
Applicants must be willing to work in Taguig City and open for a flexible working schedule.

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

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

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Your Role:

End-to-End Accounts Payable: Manage the complete accounts payable process, including invoice verification, payment processing, and reconciliation, in alignment with service level agreements.
Transaction Verification: Ensure the validity of accounts payable transactions, maintaining compliance with company policies and financial reporting standards.
Stakeholder Communication: Respond promptly to internal and external queries, escalating issues as necessary to ensure resolution.
Supplier Account Monitoring: Oversee supplier accounts to guarantee timely payments and assist with month-end closing activities.
Audit Support: Provide support for internal and external audits as required.
Process Improvement: Participate in special projects and initiatives aimed at enhancing processes, as directed by management.
Documentation Maintenance: Maintain thorough documentation for the Purchase-to-Pay (P2P) process and contribute to developing efficiency-enhancing solutions.
Analytical Problem-Solving: Utilize strong analytical skills to resolve discrepancies and offer data-driven insights.
Customer Service Excellence: Demonstrate excellent communication and customer service skills, ensuring stakeholder needs are met effectively.

Who you are:

Experience: A minimum of 2 to 6 years of experience in General Accounting or Accounts Payable, with a solid understanding of full-cycle AP processes.
Education: A graduate in Accounting, Business Administration, or related fields, or equivalent professional experience.
Functional Knowledge: Significant knowledge of accounts payable processes, procedures, and systems.
Technical Proficiency: Strong experience with SAP or other ERP systems such as Oracle and Ariba; familiarity with specific modules is a plus.
Shared Service Center Experience: Previous experience in a shared service center environment is preferred.
Communication Skills: Fluent in English, with strong verbal and written communication abilities.
Adaptability: A quick learner who is flexible, responsible, and results-oriented, capable of working effectively under pressure.
Cultural Fit: A willingness to embrace challenges and thrive in a multicultural environment.

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

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

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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!

Internship - Program support (m/f/d) (Eysins, Vaud, CH, 1262)

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Start date: May 2026

Duration: 4-6 Months

Location: Eysins, Switzerland

Your role:

As an intern in the Business Sector Controlling team, you will assist in the delivery of key milestones aimed at improving and harmonizing the RVA process. You will work closely with cross-functional teams to document methodologies, assist in parameter validation, and support the development of training materials. Your contributions will be essential in ensuring that our RVA parameters are robust, transparent, and aligned with audit requirements.

Key Responsibilities:

Assist in identifying and documenting RVA parameters requiring empirical evidence and those supported by qualitative input.
Support the development of standardized calculation templates and working instructions.
Document assumptions, calculation logic, and rationale for parameters.
Participate in the design and documentation of a sector-specific backtesting framework.
Aid in maintaining the Business Sector RVA Guideline, ensuring it is aligned with Group Accounting and audit requirements.
Support the preparation of training materials and communication packages for stakeholders.
Assist in the validation of parameter changes and documentation of results.

Your profil:

Ability to analyse data and document findings clearly and meticulous in documenting processes and ensuring accuracy in calculations.
Strong verbal and written communication skills in French and English for effective stakeholder engagement and ability to work collaboratively in a cross-functional team environment.
Familiarity with Excel and data analysis tools, word and Capacity to identify issues and propose practical solutions.
Currently pursuing a Bachelor/master degree in Finance, Business Administration, Accounting, or a related field and interest in financial analysis and process improvement.

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

Field Service Engineer (Taichung, Taichung City, TW, 43541)

與我們攜手施展你的超能力！

Job Purpose

本職位之主要目的
依公司業務需求提供客戶端之鋼瓶更換操作服務，以及公司產品售後之各項服務，包含容器、設備的維護與操作。

Your Role

<操作執行面>
客戶端Tool Side鋼瓶更換/客戶端LDS Side鋼瓶更換/各種化學品或氣體供應設備故障維修/各種化學品或氣體供應設備開機安裝 (須著無塵衣以及防護裝備)

<管理系統面>
紀錄鋼瓶更換相關資料/參加公司安排之各項相關訓練課程/積極參與技能認證提升個人職業技能/參加每月定期工作檢討、安環會議/各項品質異常事故通報與執行/維持工作區域環境整潔與衛生6S/配合上級指派任務或政策規範的執行

Who You Are

1. 無經驗可，歡迎應屆畢業生
2. 積極主動企圖心強願意學習，有基礎英文即可
3. 大專(含)以上，主修化學、電子及相關科系為佳。
4. 有無塵室工作經驗佳

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！

Expert - Indirect Taxation (Mumbai, Maharashtra, IN, 400084)

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Your Role:

You will be part of the Indirect Tax team, performing the below mentioned roles.

Compliance and Filing: Preparing, reviewing, and ensuring the timely and accurate filing of Indirect Tax returns. Performing complex tax calculations and reconciliations. Handling tax registration, amendments and refunds.
Advisory and Research: Conducting research on tax laws and regulations to provide accurate advice to internal and external stakeholders. Determining the correct taxability of company transactions, products and services.
Audit and Litigation Management: Preparing information and reconciliations required for tax audits and inquiries by tax authorities. Assisting in drafting responses to show cause notices, appeals and managing tax disputes/assessments. Liaising with tax authorities and external consiultants.
Data and Systems: Reconciling tax payable and receivable accounts to returns and financials with a strong understanding of SAP functions. Ensuring tax treatment is correctly configured in SAP systems and tax softwares.
Process Improvement: Reviewing and streamlining indirect tax processes using automations to improve efficiency thereby saving mandays and reduce audit risk. Executing internal controls over the indirect tax process.

Who You are:

1. Basic/Minimum Qualifications:

Bachelor’s Degree (B.Com) with 8+ years of experience/Master’s Degree (M.Com) with 6-8 years’ experience.
Minimum of 6-8 years of experience in Indirect Tax function
SAP knowledge
Should be working for a longer period in a company
Strong Communication Skills.
2. Preferred Requirements:
CA/LLB would be an added advantage
Well versed in regional language like Marathi
Strong proven track record of getting GST refunds for the company.
Expertise in automation processes.
Experience in project management.
Pharmaceutical/Life Science/Chemical Manufacturing background.

Preferred Requirements:

· CA/LLB would be an added advantage
· Well versed in regional language like Marathi
· Strong proven track record of getting GST refunds for the company.
· Expertise in automation processes.
· Experience in project management.
· Pharmaceutical/Life Science/Chemical Manufacturing background.

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

IT Quality Systems Expert (Mumbai, Maharashtra, IN, 400084)

As part of the global Quality, Governance and Compliance unit of SUSONITY, we are managing the IT quality systems like document-, training-, audit-, and deviation management systems (e.g. ManGo, TrackWise/Interlex or SALA) within SUSONITY. We are acting as an interface between our commercial units and corporate functions like IT, focusing on supplying a constantly high and increasing level of quality of our systems and services.

Your Role

In your role as IT Quality Systems Expert, you will take over the business coordination as global lead user for our SALA IT solution for training management. Besides the lead user roles, which contain training and support of key users, you create and maintain related system-specific procedures (SOP’s) and become the global expert for training management systems. Quality processes, like risk management, change control or deviation management, are familiar terms for you.

Furthermore, you will be the GxP expert within the new ERP project team, which is currently kicked off to implement a new ERP system within SUSONITY. In this role you develop and maintain test plans, test scripts and user acceptance test and manage the execution of test plans, validation plans and validation documents for GxP related tasks. You ensure initiation/preparation and closeout of impact on the GxP related changes.

In this position, you work with other global departments and sites to solve problems, improve service and to roll out enhancement projects within SUSONITY.

Who you are

Bachelor or master’s degree in (business) computer sciences or equivalent
Software skills in training and/or document management systems
GxP expert and knows how to implement GxP requirements into complex IT-systems
Sound knowledge and experience in quality-related function and the ability to apply quality processes to IT systems operations
Good understanding of regulatory and compliance requirements in the context of electronic systems (data integrity, data retention)
Experience in computer system validation and GAMP is a plus
Ability to understand and communicate complex issues in a simple way and to orchestrate plans to resolve issues and mitigate risks
Ability to lead & implement project initiatives
Curious about new technologies
Excitement about the SUSONITY business and joining a motivated, global and intercultural team
Fluent spoken and written English

Process Engineer (Mumbai, Maharashtra, IN, 400084)

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 Process Engineer, you will be pivotal in driving projects within the manufacturing department, focusing on the production and packing of high-quality solvents. Your technical expertise will ensure that we not only meet but exceed company’s stringent safety and quality standards. This role presents an exciting opportunity to contribute to a culture of excellence while supporting our contract manufacturing sites and leading process innovations.

Project Oversight: Lead and manage projects related to daily production and packing activities for solvents, ensuring smooth and efficient operations.
Technical Expertise: Serve as the technical authority for our contract manufacturing sites, providing guidance to optimize processes and enhance production capabilities.
Yield Optimization: Champion initiatives to improve manufacturing and packing yields through innovative strategies and continuous improvement methodologies.
Safety and Quality Assurance: Uphold company’s commitment to safety and quality by implementing best practices and ensuring compliance throughout all project stages.
Root Cause Analysis: Conduct investigations into compliance issues and deviations, utilizing root cause analysis to develop and implement effective corrective and preventive actions.
Technology Transfers: Manage the seamless transfer of technology and processes for new product introductions and modifications, ensuring smooth transitions and project alignment.
Process Innovations: Collaborate on the development and implementation of new processes for in-house manufactured products, pushing the boundaries of efficiency and quality.
Basic Project Management: Oversee project timelines and deliverables related to production improvements, ensuring alignment with operational goals and stakeholder expectations.
Data Analytics: Utilize basic data analytics to monitor production metrics, identify trends, and support data-driven decision-making processes that enhance operational efficiency.

Who you are:

B.Tech or B.E. in Chemical Engineering, Industrial Engineering, or Mechanical Engineering.
2-3 years in a relevant role within the chemical manufacturing sector, with a focus on projects and process engineering.

Apply now and become a part of our diverse team!

Business Executive (Mumbai, Maharashtra, IN, 400084)

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 :

Generate or convert doctors for our product portfolio.
Secondary sales – Ensuring to achieve secondary sales targets through prescription generation by each of his BE.
Good at relationship with KOLs (Top Physicians, Endocrinologists & Cardiologists)
Day to day sales reporting
Effective query handling and customer queries.
Ensuring 100% Implementation of Company’s strategies
Pharmacovigilance (Adverse Event Reporting) – To collect adverse drugs reaction (ADR) incidences including lack of efficacy related to medicinal products up to the maximum possible level of completeness and forward to local Patient Safety team immediately within 24 hours of ADR awareness. The additional information can be submitted as soon as possible

Who you are:

Any graduate
Freshers or minimum of 1-2 years of experience in any pharma company
Should have strong product knowledge & communication skills

Apply now and become a part of our diverse team!

SALES TRAINING MANAGER (Naucalpan de Juarez, Estado de Mexico, MX, 53370)

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Your Role

Design, develop, and implement training programs for the Sales Force across various therapeutic areas: Oncology, Neurology, Fertility, Endocrinology, Cardiology, Metabolism, and General Medicine.
Identify training needs and assess the effectiveness of training programs.
Collaborate with Medical, Marketing, and related teams to ensure training aligns with company objectives.
Ensure training complies with regulations and standards set by the Company.
Manage the training budget and resources effectively.
Maintain records and documentation of training across different sales lines.
Establish and maintain relationships with external training providers.

Who You Are

Bachelor's degree in Business Administration, Chemistry, or related fields.
Minimum of 3 years of experience in training and personnel development within the pharmaceutical industry.
Strong leadership, communication, and planning skills.
Ability to work in a highly regulated and compliant environment.
Proficient in English, both oral and written.
Experience in liaising with Regional and Global training departments.
Familiarity with digital and remote training tools, including LMS (Learning Management Systems).
Desirable experience with AI training tools, gamification, and adult education.

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

Sales Representative (Naucalpan de Juarez, Estado de Mexico, MX, 53370)

¿Te entusiasma el sector salud y el mundo comercial?

Súmate como Sales Representative, donde impulsarás el crecimiento de nuestro portafolio de Medicina General a través de visitas médicas, actividades comerciales y acciones estratégicas que generan impacto real en tu territorio. Si te motiva construir relaciones con profesionales de la salud y alcanzar resultados con excelencia, esta oportunidad es para ti.

Tu rol:

Promocionar y vender el portafolio de medicamentos y servicios de la unidad de Medicina General a los profesionales de la salud definidos por la compañía.
Impulsar la demanda en el territorio asignado mediante visitas médicas y acciones comerciales en puntos de venta.
Crear y ejecutar Planes de Acción (POA) orientados al cumplimiento de los objetivos del negocio.
Utilizar de manera eficiente los recursos asignados, cumpliendo con políticas internas y lineamientos de compliance.
Implementar actividades definidas por Marketing, dentro y fuera del consultorio (entrevistas uno a uno, talleres de entrenamiento, sesiones educativas, etc.).
Controlar, promover y vender el portafolio en los puntos de venta asignados para asegurar disponibilidad, rotación y cumplimiento de metas.
Utilizar correctamente las herramientas de promoción, análisis de mercado, control y reporte de visitas médicas proporcionadas por la compañía.
Aplicar la técnica de venta establecida y cumplir con normas, procesos y estándares corporativos.

¿Quién eres?

Universitario con título profesional.
Experiencia mínima de 1 año en ventas.
Orientación al cliente y habilidad para construir relaciones sólidas.
Mentalidad innovadora y compromiso con la mejora continua.
Licencia de manejo vigente.
Radicar en CDMX, con disponibilidad para trasladarse en la ciudad.

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

Order Processing and Customer Service Analyst (Naucalpan de Juarez, Estado de Mexico, MX, 53370)

Tu Rol

En tu rol como Analista de Procesamiento de Pedidos y Servicio al Cliente, serás responsable de garantizar la entrega oportuna de productos para satisfacer la demanda de los clientes. Registrarás órdenes de venta en el ERP, manteniendo un maestro de clientes actualizado y gestionando notas de crédito. Administrarás el repositorio documental y generarás reportes analíticos. Además, elaborarás notas de crédito según los lineamientos internos vigentes y realizarás la recuperación de cartera con clientes gubernamentales. Se requiere una experiencia a partir de 2 años en un puesto similar.

Quien eres:

Licenciatura en Administración de Empresas, Ingeniería Industrial, Contabilidad, Relaciones Comerciales, Economía o carrera afín (titulado).
Dominio del inglés básico, deseable intermedio.
Conocimientos en contabilidad, facturación y gestión de clientes.
Experiencia en quejas, devoluciones y operaciones de consignación.
Deseable conocimiento de NOM-059-SSA1 y administración de proyectos.
Habilidades en análisis de datos y facturación electrónica.
Deseable certificación en paquetería Microsoft Office.
Manejo de SAP módulo de SD y RP de facturación electrónica.

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

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.

*Sign-on bonus of $5,000 if hired for this position!

Your Role:

This diverse Manufacturing Operator 2 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. As a Manufacturing Operator 2 at MilliporeSigma, you will manufacture materials using existing production procedures and maintain a high level of safety and quality in the work environment. Additional responsibilities include:

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
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
Engage in personal and professional career development through active participation in development objectives
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 focus
Use a range of office, laboratory, and manufacturing equipment
Work near moving mechanical parts

Who you are:

Minimum Qualifications:

High School Diploma or GED
3+ years of experience in an industrial or manufacturing setting

Preferred Qualifications:

Prior industrial work experience or chemical handling
Understand chemical reactions and hazards
Understand ISO and quality systems
Mechanical and technical aptitude
Read and understand written protocols
Detail oriented and excellent multitasking ability
Strong problem solving and equipment troubleshooting skills
Excellent oral and written communication skills

Pay Range for this position: $21/hour - $37/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.

RSREMD

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

Manufacturing Operator 2 (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.

*Sign-on bonus of $5,000 if hired for this position!

Your Role:

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
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
Engage in personal and professional career development through active participation in development objectives
Shift/Hours: there are 3 shifts available:
- 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) - includes 12 hrs. of OT per pay period (every 2 weeks)
- 12-hour day shift, 6:00 AM - 6:30 PM - 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) - includes 12 hrs. of OT per pay period (every 2 weeks)
- 2nd shift - 2:00 PM - 10:30 PM, Mon - Fri

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 focus
Use a range of office, laboratory, and manufacturing equipment
Work near moving mechanical parts

Who you are:

Minimum Qualifications:

High School Diploma or GED
3+ years of experience in an industrial or manufacturing setting

Preferred Qualifications:

Prior industrial work experience or chemical handling
Understand chemical reactions and hazards
Understand ISO and quality systems
Mechanical and technical aptitude
Read and understand written protocols
Detail oriented and excellent multitasking ability
Strong problem solving and equipment troubleshooting skills
Excellent oral and written communication skills

RSREMD

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

客户主任-甲状腺-深圳 (Shenzhen, Guangdong, CN, 518010)

与我们携手施展你的超能力！

职位描述：

1. 制订有挑战性的和可行性的区域计划，并能成功地实施。

1）根据自己对所辖市场的了解, 制订区域计划和医院销售目标,活动计划和费用预算。

2）在工作中定期的回顾和修正行动计划, 以更高的达到销售目标。

3）计划和执行每天的拜访活动, 确保有效拜访时间符合公司的要求

4）建立和维护与临床医生和学术带头人的关系

5）定期拜访药剂科以保证良好的供货

6）组织GSA和其他销售和市场活动

7）如果有需要，应当协助销售经理处理经销商供货和医疗保险目录的申报

2. 发展和拓宽市场, 了解市场潜力和维护销售的持续稳定的增长

1）执行销售和市场策略并对执行后情况进行反馈

2）提供竞争对手,医疗保险目录和商业供货等信息

3. 工作态度端正，执行公司的行为要求，树立自身良好形象，维护公司品牌形象

1）体现公司的学术形象，掌握产品及相关知识并在每天的工作中运用。

2）掌握销售技巧和演讲技巧并运用到工作中。

3）工作积极努力,有责任感，保持衣冠整洁，对待客户礼貌周到

4. 报告和培训

1）按时和准确的提交各种报告和报表。

2）认真参加公司组织的各项培训和会议。

任职要求：

1. 医药及相关专业本科以上学历。

2. 熟练掌握产品知识，了解相关医学知识

3. 具备一定的市场分析和业务规划能力，具备较强的业务实施能力。

4. 有相关领域经验为佳

5. 具备RDPAC认证资格优先考虑

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！

Distribution Associate 2 - 2nd shift (Milwaukee, Wisconsin, US, 53209-3650)

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 Distribution Associate 2 – 2nd Shift role at MilliporeSigma in Milwaukee, WI plays a critical role in the fulfillment of customer orders through the activities of receiving, picking, packing, and shipping of life science materials. Job duties include:

Shift Hours: Monday – Friday, 12:00pm – 8:00pm including a 7% shift differential
Load and unload freight
Operate equipment to produce documents for workload
Locate, move, deliver, or return all materials to proper areas
Prepare materials for shipment
Accurately document all movement of materials
Audit inventory locations to maintain inventory and location accuracy
Verify chemicals, catalog number, lot number, special requests information, unit size and weights against order documentation found in packing instructions
Print and apply all required labels and markings to box to comply with hazardous materials regulations
Condense, straighten, and maintain warehouse areas
Work with team leads and supervisors to troubleshoot system issues
Report unsafe or potentially unsafe hazards to team leads or any member of management

Physical Attributes:

May involve standing for long periods of time, operating powered industrial equipment, and lifting up to 50 pounds unassisted

Who You Are

Minimum Qualifications:

High School Diploma or GED

Preferred Qualifications:

1+ years of fulfillment, customer service, or warehousing experience
Oral and written communication skills to interact with all levels of staff
Experience in a fast-paced environment and adjusting to changing priorities in the environment
Proficiency with computers, scanners, printers, and shipping equipment
Experience following good distribution practices (GDP), where applicable

RSREMD

Pay Range for this position: $19-$30/hour

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

Maintenance Technician 3 - 2nd or 3rd shift (Milwaukee, Wisconsin, US, 53209-3650)

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 Maintenance Technician 3 – 2nd or 3rd shift will maintain and install equipment, facilities, and utility systems. In addition, provide leadership, expertise, and training to other department members. Job duties include:

Shift hours: 2nd shift, Monday - Friday, 2:30pm – 10:50pm or 3rd shift, Monday – Friday, 10:30pm – 6:50am
Requires flexibility to work a variety of shifts (including nights, weekends, holidays, on-call, and call-in) and independently; requires availability for occasional work-related travel and a valid driver’s license.
Responsible for independently completing assigned work orders (P.M. tasks) upon successful completion of required training curriculum.
Performs corrective and preventive maintenance on equipment, facilities, and utility systems while proactively identifying and reporting unsafe work conditions, and strictly adhering to all safety rules and regulations.
Implements changes using the Management of Change Process and addresses deviations through Non-Conformance Reports, while consistently reading, writing clearly, understanding, and following work instructions, procedures, and drawings/schematics.
Troubleshoots, maintains, installs, and repairs electrical, HVAC, and mechanical issues, as well as instrumentation, equipment, and systems, while also assisting with process improvement initiatives and completing assigned miscellaneous duties and tasks.
Operates a variety of tools including hand tools, power tools, basic shop equipment (grinder, drill press, sand blaster, band saw), and material handling equipment (forklift/man lift), as well as hoists and rigging equipment for troubleshooting and repairing packaging machinery, and utilizes precision measuring, electrical testing, calibration, and recovery equipment.
Manages changes and non-conformances using the Management of Change (MOC) process and Non-Conformance Reports (NCR), references NEC and NFPA codes, and ensures meticulous updates to files and paperwork.
Skilled in reading gauges and units of measure, identifying repair parts, performing boiler water and cooling tower chemistry tests, conducting preventive and corrective maintenance on boilers, guiding contractors and technicians, utilizing precision measuring equipment, and understanding materials of construction and chemical compatibility.
Possesses leadership skills to direct contractors and technicians, demonstrates strong decision-making and problem-solving abilities through analysis and risk evaluation, and participates in department audits and collaborates with the engineering department.
Exemplary attendance and adherence to schedule

Physical Attributes:

Occasionally lift 50 pounds unassisted and additional weight with assistance
Walk long distances and be able to stay on your feet for eight hours
Regularly sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl for long periods of time
Use hands and feet to operate equipment
Regularly works near moving mechanical parts, outdoor weather conditions, and sources of electrical shock, vibrations, fumes, and airborne particles, toxic or caustic chemicals for which protective equipment and procedures must be used.
Workplace noise level is loud, occasionally very loud.
Occasionally wear hard hat, safety shoes, eye protection, hearing protection, protective gloves, respirator, and face shield
Close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus needed

Who You Are

Minimum Qualifications:

High School Diploma or GED
Valid driver’s license
3 + years of experience in HVAC, electrical/instrumentation, and/or mechanical (i.e., Boiler Operator’s)

Preferred Qualifications:

5 + years of experience in HVAC, electrical/instrumentation, and/or mechanical (i.e., Boiler Operator’s)
Excellent leadership, teamwork, and interpersonal skills
Strong oral and written communication skills
Self-motivation and high efficiency skills
Follows good documentation practices
Knowledgeable in the testing, operation, and repair of fire protection systems.
Proficiency with computers and experience with MS office and SAP
Excellent organizational skills and 5S skills and follows good documentation practices

RSREMD

Pay Range for this position: $30.00 - $53.00.

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

Distribution Associate 2 - AM 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:

The Distribution Associate 2 – AM Shift role at MilliporeSigma in Milwaukee, WI plays a critical role in the fulfillment of customer orders through the activities of receiving, picking, packing, and shipping of life science materials. Job duties include:

Shift Hours: Monday – Friday, 6:00am – 2:00pm
Load and unload freight
Operate equipment to produce documents for workload
Locate, move, deliver, or return all materials to proper areas
Prepare materials for shipment
Accurately document all movement of materials
Audit inventory locations to maintain inventory and location accuracy
Verify chemicals, catalog number, lot number, special requests information, unit size and weights against order documentation found in packing instructions
Print and apply all required labels and markings to box to comply with hazardous materials regulations
Condense, straighten, and maintain warehouse areas
Work with team leads and supervisors to troubleshoot system issues
Report unsafe or potentially unsafe hazards to team leads or any member of management

Physical Attributes:

May involve standing for long periods of time, operating powered industrial equipment, and lifting up to 50 pounds unassisted

Who You Are

Minimum Qualifications:

High School Diploma or GED

Preferred Qualifications:

1+ years of fulfillment, customer service, or warehousing experience
Oral and written communication skills to interact with all levels of staff
Experience in a fast-paced environment and adjusting to changing priorities in the environment
Proficiency with computers, scanners, printers, and shipping equipment
Experience following good distribution practices (GDP), where applicable

RSREMD

Pay Range for this position: $19-$30/hour

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

Distribution Associate 2 - Split 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:

The Distribution Associate 2 – Split Shift role at MilliporeSigma in Milwaukee, WI plays a critical role in the fulfillment of customer orders through the activities of receiving, picking, packing, and shipping of life science materials. Job duties include:

Shift Hours: Monday – Friday, 10:00am – 6:00pm
Load and unload freight
Operate equipment to produce documents for workload
Locate, move, deliver, or return all materials to proper areas
Prepare materials for shipment
Accurately document all movement of materials
Audit inventory locations to maintain inventory and location accuracy
Verify chemicals, catalog number, lot number, special requests information, unit size and weights against order documentation found in packing instructions
Print and apply all required labels and markings to box to comply with hazardous materials regulations
Condense, straighten, and maintain warehouse areas
Work with team leads and supervisors to troubleshoot system issues
Report unsafe or potentially unsafe hazards to team leads or any member of management

Physical Attributes:

May involve standing for long periods of time, operating powered industrial equipment, and lifting up to 50 pounds unassisted

Who You Are

Minimum Qualifications:

High School Diploma or GED

Preferred Qualifications:

1+ years of fulfillment, customer service, or warehousing experience
Oral and written communication skills to interact with all levels of staff
Experience in a fast-paced environment and adjusting to changing priorities in the environment
Proficiency with computers, scanners, printers, and shipping equipment
Experience following good distribution practices (GDP), where applicable

RSREMD

Pay Range for this position: $19-$30/hour

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

Head of Spin-On Dielectrics (SOD) R&D Thin Film / Electronics (Shizuoka, Shizuoka, JP, 437-1412)

メルクと一緒に、あなたの力を発揮しよう！

Head of Spin-On Dielectrics (SOD) R&D Thin Film

Your Role:

Technology and people leadership of Spin-On Dielectrics (SOD) R&D organization

Foster a Safety-First culture to ensure overall safety of SOD R&D facilities and team
Direct the development of new products that meet customer expectations
Partner with key stakeholders such as marketing, customer applications, and operations to understand customer needs and prioritize research activities
Drive focus on productivity, speed of execution and customer satisfaction through effective project management, budgeting and resourcing
Develop new strategic programs to build capabilities, including CAPEX planning
Develop strong collaboration with the Organosilane team to expand SOD polymer portfolio
Coach and develop managers and team leaders through regular dialog
Build and maintain strong Intellectual Property (IP) portfolio
Build a strong team by fostering an inclusive and psychologically safe environment and developing people to unleash their full potential
Represent Merck by displaying technical excellence externally and internally
Embrace and champion digital transformation

Impact & Complexity

Accountable for leading and developing a highly differentiated capability for Merck by developing new SOD polymers and applications for customers for thin films used in advanced electronic devices. Responsible for solving or directing the resolution of problems of unique complexity impacting the long-term advancement of the business by building and leading teams that apply advanced technical reasoning and practical judgment. Continued advancement is essential to maintain a technical leadership position in this business.

Internal Cooperation

Business Technology Director
Market Managers
Organosilane Synthesis Team
ALD and PECVD Applications Team
Scale up Organization
EH&S

External Cooperation

Customers
Suppliers
OEMs
Universities and research consortia

Who You Are:

Education

Master or PhD in Chemistry, Chemical engineering, Polymer Science or similar fields

Work Experience

Semiconductor experience required
Managerial experience in diverse roles and across regions
At least 5 years of R&D experience
New product development experience

Job specific Competencies & Skills

Strong knowledge of semiconductor technology (process/integration/equipment)
Demonstrated Leadership and Change Management skills
Proven ability to create and grow high performance teams
Innovation Management for growth
Ability to build trustful relationships and successfully navigate through a global matrix organization
Strong cross-functional collaboration and influencing skills
Proficiency in Japanese language strongly preferred

Job specific Competencies & 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！

Senior Specialist/Specialist_Product Management Operations (Bangalore, Karnataka, IN, 560100)

Work Your Magic 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.

Who You Are:

Minimum Requirements:

Postgraduate in Life Sciences (Biochemistry/Biotechnology/Microbiology) from a reputed University.
Experience: 5-9 Years in Scientific Industry

Preferred Requirements:

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.
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.
Project Management Support – supporting the PMO (creating dashboards, collecting all needed data, setting up meetings, sending reminder, etc)
Create and maintain appropriate documents and tracking systems for existing products update (i.e., product numbers, technical bulletins/product information sheet review, certificate of analysis, certificate of origin, specification review, create product listing on the website)
Generate Sales reports needed by Marketing representative, and other routine sales reports.
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 customer's 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 activity to support
Lead process improvement projects and support team with necessary trainings on Process Improvement.

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

Senior Specialist - Labvantage (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Your Role:

Good knowledge on the Labvantage databases.
Work on the backlogs, fixing the bugs, and working on the change requests.
Work experience on the labvantage Migration and upgrade projects.
Very good technical understanding and hands on experience with software development projects.
Proficient in usage of processes such as change control, version control, release management, service management and the related tools like JIRA, HPSM, GEAR, source code repositories.

Who you are:

Candidate should hold a Bachelor's degree in a computer system, engineer or Technical graduation.
6+ years of working experience in labvantage LIMS, Web Services (REST & SOAP),
Proficient in all technical aspects of Interfaces development (SAP), LIMSCI, preferably Instrument interfaces.

Labware skills are an added advantage
Excellent knowledge of GMP in the context of electronic systems.
Experience in international manufacturing environment, ideally in the Healthcare and Lifescience industry

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

SAP Security Expert / Service Delivery Manager Security Bridge (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

We are seeking a highly experienced Senior Security Expert / Service Delivery Manager with over 15 years of expertise in SAP system administration, security management, and Basis operations. This dual role is pivotal in leading security initiatives and managing the delivery of SAP services to ensure optimal performance and compliance with organizational standards.

Key Responsibilities:

Security Management:

Lead the implementation and management of Security Bridge tools to enhance security protocols and protect SAP environments from vulnerabilities.
Configure and customize Security Bridge tools to monitor SAP systems for compliance with security policies and standards.
Conduct comprehensive security assessments and audits using Security Bridge to identify risks and recommend appropriate mitigation strategies.
Analyze security logs and reports generated by Security Bridge to detect and respond to potential security incidents.
Design and enforce robust user access controls and authorization protocols, ensuring compliance with regulatory standards and internal policies.

Service Delivery Management:

Ensure consistent implementation of the service management framework, including business annual service reviews, Service Level Agreements (SLAs) sign-off, KPI definition, and service performance reporting.
Collaborate with cross-functional teams to integrate security measures into SAP applications and ensure adherence to best practices.
Develop and maintain security documentation, including policies, procedures, and incident response plans.
Oversee the administration and maintenance of SAP systems, ensuring seamless operation and minimal downtime through effective service delivery management.

Operational Vendor Management:

Report vendor service performance against established processes and identify improvement plans based on gaps and defined requirements.
Secure timely issuance of periodic performance reports and conduct annual service reviews.

Incident and Problem Management:

Ensure service management reporting aligns with the service catalog and stakeholder/business requirements, focusing on availability, effectiveness, and efficiency of ticket handling.
Manage disaster recovery plans and coordinate DR tests to ensure business continuity.
Support the optimization and harmonization of the service management framework.

Skills and Competencies:

Extensive knowledge of SAP technologies, including NetWeaver, HANA, and BTP.
Proficiency in managing Security Bridge tools and integrating them within SAP environments.
Strong analytical and troubleshooting skills to address complex system issues effectively.
Excellent communication and interpersonal skills, with the ability to collaborate across teams and departments.
Strong project management skills, capable of managing multiple priorities and meeting tight deadlines.
Experience in change and incident management processes, with a solid understanding of application security best practices.

Education and Qualifications:

Bachelor’s or master’s degree in information systems, engineering, computer science, or a related field.
Relevant SAP certifications (e.g., SAP Certified Technology Associate) are highly desirable.
Ability to work both independently and as part of a team.
Exceptional interpersonal and communication skills, including verbal, written, presentation, and listening abilities.

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

HR SuccessFactors PMGM & Compensation Expert (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

Your Role

You will work as HR SuccessFactors PMGM & Compensation Expert within our Technology Center in Bangalore. You will be responsible to develop or customize solutions as an individual contributor. You possess deep skills and experience in the PMP and CRC IT solutions. You will create state of the art technical specifications or configuration documents, translate solution design into software code or enhanced configuration. In fact, you will engineer, develop, maintain, test and improve the related code and solution. A key success factor for your integration will be your outstanding verbal and written communication skills, in daily use with the change requestors. Thanks to your deep understanding of the HR Performance & Compensation domain, you can understand business requirements, you have the capacity to transpose requirements into adequate solutions on time, on quality and on cost. From a technical perspective, we expect the ability to generate and maintain the needed documentation with outstanding quality in use across various SDLC methodologies (Agile, SCRUM, and others). You are a diligent, hardworking individual who is able to learn new systems and processes rapidly, can collaborate with virtual teams, and having a proven track record of delivering exceptional outcome for the Business.

Who You Are:

Bachelor/master’s degree in IT, computer sciences or business with additional qualifications in technology
5+ years of experience in HR SuccessFactors with latest 3+ years of implementation experience in SuccessFactors Compensation & Performance modules
Proven knowledge and expertise in practical application of SAP SuccessFactors through multiple implementations of Compensation & Variable Pay modules
Good hands on in the SAP SuccessFactors Employee Central Performance & Objective modules with latest templates..
Knowledge of SuccessFactors best practices, coding standards and governance
Excellent knowledge of implementation methodologies (e.g. Agile, SCRUM)
Knowledge of SuccessFactors administration, release management, and deployment expertise across various tools
Ability to analyze complex systems as well as troubleshoot and isolate system issues
Relevant certification of SAP SuccessFactors PMP and CRC
Fluent in English

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

Specialist (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

Manage credit and collection tasks for a portfolio valued at $15-$30 million, involving 300+ customers and making 25+ calls per day.
Contact customers to request payment for overdue balances and identify reasons for payment delays.
Review customer status in the accounting system and interact with various departments to resolve queries.
Responsible for collecting receivables and resolving disputes and claims.
Ensure delivery of service levels and meet SLA/KPI targets for the accounting function.
Analyze customer payment trends to forecast collections for the fiscal month.
Organize and participate in credit control, distribution center, sales, and customer meetings.
Oversee cash application, manage overpayments, and deduction management (both allowable and preventable).

Who You are

Bachelor’s degree in any field, preferably accounting.
2 to 6+ years of credit and collection experience in a corporate environment.
Strong knowledge of accounting principles and experience with SAP navigation in accounts receivable functions.
Excellent oral and written communication skills, with the ability to engage effectively with customers and stakeholders.
Good interpersonal skills coupled with basic problem-solving abilities and understanding of planning and execution processes.
Demonstrates business acumen, willingness to lead change, and ability to foster high performance in self and team.

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 those impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Head of IT Supply Chain Planning (Bangalore, Karnataka, IN, 560100)

Work Your Magic with us!

As Head of IT Supply Chain Planning, you will lead a global team and manage a complex SAP ERP and APO landscape spanning SAP R/3, ECC, S/4 and SAP APO (DP/SNP/PPDS), with expansion to SAP IBP. You will ensure robust day-to-day operations while delivering changes and aligning with transformative programs across our ERP and APS landscapes.

Key Responsibilities

Align operational and program objectives across Supply Chain functional environments, ensuring quality, consistency and continuous improvement.
Maintain operational applications to a high degree of availability, performance, quality, and compliance. Mitigate risk by demonstrating change control, release, and incident/problem management.
Lead root cause analysis across operational environments to identify underlying issues and drive structured, measurable and scalable solutions.
Manage and improve services with third party support organizations; set and monitor SLAs ensuring solution fixes are aligned to organisational objectives. ‑party support organizations; set and monitor SLAs ensuring
Collaborate across IT and the business to prioritise and implement key design decisions, utilising change control processes, and deployment approaches across operational ERP and APO landscapes.
Orchestrate delivery across complex project portfolios and operational run activities, integrating with adjacent domains (manufacturing, logistics, order management, master data).
Engage and align diverse business and IT stakeholder communities (Business Process Owners, Process Experts, Data Experts, Supply Chain Operations) to ensure value realization.
Act as a self-starter highlighting areas for improvement; evaluate and introduce new technologies (e.g., modern planning capabilities, data/analytics, automation) to enhance outcomes. ‑starter highlighting areas for improvement; evaluate and introduce new technologies (e.g., modern planning capabilities, data/analytics, automation) to enhance outcomes.
Build and develop a high performing team across SAP S/4 and SAP APO, providing inputs to budgeting, program planning, landscape maintenance, refreshes and resource planning.‑performing team
Transition our SAP APO support capability to SAP IBP in line with future programs.

Qualifications

Bachelor’s degree in Computer Science, Engineering, Business, or related field; masters degree preferred.
10+ years leading IT for supply chain planning within operational and project environments from an industry capability or consulting background – preferably from a Life Science background.
Proven experience of implementing change across complex ERP/APS landscapes (SAP ECC, S/4, APO) for supply chain functionalities; exposure to SAP IBP beneficial.
Proven operational leadership of mission critical applications with strong ITIL disciplines; expert in root cause analysis. ‑critical applications with strong ITIL disciplines; expert in root cause analysis.
Experience managing third‑party providers and complex multi‑vendor environments with contractual and performance frameworks.
Demonstrated success across complex operational and project IT landscapes; excellent stakeholder engagement and communication skills in global settings.
Self‑starter with a track record of identifying opportunities and delivering technology‑driven enhancements.

This role sits within Life Science DDIT and partners closely with business leadership to deliver reliable operations and meaningful transformation in supply chain planning.

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

Senior Specialist-Qualification Owner (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 the design and implementation of document management infrastructure solutions aligned with company’s digital strategy.
Provide expert consultation on infrastructure setup for on-premises and cloud-based document management systems.
Ensure adherence to GDP, GxP, and other relevant regulatory requirements for all document management infrastructure.
Assess and recommend appropriate hosting models and infrastructure solutions for document management applications.
Develop and maintain comprehensive technical documentation for infrastructure configurations.
Collaborate with IT, Quality, Regulatory, and business stakeholders to align document management infrastructure with business needs.
Demonstrate strong technical leadership by guiding teams and providing direction on infrastructure matters while effectively communicating complex technical concepts to various stakeholders.
Possess excellent problem-solving abilities, manage infrastructure projects from conception to implementation, and lead changes with minimal disruption to the business.

Who You Are

Bachelor’s degree in computer science, Information Technology, or a related technical field, along with a minimum of 10 years of experience in IT infrastructure management
Industry Knowledge: Experience in IT, pharmaceutical, life sciences, or regulated industries preferred

Infrastructure Expertise: Experience with on-premises infrastructure setup, cloud infrastructure deployment (AWS, Azure, GCP), hybrid cloud architecture, and Infrastructure as Code (IaC) principles.
Document Management Systems: Experience implementing and supporting enterprise document management solutions.
Virtualization: Experience with virtualization technologies and containerization (VMware, Docker, Kubernetes).
Candidates should possess knowledge of infrastructure security best practices and compliance requirements, along with a strong understanding of network architecture to ensure secure document management systems.
Understanding of GxP and GDP principles, along with regulatory requirements for document management systems, and possess expertise in implementing infrastructure that supports these compliance standards effectively.

Validation: Experience with computer system validation in regulated environments.
Risk Management: Ability to assess and mitigate infrastructure-related risks in compliance with regulatory requirements.

Preferred Certifications

ITIL certification.
Regulatory compliance certifications relevant to the pharmaceutical industry.

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 those impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Senior Specialist-Qualification Owner (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

Lead the design and implementation of document management infrastructure solutions aligned with company’s digital strategy.
Provide expert consultation on infrastructure setup for on-premises and cloud-based document management systems.
Ensure adherence to GDP, GxP, and other relevant regulatory requirements for all document management infrastructure.
Assess and recommend appropriate hosting models and infrastructure solutions for document management applications.
Develop and maintain comprehensive technical documentation for infrastructure configurations.
Collaborate with IT, Quality, Regulatory, and business stakeholders to align document management infrastructure with business needs.
Demonstrate strong technical leadership by guiding teams and providing direction on infrastructure matters while effectively communicating complex technical concepts to various stakeholders.
Possess excellent problem-solving abilities, manage infrastructure projects from conception to implementation, and lead changes with minimal disruption to the business.

Who You Are

Bachelor’s degree in computer science, Information Technology, or a related technical field, along with a minimum of 10 years of experience in IT infrastructure managementIndustry Knowledge: Experience in IT, pharmaceutical, life sciences, or regulated industries preferred.

Infrastructure Expertise: Experience with on-premises infrastructure setup, cloud infrastructure deployment (AWS, Azure, GCP), hybrid cloud architecture, and Infrastructure as Code (IaC) principles.
Document Management Systems: Experience implementing and supporting enterprise document management solutions.
Virtualization: Experience with virtualization technologies and containerization (VMware, Docker, Kubernetes).
Candidates should possess knowledge of infrastructure security best practices and compliance requirements, along with a strong understanding of network architecture to ensure secure document management systems.
Understanding of GxP and GDP principles, along with regulatory requirements for document management systems, and possess expertise in implementing infrastructure that supports these compliance standards effectively.

Validation: Experience with computer system validation in regulated environments.
Risk Management: Ability to assess and mitigate infrastructure-related risks in compliance with regulatory requirements.

Preferred Certifications

ITIL certification.
Regulatory compliance certifications relevant to the pharmaceutical industry.

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 those impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

Project Manager Electronic Quality Syste (Bangalore, Karnataka, IN, 560100)

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Your Role

Are you ready to lead the optimization and management of Veeva systems across our organization? We are seeking a dynamic and empowered leader to oversee our international team responsible for Veeva processes. In this pivotal role, you will define and implement our strategy for Veeva systems, driving compliance and innovation in our processes.
You will play a crucial role in the corporate eQMS Veeva Falcon, providing insightful reporting on process performance, KPIs, and compliance levels. Your expertise will help shape our approach to quality and ensure we meet the highest industry standards.
We are looking for a critical thinker who is not afraid of negotiation and alignment with business stakeholders. You will challenge the status quo and engage confidently with senior management, navigating organizational hierarchies effectively. Your proactive approach and motivation will be essential in driving continuous improvement initiatives and benchmarking best practices.
If you are passionate about process optimization and harmonization and want to make a significant impact in a dynamic environment, we invite you to apply.

Who You Are:

Education: Academic degree in relevant disciplines (Pharmacy, Chemistry, Engineering, Information Technologies, or related fields).
Experience: Strong knowledge of Veeva systems and related processes plus strong background in Process Ownership, IT Project- Management and Release Management (5-9 years experience)
Regulatory Knowledge: Excellent understanding of regulatory requirements for computerized systems and validation (e.g., GxP, FDA regulations).
Negotiation Skills: Proven ability to negotiate and align with diverse business stakeholders.
Critical Thinking: Exceptional critical thinking and problem-solving skills, with a willingness to challenge existing processes.
Interpersonal Skills: Excellent communication skills, with the ability to engage effectively with senior management and cross-functional teams- with empathy & emotional intelligence
Motivated: A self-starter who thrives in a fast-paced environment and is empowered to drive change.

Why Join Us?

Be part of a forward-thinking organization committed to innovation and quality.
Collaborate with a diverse team of professionals dedicated to excellence.
Drive impactful changes in a global context.

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

User Access Management Specialist (Bangalore, Karnataka, IN, 560100)

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Help safeguard data integrity and inspection readiness across our clinical systems. As User Access Management Specialist in R&D – Global Development Operations (GDO) – Clinical & Digital Innovation & Applications (CDIA), you’ll build and maintain the access model that underpins compliant, high-quality clinical trial operations.

Your role:

In this role, you’ll take end-to-end ownership of access management. You will develop and maintain a comprehensive, well-documented access model across our clinical systems, perform regular reconciliations to identify and resolve inconsistencies, and keep policies and procedures current with internal standards and regulatory expectations. You’ll partner closely with IT service management teams—providing clear role-assignment references and timely updates—while putting in place the controls and documentation that keep our systems audit‑ and inspection‑ready. At every step, you’ll collaborate with stakeholders to align access processes with the realities of clinical operations, so teams can move quickly and confidently. You’ll collaborate across R&D and GDO, DDIT R&D, data office teams, CRO partners, and other vendors to drive best practices and measurable improvements in clinical operations.

By championing best practices and strong oversight mechanisms, you’ll help teams track progress against milestones and embed quality‑by‑design principles, driving measurable improvements and a culture of continuous learning in clinical operations.

Who you are:

You bring a solid foundation—typically a bachelor’s degree in Life Sciences, Information Technology, or a related field—paired with experience in access management or adjacent domains, ideally within pharma or clinical research. You may have 5–7 years in drug development or access management in the pharmaceutical industry, and you understand how access controls protect data integrity and compliance in clinical trials. Analytical by nature, you spot discrepancies quickly and propose practical solutions. Communication is your strength: you collaborate confidently with stakeholders and provide clear, actionable reporting on access activities.

You’re also customer‑oriented and outcomes‑focused, with experience meeting stakeholder expectations. You understand data management principles—from acquisition through processing—and you’re comfortable with metrics and KPIs. Experience in data‑driven initiatives, and familiarity with data strategy and governance in pharma, are advantages. You balance project management with cross‑functional influence, managing multiple workstreams while navigating complex stakeholder dynamics with emotional intelligence. A learning mindset, strong critical thinking, and stakeholder management skills help you adapt and lead in a fast‑moving environment. Familiarity with operational data, applications, and systems used in pharma, plus attention to detail and proficiency with access tools, rounds out your profile.

If you’re ready to shape the access foundations of clinical development—enabling inspection readiness and empowering teams to deliver with confidence—we’d love to hear from you.

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

Associate Architect -SAP BW (Bangalore, Karnataka, IN, 560100)

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Your Role :

Design and develop SAP BW data models, including InfoProviders, DSOs, and cubes, to meet business requirements.
Lead the implementation of SAP Analytics Cloud (SAC) solutions for planning, reporting, and visualization.Optimize SAP BW Extractors (standard and custom) and ensure efficient data integration.
Collaborate with stakeholders to gather requirements and deliver scalable data solutions.
Develop SAC dashboards, planning models, and input-enabled stories.Integrate SAC with SAP BW/4HANA, S/4HANA, and other systems.
Utilize SAC predictive analytics and advanced formulas to provide actionable insights.

Who you are:

Qualifications:6–9 years of experience in SAP BW and SAC, with hands-on expertise in SAC planning and reporting.
Proficiency in SAP BW on HANA, SAP BW/4HANA, and ABAP debugging.Strong knowledge of SAC connectivity, data modeling, and integration with SAP systems.
Experience in planning, budgeting, and forecasting processes.Familiarity with SAC predictive and augmented analytics features.

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

ServiceNow Demand Manager (Bangalore, Karnataka, IN, 560100)

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ServiceNow Demand Manager is responsible for managing the demand intake process, progressing the backlog, and ensuring effective communication and coordination across various stakeholders. This role involves prioritizing demands, conducting feasibility checks, estimating costs, and facilitating approval processes. The Demand Manager will work closely with the application development team and the release manager to ensure timely delivery of services and features.

Key Responsibilities:

- Oversee the demand intake process to ensure all requests are captured accurately and efficiently.
- Serve as the primary point of contact for demand-related inquiries.
- Own the demand intake form in ServiceNow
- Continuously maintain and enhance the process documentation through regular reviews and timely updates to ensure accuracy and relevance
- Conduct feasibility checks to assess the viability of demands and align them with organizational goals.
- Ensure the demand is assessed with the potential business value in terms of efficiency, cost/FTE savings etc.,
- Coordinate with stakeholders to prioritize demands based on business value and urgency.
- Work with development teams and BA’s to estimate costs associated with demands.
- Communicate approval statuses and required actions to stakeholders promptly.
- Lead the collaboration with the application development team and BA’s to ensure clarity on requirements and timelines.
- Monitor development progress and address any issues that arise during the process.
- Align with the release manager on release timelines and communicate these timelines to requesters.
- Ensure that all stakeholders are informed of changes in release schedules or priorities.

Qualifications:

- Bachelor’s degree in Computer Science, Information Technology, or a related field.
- A minimum of 8 years of comprehensive IT experience, including over 2 years of specialized expertise in ServiceNow
- Proven experience in demand management, project management, or a similar role.
- Strong understanding of ServiceNow platform and its functionalities.
- Excellent communication and interpersonal skills.
- Ability to work collaboratively in a team environment and manage multiple priorities.
- Familiarity with Agile methodologies is a plus.
- ServiceNow CSA certification is a plus

Skills:

- Strong analytical and problem-solving skills.
- ServiceNow platform technical/functional skills
- Ability to communicate complex technical information to non-technical stakeholders.
- Strong organizational skills and attention to detail.

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

Sr Manager-Tech Transfer (Bangalore, Karnataka, IN, 560100)

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Your Role:

Responsible for new products transferring, technical improvement such as site expansion project management, SU new products transferring in, Hazard analysis of new product, material localization, new process & equipment design, installation, validation & qualification, technical improvement to support site business growth and new products commercial launch.

Be in charge of new project management to ensure project meets each milestone on time with high quality and project cost within budget.
Be responsible for new product technical related such as readiness of Drawing / BOM / TP, SOP / work instruction development, manufacturing data in SAP system, new products design and validation, employee technical training & qualification, etc.
Timely Technical Transfer of down filling, manufacturing technology from other global plants to support meeting production & customer demand.
Initiate continuous improvement projects to drive cost saving, quality improvement such as new equipment development, current process / equipment upgrading, automation, etc.
Responsible for assuring compliances to all regulatory requirements no matter for project phase new products transferring in or new process / equipment development - ISO, EHS, etc.
Work with PSM & quality team for raw material localization, key supplier development & maintain relationship to improve material quality standard, reduce cost & delivery lead time.
As project contact window, ensure good communication within site function team, giving site, commercial and other supporting function.
Evaluate CAPEX required and interaction with E&T team and OEM.
Support plant - wide strategic plan programs and activities.
Other assigned tasks which are required by site leader.
Organizing cross functional meeting with Global team to have smooth product transfer taking all taxation/regulatory /statutory /Change Management compliances into consideration.

Who You Are:

Requires a B.E/M. Tech. or equivalent, preferably in Chemical /Mechanical engineering, 10-12 years ' experience in technical or manufacturing process in pharmaceutical, biotechnology/Chemical -Fine/specialty/API or comparable environment.
Technical & Professional Knowledge:

Rich experience in new products transferring in, project management, process technical improvement, material localization, Process equipment Design etc.
Good communication and interpersonal skill
Lean six sigma knowledge & experience, continuous improvement mindset.
GMP and product design knowledge

Senior Expert-Pharmacovigilance IT Systems Specialist (Bangalore, Karnataka, IN, 560100)

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Job Title: Pharmacovigilance IT Systems Specialist

Your Role:

As a Pharmacovigilance IT Systems Specialist, you will be tasked with supporting, maintaining, and enhancing the pharmacovigilance system to ensure adherence to regulatory standards. You will take the lead in implementing and continuously improving safety databases, ensuring data integrity and compliance with regulations. Collaboration with cross-functional teams will be essential as you integrate new technologies and processes. Additionally, you will act as a primary point of contact for system users and technical teams, owning the entire lifecycle of system changes. This role is pivotal in shaping and optimizing safety database configurations, ensuring they are strategically aligned with evolving business needs and future growth.

The role will be based in Bangalore, India, and reporting to Team Lead, Pharmacovigilance Services.

Who You Are:

A university degree in information technology or equivalent.
Over 10 years of experience with drug safety database systems in the pharmaceutical industry, healthcare organizations, or software application vendors.
In-depth knowledge of LSMV and pharmacovigilance systems, along with drug safety regulatory requirements (ICH, GVP, FDA CFR Part 11, GxP).
Strong understanding of software validation processes and methodologies (GAMP).
Proven experience in IT project management, service delivery, or vendor management is advantageous.
Exceptional organizational skills with the ability to prioritize tasks and quickly adapt to shifting priorities.
A collaborative team player who considers the broader goals beyond individual targets.
Excellent written and verbal communication skills in English.
Strong interpersonal skills in an international setting.

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

Senior Manager - Master data (Bangalore, Karnataka, IN, 560100)

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The Senior Manager - Master Data will lead the strategy, development, and management of master data processes related to material and customer data. This position entails ensuring data integrity, compliance, and governance throughout the organization. The ideal candidate will work collaboratively with cross-functional teams to enhance data quality and support business objectives while managing stakeholder relationships, guiding teams, and demonstrating strong leadership.

This role is located in Bangalore, India.

Your Role

Master Data Management:

Oversee the creation, maintenance, and governance of material and customer master data.
Develop and implement policies and procedures for master data management.
Ensure data accuracy and consistency across various systems.

Data Governance:

Establish and enforce data governance frameworks and standards.
Collaborate with IT and business units to ensure adherence with data policies.

Process Improvement:

Identify opportunities for process enhancements and automation in master data management.
Lead projects aimed at improving data quality and operational efficiency.

Cross-Functional Collaboration:

Work closely with various functional departments to align master data with business requirements.
Facilitate training and provide support for teams on master data processes and tools.

Stakeholder Management:

Build and maintain strong relationships with key stakeholders across the organization.
Effectively communicate master data strategies and initiatives to stakeholders at all levels.

Team Management and Leadership:

Lead and mentor a team of data management professionals, fostering a collaborative and high-performance culture.
Drive team development, provide performance feedback, and create professional growth opportunities.

Who You Are:

Master’s / Bachelor’s degree in Business Administration, Data Management, or a related field
13-15 years of experience in business, master data management, data governance, or related areas.
Proven experience in managing material and customer master data processes.
Strong understanding of data management best practices and tools.
Good knowledge in SAP ERP systems, Ariba, and other relevant tools.
Excellent analytical skills with a focus on data quality and integrity.
Strong leadership and project management skills.
Excellent communication and interpersonal skills.

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

Senior DevOps Engineer (Bangalore, Karnataka, IN, 560100)

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Your Role:

As a Senior IT Systems & DevOps Engineer, you will be responsible for IT systems, incident, change, and release management. You will ensure the seamless deployment of new releases, maintaining system stability, security, and compliance in a regulated environment. You will collaborate with cross-functional teams, manage stakeholder communications, and drive automation and optimization across cloud-based platforms supporting drug discovery and development.

Key Responsibilities:

Oversee incident, change, and release management for IT systems, ensuring compliance with regulatory standards.
Manage Azure AD for identity and access management, including authentication flows for internal and third-party services.
Implement and advocate DevOps best practices, including CI/CD, automation, and observability across platforms.
Collaborate with cross-functional teams to influence architectural decisions and align infrastructure with business goals.
Ensure compliance and security within a regulated (GxP) environment, implementing RBAC, secrets management, and monitoring frameworks.
Design, develop, test, and document business requirements related to IT systems and infrastructure.
Coordinate and perform system management tasks, ensuring alignment with quality and compliance standards.
Autonomous review and clarification of business requirements, creation of technical designs, and stakeholder alignment.
Manage and optimize cloud infrastructure (AWS & Azure), including cost management and performance tuning.
Deploy and manage containerized applications using Docker, Kubernetes, Helm, and ArgoCD (GitOps).
Implement Infrastructure as Code (IaC) using Terraform and AWS CloudFormation.
Automate workflow and integration using Python and configuration management tools like Ansible.
Ensure observability, including logging, monitoring, and tracing with tools like Prometheus, Grafana, ELK Stack, and AWS-native solutions.
Participate in compliance activities, including audits, patch management, and cybersecurity initiatives.
Provide technical guidance and support for IT systems, assisting users and resolving incidents efficiently.

Your Skills & Experience:

Must-Have:

8+ years of experience in IT systems management, DevOps, cloud infrastructure, and automation.
Strong expertise in Change, Release, Incident, and Problem Management.
Hands-on experience with Azure DevOps (project configurations, repositories, pipelines, environments).
Strong knowledge of AWS services (VPC, IAM, STS, EKS, RDS, EC2, ECS, Route53, CloudWatch, CloudTrail, Secrets Manager, S3, API Gateway, Lambda, MWAA).
Experience with Linux, Windows servers, and Oracle PLSQL.
Strong understanding of IT landscapes and a willingness to work on diverse IT systems.
Hands-on experience with containerization and Kubernetes (Docker, Helm, ArgoCD).
Proficiency in Python scripting for automation and workflow integration.
Experience with Infrastructure as Code (IaC) using Terraform and AWS CloudFormation.
Strong experience in observability, security, and compliance frameworks, including RBAC, secrets management, and monitoring tools.
Global stakeholder management experience with excellent English communication skills (written & oral).

Good to Have:

Experience in a regulated industry (GxP, Pharma, Life Sciences).
Familiarity with Agile ways of working.
Knowledge of Next.js, Storybook, Tailwind, TypeScript for front-end development.
Experience with PostgreSQL, OpenSearch/Elasticsearch for data management.
Familiarity with R and SAS for data analysis and statistical modeling.
Understanding of AWS billing practices and cost optimization tools.

Why Join Us?

Work in a high-impact role contributing to cutting-edge R&D in drug discovery and development.
Be part of a multicultural, agile team with high autonomy in decision-making.
Exposure to a diverse tech stack combining Azure, AWS, Kubernetes, Python, and CI/CD tools.
Opportunities for career growth and skill development in cloud computing, security, and automation.
Work in a collaborative and innovative environment with global teams in the US, Europe, and India.

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

Cloud Solutions Architect /Senior Cloud Platform Engineer (Bangalore, Karnataka, IN, 560100)

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Your Role:

Who You Are:

A university degree in Computer Science, Engineering, or a related field.
Exceptional problem-solving skills.
With 5 plus years of relevant experience.
You are a proficient software engineer who knows the fundamentals of computer science and you master the Python programming language.
A proven track record of building and delivering secure, scalable, and resilient cloud-native systems using AWS services at an enterprise level.
Fluency in English with excellent communication skills.
Eager to learn and collaborate in a multinational environment, working with cross-functional teams across the US, Europe (primarily Germany), and India.
A strong business facing skills with a sense of accountability and ownership, with a capacity for rapid learning.

Key Technical Skills and Experience:

Programming Skills: In-depth experience in Python, relational databases, SQL, and a background in object oriented programming languages such as Scala, C#, or Java is advantageous
Services : Knowledge of distributed services, RESTful APIs and microservices built on AWS, with experience in AWS Lambda (using the boto3 library) and serverless design.
Cloud Skills: Experience working with high volume heterogenous data and preferably distributed systems like Spark, building cloud-native systems using AWS services at an enterprise level with a learning mindset.
Best Practices: Knowledge of Object Oriented Programming (OOP) and design patterns and excellent code and technical documentation as well as experience with code review.
CI/CD & Automation: Understanding of CI/CD pipelines, with experience in building and deploying CI/CD pipelines (preferably using Azure DevOps).
Data Governance: Knowledge about data governance, data access and data storage techniques
Testing Framework: Experience in testing framework
Security: Familiarity with AWS security best practices (MFA, encryption, user roles & policies).

Nice to Have:

Containerization: Experience in building and deploying container services (Docker, Kubernetes, AWS Fargate).
Data Tools: Experience with Iceberg and Snowflake.
Familiarity with Terraform, CloudFormation, or CDK for infrastructure automation.
Knowledge of NoSQL databases.

Packing Executive (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:

Co-ordinate with planning team and plan the day PO’s in 1-2 advance and hand-over the list for staging and other activities.
Weigh hazardous and non-hazardous chemicals accurately using precision equipment into specific containers.
Verify hood and safety equipment function, obtain weigh up, verify electronic balance is calibrated and maintain the necessary records.
Verify match of weigh up and bulk container lot numbers.
Obtain correct type and quantity of containers for weigh up. Weigh chemicals into containers according to packaging instructions and obtain weight checks.

Who you are:

Education: Any graduation degree
Experience: 6month to 2 years’ experience in packaging from a pharma or biochemistry background
Aware of the hazards of the chemicals and PPE requirements and safe handling and disposing methods. Basic math skills including the metric system.
Handling of semi-automated equipment.
Eye-hand coordination. Small/large tool dexterity

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!

D&A Domain Architect - Snowflake (Bangalore, Karnataka, IN, 560100)

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As a partner of company's Enabling Functions (EF), we the Enabling Functions Data and AI Organization explore, design, and deliver data, analytics, and AI solutions. With that, we are digitizing the company from the core by supporting the digital transformation for 15+ diverse Enabling Functions, including Finance, HR, Procurement, Legal, and more.

Your Role:

In this position, you will lead the design of cloud-native data & analytics solutions utilizing Snowflake, Palantir Foundry, and AWS, while guiding lighthouse implementations. A key focus will be on our strategic finance transformation Program, ‘Lumina’, where you will define the target architectural vision and govern the future implementation of the Finance Data Warehouse on Snowflake and it’s integration into our Analytics Ecosystem.

This role requires a collaboration with various teams to ensure that product architectures are scalable, secure, and aligned with the overall technology strategy. The architect plays a critical role in establishing best practices and standards that guide product development and ensure consistent quality across the EF Data, Analytics and AI portfolio.
You will contribute to the success by guiding and consulting development teams and stakeholders in selecting and implementing suitable technology solutions. Monitoring the architecture-related metrics and KPIs will ensure a continuous improvement.
Engaging actively in both internal and external people networks will be essential for sharing knowledge, mentoring colleagues, and building capabilities across the organization.
Your responsibilities will also include technology scouting, supporting of vendor RFPs, and hosting knowledge sharing sessions. An exciting aspect of this role will be representing the team and the company at various internal and external events.
You will support our Group Data Strategy, focusing on data democratization, governance, and fostering a data driven and product centric culture that empowers self-service analytics.

Who you are:

University degree preferably in Information Technology, Computer Science, Finance, Business Administration, or a related field.
5+ years experience in data engineering, application design, analytics, and visualization within a global organization.
Experience with Finance core business processes will be a must.
Strong technical skills in systems architecture, cloud computing, cybersecurity, and data management.
Proven technical leadership experience in agile software development, including leading and mentoring engineering teams.
Highly engaged expert with in-depth knowledge in Snowflake and ideally in AWS, Palantir Foundry, or SAP Business Data Warehouse / Cloud. Knowledge in Data Science is a plus.
Proficiency in ETL processes, Spark, Kafka, and Python for distributed computation (preferably PySpark).
Familiarity with SQL, R, REST APIs and basic design/visual competencies.
Ability to work both individually and collaboratively in global matrixed product teams.
Ability in establishing software engineering best practices including DevOps methodologies.
Up-to-date with digital trends and emerging technologies.
Strong ability to facilitate discussions and build consensus by simplify complex topics and creating clear, impactful messages and storylines for both, experts and non-experts
Excellent communication and presentation skills in English; knowledge of German is a plus

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

Senior Expert - Scientific Writer_Med Comm (Bangalore, Karnataka, IN, 560039)

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Expert/Senior Expert Scientific Writer:

The Global Scientific Communications Content Hub is a growing, high performing, collaborative team responsible for developing medical communications, medical education and medical information content in close collaboration with a range of teams across Healthcare. The team is based in Global Healthcare's multi-disciplinary R&D (Research & Development) Hub in Bengaluru and working together across our global medical units (Oncology, Rare Tumours, N&I, Fertility, CM&E and Global Health).

We are seeking experienced, passionate scientific writing professionals who would like to develop their career and contribute to the continued growth of our operations.

Your Role:

Working both independently and alongside other team members to develop medical content for a range of project types, audiences and writing styles including, but not limited to, medical communication content (including publications and congress materials) and medical education content
Actively contribute to improvement initiatives across the Global Scientific Communications Content Hub
Lead development of medium to high complexity content (and review the same produced by others)
Review (QA) the output of less senior writers (including scientific accuracy, tone and alignment with agreed strategic
messaging)
Lead concept and content development meetings with authors and other stakeholders.
Lead representative/SMEs for the assets/functional areas they are assigned on; develop programs to increase the depth of understanding of more junior writers
Maintain good relationship with stakeholders (e.g. within MUs)
Ensures personal efficiency and productivity targets are met
Manages and prioritizes workload to meet internal deadlines
Ensures status reporting of projects is clear

You will have:

5-8 years professional experience in medical communications/medical affairs/clinical research in an international Pharma/Biotech/agency setting
A proven track record of successful scientific writing and leading projects; are comfortable with developing a range of content types, sometimes concurrently, and able to prioritize tasks to meet timelines/deadlines
An advanced university degree in science, medicine or another related subject
Therapeutic expertise/experience in one or more of Organization's key therapy areas (Oncology, Rare Tumours, Neurology and Immunology, Fertility, Cardio-metabolic and Endocrinology)
Demonstrable stakeholder management expertise
Strong awareness of the pharmaceutical business and trends in the industry
Experience in managing projects cross-functionally and in an international setting
Strong analytical skills and ability to understand complex processes, project management and project leadership skills
Excellent verbal and written communication skills (English language)

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

Associate Director of North America Turnkey Projects (EPC) - Remote (Austin, Texas, US, 78721-2908)

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Location:

The Associate Director for Turnkey Projects is a remote position that requires the candidate to be full-time at the customer jobsite (in North America) during the construction and commissioning phase of the project. During project planning, design stage, procurement stage, the role is primarily remote, with occasional travel to meet internal teams, suppliers, and vendors.  There will be approximately 50% domestic and international travel to meet business needs, including staying at construction sites.

Your Role:

The role demands strong technical acumen, expert project management skills, and leadership in an environment where high-quality, efficient delivery is critical. The Associate Director for Turnkey Projects will be responsible for developing projects and managing project teams in the United States delivering specialty gases and chemical delivery systems in back pads, gas, and chemical buildings and subfabs for semiconductor manufacturing clients. The scope includes proposal work for new business opportunities, development of equipment modulization, leading and executing complex turnkey projects focused on engineering, procurement, construction, and commissioning. The successful candidate will work closely with Sales and Procurement while overseeing multiple project teams, including project managers, engineers, document control engineers, and a project administrator, to ensure projects meet scope, schedule, and budget targets while adhering to rigorous quality and safety standards.
 

Key Responsibilities:

As the Associate Director of Turnkey Project Management Team in U.S., you will drive strategy execution, support team growth, manage resources, enhance communication, and align team success with organizational goals.

Obtain and maintain commercial general contractor licenses from the states’ registrars of contractors. For bidding processes for new EPC (Engineering, Procurement, Construction) projects, analyze customer requirements (RFQ or RFP), review designs, estimate costs, plan schedules, and manage risks. It includes proposing technical solutions that meet customer needs, collaborating with suppliers to select optimal materials and services, and preparing bid documents. Review contract terms, provide competitive pricing, and evaluate project feasibility to secure successful awards. Additionally, manage legal and commercial risks during the bidding process and negotiate with clients to achieve the best outcomes. Interface with semiconductor clients and internal stakeholders to define project scopes, validate technical requirements, and provide strategic updates.

Oversee critical engineering deliverables across various disciplines, including process, mechanical, piping, electrical, instrumentation, and control engineering. Responsibilities include reviewing and managing Process Flow Diagrams (PFDs), Piping and Instrumentation Diagrams (P&IDs), Hazard and Operability Studies (HAZOPs), equipment specifications, plot and layout plans, piping isometrics, single line diagrams, Input/Output (I/O) lists, and logic diagrams. Facilitate design coordination among internal design engineers, subcontractors, vendors, and clients.

Develop procurement strategies leveraging professional network and working with procurement manager, coordinating with suppliers and vendors, mitigating risks, ensuring compliance with contractual and regulatory requirements, and fostering collaboration between procurement, engineering, and construction teams to secure timely delivery of materials and equipment critical to project success.

Oversee all aspects of construction activities on-site including coordinating with subcontractors, ensuring compliance with safety regulations, resolving on-site issues, and maintaining effective communication with stakeholders to achieve project objectives.

Lead cross-functional teams by mentoring and coordinating project managers, engineers, sales personnel, and support staff.

Oversee project budgets with forecast and actual cost, resource allocation, scheduling for timelines using Primavera P6 or MS Project, and risk mitigation efforts to ensure timely, on-budget delivery.

Ensure compliance with relevant engineering, quality, safety, and regulatory standards throughout project lifecycles.

Proactively identify project risks and implement corrective actions; maintain effective communication channels and reporting structures.

Champion continuous improvement initiatives by leveraging best practices and advanced project management methodologies.

Manage the development of the modularization of equipment such as gas room cabinets, mods, pods, and VMBs to enhance productivity, scalability, and cost-effectiveness. Develop and implement strategies for modular design, ensuring standardization and compatibility across systems. Collaborate with engineering, procurement, and construction teams to optimize designs for transport, assembly, and operation. Oversee the integration of modular units into existing workflows while maintaining quality, safety, and compliance standards. Identify opportunities to reduce project timelines and costs through modular solutions. Provide technical guidance, manage risks, and ensure alignment with project objectives and client requirements. Drive innovation and continuous improvement in modularization practices.

Who You Are

 Minimum Qualifications:

Bachelor's degree in chemical engineering, mechanical engineering, electrical engineering, construction management, project management, or a related technical field along with 8+ years of experience in EPC project management within process heavy industries such as semiconductor, oil and gas, petrochemical, refinery, power plant, other plant engineering required.

In lieu of a degree, the candidate must have 12+ years of progressive experience in EPC project management, preferably within the semiconductor, oil and gas, petrochemical, refinery, power plant, or other plant engineering required.

Strong network of subcontractors and experience in contract negotiation with clients and subcontractors is essential.

Eligibility to clear background check required for licensing by states’ registrars of contractors.

Preferred Qualifications:

Preconstruction, project management, engineering management, or design experience in EPC companies related to industrial or specialty gas, semiconductor, oil and gas, petrochemical, refinery, or power plant.

Demonstrates respect for individuals and fosters an inclusive work environment that values diversity. Possesses strong cultural awareness and the ability to collaborate effectively with global teams, ensuring mutual understanding and alignment across different perspectives and backgrounds.

Preference given to candidates with process, mechanical, piping, electrical and instrument engineering experience, specifically process engineering backgrounds.

Proven record of gaining market share by proposing value engineering and winning proposals in projects with intense competition.

Experience with preconstruction and proposal preparation of at least ten EPC projects worth more than $50M each.

Experience with project execution of at least three EPC projects worth more than $50M each.

Extensive experience collaborating with global teams across multiple time zones to achieve project goals and ensure seamless communication along with a proactive and diligent work ethic.

Certified Project Management Professional (PMP), MBA, or equivalent certification is strongly preferred.

Strong leadership, communication, and problem-solving skills with 10 years of experience in managing cross-functional teams.

Familiarity with industry-specific standards and technology related to semiconductor process support.

Pay range for this position: $177,200 - $265,800

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!

Analyst- Product Content Development & Optimization (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.

Analyst - Product Content Development & Optimization

The Product Content Development & Optimization Analyst/Senior Analyst creates and optimizes the web presence of the Process Solutions portfolio by efficiently generating high-quality product content and structured product data for new and existing products, ensuring it is accurate, channel-ready, and optimized for discovery (SEO/AI search) and customer decision-making. Partner with Product Management, Digital & e-Commerce, and Marketing/MarCom to improve data quality, customer experience, and commercial performance, including building and leveraging AI-driven tools to scale and automate product data and content processes.

YOUR ROLE

Ensure web product data readiness for New Product launches, collaborating with cross-functional teams to establish product requirements and timelines.
Manage product information using Product Information Management (PIM) systems, ensuring accuracy and consistency across all digital channels.
Audit and enhance product data quality, identifying and resolving discrepancies to maintain high standards in product representation.
Extract and consolidate relevant product data/content from internal sources and translate it into digital-ready product narratives and structured attributes.
Curate and maintain Product Detail Page (PDP) content that supports product discovery and customer decision-making, including scientific and marketing content.
Optimize product content for web performance, including SEO and AI-assisted search/discovery, and continuously improve findability and clarity.

WHO YOU ARE

Master’s degree in any Life Science Discipline (Biology, Chemistry, etc.).
Minimum of 2–3 years of experience in web product data management, e-commerce, digital content writing or a similar role.
Strong English writing skills with a proven track record of producing high-quality scientific and/or marketing content for a global audience / for web discovery optimization.
Highly organized, detail-oriented, and able to deliver high throughput with consistency.
Proactive, high-ownership, and solution-oriented, with a bias for action and a track record of driving issues to resolution.
Proven ability to multi-task and work autonomously and effectively in a fast-paced, deadline-oriented environment with competing priorities.
Familiarity with the Life Science industry and customer base, curiosity about product positioning.
Familiarity with Product Information Management (PIM) systems and data quality management practices.
Strong analytical skills, comfortable handling and analyzing data and using tools like e.g. Foundry, Excel, PowerBI to spot issues and trends.
Overall understanding of the Marketing funnel and Customer journey.
Practical SEO understanding; adept at diving deep into search including algorithms and technical details.
Experience with digital marketing/SEO tools (e.g., SEMrush, Google Analytics).
Experience in creating and utilizing AI tools for data analysis, generating and optimizing user-centric content and process automation.

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 those impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

OLED Application Junior Researcher (학사 이상, OLED 산업 경력 1년 이상) (Pyeongtaek-Si, Gyeonggi-do, KR, 17745)

여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!

Your Role:

OLED 소자 제작을 통해 물질(OLED 소재)의 물리적 특성을 연구, 이를 제품 아이디어로 도출
고객 사용 환경에서 소재 성능을 극대화하기 위한 최적의 OLED 소자 구조 개발
실험실, 도구 및 장비를 유지·관리하고 개선 사항 제안 및 보고
OLED 소재 개발을 위해 OLED 소자 제작 및 측정
OLED 소자의 광학 및 전기 데이터를 분석하고, 고객 요구사항에 기반하여 이를 소재 성능기준으로 도출하여 빠르게 개발에 반영
프로젝트 목표, 고객 요구사항, 리스크, 일정, 비용 등을 종합적으로 고려한 OLED 소자 제작, 측정 및 평가 실험 계획 수립과 수행
모든 데이터가 올바르게 저장되도록 OLED 특성 데이터를 시스템에 업로드
실험실 공정의 표준 운영 절차(SOP)의 문서화 및 관리
발명보고서 작성을 통한 개발 성과의 특허 보호 및 확보
실험실, 도구 및 장비의 운용 가능 상태 보장
소모품 수급의 계획 및 가용성 보장
공정 조건과 새로운 발견 사항에 대해 MDA (독일본사) 실험실과 정보 교환

Who You Are:

OLED 관련 석사 이상 학위자
또는 학사 + OLED 산업 경력 2년 이상
광학, 전자공학 및 디스플레이에 대한 기본 지식 필요
클린룸 환경에서 근무가 가능한 분
기본적인 영어 활용 능력 (이메일/문서작성 및 회의 참여 등)

<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.

National Sales Manager Fertility & CME (Budapest, Budapest, HU, 1117)

Work Your Magic with us!

Your role:

In this role you will lead, motivate and inspire the Sales Force team to maximize its contribution, performance and individual development. You will ensure excellent territory teamwork; and field execution of marketing strategies and actions that ensure the short, medium and long-term success of the Business Unit.

You will manage a team of sales representatives (REPs) and Key Account Managers (KAMs), and report to Business Unit Head.

Lead KAMs and REPs in order to achieve their goals. Coach and develop effective selling skills in line with company strategy; monitor and review territory performance regularly; gives feedback on performances on a regular basis.
Support the KAMs at developing center by center strategies and tactics and the REPs at strategical thinking and execution excellence.
Reinforce the KAMs and REPs engagement in omnichannel approach focusing on new digital initiations besides supporting the execution.
Active contribution to development of marketing strategies and tactics; annual brand plans and business reviews.
Ensures successful implementation of marketing strategies and tactics; monitors the impact and propose actions.
Analyzes and concludes on the available customer, market, and competitive data and provides feedback to the team and to the product managers and medical colleagues.
As leader contribute to deliver success through a high performing team - by supporting the Collaboration & Accountability & Execution Excellence internally among sales team members; and externally among sales, marketing and medical teams.
Continuous learning to stay updated in terms of professional and scientific information in therapeutic areas being responsible for: Cardiology, Diabetology, Fertility, Growth Hormone, Thyroids.

Who you are:

Life sciences university degree
Min 3 years Sales Manager experience at innovative pharma company with RX products
Native Hungarian
Fluent business English
Solid MS Office literacy
Driving license
Other skills: strong people leadership and talent management; strategical approach; ability to synthesize; results-oriented; work cross-functional; accountability; accurate execution; customer-oriented approach; self-initiative; ability to manage change and innovation; resilience; has capability and willingness to learn.

Preferably:

Marketing or Business degree
Experience in Key Account Management and/or managing Key Account Managers
Experience in product management and/or marketing related project management

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

OT Service Manager (Kaohsiung, Kaohsiung, TW, 821011)

與我們攜手施展你的超能力！

Your Role
An exciting new opportunity has arisen to join the IT/OT team as a sector IT/OT Service Manager. In collaboration with site IT/OT teams and peers from other sectors, you will oversee all Electronics IT/OT applications, ensuring compliance with internal processes such as Data Privacy, Data Retention, Cybersecurity, and Disaster Recovery. You will own the IT/OT Service Management with sites, linking stakeholder voices to global projects aimed at enhancing IT/OT service delivery and maximizing value through integration with the IT service management framework (ServiceNow). Your interactions will extend to other core IT/OT pillars, including Portfolio Management, Architecture, and Cybersecurity, as well as corporate IT infrastructure and application teams. You will play a crucial role in the development and implementation of an IT service management framework tailored to IT/OT needs, aligned with business priorities, budget, and risk. Additionally, you will drive IT/OT inventory and CMDB programs while designing a cross-sector training strategy for IT/OT on IT Service Management and ServiceNow. Participation in cross-sector IT/OT service management Center of Excellence & Audits will be key to your success. You will also be responsible for stakeholder management, ensuring transparency in IT/OT service decisions and managing external partnerships with key IT/OT service providers. This role reports to the Head of IT/OT Enablement.

Who You Are

Graduate degree in IT/computer science, engineering, business/economics, or a related field.
Several years (ideally 5+) of experience in IT/OT.
Proficient in implementing IT Service Management practices leveraging the ServiceNow platform.
Knowledge of leading IT Service Management frameworks such as ITIL 3 or 4.
Domain knowledge in manufacturing processes, machinery, and control systems.
Expertise in integrating IT/OT systems into IT infrastructure.
Strong communication skills to collaborate with cross-functional teams and stakeholders.
Multicultural experience, fluent in English.

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！

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

Entfalte das Besondere mit uns!

Ihre Rolle:

Als Werkstudent (m/w/d) im Bereich Automation unterstützen Sie das Engineering & Technology – Automation Team bei Aufgaben rund um die Automatisierungstechnik und IT/OT-Integration. Besonders wichtig ist uns, dass Sie Ihre technische Begeisterung und Ihr Know-how einbringen, um gemeinsam mit uns an wegweisenden Lösungen zu arbeiten.

Hauptaufgaben:

Unterstützung bei der Dokumentation und Bearbeitung von Tätigkeiten in der Automatisierungstechnik
Mithilfe bei der Vorbereitung von Präsentationen, Berichten und Analysen
Mitarbeit bei IT/OT-Themen wie Netzwerkarchitekturen oder Virtualisierungen
Beteiligung an hands-on Projekten (z. B. Integration von IoT-Geräten, Programmierung von SPS’en, Testen von Hardware wie Raspberry Pi oder ähnlichen Plattformen)
Vorantreiben von innovativen Themen rund um digitale Transformation und neue Technologien

Ihre Qualifikationen:

Eingeschriebener Student (m/w/d) im Bereich Elektrotechnik, Automatisierungstechnik, Informatik oder einem vergleichbaren Studiengang
Praktische Erfahrung im Bereich Automatisierungstechnik oder IT-Systeme (z. B. Raspberry Pi, Arduino, Virtualisierungen, Netzwerke)
Leidenschaft für Technik, insbesondere für Themen wie IoT, Smart Home oder Hardware-Prototyping
Basiswissen über Netzwerktechnologien und IT-Administration (z. B. Einrichten und Konfigurieren von Routern, NAS-Systemen oder anderen Netzwerkgeräten)
Gute Kenntnisse in MS Office, insbesondere Excel, PowerPoint und Visio
Idealerweise erste Erfahrungen mit dem Programmieren von SPS’en, beispielsweise von Siemens S-7 Steuerungen
Idealerweise erste Erfahrungen mit Programmiersprachen wie Python, Java oder ähnlichen Tools
Selbstständige und strukturierte Arbeitsweise
Sehr gute (C1) Kommunikationsfähigkeiten in Deutsch und Englisch
Teamfähigkeit und die Fähigkeit, sich schnell in neue Themen einzuarbeiten

Was wir bieten:

Einblicke in die Automatisierungstechnik eines weltweit führenden Life Science Unternehmens
Eine unterstützende und lernfördernde Arbeitsumgebung, die Raum für technisches Experimentieren bietet
Flexible Arbeitszeiten, die sich gut mit Ihrem Studium vereinbaren lassen

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

Initiativstelle - Fachkraft für Lagerlogistik (m/w/d) (Schnelldorf, Bayern, DE, 91625)

Ihre Rolle
Als unser neuer Lagerarbeiter / Kommissionierer (m/w/d) liefern und stellen Sie Rohstoffe und Packmittel pünktlich an unsere Abfüllung bereit. Sie nehmen Waren an, prüfen Anliefersendungen, bearbeiten sie im Wareneingang. Läuft, weil wir sehr gut zusammenarbeiten, Tagesabläufe gut planen und uns vollkommen unterstützen. So macht Arbeiten Spaß und die Zeit vergeht schnell. So haben Sie sich Ihren nächsten Job vorgestellt? Gerne jetzt bewerben oder mehr lesen!

Charakterköpfe: Bei uns sind alle willkommen, die zuverlässig und gut arbeiten. Ihre Persönlichkeit hängt eng mit Ihrem Job zusammen. Denn es geht um selbstverantwortliche Tätigkeiten, um Qualität und Sicherheit.

Sie mögen es! Die Rede ist von verschiedenen Aufgaben und Einsätzen in mehreren Lagerbereichen – von der Warenannahme übers Etikettieren bis zur Kommissionierung und Bereitstellung der Gebinde in Behälter. Mal arbeiten Sie mit EDV-Systemen, mal sind Sie mit Flurförderfahrzeugen unterwegs.

Finanzielle Sicherheit: Gute Arbeit. Guter Lohn. Zusätzlich zu Ihrem Tariflohn erhalten Sie Urlaubs- und Weihnachtsgeld. Ihre Fachkenntnisse in Lager, Logistik und Warenannahme entwickeln Sie weiter.

Männer & Frauen: In unserem Team gibt’s viele Möglichkeiten, mitzudenken und etwas aktiv umzusetzen. An erster Stelle stehen die Sicherheitsvorschriften. Als Mitglied unseres Reaktionsteams sind Sie auch willkommen!

Wer Sie sind:

Sie sind Fachkraft für Lagerlogistik und bringen ca. fünf Jahre Berufserfahrung in Lager, Logistik und Warenannahme mit. Sie besitzen den Staplerschein für Flurförderzeuge Stufe 1
Gut ist, wenn Sie den Staplerschein für Flurförderzeuge Stufe 2 und die Zuverlässigkeitsprüfung für Luftfahrtpersonal nach § 7 Abs. 1 LuftSiG (ZÜP) besitzen. Falls nicht, so begleiten und unterstützen wir Sie bei der Ausbildung Flurförderzeuge Stufe 2 und ZÜP
Sie haben viel auf Lager: MS-Office und eine Lagersoftware beherrschen Sie mindestens genauso gut wie die deutsche Sprache in Wort und Schrift
Ihr Typ: verantwortlich, sympathisch, gemeinschaftlich. Sie und wir – das passt

Die Stelle ist vorerst auf 12 Monate befristet mit der Möglichkeit auf Übernahme in einen unbefristeten Arbeitsvertrag.

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

Associate Director, Go-To-Market and Field Strategy, Fertility and Value & Access (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 Associate Director, Go-To-Market and Field Strategy will partner with our therapeutic areas to translate ambition and strategy to execution. You will represent the needs of the field and funnel that information to the brand team or appropriate platforms for the determination and potential deployment of critical resources.

Key Responsibilities:

Go-to-market strategy: Design, execute, and optimize GTM plans for new and existing products; track performance via KPIs and adjust based on results.
HCP & account targeting: Build and maintain targeting models (segmentation, tiering, valuation) and produce quarterly target lists to optimize resource allocation.
Account planning enablement: Support the key account management program; improve tools, capabilities, and processes to strengthen account plans and outcomes.
Territory alignment: Analyze market/sales dynamics to design and implement territory structures; manage change rollout and continuously optimize coverage and productivity.
Insights & ad hoc analytics: Deliver analyses of market trends, customer behavior, and competitive dynamics to inform decisions.
Brand planning support: Provide insights and analytics to support annual brand planning and in-year pull-through.
Program/project leadership: Lead cross-functional initiatives with clear plans, timelines, deliverables, and stakeholder communication.
Executive communication: Develop high-impact presentations; facilitate meetings/workshops (e.g., POAs, summits) to align teams and drive execution.
Cross-functional alignment: Serve as liaison across Sales, Marketing, and Operations; synthesize field and research insights into planning and priorities.

This job description is intended to provide a general overview of the role and is not an exhaustive list of all responsibilities and duties associated with the position

Who You are:

Minimum Qualifications

Bachelor’s degree
Minimum 6 years’ experience in pharmaceuticals, healthcare industry, or consulting
Advanced computer skills – excellent knowledge and experience with Excel, Word, PowerPoint, and Access
Deep expertise with data and reporting/analysis tools
Advanced knowledge of CRM technology relevant to Customer Facing Teams
Proven skills leading multiple impactful cross functional projects simultaneously

Preferred Qualifications

Biotech or pharmaceutical US marketplace launch experience
Experience in Fertility and / or Value & Access
Outstanding oral, written and communication skills with the ability to present to small and large groups
Superior team orientation and ability to influence without authority
Strong business acumen with keen analytical sense and ability to utilize quantitative analysis and sound business judgement in interpretation of sales and market data to drive strategy
Ability to think strategically and bring innovation to the organization
Ability to communicate openly and share information to foster trust while encouraging constructive debate, making informed decisions, and ensuring shared commitment to outcomes.
Demonstrated willingness to take risks and stand up for what is right while prioritizing the needs and experiences of customers and patients in all decisions.
Commitment to setting and reaching ambitious goals and setting high standards while acting in the best interest of the company and taking initiative to drive results.
Uphold ethical standards and being honest in all interactions.
Ability to streamline processes to focus on what matters and creates impact and acting quickly to adapt to changes.
Demonstrated ability to embrace new ideas, challenge the status quo, and seek innovative solutions while valuing diverse perspectives and treating others with respect and dignity.

Location: Greater Boston, MA (Seaport Office); Hybrid

Travel: <10%, International and Domestic

Pay Range for this position: $127,600.00 - $191,400.00

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

Associate Director, Market Insights, Fertility (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 Associate Director, Market Insights, Fertility is responsible for recommending, designing, and conducting US market research and leading US competitive intelligence to assess performance/perception, identify opportunities and barriers to use, and provide objective and data-driven recommendations for our in-line Fertility portfolio and future launches within the Fertility Franchise.

Working cross functionally, this position contributes to the setting of commercial and brand strategy with US TA leadership through their expertise with customer insights and objectively communicating their implications. In partnership with the Analytics and Forecasting counterparts, they will play an integral role in continuing to analyze and optimize brand performance – designing and leading research to continuously assess customer use, perceptions, and future use intentions for both EMD and competitor products, thereby enabling Senior Leadership to make optimal, data driven decisions based on in depth knowledge of the market, our customers and our products.

This role also leads the development, analysis, and dissemination of competitive intelligence for the US Fertility assets. This role ensures that US Fertility teams utilize competitive intelligence to inform decision making and action by creating transparency of information, and through collaboration with business partners, ensures an aligned view is developed and communicated to the organization.

Key Responsibilities:

Provide data-driven strategic insights to US Fertility brand teams and senior leadership; shape brand/commercial strategy and key decisions.
Lead end-to-end primary and secondary market research (study design/methodology, instruments, vendor management, analysis, readouts) to solve complex business questions.
Synthesize insights across epidemiology, claims/Rx, and other data sources; deliver clear reporting on trends, performance, opportunities, gaps, and risks.
Integrate customer/market insights into forecasting and key planning assumptions.
Drive cross-functional and Global alignment to avoid duplication, ensure US needs/compliance are met, and represent the patient/HCP perspective.
Maintain market research best practices and innovation; manage budgets and external vendors/agencies.
Lead competitive intelligence monitoring and ethical collection; manage CI agencies; translate competitive activity (including congress coverage) into assessments that inform strategy, tactics, forecasting, and lifecycle plans.

This job description is intended to provide a general overview of the role and is not an exhaustive list of all responsibilities and duties associated with the position

Who You are:

Minimum Qualifications

Bachelors Degree
Minimum 6 years of relevant experience in pharmaceutical insights generation including demonstrated ability to compare and recommend appropriate integrated approaches to address business needs
Minimum 4 years of primary market research experience
Minimum 4 years of Fertility product experience

Preferred Qualifications:

Expertise in in-line pharma market research (positioning, messaging, creative, ATU, tracking) and integrated CI/insights (primary + secondary).
Ability to assess competitive threats/opportunities and implications for clinical development and commercial potential; familiarity with ClinicalTrials.gov/Trialtrove/Cortellis.
Experience running primary CI (KIQs/KITs, vendor selection/management, congress coverage through reporting).
Strong analytical, strategic, forecasting/financial, and PowerPoint storytelling skills.
Excellent communication/presentation; able to lead and influence cross-functional teams and manage multiple priorities under tight deadlines.
Ability to communicate openly and share information to foster trust while encouraging constructive debate, making informed decisions, and ensuring shared commitment to outcomes.
Demonstrated willingness to take risks and stand up for what is right while prioritizing the needs and experiences of customers and patients in all decisions.
Commitment to setting and reaching ambitious goals and setting high standards while acting in the best interest of the company and taking initiative to drive results.
Uphold ethical standards and being honest in all interactions.
Ability to streamline processes to focus on what matters and creates impact and acting quickly to adapt to changes.
Demonstrated ability to embrace new ideas, challenge the status quo, and seek innovative solutions while valuing diverse perspectives and treating others with respect and dignity.

Location: Greater Boston, MA (Seaport Office); Hybrid

Travel: <25%, International and Domestic

Pay Range for this position: $137,800.00 - $206,600.00

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

LQPPV & Local Patient Safety Officer (Herzliya Pituach, Tel Aviv, IL, 4673325)

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About the Role

Merck KGaA, Darmstadt, Germany is seeking an experienced Local Qualified Person for Pharmacovigilance (LQPPV) & Local Patient Safety Officer (LPSO) for its Israel affiliate. As a key regulatory and patient safety role, you will be nominated as a contact person for internal and external safety-related matters and will exchange information within the Patient Safety Center (PSC) Mediterranean as well as with local key stakeholders (i.e., Medical Affairs, Regulatory Affairs, Healthcare Quality, Clinical Operations, and Commercial Organization etc.).

Key Responsibilities

Serve as the designated LQPPV and single point of contact for the Israeli MOH on all PV matters, with 24/7 availability for urgent safety communications and regulatory inspections
Ensure full oversight and timely submission of ICSRs, PBRERs, Safety Signals and other PV deliverables in line with local legislation
Monitor Israeli MOH communications and local PV legislation for changes; assess impact and drive implementation
Lead and execute local PV operational tasks, maintain the local PV file, and oversee PV system quality and compliance (KPIs, CAPAs, audits)
Manage local PV vendors and business partners, including oversight of contractual PV agreements
Ensure proper implementation of Risk Management Plans (RMPs) and additional risk minimization measures in collaboration with local and global teams
Ensure oversight of safety signals, benefit-risk evaluations, and emergency safety situations, providing LQPPV input where required
Provide PV training to local affiliate staff and third parties as required
Maintain oversight of ongoing studies conducted in the country
Represent Global Patient Safety in local cross-functional teams and act as the GPS point of contact at the affiliate

What You Will Bring

Pharmacist or physician with a valid Israeli license
Experience in the pharmaceutical industry, ideally in an affiliate setting with local PV responsibility
Knowledge of Israeli and EU PV regulations
Fluent in Hebrew and English (written and spoken); additional languages are an asset
Strong leadership, project management, and strategic thinking skills
Excellent communication, problem-solving, and organizational abilities
Proven ability to work effectively across multicultural and cross-functional teams

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

质量服务专家 (Shanghai, Shanghai, CN, 201203)

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Key Individual Accountabilities / Deliverables

In this exciting opening within our Quality Services organization, Quality Service expert role specializes in delivering Quality and regulatory support to key customers through all Life Science portfolio. You’ll be interacting with multiple biopharma companies that are pioneering this industry, to deliver quality knowledge and insight for the critical quality issues or inquiries. The role needs to closely collaborate with cross-functional teams in global, such as, Sales, Technical, Customer Excellences, Manufacturing sites, Product managers, Regulatory and other Quality functions.

We are looking for bright, enthusiastic candidates who have the ambition to success in the growing biopharmaceutical industry. Ideal candidate would be a good team-player and work well under pressure. Hands on experience from biopharma Quality or Production would be preferred. You should be fluent in English and Chinese (Mandarin).

1. Quality Services

• Is responsible for Customer Quality and Regulatory resolution and follow-up of Quality incidents.

• Foster customer intimacy and provide customers with updates to Quality complaint investigations including face-to-face meetings as needed.

• Demonstrate expertise in project management, typically in the form of coordinating complex customer inquiries or investigations across global sites.

• Possess an in-depth knowledge of Our products and industry applications and act a Subject Matter Expert for other QS Team Members.

• In-depth understanding relevant regulatory guidelines (i.e., GMP) as it relates to the Pharma, BioPharma, IVD, Medical Devices, Food, Research Markets, etc.

• Deliver Quality Services, adopting a consultative approach to understand customer needs, explain our quality systems capabilities and communicate that commitment.

• Implements standards to ensure customer satisfaction for quality and regulatory matters for the whole Life Science portfolio.

• Implements policies, procedures and methods to provide quality and regulatory product and service information and continuously improves the same.

• Collects data in partnership with Business partner for the Commercial and Business Areas to monitor, report and improve Quality performance from a customer’s perspective.

• Directs the resolution of highly complex or unusual business problems applying advanced analytical thought and judgment.

• Applies broad industry and commercial awareness to drive financial and quality performance across Life Science business sector.

• Interacting with Manufacturing site, Marketing, Sales, Supply Chain, Regulatory and other Quality teams to ensure inquiries are moving forward. Assists other QS Team Members with Inquires that have stalled.

• Contributes / Leads internal facing relevant (quality services, operations, marketing, sales, etc.) training/ education courses

2. Quality Complaint Resolutions

• Facilitate the Quality complaints from key customers in China.

• Act as a local interface for the Quality complaints, domestic troubleshooting (Quality Collaboration Program) and investigational actions (China Quality Complaint Improvement).

• Deliver specific customer Quality expectations and domestic findings to the overseas manufacturing sites.

• Directs the resolution of highly complex Quality defect and issues through effective coordination of investigation process together with Quality investigation center, site Quality and other stakeholders, such as, R&D, Product Managers, Technical experts, etc. Address customer expectations to investigation letter based on advanced analytical thought and judgment in a scientific manner.

• Monitor and report the Quality complaint metrics. Contribute to improve product Quality performance from a customer’s perspective.

• Travel ~20%

Education

Bachelors' in Biological sciences (Microbiology, Biochemistry, Molecular biology, Biotechnology, etc.). Master's degree with related scientific area would be preferred.

Work Experience

Must: 4 - 9 years of professional GMP background from pharmaceutical QC, QA or Production with Hands-on Deviation investigation experience or related Project Management experience

Desired: Certified Lead Investigator, Deviation reviewer/approver, Project management professional

Key Skills/Knowledge

• Excellent interpersonal, verbal and written communication skills. Fluent in English and Chinese.

• Good understanding on the Biopharma Quality concepts and working knowledge of FDA and/or EMA, cGMP regulatory requirements.

• In-depth understanding with the deviation, OOS investigation and CAPA planning in compliance with the Quality management and GMP standpoint.

• Strong problem solver. Ability to independently communicate and discuss complex Quality topics and regulations with customers.

• Strong Collaboration, Communication skills with mindfulness and empathy.

• Ability to work with people in cross-functional and global with diversity and inclusivity.

• Proficient in MS Office programs. Experience in SAP, Trackwise and Salesforce would be an advantage.

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

Director, Strategic Enterprise Initiatives and Enablement, Value & Access (Seaport MA) (Boston, Massachusetts, US, 02210)

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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:

The US Value & Access team (V&A) has a shared vision to create and maintain optimal product access and availability across the portfolio that supports patient care. The Director, Strategic Enterprise Initiatives and Enablement is a key member of the Value & Access leadership team with specific decision making and areas of focus, responsible for driving enterprise-level strategic initiatives and enabling operational excellence across the organization. This role serves as a trusted advisor to the SVP, ensuring alignment of priorities, seamless execution of strategic projects, and fostering a culture of collaboration and innovation.

Strategic Planning & Execution:

Lead the development and implementation of short- and long-term strategic initiatives that advance Value & Access objectives.
Partner with the SVP and leadership team to translate vision into actionable plans and measurable outcomes.
Monitor external trends and internal performance to inform strategic decisions.
Serves as a strategic thought partner with the US V&A Sr. Vice President, providing high-level support associated with complex problems, current and future initiatives, strategies, and budgets

Work closely with V&A LT to prepare and coordinate updates for SVP by synthesizing information and ensuring alignment.

Enterprise Enablement:

Design and implement frameworks, processes, and tools that enhance organizational effectiveness and operational efficiency.
Drive change management initiatives to support evolving business needs and priorities.
Ensure compliance with industry regulations and company standards.
Executive Support & Governance:
Provide high-level strategic support to the SVP, including preparation of executive briefings, presentations, and business cases.
Coordinate leadership meetings, town halls, and engagement activities to align teams and communicate priorities.
Serve as a liaison between Value & Access leadership and cross-functional stakeholders.
Generates strategic insights based on best-in-class analysis, distills outputs and recommendations which enable informed decisions of top-level leaders.
Ability to monitor and assess external trends to inform and educate stakeholders and stay abreast of macro trends in the healthcare environment, therapeutic area markets and brand business drivers. A critical aspect of this role is the ability to work seamlessly across the EMDS enterprise (both within and outside V&A and form a strong partnership with commercial) and coordinate the input of stakeholders.
Work with the GPA team to assess the potential implications of new or proposed policy changes on our inline and pipeline products.
Ensure compliance with industry regulations and ethical standards.

Cross-Functional Collaboration:

Demonstrates collaborative leadership and influence necessary to ensure alignment among key stakeholders and seamless execution of project deliverables including but not limited to: Value & Access, Patient Solutions, Pricing & Contracting, Commercial, Medical Affairs, and NEVD teams. Build strong partnerships with HR, Finance, Legal, and Government Affairs to support enterprise initiatives.

Performance & Process Improvement:

Identify opportunities to optimize processes, improve resource utilization, and enhance team productivity.
Develop KPIs and dashboards to track progress on strategic initiatives and operational goals.

Talent Development & Engagement:

Support workforce planning, succession planning, and organizational design efforts.
Champion initiatives that position Value & Access as a destination for top talent and foster a high-performance culture.
Other duties as assigned

This job description is intended to provide a general overview of the role and is not an exhaustive list of all responsibilities and duties associated with the position

Location: Seaport, MA (Hybrid)

Reports To: Senior Vice President, Value & Access

Travel: Up to 20%

Who You Are

Minimum Qualifications:

Education: Bachelor’s degree required; advanced degree (MBA, MPH, MS) preferred.
Experience: 8+ years of experience in biopharmaceutical or healthcare industry, with expertise in Market Access, Commercial Strategy, or related functions. Proven track record in strategic planning, project management, and organizational transformation. Experience leading cross-functional initiatives and influencing without authority.

Preferred Qualifications:

Exceptional strategic thinking and problem-solving skills. Strong communication and presentation abilities, including executive-level engagement. Advanced project management and organizational skills. Ability to thrive in a fast-paced, dynamic environment and manage multiple priorities. High integrity, discretion, and collaborative leadership style.
Timely and effective execution of strategic initiatives.
Improved operational efficiency and process optimization.
Positive stakeholder feedback and alignment across functions.
Development of a strong talent pipeline and enhanced team engagement.
Ability to communicate openly and share information to foster trust while encouraging constructive debate, making informed decisions, and ensuring shared commitment to outcomes.
Demonstrated willingness to take risks and stand up for what is right while prioritizing the needs and experiences of customers and patients in all decisions.
Commitment to setting and reaching ambitious goals and setting high standards while acting in the best interest of the company and taking initiative to drive results.
Uphold ethical standards and being honest in all interactions.
Ability to streamlining processes to focus on what matters and creates impact and acting quickly to adapt to changes.
Demonstrated ability to embrace new ideas, challenge the status quo, and seek innovative solutions while valuing diverse perspectives and treating others with respect and dignity.

Pay Range for this position: $145,000 - $260,300

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

Product Manager N&I (Santa Fe de Bogota, Bogota, CO, 9896)

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Your Role

The Product Manager N&I North Cone HC will develop and implement marketing strategies and programs for the Company's Neuroimmunology portfolio, ensuring sales and profitability objectives are met.
Manage the overall budget for assigned brands, defining investments and trade-offs based on strategic priorities, while ensuring detailed control over these investments.
Collaborate effectively with cross-functional teams, including medical, access, and commercial, to achieve brand objectives.
Ensure that the sales force and all brand support functions implement actions in line with the defined strategy and communication narrative.
Leverage available channels for customer communication, including multichannel and omnichannel plans.
Ensure compliance with commercial objectives, including sales, investment budget, and brand profitability, while communicating agreed positioning messages.
Lead a multidisciplinary brand team to support existing businesses and launch future products. Oversee the Brand Plan process for the upcoming year.

Who You Are

You hold a degree in business administration, industrial engineering, marketing, or health-related fields, preferably with an MBA.
You have prior experience as a Product Manager in a multinational pharmaceutical company, preferably in Colombia, with mandatory experience in leading product launches.
You possess over 5 years in the pharmaceutical/biotech industry, showing commercial leadership in marketing and sales.
Your understanding of Colombian health systems and market dynamics is complemented by effective communication and negotiation skills.
You can build and maintain relationships with key stakeholders, demonstrating a high level of collaboration and team management. Proficiency in English is essential.
Additionally, you must have experience in the same therapeutic area or in related specialties (oncology, rare diseases,...)

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)

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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:

Who You Are

Minimum Qualifications:

Doctoral and/or master’s degree (e.g., PhD, MSc) in Epidemiology, Public Health or related field
Strong experience in RWE/D within the pharmaceutical industry, particularly in the application of RWE in drug development for rare indications

Preferred Qualifications:

Preferably a background in health and life sciences (MD, pharmacist epidemiology, public health), or quantitative data sciences, biostatistics
Demonstrable experience in leading RWE generation plans and studies end-to end, including application of innovative designs and methods
Excellent oral and written communication skills and demonstrated ability to engage and communicate scientific evidence to peers and at scientific meetings
Collaborative, proactive working style, with ability to work independently.

Pay Range for this position: $169,470 - 254,100
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!

Chemical Process Engineer PIS (Nantong, Jiangsu, CN, 226010)

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Overall Objectives of the Position

The main responsibilities of the PIS process engineer are to provide process design and process technical service to PIS plant as part of on-going productivity, new product startup and commissioning and technical troubleshooting initiatives. Process engineer provides engineering leadership to drive asset performance which includes process engineering, troubleshooting, plant efficiency, process safety, equipment reliability, advanced controls, asset management and productivity project.

Your role:
Safety:
Accountable for creating and maintaining a safe &environmental-friendly operations of Production unit within responsible area including the respect of Chinese regulations and requirements.
Putting forward safety measurements during technical discussion and decision-making.
Able to find unsafe potential on site and take precaution actions to ensure safe production facilities.
Provide technical and safety reviews for Management of Changes and drive process safety compliance as part of engineering reviews. Update P&ID if any change is made.
To help/participate in accident/incident emergency response and support RCA investigations.

Operation:
Execution of POQ production, process validation and guidance of process technology of production.
Compile relevant process file, such as BPR, POQ protocol and report, PV protocol and report and so on.
Lead PIS change control and continuous improvement projects.
Responsible for process management. Strictly monitor and control the process execution and optimize the process parameters to ensure the product quality. Lead process related deviation investigation, find the root cause, draft the report and close CAPA on time.
Support to investigate the root cause of internal/external complaints, prepare the quality corrective report and track the implementation of corrective measures. Statistic and analyzing the process parameters of production.
Follow ISO9001/GMP requirements.
Create and operating procedure in PIS plant, define key process & quality related parameter, offer training to production team and regularly review and update key SOPs by following ISO system and related regulations.
Provide support for capital projects (capacity, efficiency upgrades) as requested by Project Execution Team, Plant Production/Maintenance team.

Who you are:
Bachelor degree or above, chemical engineering or equivalent knowledge of chemical processes.
Minimum 5-8 years working experience, working in a chemical/pharm plant is a plus.
Good safety knowledge and awareness.
Be familiar with office software, such as Words, PPT and Excel.
Good written and oral English.
Clear and effective oral communication skills.
Good problem solving and Self-motivated.
Strong team player with good communication and coordination.
Able to work under stress to meet tight deadlines and handle multiple tasks.

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

Senior Analyst Veeva Vault (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:

Design, Build, Configure and support Veeva Vault based applications to meet business process and application requirements.
Prepares communications and makes presentations on system enhancements and/or alternatives. Evaluates, optimizes, harmonizes, and standardizes existing systems.
Create and update system documentation. Monitors quality standards and ensures failure-free operation. Considers compatibility of different systems.
Solves a range of straightforward problems through knowledge and technical experience in own discipline with a moderate level of guidance.
Analyzes information and possible solutions and makes independent judgments, decisions, and recommendations.
Support the on-going regulatory compliance of the IT components for defined services.
Review and approve regulatory system changes and documentation.
Support periodic reviews of the entire system and compile related reports during operation phase.
Support the on-going regulatory compliance of the IT components for defined services
Support the qualification activity and documentation related to IT solutions delivery
Understands how the team integrates with other teams to achieve overall objectives of the area and builds knowledge of the organization, processes, customers, and key business drivers.

Who you are:

Minimum of 6-10 years of IT experience.
Minimum of bachelor’s Degree or applicable experience within information/Computer systems.
Must have Veeva Vault skillset and having Veeva Vault RIM experience will be preferred.
Deep knowledge of Veeva Vault configuration, developing them in live projects based on client requirement.
Working knowledge of Document and Object record migration from legacy application to Veeva Vault.
Good technical knowledge in core technologies and platforms such as Java, .Net, XML, HTML, PL/SQL & API.
Previous experience in the biotechnology / Pharmaceutical / Life Science or related industry implementing and validating computer systems that manage regulated information
Working knowledge of IT infrastructure qualification processes and IT operating procedures
Solid understanding & experience in GxP, GAMP and delivering validated applications (21 CFR Part 11)
Thoroughly familiar with Quality & GxP IT compliance requirements.
Strong planning and analytical skills combined with ability to work with geographically distributed teams in a rapid development model.
Awareness of ITIL and Support Project Methodology.
Ability to familiarize himself / herself independently with entirely new subjects and thus provide comprehensive and innovative solutions
Excellent written and verbal communications skills
Working knowledge of Information security and best practices

Apply now and become a part of our diverse team!

Senior Filed Application / Senior Customer Application Engineer (Shanghai, Shanghai, CN, 200031)

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Job Listing Detail

Job Descriptions/Purpose:

We are seeking a talented Senior application Engineer to join our products management Thin Film department at ZJG site. This role will focus on leading the following main initiatives:

The Container BCP project, which involves developing alternative sources for containers and valves.
Assist the site and R&D units in the development of new products and provide technical support for client usage.
Help deal with FA analysis of customer complain cases.

Location: The Senior Container Engineer position will be based in ZJG site, & Shanghai ETCC CN, and cooperation with other sites application team. It will primarily support the China market.

Your Role:

Products application development with customers: Analyze the situations arising from the product's application on the customer side, collaborate with relevant production units, QA and R&D units to solve the problems at the user application end, and propose relevant solutions.

FA analysis: Assist in conducting the relevant failure analysis, including designing the analysis process, leading the analysis, cooperating with the QA team to prepare relevant reports, and participating in client discussions

Project Management: Lead or actively participate in cross-functional teams to ensure project timelines, cost efficiency, and quality standards are met.

Technical Support: Provide technical support to internal and external customers, ensuring products application meet customer requirements.

Collaboration: Coordinate closely with multiple teams, including sales, OEM, vendors, project managers, process engineers, production teams, and quality assurance personnel, to ensure optimal product performance and quality.

Experimental Design: Design and conduct hands-on experiments to develop new products or enhance existing ones, while analyzing data and interpreting results independently.

Research and Development: Conduct independent research for papers or patents. Prepare and present research findings, reports, and publications to internal and external stakeholders.

Intellectual Property: Contribute to the development of intellectual property and assist in preparing patent applications as needed.

Regulatory Compliance: Ensure compliance with safety and environmental regulations in all laboratory activities.

Who You Are

Minimum Qualifications:

Education: Bachelor’s or master’s degree in engineering, science, or a related technical discipline (SEMI TF process engineering preferred).
Experience: 5+ years of SEMI industry experience in areas such as Thin-film processing, especially having a good understanding of the principles and applications of ALD, MCVD or CVD processes. or related mechanical design, particularly within the semiconductor manufacturing or chemical industries is plus.
Communication: Excellent verbal and written communication skills, with fluency in English preferred.

Preferred Qualifications:

Education: Master or PhD in engineering, science, or related technical discipline (Semiconductor film process preferred).
Experience: 5+ years of industry experience in areas such Fab TF module and process development, DOE experimental design, understanding of statistical analysis, and root cause analysis.
Research and Development: Experience in conducting independent research, including designing experiments and analyzing data.
Intellectual Property: Familiarity with intellectual property development and patent applications.
Industry Knowledge: Experience in the semiconductor industry or semiconductor materials industry, with an understanding of semiconductor customers' needs for material/container quality and reliability.
Skills: Strong organizational and planning skills with attention to detail, coupled with excellent leadership, communication, and interpersonal skills.
Language Proficiency: Excellent communication skills in both English and Mandarin, both oral and written.

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

应用工程师-量测设备 (Shanghai, Shanghai, CN, 200131)

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FAE will be responsible for assuring proper execution of demo at our demo center facility located in Shanghai. This includes planning, execution, reporting, and customer management when at demo center.

Proper testing of each product on demo center site, including definition of Test plan for each tool and therefore guarantees the quality of our products.

Collaboration with other team in the company & customers to identify new business opportunities.

Backup regional application team whenever needed if needed

The principal roles include:

• Executing FAT plans (measurements, data analysis and result dissemination) while respecting key deadlines to guarantee that each new tool complies with well-defined performance specifications.

• Train the customer and team employees.

• Closely collaborating with the application team and customers to identify new use cases

• Testing new solutions and related software / hardware release.

• Helping to improve the documentation

• Working with the Field Service Engineer team and engineering team on continuous improvement programs to enhance the product quality.

• Documenting any non-conformity detected at customer site

Your profile:

• Engineer (BSC, MS) plus 3 years in Semiconductor Industry with strong knowledge in semiconductor processes & statistical analysis.

• Basic knowledge of Physics of Interferometry, Reflectometry, Defectivity and optics.

• Strong communication, and interpersonal skills, with the ability to work in autonomy and meet scheduled deliverables.

• Strong analytical aptitude and problem-solving capabilities

• Good knowledge of semiconductor manufacturing processes

• Fluent in English

• Occasional international travel is required

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

Senior Medical Science Liaison Italy Rare Tumor (Rome, Rome, IT, 00189)

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Your Role:

As the Senior Medical Science Expert for our newly acquired company, SpringWorks, you will play a pivotal role in driving operations and strategic growth within your designated area in Italy.
You will be responsible for managing a company product(s) within a defined area. This entails establishing and maintaining key scientific relationships with Key Opinion Leaders (KOLs) within their territory and serving as a scientific expert to the medical community and facilitating the appropriate exchange of scientific information.Key expectations include being able to develop and maintain an advanced scientific, medical, and product knowledge base, ability to communicate key insights learned, and disseminate critical scientific data to external stakeholders; including but not limited to academic/scientific/clinical experts and patient organizations.You will be responsible for ensuring timely and appropriate input on the field medical engagement plans in support of our clinical development andcommercialization programs and activities. In addition, you will assist, lead, and drive the support of the company’s clinical trials in partnership with technical development team and with researchers as appropriate. You will be expected to master the MSE responsibilities and be able to take on additional leadership roles on projects and initiatives within the country. You will be expected to work independently with little direction/oversight, be accountable, and assist the Medical Director as needed.

Key Responsibilities will include:

Identify KOLs and establish and maintain strong and deep scientific relationships with KOLs across multi-specialty disciplines, connecting to KOLs in academic and non-academic centers at the local, regional, and national level.
Serve as a scientific expert to the medical community and facilitate the appropriate exchange of scientific information
Communicate experts’ opinion and feedback on new data and clinical trends to Medical Affairs and translate this information into strategic recommendations to enhance science and advance patient care
Act as primary liaison to investigators interested in developing and performing investigator-initiated research
Collaborate with the Clinical Operations organization to enhance patient enrollment in company-sponsored clinical trials by identifying appropriate clinical trial sites, supporting clinical trial awareness, and interacting with investigators in ongoing studies
Serve as medical lead and provide scientific support at medical congresses, support national and European medical booths staffing, participate and lead clinical support, and facilitate medical discussions at advisory boards and local scientific/medical programs
Lead national projects such as national congresses, PAG engagement, as delegated by Country or European medical leadership
Be familiar with country specific pharma rules and regulations, particularly as they apply to MSE activities
Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, non-academic, and healthcare provider settings
Develop and execute territory plans in alignment with regional and national strategy
Develop and maintain strong and deep relationships with clinical decision makers at local and national institutions
Partner with cross functional teams, including HEOR/market access to develop the strategy and generation of health economic and outcomes data as needed, and presentation of such data to relevant audiences
Serve as mentor for other new hires and/or less-experienced MSEs
Manage/lead relevant medical activities/projects including, but not limited to:
- Facilitate and lead field medical onboarding programs, and support training of commercial (including sales) colleagues
- Support Country Medical Director in translating the medical affairs strategy to a national KOL engagement plan and ensures the KOL development translates toindividual territories
- Partner with Global Medical Information colleagues to continuously improve Standard Response Letters and efficiency of MIRF process
- As a senior member of the medical team, contribute to the national, and as needed regional, medical strategy and medical plan
- Provide scientific support to Regional Medical Director and facilitate medical discussion for national medical advisory boards
Other duties as assigned

Who you are:

Advanced Scientific degree or equivalent experience required. (MD, PhD, PharmD)
Minimum of 5 years MSE experience in the pharmaceutical industry
Rare disease experience preferred, particularly in Oncology and/or Neurosciences
Demonstrated mastery of effectively presenting clinical/scientific information
Fluent in both Italian & English

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

Key Account Manager (Moscow, Moscow, RU, 115054)

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г. Москва

На данной роли Вам предстоит:

-Продвижение препаратов компании направления Онкология на вверенной территории;

-Работа со специалистами (представителями администрации здравоохранения, медицинскими и фармацевтическими работниками):

-Реализация бизнес-плана развития территории ответственности;

-Реализация маркетинговой стратегии;

-Организация мероприятий, конференций, круглых столов;

-Взаимодействие с дистрибьюторами;

-Регулярная отчетность в соответствии с внутренними политиками компании.

Наши пожелания к кандидатам:

-Высшее фармацевтическое/медицинское образование;

-Высокий уровень владения медицинской информацией;

-Опыт работы в госпитальном сегменте от 2-х лет;

-Ориентация на результат, развитые коммуникативные навыки, умение работать со сложными клиентами;

-Готовность к командировкам.

Нашим сотрудникам мы предлагаем:

-Оклад + бонус;

-Корпоративный автомобиль;

-ДМС на сотрудника и детей до 23 лет;

-Компенсация питания;

-Страхование жизни, выезжающих за рубеж, от критических заболеваний;

-Различные программы поддержки сотрудников.

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

Medical Science Liaison (MSL) - Temporary Maternity Cover (Madrid, Madrid, ES, 28006)

Apply your magic with us!

Are you ready to explore, break barriers, and discover so much more? We know you have big plans, and so do we—innovating with science and technology to enrich people's lives with solutions in Healthcare, Life Science, and Electronics excites our colleagues around the world. Together, we dream big and share the enthusiasm for caring for a diverse range of people, clients, patients, and the planet. That’s why we are always looking for curious minds to imagine the unseen with us.United as one for patients: our goal in Healthcare is to help create, improve, and prolong lives. We develop treatments, smart devices, and innovative technologies in therapeutic areas such as oncology, neurology, and fertility. Our teams collaborate across six continents with passion and relentless curiosity, aiming to assist patients at every stage of their lives. Joining our Healthcare team means being part of a diverse, inclusive, and flexible work culture that offers fantastic opportunities for personal and professional development around the globe.

Job Description:

As a Medical Science Liaison (MSL) specializing in oncology, you will act as a trusted scientific partner to healthcare professionals and relevant stakeholders across the eastern region of Spain (Comunidad Valenciana, Murcia, Albacete). You will provide credible, up-to-date scientific information to support the optimal use of oncology products and contribute to improving patient outcomes. Your role involves building strong, collaborative relationships, facilitating open scientific exchange, and working closely with regional access and commercial teams to ensure alignment in oncology strategy implementation.

You will gather diverse perspectives and feedback from the field related to oncology treatments to inform inclusive internal decision-making and contribute to shaping future activities. This role requires a field-based presence and adaptability, with a willingness to travel up to 50% within the assigned territory.

Requirements:

Degree in Life Sciences (e.g., biomedical, biotechnology, pharmacy, PhD) or equivalent
Minimum of 1 year experience in a similar role, ideally in oncology
Knowledge of pharmaceutical regulations, clinical research, and Good Clinical Practice (GCP)
Strong scientific knowledge, communication skills, and ability to build inclusive, collaborative relationships in oncology
Organized, analytical, and able to work independently as well as part of a team
Proficient in MS Office and virtual communication tools (e.g., MS Teams, Zoom)

Location: Field-based covering Eastern Spain; remote base possible (e.g., Madrid)

Duration: Until end of 2026 (8-9 months)

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