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Project Scheduler/Steerer (CDM 18 months) - All Genders

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.

Fixed-term contract from July 2026 to December 2027

 

As the Project Scheduler/Steerer for Helvetia, you will be responsible for the integrated detailed project scheduling and drive progress across a strategic investment project in the pharmaceutical industry. You will be the sole Scheduler, reporting to the Project Manager, working closely with the Work Package Owners and other stakeholders to ensure alignment with the project goals. Your role encompasses end-to-end scheduling across the three main project streams (buildings/infra, biotech process, IT/automation) in a fast-paced, regulated environment, with a clear impact on timelines, budgets, and resource allocations.

 

Key Responsibilities:

  • Develop and maintain the integrated detailed Level 4+ schedule (logic-linked) aligned with Level 3 schedule issued in Basic Design phase, identifying critical paths 
  • Optimize schedules impacting manufacturing operations and manage interdependencies between Work Packages to prevent bottlenecks 
  • Regularly update the schedule to reflect scope changes, delays, and shifting priorities; ensure real-time accuracy 
  • Ensure schedule alignment with resource constraints, budget, and overall project objectives 
  • Organize and lead coordination meetings, prepare agendas, document decisions, and track actions and deadlines; act as liaison between teams 
  • Lead the Change Order Process : Define workflow for scope changes, assess impacts on schedule, budget, and resources, and communicate and integrate approved changes 
  • Maintain the risk register, implement mitigation strategies, and escalate high-priority risks as needed 
  • Track progress (schedules, resources, milestones) and produce monthly performance reports with KPIs; support updates for the Steering Committee
     

Expected Skills and Competencies:

 

  • Education: Bachelor’s or Master’s degree in engineering, life sciences, or a relevant technical/scientific field. Languages: English and French (bilingual) proficiency required.
  • Experience: 5–10 years in project scheduling, coordination, or project management, preferably in large-scale industrial or pharmaceutical projects.
  • Expertise: Proven ability to manage complex schedules and coordinate large, multidisciplinary projects.
  • Advantage: Experience in steering large, strategic investment projects is a plus.
  • Technical skills: Proficiency in MS Project and knowledge of technical disciplines and their workflows and constraints.
  • Analytical ability: Strong skills to interpret data and generate actionable insights.
  • Project management: Demonstrated experience with multiple work packages and cross-functional teams; knowledge of PM best practices.
  • Key Deliverables: Detailed schedule with critical paths, site shutdown coordination, risk mitigation plans, robust change-order workflow, and monthly KPI reports.

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! 
Job Requisition ID:  298735
Location:  Aubonne
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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Job Segment: Pharmaceutical, Project Manager, Scheduler, Oncology, Science, Technology, Administrative, Customer Service, Healthcare

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