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Project Manager Hoofddorp • SIRE Life Sciences
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Gevraagd
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37 - 40 uur
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Medior/Senior
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Engels (taal)
Aanbod
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Vast contract
Vacature in het kort
Over het bedrijf
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About the Company
Our client is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors.
Role Description
As a Project Manager, you will be responsible for leading and executing critical small to medium-sized biopharmaceutical technical projects from initial definition through to final handover, all aligned with the site’s strategic goals. You will lead the full project lifecycle design, planning, and execution of equipment, facilities, and utilities CapEx projects. The role aims to deliver best-in-class project outcomes that meet stringent requirements for safety, quality, budget, and schedule.
Responsibilities
- Conduct feasibility studies, develop business cases, and present proposals aligned with project scope and strategy
- Create and manage project plans, ensuring timely, budget-conscious, and high-quality delivery
- Supervise on-site construction and technical execution, ensuring alignment with GMP, GAMP, and industry standards
- Guide cross-functional teams across the full project lifecycle and foster collaboration with key stakeholders
- Ensure compatibility and consistency with existing organizational and industry standards
- Lead ongoing project risk analysis as well as mitigation plan and lead continuous improvement process through lessons learned sessions
- BSc or MSc in Engineering or related technical field
- 4+ years of experience in Technical Project Management within Pharma, Biotech, - Medical Device, Food, Chemical, or Semiconductor industries
- Familiarity with project management methodologies (CAPM, PMP, PRINCE2 preferred)
- Strong knowledge of cGMP manufacturing, GAMP validation model, and ASTM E2500.
- Experience with validation lifecycle activities (FAT, SAT, IQ, OQ, PQ)
Apply to our vacancy for more information. Looking forward to getting in touch!
55067
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