| Location | Leiden, Netherlands |
|---|---|
| Business Sector | Biotechnology |
| Contact email | |
| Job ref | 25167 |
| Published | 1 day ago |
Role: Project Manager Global MSAT
Location: Leiden
Start date: ASAP
Contract duration: 6 months (highly likelihood of extension)
Project Scope
We are seeking a skilled Project Manager to join the Global MSAT team. In this role, you will collaborate closely with a seasoned team of engineers to define plans and procedures that support the implementation of process changes across a global manufacturing network. You will also play a key role in advancing the development of CAR-T and TCR-T manufacturing processes and products from early clinical stages to commercial readiness.
Your Mission
Act as the MSAT project lead for cell therapy change implementations, coordinating efforts from the central reference site in close collaboration with regional operations teams.
Develop and maintain comprehensive global MSAT project plans and timelines to ensure alignment and successful execution across all regions.
Translate technical and operational process changes into structured implementation packages, and guide their deployment across manufacturing sites.
Lead investigations into product and process issues, and define effective corrective and preventive actions.
Build trust and maintain positive relationships with cross-functional teams and key stakeholders in Regional Manufacturing, CMC, QA, and Regulatory Affairs.
Facilitate knowledge transfer between global and regional teams, promote issue resolution, and share best practices across the network.
This position reports to the Associate Director of Global MSAT.
Job Requirements
PhD in life sciences, biotechnology, engineering, or a related field with at least 7 years of relevant experience; or an MSc with equivalent industry experience.
Proven experience in project management within the biotech or pharmaceutical industry, ideally with a focus on cell therapy technology transfers.
Strong understanding of regulatory frameworks such as FDA and EMA guidelines, as well as GMP requirements.
Excellent verbal and written communication skills with the ability to work effectively across functions and international teams.
Results-oriented mindset with a strong sense of accountability, without compromising on quality or compliance.
Strategic thinker with the ability to drive initiatives from concept through to implementation.
Comfortable in a dynamic, fast-paced environment with the ability to manage multiple priorities and adapt to changing needs.
Strong interpersonal skills and fluency in written and spoken English.