Join a leading global pharmaceutical organization focused on advancing science and developing innovative therapies that make a real difference for patients. At the Leiden site, multidisciplinary teams work in a highly regulated laboratory and production environment, supporting cutting‑edge therapeutic development.
About the RoleAs an Associate Scientist – Compliance Management, you will support quality and compliance activities within an Analytical Development laboratory environment. You will work closely with cross‑functional stakeholders to ensure GMP compliance, manage quality systems, and continuously improve processes in a dynamic, science‑driven setting.
Key Responsibilities- Review, lead, and manage document revisions in line with GMP standards
- Manage change controls, non‑conformances, and CAPA records
- Maintain and manage training curricula for laboratory employees
- Perform self‑inspections and support continuous quality improvements
- Collaborate closely with internal stakeholders to ensure compliance and alignment
- MLO-4 or Bachelor/HBO level education (no Master’s degree required)
- 2–5 years of experience in GMP compliance or quality‑related roles
- Experience with laboratory systems such as COMET, TruVault, or SUMMIT
- Background in a quality‑driven, regulated laboratory environment
- Strong communication skills in both English and Dutch
This is an on‑site role in Leiden with a strong focus on collaboration, quality, and compliance. Contract extension is possible based on performance.
Looking forward to speaking with you!
#J-18808-Ljbffr€45000 - €65000 monthly