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GMP Quality Engineer – Biopharma LVV Production; Hybrid
Job in
2170, Sassenheim, South Holland, Netherlands
Listed on 2026-03-08
Listing for:
Panda International
Full Time
position Listed on 2026-03-08
Job specializations:
-
Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer
Job Description & How to Apply Below
Location: Sassenheim
An international biopharmaceutical organization in Sassenheim is seeking a GMP Specialist to ensure compliance within their new production facility for lentiviral vectors. This key role involves reviewing GMP documentation, managing change controls, leading investigations, and coordinating audits and batch release activities. Candidates should have a degree in Science or Engineering and 2–8 years of experience in a biopharmaceutical GMP environment.
Proficiency in English is required, and knowledge of Dutch is preferred. This position offers a hybrid working model with significant impact in the sector.
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