CSV Specialist — GMP Validation Lead IT/OT Pharma
Job in
3012 XX, Rotterdam, South Holland, Netherlands
Listed on 2026-04-01
Listing for:
Panda International
Full Time
position Listed on 2026-04-01
Job specializations:
-
Pharmaceutical
Job Description & How to Apply Below
A leading pharmaceutical company in the Netherlands is looking for a CSV Specialist to join their Engineering department. This role focuses on the optimization and maintenance of computerized systems management within a GMP-regulated environment. You will lead CSV activities for IT/OT automation projects, ensuring compliance with industry standards such as GAMP 5 and 21 CFR Part 11. The ideal candidate has a relevant degree, 3-4 years of experience, and expertise in risk management and validation testing.
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