CSV Specialist — GMP Validation Lead for IT/OT Pharma

Panda International

Location

Remote, Netherlands
Published

23.09.2026
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1
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Role description

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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CSV Specialist — GMP Validation Lead for IT/OT Pharma

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