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Regulatory Compliance Specialist Pharmaceutical Manufacturing Pharma Engineer Validation Engineer

Senior Validation Manager – Biopharma CQV & GMP

Job in 2130, Hoofddorp, North Holland, Netherlands
Listing for: Oxford Global Resources
Full Time position
Listed on 2026-05-14
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Pharma Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 EUR Yearly EUR 80000.00 100000.00 YEAR
Job Description & How to Apply Below
A leading biopharmaceutical company in the Amsterdam area is seeking a Senior Manager Validation to oversee validation operations and manage CQV projects. The ideal candidate will have a Bachelor's or Master's in Engineering or Life Sciences and 8-10 years of experience in a GMP-regulated environment. They will lead a team, defining validation strategies and ensuring compliance with regulatory expectations. This position offers a project-based contract until the end of the year with a competitive salary and opportunities for professional development.
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Position Requirements
10+ Years work experience
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