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Lead GMP QA operations for clinical trial materials and companion diagnostics in Mechelen. You will build and mentor a team, ensure EU/FDA compliance, and oversee batch release. Requires 7+ years' GMP QA experience in pharma/medical devices, team leadership, and fluency in English and Dutch. Join...
Location
Belgium , Mechelen
Salary
Not provided
Amaris Consulting
Expiration Date
Until further notice
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