GMP Documentation Specialist
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GMP Documentation Specialist GMP Documentation Specialist Jobdescription For one of our clients, an international pharmaceutical company, we are seeking a GMP Documentation Specialist.
General Information: Start date: 26.10.2026 End Date: 30.06.2027 Workplace: Schachen, Luzern Workload: 100% Working hours: Standard Home Office: primarily onsite About the work: The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records an…
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