Downstream GMP Specialist - Onsite Pharma Manufacturing
Job in
6000, Luzern, Kanton Luzern, Switzerland
Listed on 2026-06-20
Listing for:
Randstad Switzerland
Full Time
position Listed on 2026-06-20
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Regulatory Compliance Specialist, Validation Engineer -
Pharmaceutical
Pharmaceutical Manufacturing, Regulatory Compliance Specialist, Validation Engineer
Job Description & How to Apply Below
Randstad Switzerland is seeking an Associate Process Specialist in Luzern. This role involves supporting the manufacturing team with GMP operations while ensuring compliance with regulatory standards. Candidates should have a relevant degree and experience in pharmaceuticals.
The position requires a full-time presence at the workplace, with tasks including the execution of manufacturing processes and documentation management. Proficiency in both English and German is essential and candidates must be willing to relocate or commute to Schachen.
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