CK QLS in Lucerne is seeking a Quality Auditor to join their Clinical Supplies Quality team. The role involves reviewing and releasing packaged drugs for clinical studies, with responsibilities including GMP review and managing label stock.
This position offers a hybrid work model, allowing up to 3 days in the office per week. Candidates should have a bachelor's degree, 2–3 years of experience in a regulated environment, and strong knowledge of GMP standards.
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