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CK Group seeks a Quality Auditor to join its CK QLS division in Schachen, working within the Global Development Quality Operations team. The role focuses on GMP documentation review, supporting batch release decisions, and maintaining high standards of GMP compliance.
The candidate should have QA/Quality Operations experience in a regulated environment, strong attention to detail, and a Bachelor’s degree or higher.
Quality Auditor
CK QLS is recruiting a Quality Assurance Specialist to join the Global Development Quality Operations team at a leading pharmaceutical company in Schachen.
This opportunity is suited to a quality-focused professional who enjoys reviewing GMP documentation and supporting compliance within a pharmaceutical environment.
You will work within a collaborative team, with regular meetings to discuss ongoing activities. The role offers hybrid working, requiring at least three days per week on site, with additional attendance depending on business needs.
Applicants must be an EU citizen or hold a valid Swiss work permit.