PpThe Clinical Supplies Quality team is responsible for release of the packaged and labeled drugs for usage in clinical studies. The team is responsible from release of clinical and commercial drugs, incoming label stock and primary packaging components to release of clinical finished good. /p pbProject title: /b Clinical Supplies Quality Specialist m/f/d /p pbType of employment: /b Payroll /p pbSkills: /b clinical, GMP, clinical supplies /p pbProject start: /b /p pbLocation: /b Lucerne, Switzerland (hybrid - 3 days onsite) /p pbTasks: /b /p ul liReview and release of incoming label stock /li liReview, and release of clinical finished goods, including review of the printed and applied label /li liGMP review of the batch record and review of the regulatory filings and the final release. /li /ul pbQualifications: /b /p ul liPrevious experience in a similar role /li liDeep understanding of working in GMP regulated environment /li liUniversity degree (bachelor or higher) is required /li li2-3 years’ experience in regulated environment /li liEnglish C1 mandatory, German is nice to have. /li /ul /p #J-18808-Ljbffr