ph3Quality Auditor, Specialist Clinical Supplies Quality, Lucerne, Fulltime /h3 pCandidates immediately available are strongly preferred. The latest start date that can be considered is 01 August 2026. /p h3Home office hybrid working /h3 pWe have a hybrid work model. The candidate will begin training fully on‑site, then transition to hybrid (up to 3 days in the office, 2 days home office) and may adjust depending on business needs. /p h3Description of the department /h3 pThe Clinical Supplies Quality team is responsible for the release of packaged and labeled drugs for use in clinical studies. The team manages release of clinical and commercial drugs, incoming label stock, primary packaging components, and clinical finished goods. /p h3Job tasks and responsibilities /h3 ul liReview and release of incoming label stock /li liReview and release of clinical finished goods, including printed and applied labels /li liGMP review of the batch record, regulatory filings, and final release /li /ul h3Requirements for the position /h3 ul liPrevious experience in a similar role is highly appreciated. Candidates should have a deep understanding of GMP‑regulated environments, hold a bachelor’s degree or higher, and possess 2–3 years of regulated‑environment experience. /li liLanguage requirements: English C1 mandatory, German is a plus. /li /ul h3Day in the job /h3 pThree times per week the day starts at 9 am with a team meeting to discuss ongoing releases. During the day, the person will focus on completing release activities. /p /p #J-18808-Ljbffr
