For one of our clients, an international pharmaceutical company, we are seeking a Clinical Supplies Quality Specialist.
General Information:
- Start date: ASAP
- Latest possible start date: 03.08.2026
- End Date: 31.07.2027
- Workplace: Schachen, Luzern
- Home office: possible
- Workload: 100%
- Working hours: Standard
About the work:
The 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.
3 time per week the day starts at 9 with a team meeting to discuss ongoing jobs to be released (batch). During a day, the person will work on releases.
Tasks & Responsibilities:
- Review and release of incoming label stock
- Review, and release of clinical finished goods, including review of the printed and applied label
- GMP review of the batch record and review of the regulatory filings and the final release
Requirements:
- University degree (bachelor or higher)
- Deep understanding of working in GMP regulated environment
- 2-3 years’ experience in regulated environment
- Previous experience in a similar role is highly appreciated
- English C1 mandatory, German is nice to have
Sounds interesting? Apply now – we’re looking forward to receiving your applications!
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