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Specialist Clinical Supplies Quality (M/F/D)
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.
Tasks:
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
Qualification:
Previous experience in a similar role is highly appreciated, candidate should have a deep understanding of working in GMP regulated environment, university degree (bachelor or higher) is required, 2-3 years’ experience in regulated environment
English C1 mandatory, German is nice to have
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
Hybrid work model: candidate will start for training purposes fully on site and then switch to hybrid (up to 3 days in the office, 2 days home office) and might change depending on business needs
Candidates immediately available are strongly preferred. Nevertheless, latest start entry date that can be considered is 01 August 2026
Requirements:
Start: 03.08.2026
Duration: 12 months
Capacity: 5 days per week
Location: Werthenstein, Switzerland
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