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Specialist Clinical Supplies Quality (M/F/D)
Tasks:
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 for packaging, incoming label stock and primary packaging components to release of clinical finished good.
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, university degree (bachelor or higher) is preferred
experience in regulated environment is an advantage (min 2 years)
English C1 mandatory, German is nice to have
Hybrid work model. The candidate will start for training purposes fully on site and then switch to hybrid (currently 2 days in the office, 3 days home office) and might change depending on business needs.
Requirements:
Start: 01.05.2025
Duration: 7 months
Capacity: 5 days per week
Location: Werthenstein, Switzerland
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