Specialist Clinical Supplies Quality (m/f/d)
For our international pharma client we are looking for a Specialist Clinical Supplies Quality (m/f/d).
Duration: 12 months (possibility of extension)
3 days per week home office
Location: Lucerne
The Clinical Supplies Quality team is responsible for the release of the packaged and labeled drugs for usage in clinical studies. The team handles the release of clinical and commercial drugs for packaging, incoming label stock, and primary packaging components to the release of clinical finished goods.
Tasks and responsibilities:
* Review and release of incoming label stock
* Review and release of clinical finished goods, including the review of the printed and applied label
* GMP review of the batch record and review of the regulatory filings and the final release
Requirements:
* Experience in a regulated environment (pharma, medtech preferred)
* Previous experience in a similar role is highly appreciated; a university degree (bachelor or higher) is preferred
* English C1 mandatory, German is a plus
Deadline: 04.03.2025
Seniority level
Not Applicable
Employment type
Full-time
Job function
Other
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Chemical Manufacturing
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