For our client, a leading international pharmaceutical company, we are seeking a Clinical Supplies Quality Specialist.
General Information:
* Duration: until 31.12.2025 with the possibility of extension
* Working hours: Standard
* Home office: Possible, 2 days on-site, 3 days home office
About the job:
The Clinical Supplies Quality team is responsible for releasing packaged and labeled drugs for use in clinical studies. The team handles the release of clinical and commercial drugs for packaging, incoming label stock, and primary packaging components, up to the release of clinical finished goods.
The workday begins three times a week at 9 am with a team meeting to discuss ongoing jobs for release (batches). Throughout the day, the specialist works on these releases.
Tasks & Responsibilities:
* Review and release of incoming label stock
* Review and release of clinical finished goods, including verification of printed and applied labels
* GMP review of batch records and regulatory filings for final release
Must-haves:
* Minimum of 2 years experience in a regulated environment (pharma, medtech preferred)
* Proficiency in English (C1), German is a plus
* Bachelor’s degree or higher preferred
* Prior experience in quality roles within GMP environments is highly desirable
Does this sound interesting to you? Apply now — we look forward to receiving your application!
Additional Details:
* Seniority level: Associate
* Employment type: Contract
* Job function: Other
* Industry: Pharmaceutical Manufacturing
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