Clinical Supplies Quality Specialist

For our client, a leading international pharmaceutical company, we are seeking a Clinical Supplies Quality Specialist.

General Information:

• Start date: ASAP, 01.05.2025
• Duration: until 31.12.2025 with the possibility of extension
• Workplace: Schachen, Lucerne
• Workload: 100%
• 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 release of the packaged and labeled drugs for usage in clinical studies. The team is responsible for release of clinical and commercial drugs for packaging, incoming label stock and primary packaging components to release of clinical finished goods.

3 times per week the day starts at 9 am 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

Must-haves:
 

• Minimum of 2 years experience in a regulated environment (pharma, medtech preferred)
• Proficiency in English (C1), German is nice to have
• Bachelor’s degree or higher preferred
• Prior experience in quality-related roles within GMP environments is highly desirable

Does this sound interesting to you? Apply now – we look forward to receiving your application!
 

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