Clinical Supplies Quality Specialist.

For our client, an international pharmaceutical company, we are looking for a Clinical Supplies Quality Specialist.
 

General Information:

• Start date: 01.04.2025
• Latest start date: 01.05.2025
• End date: 31.12.2025 (with the possibility of extension)
• Workplace: Schachen, Lucerne
• Workload: 100%
• Remote/Home office: 2 days in the office, 3 days working from home

About the job:

As a part of the Clinical Supplies Quality team you will be 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 workday typically begins at 9:00 AM with a team meeting to discuss ongoing batch releases. You will then focus on reviewing and releasing various items related to clinical supplies.

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

Requirements:

• Minimum of 2 years experience in a regulated environment (pharma, medtech preferred).
• Previous experience in a similar role is highly desirable.
• University degree (Bachelor’s or higher) preferred.
• Fluent in English (C1), German is a plus.

If this sounds like you, we’d love to hear from you! Submit your CV today and become part of a leading pharmaceutical company driving innovation.