Specialist Clinical Supplies Quality m/f/d

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, incoming label stock and primary packaging components to release of clinical finished good.

Project title: Specialist Clinical Supplies Quality m/f/d

Type of employment: Payroll

Industry: Engineering

Skills: clinical,GMP,clinical supplies

Project start: 01.07.2026

Project duration: 12 months+

Location: Lucerne, Switzerland, hybrid, 3days onsite

Tasks:

• 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.

Qualifications:

• Previous experience in a similar role is highly appreciated
• candidate should have a deep understanding of working in GMP regulated environment
• university degree (bachelor or higher) is required
• 2-3 years’ experience in regulated environment
• English C1 mandatory, German is nice to have.