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:
Clinical Supplies Quality Specialist m/f/d
Type of employment:
Payroll
Skills:
clinical, GMP, clinical supplies
Project start:
01.07.2026
Location:
Lucerne, Switzerland (hybrid - 3 days 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
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.
#J-18808-Ljbffr
Project title:
Clinical Supplies Quality Specialist m/f/d
Type of employment:
Payroll
Skills:
clinical, GMP, clinical supplies
Project start:
01.07.2026
Location:
Lucerne, Switzerland (hybrid - 3 days 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
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.
#J-18808-Ljbffr
