Specialist Clinical Supplies Quality.

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

• Start date: ASAP
• End: 30.06.2024
• Extension: possible
• Workplace: Luzern
• Workload: 100%
• Home office & hybrid working: The candidate will start for training purposes fully on site and then switch to hybrid (2 days in the office, 3 days home office) which might change depending on business needs.

 

Department description:
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.

 

Your Responsibilities:

1. Review and release of incoming label stock
2. Review, and release of clinical finished goods, including review of the printed and applied label
3. GMP review of the batch record and review of the regulatory filings and the final release

 

Your profile:

• Previous experience in a similar role is highly appreciated, university degree (bachelor or higher) is preferred, experience in regulated environment is an advantage
• English C1 mandatory, German is nice to have