Quality Auditor III

CK QLS are looking for a Specialist Clinical Supplies Quality, to join a Global Biopharmaceutical company, based in Lucerne.


Duration:
From 1st of May to 31st of December 2025.

Home Office:
We do have a hybrid work model. The candidate will start for training purposes fully on site, and then switch to hybrid (currently 2 days in the office, 3 days home office), and might change depending on business needs.

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

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.

Candidate s Requirements:

• Previous experience in a similar role is highly appreciated, university degree (bachelor or higher) is preferred, experience in regulated environment is an advantage.
• Minimum of 2 years experience in a regulated environment (pharma, medtech preferred).
• English C1 mandatory, German is nice to have.

Day in the job:
3 times per week the day starts at 9, with a team meeting to discuss ongoing jobs to be released (batch). During a day, the person will work on releases.

Apply:
If you are interested, please send a CV in English at . Please quote job reference in all correspondence.