Assignment Period
– , with option for extension
About Our Client
For our client, a globally active pharmaceutical company with a strong focus on clinical research and drug supply, we are looking for a dedicated Specialist Clinical Supplies Quality (f/m/d). The organisation is renowned for its rigorous quality standards, innovative pipeline, and a collaborative culture that places patient safety at the heart of every decision.
Responsibilities
- GMP‑compliant batch record review and formal release of clinical finished goods
- Incoming inspection and release of label stock and primary packaging components
- Verification of printed and applied labels as part of the finished goods release process
- Review of regulatory filings in connection with batch release activities
- Active participation in daily team coordination meetings to align on ongoing release priorities
- Ensuring full compliance with GMP regulations throughout all quality activities
Qualifications
- University degree (Bachelor's or higher) in pharmacy, life sciences, chemistry, or a related field
- 2–3 years of professional experience in a GMP-regulated environment, ideally in clinical or commercial drug supply
- Solid understanding of GMP principles and quality release processes in the pharmaceutical industry
- Proficiency in English at C1 level (mandatory); knowledge of German is an advantage
- Structured, detail-oriented working style with a strong sense of quality and compliance
- Ability to work independently as well as collaboratively in a dynamic team environment
