Assignment Period
03.08.2026 – 31.07.2027, 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
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