Our client, a global CDMO, is growing their Quality control team. In this role, you will closely collaborate with other laboratory departments on-site, as well as with the Production, Quality, and Supply Chain teams. You will report directly to the Head of Quality Control.

Job Duties:

-Managing and coordinating the incoming goods inspection laboratory (active and auxiliary substances).
-Ensuring accurate sampling, analysis, and documentation of raw materials in accordance with authorized specifications, pharmacopeias, work instructions, and other internal guidelines.
-Guaranteeing compliance with current GLP (Good Laboratory Practice) and occupational safety requirements.
-Providing training for employees.
-Advocating for the laboratory area during regulatory and customer audits.
-Handling and reviewing work instructions, SOPs (Standard Operating Procedures), deviations, OOS (Out of Specification) cases, and other pharmaceutical documentation.
-Contributing to the enhancement of efficiency processes.

Your Qualifications:

-Completion of a degree in natural sciences or engineering, preferably in chemistry, food chemistry, pharmacy, or a related field; several years of professional experience is preferred.
-In-depth knowledge of analytical chemistry.
-Thorough understanding of GMP (Good Manufacturing Practice) regulations related to the release testing of pharmaceutical bulk products.
-Strong analytical thinking and a systematic work approach.
-Exceptional dedication, teamwork, resilience, and decision-making ability.
-Fluent in German and Proficiency in the English language (both written and spoken) and a confident command of MS-Office (Word/Excel).