Quality Engineer for Pharmaceutical Development | Quality Engineer (m/w/d) Arzneimittelentwicklung (1657)

Job Summary

As a Quality Engineer in drug development, you will play a critical role in ensuring the safety and efficacy of clinical trial preparations. Your day-to-day responsibilities involve managing product complaints in compliance with Good Manufacturing Practice (GMP) standards, conducting root-cause analyses, and defining CAPA measures. You will also coordinate laboratory tasks, produce detailed result reports, and provide administrative support for the release of clinical trial materials, including the preparation of import/export documentation and QP declarations. This role is highly collaborative, requiring close interaction with production, laboratory, and regulatory departments. This position is particularly attractive for professionals seeking a permanent, full-time role in Ludwigshafen am Rhein with a company that values personal growth and interdisciplinary cooperation. You will have a direct impact on global patient safety by maintaining rigorous quality standards throughout the pharmaceutical development lifecycle.