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

Job Summary

This role involves taking responsibility for quality assurance within pharmaceutical development, specifically focusing on clinical trial preparations. Day-to-day activities include the GMP-compliant handling and documentation of product complaints, conducting thorough root-cause analyses, and implementing appropriate Corrective and Preventive Actions (CAPA). The Quality Engineer will also independently coordinate and execute laboratory tasks, generate detailed results reports, and provide administrative support for the release of clinical trial preparations, including generating necessary import/export documents and QP declarations. The ideal candidate holds a degree in Pharmacy, Chemistry, or a related scientific field, possesses several years of professional experience in pharmaceutical quality assurance, manufacturing, or testing, and demonstrates expert knowledge of cGMP (EU, US) and Clinical Trial Regulation. This permanent, full-time position in Ludwigshafen am Rhein offers the opportunity to actively contribute to the safety and efficacy of global medicines within a dynamic and supportive engineering environment.