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

Job Summary

As a Quality Engineer in Pharmaceutical Development at BRÜGGEN ENGINEERING, you will play a critical role in ensuring the safety and efficacy of medicinal products. Your day-to-day responsibilities involve the GMP-compliant processing and documentation of product complaints related to clinical trial supplies. You will lead root-cause analyses, define Corrective and Preventive Actions (CAPA), and coordinate laboratory tasks to assess impacts on drug quality. Beyond technical analysis, you will provide administrative support for the release of clinical trial products, including the preparation of import/export documentation and QP declarations. This role is highly collaborative, requiring seamless interaction with production, laboratory, and regulatory departments. It is an attractive opportunity for professionals who want to work at the intersection of quality assurance and clinical research within a permanent, full-time position that offers significant responsibility and international exposure in the pharmaceutical sector.