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

Job Summary

This role is critical for ensuring the quality and safety of clinical trial drugs within the pharmaceutical industry. The Quality Engineer will manage and document product complaints for clinical investigational products in compliance with GMP standards. Key responsibilities include supporting root-cause analysis, defining corrective and preventive actions (CAPA), and assessing the impact on drug safety and quality. The position also involves independently coordinating and executing laboratory tasks, generating comprehensive result reports, and providing administrative support for the release of clinical trial drugs, including creating import/export documentation and QP declarations. This role requires strong regulatory knowledge, excellent organizational skills, and collaborative engagement with Quality Assurance, Production, Laboratory, and Regulatory functions.