Quality Engineer, Pharmaceutical | Qualitätsingenieur (m/w/d) Pharma

Job Summary

This role involves ensuring the quality and compliance of clinical trial preparations within the pharmaceutical and life science sectors. The Quality Engineer will be responsible for GMP-compliant complaint management, conducting root cause analyses, and coordinating laboratory analyses, including the implementation of Corrective and Preventive Actions (CAPAs). Key duties also include creating and maintaining Quality Management System (QMS) documents, performing pharmaceutical risk assessments, and managing product releases. The ideal candidate holds a degree in natural sciences, possesses experience in the pharmaceutical industry, and is proficient in drug development, clinical trial management, and international pharmaceutical law, particularly cGMP (EU/US) and the Clinical Trial Regulation (CTR). The position requires fluent German and English skills, both written and spoken, to effectively contribute to complex development projects and drive technological advancement.