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

Job Summary

This role offers a career in pharmaceutical quality assurance, focusing on ensuring the quality and safety of clinical trial materials within drug development. The Quality Engineer is responsible for GMP-compliant management and documentation of product complaints, including supporting root-cause analysis and defining appropriate Corrective and Preventive Actions (CAPA). Day-to-day tasks involve coordinating and performing essential laboratory duties, generating comprehensive result reports, and providing critical administrative support for the release of clinical trial materials, such as creating import/export documents and QP declarations. Success in this position requires a degree in Pharmacy, Chemistry, or a related scientific field, coupled with several years of professional experience in pharmaceutical quality assurance or manufacturing. Candidates must possess strong knowledge of cGMP (EU, US), Clinical Trial Regulation, and international pharmaceutical law, alongside excellent English proficiency, organizational skills, and a precise, solution-oriented working style.