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

FERCHAU GmbH Niederlassung Mannheim

Mannheim, Baden-Württemberg, Deutschland
Published Apr 17, 2026
Full-time
No information

Job Summary

As a Quality Engineer in the pharmaceutical sector, you will be responsible for GMP-compliant complaint management specifically for clinical trial products. Your daily activities will involve conducting root cause analyses, generating detailed reports, and coordinating laboratory analyses to implement effective Corrective and Preventive Actions (CAPAs). You will play a vital role in maintaining Quality Management System (QMS) documentation, performing pharmaceutical risk assessments, and overseeing product releases. Additionally, the role involves preparing clinical trial applications and submission documents, as well as translating testing specifications into in-process and final inspection guidelines. This position is particularly attractive due to the opportunity to work on complex development projects for renowned life science clients, supported by extensive professional development through the FERCHAU Academy and a comprehensive benefits package including childcare subsidies and special leave.

Required Skills

Education

Completed university degree in Natural Sciences (e.g., Biology, Chemistry, Pharmacy) or a related field.

Experience

  • Professional experience in the pharmaceutical industry
  • Practical experience in drug development and the management of clinical trial products
  • Proven track record in GMP-compliant quality management and documentation
  • Experience in handling clinical trial applications and regulatory submission documents

Languages

German (Fluent)English (Fluent)

Additional

  • Knowledge of international pharmaceutical law and Clinical Trial Regulation (CTR) is required. The role involves coordination between laboratory teams and regulatory bodies.