Specialist QA Manufacturing | Specialist (m/w/d) QA Manufacturing

Simtra Deutschland GmbH

Halle (Westfalen), Nordrhein-Westfalen, Deutschland
Published Nov 14, 2025
Full-time
Permanent

Job Summary

This role acts as a critical interface between Production and Quality Assurance, ensuring strict adherence to current Good Manufacturing Practice (GMP) guidelines within a facility producing pharmaceuticals for cancer and other life-threatening diseases in Halle/Westphalia. The Specialist will perform Quality Oversight, support production staff in identifying preventive measures to avoid deviations, and execute batch documentation review and QA release. Key responsibilities include observing and evaluating media fill runs in sterile areas, organizing the QA Media Fill Review, and managing associated documentation. Candidates should possess a degree in Chemistry, Pharmaceutical Technology, Biotechnology, Pharmacy, or related fields, ideally with initial professional experience and knowledge of GMP and aseptic manufacturing. Success in this role requires excellent German and English proficiency, flexibility, strong teamwork skills, and a meticulous, structured approach to work.

Required Skills

Education

Completed university degree in Chemical or Pharmaceutical Technology, Biotechnology, Pharmacy, Food Technology, or related fields

Experience

  • Initial professional experience (desirable)
  • Experience with GMP guidelines (desirable)
  • Knowledge of aseptic manufacturing (desirable)

Languages

German (Fluent)English (Fluent)

Additional

  • Not specified