Specialist QA Manufacturing | Specialist (m/w/d) QA Manufacturing
Simtra Deutschland GmbH
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
Additional
- Not specified
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