Manufacturing Quality Assurance Specialist | Specialist (m/w/d) QA-Manufacturing
Simtra Deutschland GmbH
Job Summary
This role acts as a critical interface between production and quality assurance at a pharmaceutical manufacturing site in Halle/Westfalen, specializing in oncology and life-saving medications. The successful candidate will ensure strict adherence to GMP guidelines and perform quality oversight directly on the shop floor. Key responsibilities include supporting production staff in identifying preventive measures to avoid deviations, monitoring and evaluating media fill runs (both in-person in sterile areas and via video review), and managing the associated documentation. You will also be responsible for reviewing batch documentation, granting QA releases, and approving production-related GMP documents such as manufacturing instructions and cleaning protocols. This position is ideal for professionals with a background in pharmaceutical technology or biotechnology who enjoy a structured, detail-oriented environment. The role offers an attractive 37.5-hour work week, 30 days of vacation, and comprehensive social benefits within a diverse and inclusive corporate culture.
Required Skills
Education
Completed degree in Chemical or Pharmaceutical Technology, Biotechnology, Pharmacy, Food Technology, or a related field of study.
Experience
- Initial professional experience in a pharmaceutical or chemical manufacturing environment is desirable
- Practical knowledge of GMP (Good Manufacturing Practice) standards
- Experience or knowledge in aseptic manufacturing processes is preferred
- Experience in creating and revising Standard Operating Procedures (SOPs)
Languages
Additional
- Willingness to work in sterile production areas; ability to perform video-based reviews of manufacturing processes; location-based in Halle/Westfalen.
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