Quality Engineer for Pharmaceutical Biotechnology | Qualitätsingenieur Phamazie Biotechnologie (m/w/d)
Brunel GmbH NL Würzburg
Job Summary
As a Quality Engineer, you will play a critical role in the production, testing, and storage of cell banks, drug substances, and drug products for proprietary development products. Your daily responsibilities involve managing deviations and change controls, acting as a key representative in team rooms, and drafting Product Specification Files. You will serve as a vital point of contact between manufacturing departments and the quality unit, ensuring all processes align with rigorous standards. This position is particularly attractive for professionals looking to build a broad base of expertise in the medical technology and biotech sectors within an internationally successful engineering service provider. Brunel offers a permanent contract, 30 days of vacation, and a structured career path with individual training and feedback sessions, providing both stability and professional growth in a highly regulated and innovative environment.
Required Skills
Education
University degree in Medical Technology, Biology, or an equivalent vocational training combined with relevant professional experience.
Experience
- Initial professional experience in the production or testing of biological agents and products.
- Proven knowledge of quality processes including Deviation, Investigation, and CAPA.
- Experience working within GMP regulated environments.
- Practical experience using electronic systems for recording quality events.
Languages
Additional
- Permanent full-time contract. Location-based role within the DACH-CZ region.
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