Quality Assurance Engineer – Batch Record Review | Ingenieur (m/w/d) Qualitätssicherung – Batch Record Review (1604)
Brüggen Engineering GmbH
Job Summary
As a Quality Assurance Engineer, you will play a pivotal role in ensuring the highest production standards within the pharmaceutical industry. Your day-to-day responsibilities will include reviewing and approving manufacturing instructions, managing batch records to meet Order Lead Time, and supporting GMP audits. You will also develop and update Standard Operating Procedures (SOPs), conduct internal training, and analyze production data to identify areas for improvement. This position is attractive as it offers an opportunity to directly influence product and process optimization in pharmaceutical quality assurance, working within a dynamic and supportive team environment. You will be instrumental in maintaining regulatory compliance and contributing to the implementation of new Electronic Batch Record (EBR) systems.
Required Skills
Education
Degree in Biotechnology or a comparable field
Experience
- Professional experience in pharmaceutical production
- Experience in parenteral manufacturing (ideally)
- Experience with GMP regulations and hygienic standards
- Experience in pharmaceutical documentation
Languages
Additional
- Not specified
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