GMP Specialist / Batch Record Reviewer | GMP Spezialist (m/w/d)
Randstad Professional
Job Summary
This role involves working as a qualified Chemical Technician focused on ensuring pharmaceutical quality control and compliance within the Life Science sector in Berlin. The specialist will primarily handle the planning and processing of batch documents, including the critical Batch Record Review (BRR) process, ensuring all documentation is complete and compliant with GMP standards. Key daily tasks include conducting chemical and physical quality tests on intermediate and finished medicinal products for release investigations, controlling finished products for appearance and completeness, and meticulously documenting and evaluating all test and control results. The ideal candidate possesses a technical or scientific background, excellent knowledge of GMP requirements, and professional experience in pharmaceutical analysis and BRR. This position offers a stable, permanent contract with performance-based compensation and opportunities for professional development.
Required Skills
Education
Completed technical or scientific vocational training, including proven advanced qualification (e.g., in Pharmaceutical and Chemical Technology or Pharmaceutical Chemistry)
Experience
- Foundational professional experience in Batch Record Review is advantageous
- Experience in medicinal product analysis
- Experience in applying applicable GMP regulations
- Experience with pharmaceutical technologies
Languages
Additional
- Not specified
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