GMP Quality Specialist | GMP Spezialist (m/w/d)
Randstad Professional
Job Summary
As a GMP Quality Specialist (Batch Record Reviewer) based in Berlin, you will play a critical role in the pharmaceutical manufacturing process by ensuring all production documentation meets rigorous regulatory standards. Your daily responsibilities will involve the detailed planning and processing of batch records, performing physical and chemical quality tests for the release of intermediate and finished medicinal products, and maintaining GMP-compliant workflows within the laboratory complex. You will be responsible for documenting test results, managing retention samples, and verifying that final products match all registration requirements. This position is ideal for professionals with a technical or scientific background who possess a high attention to detail and a commitment to pharmaceutical safety. Joining this global leader in recruitment services offers a secure, permanent contract with attractive social benefits, including holiday pay and professional development through extensive e-learning opportunities, all while working within a supportive and inclusive team environment.
Required Skills
Education
Completed technical or scientific vocational training with verifiable further qualifications, specifically in fields such as Pharmaceutical Technology, Chemical Technology, or Pharmaceutical Chemistry.
Experience
- Professional experience in Batch Record Review is highly advantageous
- Experience in the field of pharmaceutical analytics
- Proven experience applying current GMP regulations and pharmaceutical technologies
- Experience in conducting chemical and physical quality testing for product release
Languages
Additional
- Must have the ability to work independently with a structured approach; requires high levels of responsibility and assertiveness; position is based in Berlin.
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