GMP Specialist | GMP Spezialist (m/w/d)
Randstad Professional
Job Summary
As a GMP Specialist, you will be responsible for batch record review and quality control in a pharmaceutical environment. Your day-to-day tasks include planning and processing batch documentation, conducting chemical and physical quality tests on intermediates and finished products, and ensuring GMP-compliant workflows. You will also manage sample entry/exit, document and evaluate test results, and compile complete batch records. The role requires a technical or scientific education with proven further training in pharmaceutical or chemical technology, strong GMP knowledge, and experience in batch record review or pharmaceutical analytics. This position offers a performance-oriented salary, up to 30 vacation days, and potential for permanent hire. Join a leading pharmaceutical company in Berlin and advance your career in a specialized field.
Required Skills
Education
Completed technical or scientific education with verifiable further training qualification, e.g., in pharmaceutical and chemical technology or pharmaceutical chemistry
Experience
- Proven professional experience in batch record review preferred
- Experience in pharmaceutical analytics, GMP regulations, or pharmaceutical technologies
Languages
Additional
- Location: Berlin, Germany. Work permit required for non-EU citizens.
More Jobs from Randstad Professional
Electrical Engineer | Elektrotechniker (m/w/d)
May 25, 2026
As an Electrical Engineer at a pharmaceutical company in Biberach, you will be responsible for recor...
Technical Assistant | Technical Assistant (m/w/d)
May 22, 2026
Randstad Professional is seeking a Technical Assistant for a permanent, full-time role in the pharma...
Project Office Specialist | Project Office Specialist (m/w/d)
May 21, 2026
Join a leading talent company as a Project Office Specialist in the pharmaceutical industry, based i...