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Quality Assurance Specialist in Clinical QA for pharmaceutical studies

Join a dynamic company offering daily challenges in clinical quality assurance. Your role includes handling GMP-compliant product complaints, coordinating lab investigations, and preparing reports. You will also support deviation analysis, define CAPA measures, and assist in clinical trial material release and regulatory documentation. A scientific degree and experience in pharmaceutical quality assurance are required.

Location

DEA, Deutschland

Contact

Brunel GmbH NL Mannheim

Added

16 October 2026

View source (europa.eu)

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