Real Staffing Brussels (International) is seeking a QA GMP Compliance Support in Neuenburg, Switzerland. In this role, you will act as a Person-in-Plan (PIP) at a Contract Manufacturing Organization (CMO) and provide on-site quality oversight for clinical drug product manufacturing activities. Your responsibilities include ensuring compliance with GMP standards and Quality Agreements, overseeing drug manufacturing processes, and reporting on progress. Ideal candidates should have an understanding of quality compliance in a pharmaceutical context.
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