As a QA GMP Compliance Support, you will act as a Person‑in‑Plan (PIP) at a Contract Manufacturing Organization (CMO) in Germany. A leading global pharmaceutical organisation, recognised for its high standards in quality, GMP compliance, and patient safety, operating in a highly regulated environment and working closely with external manufacturing partners for the production of pharmaceutical products, including sterile drug products. * Support the investigation, follow‑up, and closure of deviations, including associated CAPAs * University degree in a scientific discipline (Pharmacist, PhD in Life Sciences, Bio‑Engineer, or equivalent) * Relevant experience in the pharmaceutical industry within a GMP environment * Fluent in English (written and spoken); German is a plus - The position can be offered either on a contract or permanent basis, depending on the candidate's preference and profile.
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