As a QA GMP Compliance Support, you will act as a Person‑in‑Plan (PIP) at a Contract Manufacturing Organization (CMO) in Germany. You will provide on‑site quality oversight of clinical drug product manufacturing activities and ensure compliance with GMP requirements and applicable Quality Agreements. 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. * Ensure that clinical batches are manufactured in compliance with GMP standards and Quality Agreements - o Performing GEMBA walks when required to ensure process compliance o GMP compliance
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