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 * Escalate critical quality issues and support impact assessments in collaboration with the * University degree in a scientific discipline (Pharmacist, PhD in Life Sciences, Bio‑Engineer, or equivalent) * Experience in QA and/or Production, with strong exposure to quality systems and/or batch release
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