QA GMP Compliance support Consultant

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.