Use Your Power for PurposeEvery day, Pfizer''s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. What You Will Achieve As a member of Pfizer''s dedicated and highly effective Pharmaceutical Sciences Operations Quality (PSOQ) team, you will evaluate and review Pfizer''s investigational products by acting as a Qualified Person (QP) in accordance with The Human Medicines Regulations 2012 (SI 2012/1916) and T he Medicines for Human Use (Clinical Trials) Regulations 2004 (SI 2004/1031) as amended. How You Will Achieve ItAs a QP within PSOQ, the primary job function will be the QP certification and release of Investigational Medicinal Products (IMPs) for use in clinical trials in accordance with UK legislation. Duties are expected to include the following: QP certification of finished IMPs (release for clinical use in a specific study and country) in accordance with The Medicines for Human Use (Clinical Trials) Regulations 2004 (as amended). QP confirmation of partially manufactured IMPs (release for further processing) in accordance with the principles and guidelines of good manufacturing practice (GMP). Maintain detailed knowledge of relevant pharmaceutical legislation and GMP guidel