Senior Qualified Person (QP) Manager

Are you a proven leader in pharmaceutical Quality Assurance with a strong background in QP oversight and team development?Do you have the vision and drive to lead Qualified Person operations across multiple sites, shaping strategic quality direction while mentoring high-performing teams?We are recruiting for a Senior QP Manager to take on a pivotal leadership role within a dynamic and highly regulated radiopharmaceutical manufacturing environment. This position offers the opportunity to lead a team of Qualified Persons, influence quality strategy at a national level, and ensure excellence in GMP compliance across UK operations.About the RoleAs a Lead QP, you will play a critical role in ensuring the safe release of radiopharmaceutical products across multiple sites in the UK. You will be responsible for:Managing and leading a team of permanent and contract Qualified Persons (QPs) across multiple UK manufacturing sites.Acting as a Releasing QP for radiopharmaceuticals/sterile products under a UK MHRA licence.Chairing the QP Forum and contributing to site Quality Management Meetings.Ensuring compliance with GMP, UK/EU regulations, and local/global procedures.Reviewing and certifying batches in a timely manner while overseeing deviations, complaints, CAPAs, and OOS/OOT investigations.Supporting MHRA inspections at key manufacturing sites.Acting as a mentor and coach for quality teams, fostering a culture of compliance and continuous improvement.Working closely with the Head of Quality to enhance and maintain the Global Quality System.Experience & QualificationsEligible to be named as a Qualified Person (QP) on a manufacturing licence.10+ years’ Quality Assurance experience within a UK-licensed pharmaceutical organisation.5+ years’ experience managing Quality teams in Quality Assurance or Quality Control.Previous experience in QP certification of medicinal products.Background in pharmaceutical manufacturing, preferably in sterile or radiopharmaceutical production