Join a leading logistics partner to the healthcare and pharmaceutical industry, as a Quality Manager and Responsible Person (RP). This is a crucial leadership role, responsible for site-level Quality operations, ensuring full compliance with GDP, MHRA, ISO, and internal quality systems. Key ResponsibilitiesLead and manage the on-site Quality department, overseeing personnel, operations, and performance.Act as the named Responsible Person for MHRA licences, ensuring adherence to GDP (2013/C 343/01).Ensure robust implementation of the Quality Management System including deviations, CAPAs, change control, and self-inspections.Maintain compliance with GxP, ISO 9001, ISO 13485, and regulatory standards.Conduct internal and external training on key QA topics and regulatory requirements.Oversee supplier management, quality risk assessments, validation processes, and complaint handling.Lead audit readiness and host MHRA, ISO, and client audits, ensuring timely resolution of any findings.Act as a key quality liaison for clients, attending meetings and maintaining strong working relationships.Prepare, review, and approve Technical and Quality Agreements.Ensure traceability of recalls and release of returned and quarantined stock in accordance with MHRA guidelines.About YouExtensive experience in pharmaceutical or medical device quality assurance, preferably in a logistics/distribution setting.Eligible to act as Responsible Person (RP) under MHRA WDA(H) and WQP guidelines.Solid ..... full job details .....