Looking for a QA role that challenges your thinking as much as it values your expertise? Join an award-winning global Pharmaceutical company dedicated to improving patient outcomes through quality excellence and state-of-the-art technology. We have an exciting opportunity for an experienced Quality Assurance Manager to join the established Quality team The Role: Full Time, Monday to Friday, On-site As a QA Manager, you will be an active member of the Quality Department and Site Management Team People management for the QA Department as required, including managing of workloads, setting objectives and performance development Operational oversight of Quality Assurance Officers, Document Controller, Admin and Quality Support Officer, including responsibility for absence, sickness, and overtime Coordinate with the Head of Quality, Lead QP, QPs, Senior QA Manager and other QA Managers in maintaining and improving the Global Quality system Lead Site Quality Management Meetings, document and track actions, and proactively drive the resolution of identified issues Perform and/or oversee internal audits in accordance with the internal audit schedule and ensure spot checks are being performed Participate in MHRA inspections and client audits as site host alongside the Head of Quality Support the introduction and development of an eQMS and/or LIMS system Serve as the Quality SME (Subject Matter Expert) for site and global projects Drive compliance with the site maintenance schedule through close collaboration with Production and QC teams Review and approve deviations, complaints, CAPAs, change controls and Out of Specification (OOS) / Out of Trend (OOT) investigations Maintain control of Quality documentation through the review and approval of SOPs, forms, logbooks, and templates Escalate serious quality matters to the Quality Leadership Team Support the QP in the withdrawal and recall process and reporting of quality defects to the DMRC About You: Degree or higher in relevant scientific area or equivalent experience in a pharmaceutical setting A strong background in Quality Assurance (4 years+) Aseptic or Sterile manufacturing background Good regulatory knowledge (GMP, Safety) Previous managerial experience Understanding of PrOFS Self-motivated
QA Manager in Reading employer: ARx Recruitment Services
CMDO is an exceptional employer for those seeking to make a meaningful impact in the pharmaceutical industry. With a strong commitment to employee development and a collaborative work culture, we offer extensive training opportunities and a supportive environment that fosters innovation. Located in a vibrant area, our team enjoys not only competitive benefits but also the chance to contribute to groundbreaking medicines that improve patient lives across the UK and EU.
