3 of 3 CAPA Jobs in the North of England

and release of IMP to clinical studies on clients' behalf. To provide support and leadership on a range of activities including but not limited to: non-conformance management, including CAPA, events, root cause analysis, continuous improvement, key supplier issues, complaint investigations etc. Take the lead on regulatory inspections and client audits, taking accountability (with the Site Leadership Team) for the … and release of IMP to clinical studies on clients' behalf. To provide support and leadership on a range of activities including but not limited to: non-conformance management, including CAPA, events, root cause analysis, continuous improvement, key supplier issues, complaint investigations etc. Take the lead on regulatory inspections and client audits, taking accountability (with the Site Leadership Team) for the More ❯

to maintain regulatory compliance Provide QA/RA expertise throughout product development and change control processes Guide risk management and post-market surveillance activities Conduct root cause analyses for CAPA investigations Review SOPs, software development documents, and regulatory submissions Deliver training to ensure quality and regulatory understanding across the business Perform internal and supplier audits and support external inspections Validate More ❯

in manufacturing/assembly/testing/service related tasks with aptitude for metrology and mechatronics; preferably working in interdisciplinary and international teams. - Knowledge of quality methods such as CAPA, cGMP, FMEA, ISO would be beneficial. - Experience with product development and/or life cycle management in a regulated environment (Design Controls according to European and U.S./FDA guidelines … in manufacturing/assembly/testing/service related tasks with aptitude for metrology and mechatronics; preferably working in interdisciplinary and international teams. - Knowledge of quality methods such as CAPA, cGMP, FMEA, ISO would be beneficial. - Experience with product development and/or life cycle management in a regulated environment (Design Controls according to European and U.S./FDA guidelines More ❯