2 of 2 GMP Jobs in Oxfordshire

this role would be: Reviewing and approving deviations, CAPAs and change controls within defined timelines. Supporting manufacturing teams as a QA partner to ensure GMP compliance during production activities. Reviewing batch documentation and support preparation for Qualified Person batch disposition. Participating in investigations, root cause analysis and risk assessments … quality events. Reviewing and approving SOPs, protocols, reports and other GMP documentation. Supporting implementation of new manufacturing processes for incoming client programs. Contributing to continuous improvement initiatives to strengthen quality systems and operational processes. We are looking for: Experience in a GMP-regulated pharmaceutical, biotechnology or similar manufacturing environment. Significant ...

candidate will act as a technical leader for manufacturing systems, process optimisation, equipment performance, and implementation of new technologies while ensuring full compliance with GMP, quality system, and regulatory requirements. Key Responsibilities: Team Leadership & Development: Lead, mentor, and develop a team of Automation Engineers and Continuous Improvement (CI) Engineers … quality, maintenance, and process data to identify trends and improvement opportunities. Quality, Compliance & Regulatory Support: Ensure all engineering activities are performed in accordance with: GMP requirements, ISO 13485 requirements, FDA Quality System Regulations, Internal quality procedures. Cross Functional Collaboration: Work closely with Operations, Quality, Validation, Maintenance, Supply Chain, Regulatory ...