3 of 3 GMP Jobs in the Thames Valley

budget spend against timelines. Risk & Compliance Awareness: Support the team in ensuring project documentation strictly adheres to global regulatory standards (e.g., FDA, ISO 13485, GMP). Flag early risks or bottlenecks to senior leads. Stakeholder Communication: Maintain action logs, prepare progress updates, and assist with draft presentations for local ...

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 ...

secondary packaging and labelling activities and support the QP with release activities. Provide guidance and support on GDP and GMP compliance to ensure product quality is not compromised Provide Guidance and Support on Good Documentation Practice and Data Integrity to ensure GxP records are generated and retained appropriately Carry … risk assessments on business, GDP and GMP critical areas and has experience in conducting risk assessments Provide backup support in case of other quality members absence Conduct Quality tasks as requested by the line manager in support of business activities Position Requirements To be successful in this role you must ...