Role Functions (Functions include, but are not limited to, the following) Review and approve production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to appropriate SOPs, GMP and regulatory requirements, including supporting QP certification. Actively communicate and collaborate with functional areas to develop a strong working relationship and understanding of roles and responsibilities. Utilise this network to help resolve comments and issues that arise during audit and review. Support product recalls and stock recoveries as appropriate. Identify compliance gaps and make recommendations for continuous improvement Creates and maintains assigned SOPs. Perform and review complaints and deviation investigations, change controls and CAPAs. May assist in the induction process for new starters. Follows standard procedures and consults with manager/supervisor on exceptions. Compiles data for reports and presentations - May interpret data and draw conclusions. Carries out all assignments to the standards of compliance, efficiency, innovation, accuracy and safety in accordance with Company and regulatory requirements. Completes audits of data, information, procedures, facilities, equipment and systems (inc computer systems) to ensure compliance to SOPs, GMPs and applicable regulations. Keep abreast of cGMP requirements as described in applicable worldwide regulations. Additional activities may be assigned by the manager/supervisor Experience, Knowledge & Skills The contractor is required to possess a degree in an Engineering or Science discipline. Alternatively, they must possess significant industrial experience. (Pharma Experience required) Skills: Pharma Experience GMP SOP CAPA