4 of 4 GMP Jobs in the East Midlands

are collected for testing schedules and testing schedules are met Logging micro samples Accurate carrying out of positive release checks for all finished products GMP audits/Glass and plastic audits, including generation of improvement areas, completing database Ensure close outs of non-conformances Sampling and recording of finished product More ❯

taking a lead in generating and building a quality culture. Accountabilities: To participate and direct QA team to observe and audit production processes and GMP, ensuring products are made to specification and within customer codes of practice and Bakkavor standards - reporting findings to managers as appropriate To assist in delivery … Line Manager, manage QA activities required to deliver improvement of Technical KPIs e.g. audit of non-conforming processes, complaint investigations, update of swab schedules, GMP audits, glass, and plastic audits To plan and co-ordinate work of the QA team to meet requirements of the quality management system and the More ❯

taking a lead in generating and building a quality culture. Accountabilities: To participate and direct QA team to observe and audit production processes and GMP, ensuring products are made to specification and within customer codes of practice and Bakkavor standards - reporting findings to managers as appropriate To assist in delivery … Line Manager, manage QA activities required to deliver improvement of Technical KPIs e.g. audit of non-conforming processes, complaint investigations, update of swab schedules, GMP audits, glass, and plastic audits To plan and co-ordinate work of the QA team to meet requirements of the quality management system and the More ❯

an exciting opportunity to work in a fast-paced environment, ensuring the quality and compliance of laboratory work in line with ISO 17025 and GMP standards. Key Responsibilities : Ensure compliance with company policies and procedures, including Health and Safety, ISO 17025, and GMP. Review, write, and amend documentation such as … SOPs. Manage controlled documentation and maintain its circulation and availability. Audit GMP data, including reviewing raw data prior to releasing GMP CoA or CoP. Coordinate quality issues, investigations, and CAPA. Assist with OOS, NC, NTF, CMP, RA, and CAPA investigations. Participate in the change control process to ensure changes maintain … GMP compliance. Track, trend, and gather data for meetings as per procedures. Conduct staff training on quality matters when required. Liaise with customers or regulatory representatives. Host and manage external audits by customers or regulatory bodies. Respond to external audit... More ❯