26 to 31 of 31 GMP Jobs in the UK

across raw materials, production processes, and finished products. Maintain accurate and compliant documentation in line with industry and company standards. Ensure adherence to HACCP, GMP, and site-specific quality procedures. Support internal and external audits through meticulous record-keeping and process compliance. Investigate non-conformances and assist in implementing corrective ...

documentation. Desirable Requirements of Specification Technologist Experience using retailer specification systems. Knowledge of supplier approval processes and risk assessments. Exposure to audits (internal, customer, GMP, traceability). Experience supporting NPD projects. The Specification Technologist will benefit from: Joining a stable and respected FMCG manufacturer. Ongoing training and development Involvement ...

significant recurring annual budgets and orchestrating large blended teams across 8–12 workstreams and multiple regions. - Technical Context: Familiarity with enterprise manufacturing IT landscapes, GMP, and CSV is preferred. - Availability: Start within 6–8 weeks of an offer. Suppliers must confirm the candidate's notice period and earliest possible start ...

environment. This role offers the opportunity to work closely with manufacturing, quality, and supply teams to ensure products are released in full compliance with GMP and regulatory requirements. The Role The QA Release Officer will provide quality oversight across manufacturing, production, and packaging operations. The role focuses on the timely … quality. Key Responsibilities Review and approve batch documentation for bulk, finished product, and IMP batches Ensure timely and compliant batch release in accordance with GMP, GDP, and GCP requirements Provide QA support to manufacturing, production, and packaging activities Review production records prior to Qualified Person (QP) release and escalate issues ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

pharmaceutical manufacturer is seeking a Quality Systems & QC Laboratory Electronic Systems Administrator to support and maintain electronic quality and laboratory systems in line with GMP, GAMP, and data integrity requirements. This role will play a key part in ensuring systems such as electronic QMS and QC laboratory applications remain compliant … SOPs Troubleshoot system issues and provide user support and training Requirements Experience supporting electronic QMS and/or QC laboratory systems in a GMP environment Working knowledge of CSV, GAMP, and data integrity principles Understanding of qualification and validation for equipment and electronic systems Strong analytical, documentation, and communication skills ...