1 to 25 of 39 GMP Jobs in the UK excluding London

with diverse cultures Necessary legal status to work in the UK. Beneficial requirements: The closest relevant experience would be MES/EBR, eQMS, LIMS, ERP or other systems for GMP regulated manufacturers. Experience of different project delivery methodologies including waterfall and agile Experience of client account management Knowledge of Computer System Validation is an advantage. Key Responsibilities: Become an expert More ❯

a scientific discipline (e.g., microbiology, biology, biomedical sciences) or equivalent. Proven experience in quality assurance within a regulated manufacturing or laboratory environment. Strong knowledge of quality systems, ISO standards, GMP/GDP principles, and regulatory compliance. Skilled in leading audits, managing CAPAs, and interpreting quality metrics. Excellent leadership, communication, and problem-solving abilities. Proficient in data analysis tools, LIMS, and More ❯

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive More ❯

Candidate: Proven experience in a quality systems or quality assurance role within a manufacturing or production environment - precision environment Strong knowledge of quality standards and regulations such as ISO, GMP, FDA if applicable). Experience with quality tools and methodologies such as CAPA, FMEA, Root Cause Analysis Certification in quality management systems - desirable Excellent communication, analytical, and problem-solving skills. More ❯

teams. ?? Support change management and training initiatives to ensure smooth adoption of new tools and processes ? Ensure all business processes and documentation comply with FDA, ISO, EU MDR, and GMP standards. ?? Qualifications & Experience ?? Bachelor's degree in Engineering, Supply Chain, Business, Data, IT , or a related field. ?? 10+ years' experience as a Business Analyst within manufacturing, supply chain, medical devices More ❯

and embedded analytics for production KPIs. Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable. Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.). Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs. Ability to translate complex operational processes into streamlined SAP-enabled solutions. More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

cycle methodologies, 21 CFR Part 11, and GAMP. 4. Development of detailed specification, engineering documents, SOP and operating standards. 5. Ownership and administration of process control automation in a GMP regulated manufacturing setting. 6. Engage in, and process change control requests per established SOP and processes. 7. Lead technical root cause analysis, incident investigations, and troubleshooting on process control issues More ❯

packaging and goods-in areas in the event of staff shortages Address non-conformances and corrective actions immediately Handle customer complaints and supplier NCRs Weekly Duties Probe & scale calibration GMP audits (3–4 per week) Staff induction, manual handling, and refresher training Machinery and health & safety training with supervisors Traceability and raw material paperwork checks Forklift, cleaning, and first aid More ❯

data platforms) Understanding of data governance and compliance (ideally obtained from a highly-regulated environment) Excellent problem-solving skills and attention to detail Preferred Qualifications: Knowledge/experience of GMP would be highly advantageous. Benefits GSK offers a range of benefits to its employees, which include, but are not limited to: Competitive base Salary Annual bonus based on company performance More ❯

policies and procedures Ensuring samples 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 shelf life Carryout of routine More ❯

resolving day to day issues/escalation points. How Will You Make An Impact? Ensuring a safe, clean, and good working environment by utilising 5S principles, implementing and monitoring GMP standards, and ensuring compliance with Arlas standards in terms of Food Safety, Health & Safety, and Environment, including conducting internal audits. Assisting the team to achieve their objectives through training, coaching More ❯

in Cheshire. Our client requires someone who has experience managing a team and QMS. This position plays a leading role in improving the QA function and ensuring compliance to GMP standards. Experience of internal audits, CAPAs, deviations, root cause analysis and change control are essential for this role. Key Responsibilities: Manage and improve the Quality Management System (QMS). Ensure … experience of directly managing individuals is essential for this role. Previous direct experience of CAPA, Change control, root cause analysis & deviations Experience in a sterile environment. Strong knowledge of GMP and quality system regulations. Excellent communication, leadership, and problem-solving skills. Audit and regulatory inspection experience. Important Information: We endeavour to process your personal data in a fair and transparent More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

checks, supplier and internal non-conformance, customer complaint investigations, glass & plastic audits, and fabrication audits. - Supporting the training of staff and verification against CCPs, policies and procedures. - Conducting internal GMP audits across departments and conducting hygiene verifications. - Assisting with external audits. The role will be a mix of factory and office-based work to meet the needs of the business More ❯

applications and embedded analytics for shop floor and KPI reporting. Advantageous: exposure to IBP, PP/DS, or advanced scheduling tools. Awareness of manufacturing standards and compliance (e.g., ISO, GMP). Soft Skills & Leadership Strong communication and stakeholder management, particularly with operations, production, and executive-level teams. Ability to translate complex business processes into practical SAP-based solutions. Confident presenting More ❯

follow-up, and root cause investigations. What We’re Looking For: 5+ years of experience in Site Reliability Engineering or a related field. Hands-on experience with Biosafety and GMP environments. Strong foundation in Lean Six Sigma principles. Proven problem-solving skills with a knack for performance tuning. Effective communicator and team player. Formal education in an engineering-related discipline. More ❯

follow-up, and root cause investigations. What We’re Looking For: 5+ years of experience in Site Reliability Engineering or a related field. Hands-on experience with Biosafety and GMP environments. Strong foundation in Lean Six Sigma principles. Proven problem-solving skills with a knack for performance tuning. Effective communicator and team player. Formal education in an engineering-related discipline. More ❯

equivalent experience in Controls, Mechanical/Electrical, or Software Engineering. Proven experience in Systems Engineering, specification writing, and validation. Strong organisational, communication, and coordination skills. Familiarity with regulatory standards (GMP, ISO, Medical Devices). Experience with MS Project, MS Office, Visio, and 3D CAD or AutoLab. What you'll get in return Competitive salary and benefits package. Opportunity to work More ❯

Carry out routine quality checks 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 actions. Work closely with production More ❯

patient outcomes. About the Role We're hiring a QA Compliance Manager to lead a team focused on maintaining and enhancing the Quality Management System (QMS) in compliance with GMP, ISO 9001, ISO 13485, and other regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits, while also supporting … opportunity with potential Qualified Person (QP) sponsorship for the right candidate. Key Responsibilities: Lead and develop the QA Compliance team Maintain and improve the QMS in line with EU GMP and ISO standards Oversee internal audits, CAPA management, and batch documentation review Host customer audits and support regulatory inspections Drive continuous improvement and contribute to strategic quality initiatives Support training … change control, and compliance projects Candidate Requirements Essential: Degree in a scientific discipline (e.g. Chemistry, Biology, or related field) 10+ years' experience in GMP-regulated environments Strong leadership and people management skills In-depth knowledge of EU cGMP, ISO 9001, and ISO 13485 Experience supporting or conducting batch release under QP supervision Lead Auditor training and a proactive approach to More ❯

continuous improvement in patient outcomes. Your new role As QA Compliance Manager, you'll lead a team responsible for maintaining and improving the Quality Management System in line with GMP, ISO, and regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits. You'll also contribute to strategic quality … Qualified Person (QP) sponsorship for the right candidate. What you'll need to succeed A degree in a scientific discipline (e.g. Chemistry, Biology, or related field) Extensive experience in GMP-regulated environments (10+ years preferred) Strong leadership and people management skills In-depth knowledge of EU cGMP and ISO standards (9001, 13485) Experience supporting or conducting batch release under QP More ❯