1 to 25 of 43 GMP Jobs in the UK

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 ❯

in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National Regulatory Authority (AIFA) and is compliant with the FDA 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 ❯

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 ❯

Microsoft Office 365 Desirable Experience of working in a first, second and third line technical support role Experience working with NHS Wales clinical and administrative applications Working knowledge of GMP and GAMP Experience of taking lead role in system design projects Skills Essential Excellent presentation and report writing skills Excellent understanding of problem, change and release management Ability to learn 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 ❯