26 to 43 of 43 GMP Jobs in the UK

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 ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures More ❯

regulated manufacturing environment. This opportunity is ideal for someone with a science or pharmaceutical-related degree and exceptional people management skills, looking to make a meaningful impact in a GMP-licensed facility. Key Responsibilities: Lead and manage a team of QA Officers to ensure product release meets GMP and QMS standards. Support the QA Manager with site inspections, internal audits … risks are mitigated. Experience: Degree in Microbiology, Biology, Biomedical Sciences, or equivalent. Pharmacy Technician Level 3 (GPhC registration desirable). Proven experience in pharmaceutical manufacturing and working within a GMP-regulated environment. Strong leadership and coaching skills with a track record of team development. Excellent understanding of MHRA regulations, ISO standards, and quality systems. Skilled in risk management, root cause More ❯

instructions, change controls, deviations, investigations, validation, customer audits/quality requests, and material and product disposition. The QA officer is expected to identify, escalate and work to address any GMP/GxP issues with potential impact to product quality or quality compliance. Together we offer fantastic opportunities for committed employees to learn and develop their career with us. At Piramal … to performing the relevant disposition of products. Where potential issues exist, these are to be highlighted to the QA manager. Promote and work to ensure compliance with all relevant GMP/GxP requirements. Support and lead as required, quality process improvements and quality management system improvements within the department and on site. Escalate any identified GMP/GxP areas of More ❯

we want you to be part of our team. Quality Assurance & Compliance Ensure compliance with Food Safety and Quality Management System (QMS) procedures, including allergen controls. Conduct GMP (Good Manufacturing Practice) and COP (Compliance Observation Process) audits. Verify product compliance with factory specifications; report any deviations in legality, quality, or consistency. Monitor staff hygiene practices and report issues to the More ❯

the functioning of the QMS, providing oversight to key stakeholders alike (including senior staff members). Accountability across (but not limited to); change control, stability, documentation control, internal audits, GMP, supplier approval, complaints, PQRs, NPI, route cause analysis and controlled drug returns. Ensuring compliance/correct documentation practices, i.e batch records, laboratory tests and quality agreements too. Overseeing supplier verification … batch review process. Keeping abreast of evolving UK & EU retained regulations (for the purposes of pharmaceutical and/or food/ingredients manufacturing). To ensure compliance with EU GMP standards & BRC food safety requirements. Managing the preparation process (and heavily involved in hosting activities) for MHRA inspections, customer (third party audits) and acting as the lead person. Enrsuring quality … bodies. Deputising for the HOQ when required. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experience managing QA team/s in an GMP/Pharmaceutical setting. Management experience essential (will consider Team Leader or similar). Experienced in batch review and batch release Experience in auditing and audit hosting Experience in CAPA, deviations More ❯

customers and answering queries and product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder in an auditable state Maintaining quality … limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills and strong written/verbal report More ❯

Systems Manager Upperton Pharma Solutions is a Nottingham-based CDMO that specialises in the development and manufacture of pharmaceutical products, providing a complete service from early-stage feasibility to GMP clinical manufacture. Formulations cover a range of delivery routes, typically including oral (tablets & capsules), nasal and inhaled. Continued growth and investment into the business has led to the creation of … exciting new job opportunities; in our new GMP Manufacturing headquarters in Beeston, Nottingham. Upperton Pharma Solutions is undergoing a period of significant expansion to meet international customer demand and offer a comprehensive drug development portfolio, so now is a great time to join our team. Reporting to the Quality and Compliance Director this role will be responsible for leading the … support the growth of the business and deliver a compliant IT platform for business-critical systems and processes. Main duties and responsibilities: Ensure compliance with the company quality systems, GMP requirements and all regulatory body requirements. Responsible for ensuring all computerised systems at Upperton remain in a qualified state in accordance with the validation/qualification schedule Responsible for ensuring More ❯

customers and answering queries and product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder in an auditable state Maintaining quality … limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills and strong written/verbal report More ❯

with health authorities, contract manufacturers, and internal stakeholders to ensure compliance across the product lifecycle. Key Responsibilities Lead product release and compliance activities, ensuring documentation accuracy and adherence to GMP/GDP standards. Maintain and improve Quality Systems including Change Control, Deviations, Complaints, Product Quality Reviews (PQRs), Recalls, and Returns. Act as a key liaison with Health Authorities, ensuring timely … Pharmaceutical Sciences, Chemistry, Biotechnology, Biochemistry, or a related discipline. 5+ years' experience in Quality Assurance, Quality Control, or a similar function within the pharmaceutical or healthcare sector. Certifications in GMP and GDP. Strong knowledge of regulatory affairs, pharmaceutical guidelines, and quality systems. Proven experience in compliance activities including CAPAs, Change Control, and Deviations. Exposure to regulatory audits and interactions with More ❯

of Solstice. Key Responsibilities Monitoring ongoing compliance with food safety, legislation, quality & customer requirements, and industry regulatory requirements. Interpret and implement quality assurance standards and procedures. Monitor and promote GMP, Hygiene, Quality Standards, and adherence to all Quality Management & Food Safety related procedures. Managing Microbiology testing schedule, including product samples and environmental swabs collections Conducting and document internal audits (GMP More ❯