1 to 25 of 33 Permanent GMP Jobs in the UK

data integrity across both paper-based and electronic systems. We are looking for: Significant experience in Quality Systems within the biopharmaceutical/pharmaceutical industry, with a strong understanding of GMP and regulatory standards. Proven background in Pharmaceutical QA, including audits, inspections, investigations, root cause analysis, and change control. Experience managing electronic Quality Management Systems and document/records management in 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 ❯

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 ❯

capture and patent support. Consistently demonstrate a strong commitment to both lab and process safety. Adhere to and promote biosafety, hygienic design and quality management standards (e.g. BSL-2, GMP, FSMA, HACCP, ISO food-grade). What you can bring to the role Ideally PhD qualified in Biochemical Engineering, Biological Engineering, Fermentation Engineering, or a related technical degree. Proven industry 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 Excellent 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 ❯

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 ❯

A minimum of ten years' experience leading IT at a senior management level Track record of delivering results quickly Experience in delivering IT services to customers Work in a GMP or highly regulated environment Preferred Experience: Experience of agile product development Experience of Lean Six Sigma Infrastructure delivery (networking, hardware) to customers Experience with data science project delivery Knowledge/ 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 ❯

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 ❯

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 ❯

looking for a QA Manager to join their Technical team. In this QA Manager position you will lead the QA team and be responsible for delivering high levels of GMP, food safety and integrity standards within the factory. You will also be responsible for updating and maintaining the QMS, conduct audits and ensure any corrective actions are implemented. As the 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 ❯

negotiation, and presentation skills. Highly self-motivated, organised, and target-driven. Experience with clients in life sciences, healthcare, or education. Knowledge of cleanroom or controlled environment standards (e.g., ISO, GMP). Technical or engineering background advantageous. Benefits Competitive base salary of £40,000 + performance-related bonus Hybrid working: 3 days in office/2 days from home Pension scheme More ❯

systems running during any kind of disruption. Why this matters in pharma Regulators such as the MHRA and EMA expect firms to have strong business continuity plans to protect GMP, GDP, and data integrity. Manufacturers and suppliers are being asked by clients to show proof of continuity and disaster-recovery arrangements. Government and NHS supply concerns have made resilience a 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 ❯

act as point of contact for the Archives facility (Archives Champion) for documentation queries. This will include preservation notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries. Qualifications & experience: · SVQ Level 3: Highers/higher national certificate/apprenticeship or equivalent More ❯

Pensions data and transformation projects. You'll work directly with clients to analyse, cleanse and migrate data, design and test Pension calculations, and support key industry programmes such as GMP rectification and equalisation. Key Responsibilities Analyse complex Pensions data using SQL and Excel Deliver data mapping, migration and cleanse activities Produce and test calculation specifications based on scheme rules Present 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 ❯

Set Proven leadership in digital performance, measurement and data strategy roles. Hands-on experience with MMM, incrementality testing and advanced attribution. Strong understanding of ad tech and martech ecosystems (GMP, GA4/BigQuery , Meta CAPI, server-side GTM etc.). Fluent in using data to tell compelling stories and influence both internal teams and C-suite clients. Success Indicators (First 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 ❯

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 ❯