26 to 44 of 44 GMP Jobs in the UK excluding London

biotechnology and/or pharmaceutical industry, including senior Quality leadership roles in regulated manufacturing environments. Strong knowledge of global regulatory authorities including FDA, GMP, GCP and GLP requirements. Proven expertise in Quality Management Systems (QMS), with a particular focus on GMP compliance and data integrity. Demonstrated experience with regulatory inspections ...

providing the required documents and records. Track corrective and preventive actions and ensure they are completed within agreed timescales. Support compliance with relevant ISO, GMP, BRC or other applicable quality standards. REQUIRED EXPERIENCE AND QUALIFICATIONS Previous experience in quality assurance or quality control within a warehouse, logistics, manufacturing or supply … record management. A diploma or degree in Quality, Science, Engineering or a related subject would be beneficial. Quality Management System certification, including ISO, GMP or BRC, would be advantageous. SKILLS REQUIRED Excellent attention to detail. Strong organisational and record-keeping skills. Confident communication and training abilities. Good working knowledge ...

product quality to ensure customer specifications and quality requirements are consistently achieved. Maintain and continuously improve food safety and quality management systems, including HACCP, GMP, and customer-specific standards. Ensure compliance with all food safety, legal, regulatory, and customer requirements. Auditing & Traceability Plan, conduct, and close out internal audits. Maintain … performance. Monitor quality KPIs and drive initiatives that enhance product quality, reduce waste, and improve efficiency. Essential Strong knowledge of food safety systems, HACCP, GMP, quality standards, and audit requirements. Demonstrated experience managing traceability systems and conducting traceback investigations. Strong analytical, problem-solving, and root cause investigation skills. Excellent attention ...

will translate complex processes and investigations into structured, easy-to-follow documentation. This role is critical to ensuring operations remain inspection-ready and GMP/GDP compliant . This is a factory-based role , with time spent both on the production floor and in a dedicated computing/documentation area. … SMEs) to ensure accuracy and relevance Support document updates in line with process changes, audits, and system improvements Compliance & Governance Ensure all documents meet GMP and GDP standards , including version control and traceability Identify gaps or risks in documentation and drive improvements Maintain documentation aligned with site Quality and document ...

Specialist will play a key role in supporting site validation activities across a range of projects. This is a great opportunity for someone with GMP validation experience looking to build on their existing knowledge within a supportive and expanding team. Candidates with equipment or process validation experience from pharmaceutical … other GMP-regulated manufacturing environments are encouraged to apply. The role: Plan and execute validation activities in line with site validation plans and project timelines. • Author and maintain validation protocols and reports across multiple validation areas such as: Cleaning validation Computerised systems validation Equipment and utilities qualification Process validation Interpret ...

Specialist will play a key role in supporting site validation activities across a range of projects. This is a great opportunity for someone with GMP validation experience looking to build on their existing knowledge within a supportive and expanding team. Candidates with equipment or process validation experience from pharmaceutical … other GMP-regulated manufacturing environments are encouraged to apply. The role: Plan and execute validation activities in line with site validation plans and project timelines. Author and maintain validation protocols and reports across multiple validation areas such as: Cleaning validation Computerised systems validation Equipment and utilities qualification Process validation Interpret ...

patient focus service. The prime function of the unit is the preparation of diagnostic radiopharmaceuticals, in a safe and efficient manner according to Good Manufacturing Practice and National Standards. Main duties of the job Perform duties in Radiopharmacy to aid the safe and efficient preparation of radiopharmaceuticals … radioactive materials oTrained in the Transportation of Dangerous Goods oExperience of using MS packages or similar databases oAn awareness of Good Manufacturing Practice (GMP) and GCP guidelines (Good Clinical Practice) and the EU Clinical Trials Directive Skills Essential oAbility to work within set timeframes working to priorities and deadlines oDemonstrates ...

looking to appoint an experienced Project Engineer - Automation to support the delivery of a major pharmaceutical manufacturing expansion project. Working within a highly regulated GMP environment, you will play a key role in the development, implementation, testing and commissioning of automation systems across process equipment, cleanrooms and critical utilities. This … qualification and validation activities. Review vendor and contractor designs and technical submissions. Participate in design reviews, risk assessments and FMEA workshops. Ensure compliance with GMP, CSV, data integrity and cybersecurity requirements. Maintain accurate project documentation and system handover records. Experience Required Degree qualified in Automation, Control Systems, Electrical Engineering ...

CMMS experience Strong health & safety awareness Ability to work rotating days and nights Desirable Experience Food Manufacturing or FMCG SAP and/or SCADA GMP and Food Safety standards LOTO procedures Permit to Work systems Root Cause Analysis (5 Why, 5W1H) Contractor management Industries Considered Ideal Food Manufacturing FMCG Also … Environment You'll be working in a highly automated, fast-paced food manufacturing facility focused on: Asset reliability Downtime reduction Continuous improvement Health & Safety GMP and Food Safety compliance Equipment You'll Work On Experience with any of the following would be advantageous: Automated production lines PLC-controlled machinery Conveyors ...

Contract | Part-Time | Pirbright, Surrey | Inside IR35 We're looking for a System Administrator with experience supporting validated systems in regulated environments (GxP/GMP) . Key Responsibilities: System administration, maintenance, and patch management Testing and validation activities (CSV/GxP) System implementation and release support Change control and compliance … Computer System Validation (CSV) Change Control & Patch Management Compliance & Audit Readiness System Lifecycle Management CAPA & Risk Management Vendor & Stakeholder Management Project Delivery & Coordination Desirable: GMP, GxP, FDA 21 CFR Part 11, Annex 11 Working Pattern: 2-3 days per week Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting ...

upgrades. Lead fault finding and implement right-first-time, long-term solutions. Oversee new equipment installations, upgrades and GAP assessments. Ensure equipment meets GMP, safety and regulatory requirements. Develop preventive maintenance strategies and monitor equipment performance, including MTBF. Work closely with engineering teams and third-party suppliers to deliver maintenance … mentorship across the engineering team. Requirements: HNC/HND or equivalent in an engineering discipline. Proven maintenance engineering experience, ideally within pharmaceutical or GMP manufacturing. Strong understanding of pharmaceutical processing equipment and/or GMP infrastructure. Experience in equipment lifecycle management, troubleshooting and continuous improvement. Strong problem-solving, communication ...

early • Ensure full supplier approval, including audits, and certification requirements • Support raw material elements of internal, customer, and group audits • Audit compliance with QMS, GMP, and HACCP standards, driving corrective actions to closure • Monitor KPIs, identify trends, and drive continuous improvement initiatives • Communicate customer and business requirements clearly to suppliers … ensure compliance and robustness • Ability to work cross-functionally with Technical, Operations, NPD, and suppliers • Strong audit capability with a clear understanding of GMP and HACCP requirements • Highly organised with excellent attention to detail • Strong communication skills, able to influence at all levels • Proactive mindset with the ability to anticipate ...

Job summary You will be joining NHSBT at a particularly exciting time as we embark on a journey of change, enhancing our current IT service provision. You will lead the systems testing required to ensure ...

Specialist to deliver data services to our clients, which include data and benefit audits, preparing data strategies and plans, undertaking various pension rectifications including GMP rectification and equalisation. While we continue to help clients meet their GMP objectives, the data challenges our clients face are becoming more diverse which gives … advantageous as well as more advanced data and benefit auditing and cleansing of Pension data. While we continue to help clients meet their GMP objectives, the data challenges our clients face are becoming more diverse which gives you a great chance to work in a team across a broad spectrum ...

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 ...

will lead a team to: Provide technical expertise & support for QC equipment & Instrumentation. Manage the qualification, procurement, implementation & validation of new equipment. Manage GMP QC computer systems, ensuring compliance with quality & data integrity regulations. Lead equipment related deviation investigations. Required: A degree or similar qualification in Chemistry or a relevant … scientific field. Proven experience in a GMP Quality Control (QC) laboratory setting. Excellent technical knowledge relating to laboratory equipment, and QC instrumentation Experience in Instrument & equipment qualification, change management & troubleshooting. Strong computer skills & knowledge of QC Pharmaceutical Automated Systems & Automated Systems Validation. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio ...

Quality Assurance Officer (GMP/Cannabinoids) Sandwich Up to £40,000 + Company Bonus + Private Healthcare + Pension + Training Are you a Quality Assurance Officer or similar with GMP experience looking to join an innovative pharmaceutical manufacturer operating within one of the fastest-growing areas of the life ...

within a highly regulated life sciences environment. This role requires someone who has successfully delivered LIMS projects and can operate effectively in GxP and GMP-regulated environments , where data integrity, compliance, and patient safety are central to the programme's success. Key Requirements Proven experience delivering LIMS implementation projects Experience … with LabVantage LIMS Strong understanding of GxP and GMP regulations Experience managing complex stakeholder groups across business and technical teams Track record of delivering projects in highly regulated environments Contract Details 6-month initial contract Outside IR35 Potential for a multi-year engagement , with further European and US projects planned ...

sponsors on some of the most complex data challenges facing UK pension schemes. Working closely with clients, you will lead and deliver projects across GMP Equalisation, benefit rectification, data audits, data remediation, buy-in and buy-out readiness, pensions dashboards and wider de-risking initiatives. In this client-facing role … pensions knowledge with a consultative approach, excellent stakeholder management skills and the ability to build trusted relationships with trustees, sponsors and advisers. Experience of GMP Equalisation, benefit audits, data remediation, buy-in/buy-out activity or wider pensions data consulting projects is essential. Apply here or get in touch ...