1 to 25 of 104 GMP Jobs in the UK excluding London

Team Leader and continue to always perform as a leader within the group. You will work according to all necessary Good Manufacturing Practice (GMP), Hygiene and Health & Safety (H&S) requirements to ensure high quality products are produced in accordance with standard operating procedures (SOPs) and regulatory requirements. You will … make sure these are covered off in an acceptable and timely manner. Ensure all activities are conducted in compliance with Good Manufacturing Practice (GMP) standards Complete and review all documentation in a timely manner and ensure accuracy is maintained in line with batch right first-time targets (BRFT) Drive ...

user requirements gathering, risk assessments, validation planning and test execution. Maintain documentation including SOPs, validation records, configuration specifications and change records. Ensure compliance with GMP, GAMP 5, Annex 11, 21 CFR Part 11 and company quality procedures. Support internal audits, external audits and regulatory inspections. Project and Vendor Management Work ...

skills. - Experience dealing directly with customers on quality matters. - Excellent communication and stakeholder management skills. - The ability to work independently while managing multiple priorities. - GMP experience (desirable). - Degree or equivalent in a science, engineering or manufacturing discipline (desirable). This is an excellent opportunity for an experienced Quality Assurance ...

endpoint management solutions Experience working within a pharmaceutical, biotechnology, medical device or similarly regulated environment would be highly desirable An understanding of GxP, GMP, GAMP 5, Annex 11 and 21 CFR Part 11 would be advantageous Strong understanding of IT service management and ITIL principles Excellent analytical and troubleshooting skills ...

site is audit-ready at all times. Maintain accurate quality records & contribute to the reporting of site quality KPIs. Manage the site's GMP auditing programme & actively participate in the internal audit team. Drive continuous improvement initiatives that enhance product quality, food safety and operational performance. Ensure Health & Safety, Hygiene ...

Investigational Medicinal Product (IMP) manufacturing and associated Quality Management Systems at MedPharm. The role is responsible for supporting compliance with Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), applicable regulatory requirements and internal quality procedures through the review of quality documentation, management of quality systems … analytical methods, sampling instructions and protocols. Support review of analytical investigations including OOS, OOT and atypical results. Review laboratory documentation to ensure compliance with GMP, GLP and internal procedures. Support QA oversight of reference standards, retained samples and stability documentation where applicable. Materials Management Perform QA review and disposition ...

will be critical as you contribute to process innovations and operational excellence. Here’s What You’ll Need 3+ years of experience in a GMP manufacturing environment This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. ...

problem-solving skills. Good IT skills, including Microsoft Office and MRP/ERP systems. Desirable 5+ years' mechanical inspection experience. Knowledge of FDA, GMP and ISO 13485 standards. Engineering qualification, apprenticeship, or equivalent industry experience. Experience working within regulated manufacturing environments. Key Skills CMM Programming & Inspection (Essential) LK & Mitutoyo CMMs ...

time. To manage internal taste panel and shelf-life sample assessments. Assist in the management and completion of internal audits including CCP, GMP, fabrication, hygiene, plastic, and system audits. Skills and Experience Required Relevant certification - HACCP Level 3 Basic Food Hygiene Attention to detail and able to prioritise workload. Organised ...

root cause analysis. Support supplier approval processes and supplier questionnaires. Ensure quality control equipment is calibrated and maintained. Promote continuous improvement, quality culture and GMP standards. Deliver quality-related training across site where required. Essential Skills & Experience Previous experience within a manufacturing environment. Knowledge of quality systems and food safety ...

operations Excellent knowledge and understanding of Lab systems, Lab data, and the workings of a lab on a day-to-day basis in a GMP environment (Pharma or Consumer Health Care business). Understanding and experience in the deployment of key lab digital systems (e.g. QC E-planning, QC Electronic ...

faulty material. When required support sorting activity. Conduct where appropriate, testing of raw material. Carry out internal audits to the standards - Monitor and maintain GMP/BBQ. G&P, Internal audit performance. Publish results, raise and manage non-conformances. Oversee and conduct quality inspection rounds during the designated shifts. Monitor ...

Oriented Programming Git version control Basic electrical, mechanical and pneumatic knowledge Robotics Machine Vision SCADA/MES systems Pharmaceutical or regulated manufacturing environments GAMP, GMP, 21 CFR Part 11 or EU Annex 11 Industrial communication protocols including EtherCAT, Profinet, CAN, Ethernet/IP and Serial communications .NET ...

records, maintenance schedules, equipment hierarchies, and work order data remain accurate and up to date. Record, monitor, and close maintenance activities in line with GMP and regulatory requirements. Develop, maintain, and optimise preventative maintenance programmes to support site compliance and asset performance. Manage the maintenance service desk, ensuring maintenance requests ...

execute commissioning, qualification, and SAT protocols. Prepare system impact assessments, qualification documentation, and validation reports. Review project documentation for technical accuracy, compliance, and GMP requirements. Ensure systems are safe and ready for start-up, testing, and qualification activities. Perform installation verification, system start-up, and functional testing. Monitor progress, coordinate ...

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 ...

quality systems are adhered to, support investigations, conduct audits and help drive continuous improvement initiatives across the site. Key Responsibilities Conduct internal audits covering GMP, hygiene, traceability, product quality, documentation and manufacturing processes, ensuring corrective actions are completed effectively. Investigate quality, food safety and compliance issues, including customer complaints ...

responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site. This role ensures ongoing compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, GAMP5 principles, and applicable global regulatory requirements. The position provides technical oversight of electronic systems, manages validation activities, assesses system … validated state. Identify and close existing CSV gaps to ensure compliance with Annex 11 and data integrity requirements. EudraLex Volume 4 Good Manufacturing Practice (GMP) guidelines, laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/ ...

manufacturing experience are unlikely to be suitable for this position. Experience with Siemens S5/S7 PLCs, inverter drives, COMPEX, hazardous areas, pneumatics or GMP environments would be beneficial, but not essential. The role You will respond to production breakdowns, carry out planned maintenance, support equipment modifications and small projects ...

system. Participate in daily maintenance meetings and continuous improvement initiatives. Assist with root cause analysis and equipment reliability projects. Maintain high standards of housekeeping, GMP and health & safety compliance. Ensure equipment is operating safely and efficiently to minimise downtime. Experience/Skills/Knowledge/Qualifications: Strong electrical maintenance background ...

improvement initiatives, including automation developments and SMED projects. Maintain accurate maintenance records and documentation. Ensure all work is completed in accordance with Health & Safety, GMP, quality and environmental standards. Support colleagues through knowledge sharing and contribute to maintaining high engineering standards across the site. About You To be successful ...

coach, develop and inspire technical teams. Desirable Experience within medical devices, healthcare technology or other safety-critical industries. Knowledge of IEC 62304, ISO 13485, GMP and FDA-regulated environments. Experience with cloud platforms such as Azure, AWS or GCP. Understanding of cybersecurity for connected devices and IoT systems. Exposure ...

MedPharm Ltd in Guildford is seeking a CSV Specialist to govern and manage validated computerised systems (GxP) across the site, ensuring compliance with EU GMP Annex 11 and MHRA guidance. You will oversee the validation lifecycle (URS, IQ/OQ/PQ, reports), assess updates, perform risk assessments, and support ...

electrical schematics and technical drawings Good understanding of mechanical systems (gearboxes, bearings, conveyors, pneumatics) Knowledge of food safety standards such as BRC, HACCP, or GMP Strong problem-solving skills and ability to work independently Benefits Opportunity to work in a modern food manufacturing facility Ongoing training and development Pension scheme ...

will have experience in raw materials, technical or quality roles within food manufacturing. Bringing a strong understanding of food safety, legality, allergens, HACCP, GMP and customer codes. Being confident working with technical systems, specifications and supplier documents. You will have good analytical skills and the ability to spot risks early. ...