1 to 25 of 98 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 ...

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 ...

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 ...

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 ...

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 ...

Role Accountabilities • Deliver a risk-based programme of internal and supplier audits to assess compliance with food safety, quality, legality and customer standards • Evaluate GMP, hygiene, HACCP, allergen controls and traceability during audits to ensure sites meet required standards • Plan, conduct and report audits independently across multiple categories, processes ...

Cambridge, Waterbeach site! As the Senior Quality Engineer, you will support the development and manufacture of innovative instrumentation and single-use consumables for GMP cell and gene therapy manufacturing, as well as research use only (RUO) applications. Working closely with Engineering, Manufacturing, and the broader Quality team, you will provide ...

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 ...

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 ...

PowerPoint A proactive approach to problem solving, risk management and decision making Desirable criteria include PRINCE2 or PMP certification Experience working within a GMP or regulated environment Experience delivering projects across multiple global locations Experience managing third-party suppliers and external resources Experience communicating with senior leadership and executive stakeholders ...

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 ...

embedding Greencore, customer, and legal standards, ensuring compliance is consistently achieved and maintained. This role plays a critical part in driving improvements in GMP performance and audit readiness, helping to raise quality standards and strengthen food safety culture across the site. Role Accountabilities Understand and apply Greencore, customer ...

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 ...

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 ...

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 ...

conjunction with Production Management To assist with preparation of the site for audits from both internal and external expectation To manage the site GMP audit system and be a member of the site internal auditing team To assist with the recording of all necessary KPI information weekly In the absence ...

procedures. Conduct risk assessments and ensure all engineering activities are compliant with safety protocols. Food Safety and Hygiene: Ensure all engineering activities align with GMP and food safety regulations, maintaining impeccable hygiene standards during maintenance. Skills, Knowledge, and Experience Qualifications: Recognized engineering degree in Electrical, Electronic, Automation, or Multi-Skilled ...

. Experience with process control and automated systems for production lines. Familiarilty with PID tuning for production lines. Familiarity with industry-specific regulations (HACCP, GMP, etc.) and food safety standards. Knowledge of instrumentation and process equipment . Knowledge of Java, Python, C++ and VB Scripting Familiarity with Flow Charts ...

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 ...

Catalent Swindon site seeks an Associate Director, QMS & Compliance to lead the Quality Management System and regulatory affairs, ensuring GMP/FDA/MHRA compliance and continuous improvement at a leading biologics/pharmaceutical operations hub in Swindon, UK. You will develop high-performing teams, manage QMS budgets, and partner ...

accuracy and attention to detail Reporting hazards or near-misses using iAuditor Suggesting improvements and supporting continuous improvement activities Following production processes, quality standards, GMP/GDP and good housekeeping Taking part in training to build your skills and knowledge What We re Looking For Previous experience in a machine ...