76 to 100 of 104 GMP Jobs in the UK

improvement of QC equipment and electronic systems.Manage the procurement, validation, qualification, and deployment of new or upgraded QC equipment and systems.Ensure compliance with GMP, data integrity guidelines, and corporate standards for QC operations.Develop and maintain a long-term equipment replacement plan to meet testing requirements.Oversee new product introductions, method transfers … electronic systems, including their qualification and validation.Experience in managing QC equipment and systems, including acting as a laboratory administrator or end-user.Proficiency in GMP guidelines, data integrity requirements, and regulatory compliance.Excellent communication, leadership, and project management skills.Ability to analyze complex data and present findings clearly.Proficiency in computer applications such ...

equipment and electronic systems. Manage the procurement, validation, qualification, and deployment of new or upgraded QC equipment and systems. Ensure compliance with GMP, data integrity guidelines, and corporate standards for QC operations. Develop and maintain a long-term equipment replacement plan to meet testing requirements. Oversee new product introductions, method … systems, including their qualification and validation. Experience in managing QC equipment and systems, including acting as a laboratory administrator or end-user. Proficiency in GMP guidelines, data integrity requirements, and regulatory compliance. Excellent communication, leadership, and project management skills. Ability to analyze complex data and present findings clearly. Proficiency ...

U.K. Full-time Permanent Lead the heartbeat of pharma manufacturing on the shopfloor. In this hands-on leadership role, youll act in line with GMP and Quality regulations, making sure internal and external audit observations are closed on time and in full. Youll champion full compliance with all STADA requirements … efficiency/cost-saving initiatives, all while maintaining full adherence to global and local Health, Safety & Environmental requirements. If you thrive in a GMP environment and want your leadership to directly impact patients and product supply, this is the role for you. How You Will Make an Impact Lead ...

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 ...

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 ...

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 ...

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 ...

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 ...

with the site-based commercial leadership team, general contractors, supply chain partners and the wider project team to help drive robust commercial outcomes across GMP procurement, FIDIC contract administration, change control, valuations, forecasting and final accounts.What You’ll Be DoingSupporting the Commercial Director in the commercial management of major … capital work packages from procurement to final accountSupporting, and where agreed leading, GMP development, negotiation and conversion to agreed package valuesPreparing and reviewing valuations, payment recommendations and change control with the wider site commercial teamContributing to cost reports, forecasts, CVRs and executive dashboardsSupporting the administration of FIDIC contracts and wider ...

visual and instrumental inspections of raw materials and finished goods. You'll play a vital role in identifying defects and maintaining Good Manufacturing Practice (GMP). Safety & Standards: Maintain a "Safety First" mindset by adhering to COSHH and EHS guidelines and keeping your workspace pristine using 6S principles. Data Integrity ...

lead a multidisciplinary team, oversee validation across equipment, facilities, utilities, sterilisation, aseptic processing and GxP computerised systems, and ensure compliance with EU/US GMP and industry standards. The role requires a degree in a relevant scientific or engineering discipline, extensive GMP validation #J-18808-Ljbffr ...

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 ...

optimal stock levels of consumables to support the team and ensure maximum throughput and efficiency. Safety & Compliance: Uphold excellent housekeeping to Good Manufacturing Practice (GMP)/Good Laboratory Practice (GLP) standards, strictly adhering to all safety recommendations, including proper PPE usage, and contributing to safety assessments. Process Improvement: Proactively identify ...

Eblex Group is supporting a growing biotechnology company with an expanding clinical pipeline in the search for a Director Clinical Quality Assurance with GMP exposure. This broad QA role sits within a lean biotech environment and works closely with Clinical Development and other functions across clinical quality, audits, CAPA, investigations ...

Nexus Life Sciences seeks an experienced QC Validation & Systems Lead to own QC systems, equipment lifecycles and computerised platforms in a GMP laboratory. You will lead IQ/OQ/PQ validation, calibration programs, and act as system owner for Empower and LabX, ensuring data integrity and audit readiness. This ...

Convatec Oxford laboratory is seeking a senior leader to manage operations, oversee CNAP R&D programmes, and ensure regulatory compliance across CSV, QMS, GMP, and related standards. The role leads a multidisciplinary team including technicians and scientists, driving capability, partnerships, and a culture of high performance. We seek a Doctorate ...

cost, lead time, efficiency and best practices. They will support compliant, reliable, and efficient operation of processing equipment in line with regulatory requirements (e.g., GMP, FDA, MHRA ) and other business objectives. The role requires the ability to work in a cross-functional matrix organisation, fostering a continuous improvement culture, with … location of which will be varied. Review performance and KPI’s for key OEMs.Ensure Self Care, and IW processing installations meet hygienic design, GMP, and regulatory requirements. In collaboration with RPS and Reliability Engineering monitor equipment performance, reliability, and compliance and link to continuous improvement initiatives. Capture inputs from Reckitt ...

audit events, conversions, and consent, server-side GTM evaluation, manage parameter standards and de-duplication rulesPlatform integrations: Build robust connectors/APIs for GA4, GMP (CM360/DV360/SA360), Meta and other platforms. Unify with Databricks, COGNOS and SalesforceData engineering: Model clean tables/views, implement data quality checks … Science, Analytics or Data ScienceProfessional Experience: 6-8 years in analytics/data engineering or marketing analytics engineering rolesExpertise in GTM/GA4/GMP/Meta tracking; strong SQL, experience with BigQuery or equivalentHands on APIsProficiency with dashboarding (Looker studio/Tableau) and at least one scripting language (Python ...

Onyx-Conseil in Stevenage offers a hybrid IT Director role to shape the IT strategy and governance for a GMP-regulated environment. The position leads external and internal customers, directs a 15-person IT team, and partners with senior leaders to enable clinical, regulatory and manufacturing workflows. You will drive ...

critical process equipment, with three days on site per week, and the rest remote. You will drive design assurance, stakeholder engagement, and compliance with GMP and SHE requirements across all design stages. #J-18808-Ljbffr ...

GMP Recruitment Agency Limited are proud to be partnered with one of the leading law firms in the UK. We are looking for a confident, approachable and enthusiastic IT Trainer to become the go-to person for IT training across multiple sites. You’ll help colleagues get the most … What's important is that you're confident with technology and able to learn new systems quickly and then explain them clearly to others. GMP Recruitment Agency Limited are recruiting for this role on behalf of their client and are acting as an Employment Agency. GMP Recruitment Agency Limited ...

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 ...

contractor pre-qualification, technical assessment and selection. Produce regular Design Assurance Reports to ensure ongoing technical alignment. Identify and support value engineering opportunities. Ensure GMP and SHE requirements are appropriately reflected within design deliverables. Participate in SHE and technical risk assessment activities and ensure appropriate mitigations are incorporated into … manufacturing environment. Strong experience across controls and instrumentation engineering within major capital projects. Experience providing technical leadership, design assurance and governance. Strong understanding of GMP and engineering requirements within a pharmaceutical environment. Experience working with Design Contractors, suppliers and Work Package Owner teams. Experience reviewing technical specifications, drawings, calculations ...

GMP Application and Analytics Manager - Salesforce & Microsoft Power BI Summer-Browning Associates is currently supporting our central government client, who is seeking a GMP Application and Analytics Manager for an initial six-month assignment with the option to extend. Location: Milton Keynes - Hybrid working The ideal candidate will possess ...

include pitching technical products, negotiating pricing and supply agreements, preparing sales forecasts, managing customer trials and maintaining accurate CRM records. Sector - Chemical, Process or GMP Manufacturing Non-Negotiable Requirements of the Business Development Manager Proven B2B sales and key account management experience Successful new-business generation experience Experience within chemical … process, GMP or technical manufacturing Requirements for the Business Development Manager Strong pricing and commercial negotiation experience Confident pitching to senior-level customers Strong CRM, pipeline management and forecasting experience Able to independently manage a national territory Willingness to travel nationally and internationally for client meetings Desirable Requirements ...