126 to 146 of 146 GMP Jobs in the UK

Commercial Director in the commercial management of major CSA capital work packages from procurement through to final account. Support and, where appropriate, lead GMP development, negotiation and conversion into agreed package values. Prepare and review valuations, payment recommendations and change control. Contribute to cost reports, forecasts, CVRs and executive-level … successful candidate will ideally have: Significant experience in cost or commercial management on major capital projects. Strong post-contract cost management experience. Experience with GMP procurement, development and negotiation. Working knowledge of FIDIC contracts and contract administration. Strong experience in change control, variations and commercial management. Experience managing valuations ...

play a key role in data preparation in advance of transactions (e.g. buy‐ins); 2) conduct data audits, benefit audits and calculations; 3) undertake GMP projects. For this reason, prior GMP experience is essential. You will also have a good understanding of the technical aspects of defined benefit pensions, with ...

STEMCELL Technologies Inc., Cambridge-based, seeks a Senior Quality Engineer to support GMP cell and gene therapy product lifecycle from development through manufacturing. You will lead design control, risk management, and QA activities, aligning documentation, tests, and audits with ISO and CFR standards. The role emphasizes cross-functional collaboration with ...

East Grinstead, United Kingdom, is seeking a Validation Engineer to ensure manufacturing processes, equipment, utilities, facilities, and systems remain qualified and compliant with GMP and quality requirements. You will prepare and maintain validation documentation, collaborate with Manufacturing, Engineering, Quality, and Regulatory Affairs, and support audits while contributing to product quality ...

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 ...

dedicated Quality Analyst to support the digital transformation journey of a manufacturing site, focusing on implementing and maintaining IT systems that align with GMP regulations. This role will primarily involve working with Quality Systems such as LIMS, CDS, and other QC equipment applications, while also supporting broader manufacturing IT needs. ...

manufacturing processes, equipment, and systems validated and compliant. The role emphasizes quality, regulatory compliance, and reliability while collaborating with cross-functional teams in a GMP environment. The engineer will plan, execute, and maintain validation docs, support qualification activities, perform risk and impact assessments, and assist audits and inspections to continuously ...

reviews for equipment, facilities, utilities, processes, cleaning validation, analytical methods and computerised systems. Role involves planning, coordinating and delivering validation activities, ensuring regulatory compliance (GMP, MHRA, EU and FDA), and supporting investigations, audits and continuous #J-18808-Ljbffr ...

Accord Healthcare Europe is seeking a suitably skilled Calibration/Instrumentation Engineer to ensure calibration systems operate to GMP, SOPs and regulatory standards. You will troubleshoot, calibrate, repair, and install equipment, while supporting the site’s electrical infrastructure and audit readiness. The role requires ONC level or equivalent in Electrical ...

Radiopharmacy team in the UK. The role focuses on radiopharmaceutical testing for release, including HPLC, GC, r-TLC and gamma spectroscopy, with extensive GMP and safety training. New graduates and experienced Analytical Chemists are welcome. The position involves shift work to accommodate the short shelf-life of radiopharmaceuticals, with ...

team responsible for computer systems validation across facilities and software. You will monitor milestones, ensure documented evidence, and manage quality documentation in line with GMP and SOPs. The role requires proven CSV experience, a background in supervising teams, and strong attention to detail. You will engage in audits, risk assessments ...

team in Shawfair. You will supervise a small CSV team, manage validation activities for facilities and software, and ensure milestone evidence is maintained to GMP standards. You will review and approve CSV docs, including plans, protocols, reports, and risk assessments, and help set up the validation schedule for new facilities. ...

into delivery, processes and capability Own commercial performance, identifying growth opportunities and supporting pitches Provide technical leadership across analytics, tagging, MMM, BI and GMP Lead and develop a senior leadership/practitioner team, with responsibility for a large wider function Represent the data practice with C-suite clients and senior … multiple data/marketing disciplines Agency experience preferred, particularly within the media/marketing ecosystem Technical credibility across analytics, BI, MMM and/or GMP - you don't need to be hands-on day-to-day, but must be able to challenge and guide technical teams A strong commercial track ...

major pitches and working with senior clients to identify opportunities to expand data services. Providing technical leadership across analytics, tagging, measurement, MMM, BI and GMP, with enough technical depth to challenge senior practitioners and make sound decisions. Building and developing the leadership team, creating strong development pathways and succession plans. … discipline. You'll ideally have: Experience leading data or analytics teams across multiple disciplines such as Analytics, BI, Data Science, MMM/Econometrics, or GMP Strong experience managing and developing high-performing teams and senior practitioners. A background in an agency environment would be highly relevant, although strong in-house ...

About The Role Training Management Systems Lead We're looking for a Training Management Systems Lead to help shape the future of GMP training and competency management at Bespak. This is an exciting opportunity to lead the transformation of our training processes, moving from a manual approach to a modern … automated Training Management System that supports compliance, efficiency and continuous improvement. You'll play a key role in developing a robust, role-based GMP Training Curriculum Framework, completing Training Needs Analyses (TNA) and defining role-specific training pathways. Working as part of the AlignQ programme, you'll support the implementation ...

Bespak Limited is seeking a Training Management Systems Lead to shape GMP training and competency management, driving the move from manual processes to a modern automated Training Management System that supports compliance and efficiency. You will develop a robust GMP Training Curriculum Framework, complete Training Needs Analyses, and define role ...

Perceptive is seeking a QC Chemist to perform method development and routine analysis of PET radiotracers in a GMP setting. You will implement QC for new radiotracers, support clinical and pre-clinical studies, and contribute to data processing including HPLC and GC. The role requires at least 2 years … laboratory with HPLC experience and GMP knowledge. GC experience is advantageous; familiarity with short‐lived isotopes is desirable. #J-18808-Ljbffr ...

Benjamin Moore is seeking an experienced maintenance engineer to join our engineering team in Prudhoe. You will lead reactive and preventative maintenance across a GMP-regulated site, ensuring uptime, quality and safety standards are met. You will diagnostic faults on mechanical and electrical systems, plan and execute improvements, and coordinate ...

seeking a Cell Scientist to join our biopharmaceutical testing team. You will perform cell-based bioassays and contribute to method development within a GMP-accredited laboratory. You will develop expertise in cell culture, data reporting and documentation while collaborating with experienced colleagues to support long-term client projects and ensure ...

support microbiological testing activities and environmental monitoring programmes that contribute to the manufacture and release of veterinary vaccines, working alongside experienced microbiologists in a GMP-regulated environment. This fully onsite role is a fixed-term contract until end December 2027. #J-18808-Ljbffr ...

Pearl Control Systems Limited in the UK is seeking a Senior Control Systems Engineer to design, program and maintain advanced control systems for production facilities. You will help automate processes, troubleshoot issues and enhance operational ...