19 of 19 Permanent GMP Jobs in the North of England

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 ...

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 ...

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 ...

related field 3+ years experience in Control Systems Engineering Hands on experience with DCS systems (ideally Siemens SIMATIC PCS7) Previous work experience in a GMP manufacturing environment (Pharmaceutical experience is desireable) Knowledge of GAMP frameworks Willing to work on customer sites across the Northwest Code: INDENM If you are interested ...

within a QA, Quality Assurance, or Quality Control role. Experience within the food manufacturing industry is essential. Good understanding of HACCP, Food Safety, and GMP standards. Strong attention to detail and excellent record-keeping skills. Confident communication skills and ability to work collaboratively. Ability to work independently and make informed ...

ensure the continued operation of the calibration systems and equipment within the company. To ensure that all work is performed in full compliance with GMP, SOPs, FDA, MHRA, work instructions and established safety standards. The primary focus of the role will be instrumentation and calibration but the candidate will ...

join the Cost & Commercial Management team, supporting the post-contract commercial management of a major hyperscale data centre programme. You will work on GMP development, contract administration, change control, valuations, forecasting and final accounts with site-based teams and client representatives. The role requires strong post-contract experience, ability ...

programme in the North East. This site-based role focuses on post-contract cost management across Civil, Structural and Architectural packages. You will influence GMP procurement, FIDIC contract administration, change control, valuations and final accounts, working alongside the site leadership, contractors and design teams to drive robust commercial #J ...

experience in programmatic advertising, with a deep knowledge of the Google Stack, Google Ads (Display/Video), DSP (e.g. Adform, Tradedesk, DV360, Amazon DSP), GMP and Analytics Strong understanding of the digital advertising ecosystem, including DSPs, DMPs, and ad exchanges Strong analytical skills and ability to provide insights and recommendations ...

Conveyor Systems and Thermal processing equipment. 3. City & Guilds 2382 (minimum of 18th Edition Regulations) 4. Familiar with the requirements of working within a GMP facility. 5. Excellent internal and external communications skills 6. Experience of working an on-call maintenance system. ...

heights. Making animals’ lives better makes life better – join our team today! Your Role: Advisor, Quality – R&D Position Description: Provides Quality Leadership and GMP compliance guidance across global R&D teams, project groups, and CMOs to support product development, technical transfers, registrations, and successful launches. Partners cross-functionally … Biology, Biotechnology, Chemistry) 5+ years’ experience in Quality Assurance, Quality Control or related technical field (Pharmaceutical Development, Manufacturing, Chemical Engineering etc.) Expert knowledge of GMP and global regulatory requirements (e.g., FDA/CVM, EMA, MHRA/VMD), CMC-related activities, and R&D Quality Assurance from development through registration. Proven ...

Monitoring equipment and facilities to ensure they remain compliant and operational Managing spare parts and consumable stock levels Producing clear, accurate documentation that supports GMP and UKAS requirements Contributing ideas that improve processes, efficiency and reliability This role supports activities across both our Oak Tree House and Coleby House sites … full UK driving licence Bonus Points If You Have Experience With Chromatography systems Mass spectrometry instrumentation Chromatography Data Systems (CDS) Equipment validation and qualification GMP, UKAS or ISO 17025 regulated environments Why Join Us This is an ideal opportunity for someone early in their technical career who enjoys taking things ...

mRNA manufacturing capabilities and seeks a Manufacturing Scientist to help establish a robust, client-ready service offering. You will translate development-scale processes into GMP manufacturing, delivering high-quality mRNA drug substance and formulated products for vaccines and therapeutics. You will work with Analytical Development, QA/QC, Validation ...

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 ...

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 ...

Elanco is seeking an Advisor, Quality – R&D to provide strategic quality leadership across global R&D teams, ensuring GMP compliance for product development, transfers, registrations, and launches. The role partners across functions to shape quality strategy and optimize systems, training, and processes. The role focuses ...

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 ...

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 ...