26 to 50 of 64 GMP Jobs in the UK

continually enhance our relationships with key platform partners. Working to ensure we deliver against agreed JBPs with all key partners. Including Google, SA360/GMP & Microsoft. Team Leadership & Operational Excellence Being a visible role model to PPC Account Directors and Senior Account Managers. Demonstrating a proactive, highly positive/mature More ❯

Engineering, or a similar subject. Extensive industry experience in validation, engineering, or operations within a cGMP environment. A working knowledge and practical experience with GMP utilities, equipment, DIA, and CSV. Key Words: Senior Validation Engineer/Biotech/Validation/cGMP/CQV/DIA/CSV/Qualification Protocols More ❯

a similar MEP-focused role, ideally within Data Centres, Pharmaceutical, or Cleanroom environments Previous experience delivering projects for hyperscale or co-location data centres, GMP/pharma clients, or other critical infrastructure is highly desirable Knowledge of commissioning protocols, integrated systems testing (IST), and regulatory compliance in regulated environments Proficient More ❯

such as Controls & Instrumentation 2. Proven calibration experience working in a highly regulated manufacturing environment, such as Pharmaceutical, Food, Beverage or Chemical. Ideally to GMP standards. 3. A working knowledge and practical experience with PLC, SCADA, and HMI systems. Ideally Allen Bradley or Siemens. More ❯

such as Controls & Instrumentation 2. Proven calibration experience working in a highly regulated manufacturing environment, such as Pharmaceutical, Food, Beverage or Chemical. Ideally to GMP standards. 3. A working knowledge and practical experience with PLC, SCADA, and HMI systems. Ideally Allen Bradley or Siemens. More ❯

information and managing on the online label verifier, including reel changes and troubleshooting. Develop in-depth knowledge of automatic labeller and verifier machine. Formal GMP and process control document completion. Requirements: Ideally have experience of working within a fast- paced food manufacturing environment. A good level of both written and More ❯

The ideal candidate must have a good DB pension's technical knowledge, ideally 5 years experience working in a Defined Benefit role, knowledge of GMP reconciliation, equalisation calculations and PPF. Excellent computer, communication, and organisation skills are required. Candidate should be able to work independently as well as part of More ❯

investigations. What We’re Looking For: 5+ years of experience in Site Reliability Engineering or a related field. Hands-on experience with Biosafety and GMP environments. Strong foundation in Lean Six Sigma principles. Proven problem-solving skills with a knack for performance tuning. Effective communicator and team player. Formal education More ❯

CSV related policies and procedures. Responsible for managing vendor enquires and the troubleshooting and monitoring of process systems. Perform all duties in accordance with GMP requirements, SOPs and controlled documents. Provide guidance, mentorship, and support to team members, fostering a collaborative and high-performance work environment. Report on key metrics More ❯

CSV related policies and procedures. Responsible for managing vendor enquires and the troubleshooting and monitoring of process systems. Perform all duties in accordance with GMP requirements, SOPs and controlled documents. Provide guidance, mentorship, and support to team members, fostering a collaborative and high-performance work environment. Report on key metrics More ❯

fast-paced, ever-changing environment. Strong communication skills. Excellent time management. Desirable skills and experience SQL, R and/or Python coding Experience of GMP rectification and/or equalisation projects Experience working with pension scheme data Knowledge of the journey through Pensions Risk Transfer transactions Experience providing consultancy services More ❯

such as Controls & Instrumentation 2. Proven calibration experience working in a highly regulated manufacturing environment, such as Pharmaceutical, Food, Beverage or Chemical. Ideally to GMP standards. 3. A working knowledge and practical experience with PLC, SCADA, and HMI systems. Ideally Allen Bradley or Siemens. More ❯

vision for modernization in this space Ability to travel for customer meetings and presentations up to 40% Nice to Have Industry experience with QC, GMP quality content, training management, quality systems processes, or manufacturing Leadership of global Sales teams to drive opportunities with intensity Seasoned at developing and maintaining relationships More ❯

vision for modernization in this space Ability to travel for customer meetings and presentations up to 40% Nice to Have Industry experience with QC, GMP quality content, training management, quality systems processes, or manufacturing Leadership of global Sales teams to drive opportunities with intensity Seasoned at developing and maintaining relationships More ❯

As a technician, you'll follow precise mechanical CAD drawings to assemble, perform testing (including force and measurement), inspect assemblies, and document processes to GMP standards. Experience working in safety-critical industries (e.g., medical, aerospace, or automotive) is a plus. Key Responsibilities: Interpret and follow mechanical CAD drawings (SolidWorks preferred More ❯

activities. Acting as Subject Matter Expert for validation during Regulatory and customer inspections. Key attributes and skills: Essential: Prior experience in a Pharmaceutical/GMP environment Good understanding of Qualification & Validation lifecycles Up-to-date knowledge of current regulatory requirements and industry standards associated with Validation activities Experienced in the More ❯

and converting opportunities into successful outcomes. Consult - give strategic support and guidance to clients, delivering high quality and forward-thinking solutions. Pension Projects - including GMP equalisation, data and administration. Propositions development - influence strategic plans for growth of the Operational Solutions business support. Drive innovation - contribute to new tools and technologies More ❯

clearly at every level WHAT WE ARE LOOKING FOR Have extensive, relevant programmatic experience (Google Ads (Display/Video), DSPs (e.g. Adform, Tradedesk, DV360), GMP and Analytics) Have experience with, and gain a lot of energy from, guiding other people Have experience with the Dutch and/or Nordic publisher More ❯

DMPs, CDPs, ad servers, and programmatic advertising. • Proficiency in AI/ML applications for ad targeting, personalization, and optimization. • Experience with Google Marketing Platform (GMP), Amazon Ads, The Trade Desk, or similar ecosystems. • Strong understanding of cloud architectures (AWS, Azure, GCP) and big data technologies. • Experience with privacy-first advertising More ❯

DMPs, CDPs, ad servers, and programmatic advertising. • Proficiency in AI/ML applications for ad targeting, personalization, and optimization. • Experience with Google Marketing Platform (GMP), Amazon Ads, The Trade Desk, or similar ecosystems. • Strong understanding of cloud architectures (AWS, Azure, GCP) and big data technologies. • Experience with privacy-first advertising More ❯

and take ownership of site-wide quality processes, with particular focus on data integrity, validation oversight, documentation, and continuous improvement of systems that support GMP/GDP operations. You’ll also work closely with colleagues across Quality, Validation, Manufacturing, and IT, providing compliance guidance and driving a strong quality culture. … to Quality leadership team projects and initiatives to enhance overall site compliance Ideal Experience: Extensive experience in pharmaceutical QA, with a strong understanding of GMP and GDP Proven track record in managing QMS elements, including validation, documentation, and data integrity Experience supporting inspections and audits, both internal and external Excellent More ❯

workloads and work on multiple projects as required Ideally degree qualified in BioChemistry or Chemistry (or related scientific discipline) A sound working knowledge of GMP and other analytical related quality standards is preferable Proven industry experience of performing detailed experimental checks within the above regulatory framework Industry experience in analytical … extensive range of analytical instrumentation and that provides analytical services to customers in the pharmaceutical, biopharmaceutical, personal care and speciality chemical sectors in a GMP regulated laboratory. This role will review deviations, OOS and change control records, perform internal audits and review of equipment qualifications as well as perform checks … GMP data as necessary in accordance with experimental checking procedures. Key activities: Perform GMP and related quality system checks necessary to ensure that appropriate standards and effective working systems are employed to meet our company and customer requirements Assist the Quality Assurance Team Leader in the overall implementation of the More ❯

validation in the pharmaceutical sector. Experience and knowledge of working in a regulated environment, specifically with regards to record retention. Knowledge of GCP and GMP with regards to QMS activities. Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in … accordance with applicable procedures. Responsible for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken. Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions are closed More ❯

dependant on performance), company pension, onsite parking Major Duties and Responsibilities Reviewing Batch records and creating the associated checklists to support batch certification Archiving GMP critical documents in line with company policy Ensuring current versions of controlled documents are available to site personnel Assist in Audits Proactively identifying risks within … release testing in a timely manner The Person Minimum degree in pharmacy, biomedical sciences, or any other scientific degree. 2 years' experience in a GMP/GLP role. Experience in CAPA, OOs, OOt, deviations, change controls etc in a GMP setting Willingness to learn. Strong administrative skills and the ability More ❯

standards. Your new role As a Quality Assurance Specialist, you will be responsible for managing quality activities to ensure compliance with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) for medicinal products. Your key duties will include: Overseeing the product release and compliance process, verifying documentation completeness, and ensuring … field. Minimum of 5 years of experience in Quality Assurance, Quality Control, or a related function within the pharmaceutical or healthcare industry. Certifications in GMP and GDP Strong understanding of regulatory affairs, quality assurance, and pharmaceutical guidelines. Proven experience managing quality systems, pharmaceutical product releases, and compliance-related activities such More ❯