26 to 50 of 53 GMP Jobs in England

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 ❯

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 ❯

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 ❯

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 ❯

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 ❯

and Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and company expectations. Provide input to the review and writing of any associated quality policies, systems and procedures as required and prepare and update SOPs … applications providing independence of access for administrator activities Ensure Qualification and Validation of equipment, processes, systems is/are performed in line with procedures, GMP and GAMP guidelines for process, equipment and electronic systems, as and when required. Ensure the maintenance of procedures supporting Qualification and Validation and review and … of data integrity and application to system management Good understanding of Quality Control Systems and analytical software and electronic Quality Systems Good understanding of GMP Guidelines and Regulations Knowledge of the qualification and validation requirements for equipment and electronic systems Excellent verbal and written communication skills. Apply: It is essential More ❯

and Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and company expectations. Provide input to the review and writing of any associated quality policies, systems and procedures as required and prepare and update SOPs … applications providing independence of access for administrator activities Ensure Qualification and Validation of equipment, processes, systems is/are performed in line with procedures, GMP and GAMP guidelines for process, equipment and electronic systems, as and when required. Ensure the maintenance of procedures supporting Qualification and Validation and review and … of data integrity and application to system management Good understanding of Quality Control Systems and analytical software and electronic Quality Systems Good understanding of GMP Guidelines and Regulations Knowledge of the qualification and validation requirements for equipment and electronic systems Excellent verbal and written communication skills. Apply: It is essential More ❯

week) You will be responsible for: The Data Integrity Analyst Co-Op works alongside Quality Control (QC) laboratory staff learning about Good Manufacturing Practices (GMP) associated with the Pharmaceutical Industry and has responsibility for assisting (or independently performing) various laboratory processes within the QC environment. All tasks performed as part … of this position are completed in compliance with all applicable procedures, standards and GMP regulations. This position may also contribute to improvement projects within the QC organization related to data integrity processes. Key responsibilities include the following: Maintaining a safe work environment in compliance with all applicable environmental, health, and More ❯

and Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and Corporate expectations. Provide input to the review and writing of any associated quality policies, systems and procedures as required. Support the maintenance and administration … independence of access for administrator activities. Ensure Qualification and Validation of EML equipment, processes, systems is/are performed in line with EML procedures, GMP and GAMP guidelines for process, equipment and electronic systems, as and when required. Ensure the maintenance of EML procedures supporting Qualification and Validation ensuring they … Quality Systems. Ability to interpret complex data and present key findings. Ability to describe technical information in easy-to-understand terms. Good understanding of GMP Guidelines and Regulations. Knowledge of the qualification and validation requirements for equipment and electronic systems. Maintain knowledge and understanding of technical advancements in electronic systems. More ❯

systems at our Holmes Chapel site. You'll provide hardware and software support, resolve breakdowns, implement preventative maintenance, and ensure compliance with GMP (Good Manufacturing Practice), EHS, and company standards. Your role also involves supporting computer system validation, quality improvement initiatives, and training other team members. This is a hands … and coding support to maintain system performance. Resolve equipment breakdowns and conduct root cause analysis. Support engineering CAPEX and improvement projects. Ensure compliance with GMP, EHS, and company standards. Support computer system validation and lifecycle management. Contribute to engineering best practices and project execution. Train team members on equipment, systems More ❯

Comfortable operating autonomously once goals and objectives are set. Excellent interpersonal, written and verbal communication skills. Confidence and ambition to provide pragmatic and considered GMP advice. Having current and up to date professional knowledge, expertise and best practice. Proven ability to engage constructively with colleagues at all levels across different More ❯

To complete customer line forms, questionnaires and specification requests. To set up and maintain data in the companys ERP system(s). To undertake GMP audits according to agreed audit schedule, distribute the results and ensure the closure of actions raised. To lead and/or participate in root cause … methodical, with excellent administrative and strong communication skills. Good relationship building skills with both internal and external stakeholders. An understanding of the principles of GMP and Global Food Safety Initiatives. Personal Skills An excellent multi-tasker, able to manage multiple projects simultaneously and who thrives in a fast paced role More ❯

education and professional registration. In this role you will Specification, Procurement, Installation, Acceptance Testing (e.g. FAT/SAT) of automation systems in a licensed GMP commercial plant Ensure compliance with engineering and EHS standards relevant to the service provided. Engage with external specialist companies engaged to deliver projects or provide … for supporting senior automation engineers in delivery of site automation strategy. Work with site Quality and Validation personnel to ensure automation and control system GMP compliance. Implement and complete change controls, CAPAs, and Deviations for automated GMP systems and equipment. Why you? Basic Qualifications & Skills: We are looking for professionals … P&ID nomenclature Process and Machinery Safety (UKCA/CE, PUWER, HAZOP, SIL) Appreciation of Operational Technology Cyber Security Standards and knowledge of current GMP regulations and an understanding of regulatory agencies expectations and change management in a regulated environment. Closing Date for Applications: 15/5/2025 Please More ❯

/office arrangement as the business requires. The role of the Senior Technical Editor is to manage the creation of new documents and revise GMP documents for complex technical changes. Key responsibilities: Independently manage the creation of new documents and revise GMP documents for complex technical changes according to documented … Tasks and CAPAs Creation and coordination of Change controls and completion of change assessments in Trackwise in conjunction with internal Lonza donors Maintenance of GMP document templates and document style and format standards Advise on document style and content, use of DMS, documentation procedures and documentation best practice and provide More ❯

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, giving you More ❯