26 to 50 of 62 GMP Jobs in England

toxicological assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility assessment methodology Basic knowledge of FDA and international medical device regulations/directives and working knowledge of GMP/ISO/GLP guidelines as applied to medical device testing and documentation. Have the ability to work with people and teams in a complex, changing environment and be able More ❯

time and to a high quality In addition, you’ll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement Our More ❯

time and to a high quality In addition, you’ll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement Our More ❯

an award-winning and growing business In addition, you'll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement The More ❯

that the relevant documents have been completed, e.g., hold log, non-conformance log. Reporting any complex issues to QA Supervisor. Hygiene Audits, micro swabbing, and micro sampling product Formal GMP and Process Control document completion About the shift pattern: This Monday - Friday QA role is based in our technical department but working in all areas of the factory as required More ❯

in process control skills, including some of the following: PLC (AB Rockwell, Siemens), SCADA systems (Rockwell Historian), CAD, Trend BMS/Set, Lighthouse EMS, JDEdwards. Experience: Good Manufacturing Practice (GMP) experience. Attributes: Proactive, methodical, and a strong problem solver. Why You Should Join Catalent: Competitive Salary - Reflecting your experience and skills. Bonus & Benefits - Includes an annual performance bonus, a pension More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

Developing specifications and leading multidisciplinary teams to clearly communicate the requirements for the Store and capture client requirements. The industries we serve have growing requirements for regulatory quality control (GMP, Medical Devices, ISO etc). The System Engineering role provides opportunity to develop the fully documented lifecycle to support adherence to these standards. What You'll Be Doing Designs, defines More ❯

Mobilize the Enterprise . Deep PPC knowledge and experience, with current dated certifications (Google and Microsoft) . Excellent and detailed understanding of bid management and core PPC technology platforms (GMP preferred) . Self-motivated and able to manage their time effectively . Operationally proficient, with an affinity for numbers, an analytical thought process and keen to drive continued excellence . More ❯

plans that can be presented 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 landscape Are analytical, flexible and More ❯

Manager is responsible for the qualification, oversight, and auditing of third-party suppliers and vendors supporting GxP activities, including pharmaceutical manufacturing, distribution, and clinical operations. This includes providers across GMP, GDP, GCP, GLP, and GVP domains. The role ensures partners meet regulatory requirements and internal standards to support the safe and compliant delivery of key service lines, such as Expanded … Own and lead global compliance monitoring programs for all GxP third parties, ensuring timely qualification, requalification, or disqualification. Design and manage a global, risk-based GxP audit program covering GMP, GDP, GCP, GLP, and GVP audits, both remote and on-site. Oversee third-party audits, ensuring findings are risk assessed, reported, and closed with appropriate CAPAs; follow up on CAPA … party audits and qualifications, maintaining audit readiness. What You'll Need: Bachelor's or Master's degree in Life Sciences, Pharmacy, Chemistry, or a related field. Extensive knowledge of GMP, GDP, and GCP activities, including qualification, requalification, and auditing best practices. Formal lead auditor certification required (e.g., IRCA/CQI, ISO 9001 or equivalent). Minimum 6-7 years of More ❯

the business will develop in the next coming years.Here is a brief overview of what they're looking for:- Strong retirement calculations experience for DB pensions- Thorough understanding of GMP equalisation- Exposure to or an understanding of new pension dashboard legislation- Strong capabilities in Excel VBA or SQL If you're keen to hear more, please contact Ella Halliday or More ❯

these projects might include; IT infrastructure changes Business process enhancement Administration system software upgrades Web site (member self-service) development Communication exercises on changes to pension benefits/arrangements GMP equalisation Changes to internal control framework (including compliance with the new General Code) To effectively build strong relationships with the different teams and successfully complete any required projects, it is More ❯

Data Scientist - Police Staff - Data Science Unit - Counter Terrorism Policing NW Location: GMP Force Headquarters, Central Park Complex, Northampton Road, Manchester, M40 5BP Contract type: Full Time, Permanent Grade: H/J About the role: This role offers an exciting opportunity for the successful candidate to help shape a new department dedicated to delivering innovative services to the counter terrorism More ❯

these projects might include; IT infrastructure changes Business process enhancement Administration system software upgrades Web site (member self-service) development Communication exercises on changes to pension benefits/arrangements GMP equalisation Changes to internal control framework (including compliance with the new General Code) To effectively build strong relationships with the different teams and successfully complete any required projects, it is More ❯

and experience ideally across all digital media channels but in particular paid search. You will have excellent knowledge of bid management and core technology platforms such as Google Analytics, GMP Platform, SA360 for example. Data analysis and an understanding of the strategic application of digital marketing channels will be a strength. More ❯

topics. Key Experience & Skills Required: Proven success in building effective digital solutions within an agency environment. Ability to consider digital and data across the entire customer journey. Experience with GMP stack. Strong proficiency in Excel. Desired: Experience managing international clients. Understanding of ad tech platforms. Contract Type : Permanent Agency : Havas Media Group Our Commitment: Here at Havas, we pride ourselves More ❯

Set Proven leadership in digital performance, measurement and data strategy roles. Hands-on experience with MMM, incrementality testing and advanced attribution. Strong understanding of ad tech and martech ecosystems (GMP, GA4/BigQuery , Meta CAPI, server-side GTM etc.). Fluent in using data to tell compelling stories and influence both internal teams and C-suite clients. Success Indicators (First More ❯

. Manage contractors to ensure work is carried out safely, efficiently, to the highest quality standards with minimal disruption to the process. Support and expertise in the application of GMP and Sanitary design standards across the sites is provided, developing and sharing best practices across the MEU network Work with Cluster, Regional and global teams to align Capital plans across … . Manage contractors to ensure work is carried out safely, efficiently, to the highest quality standards with minimal disruption to the process. Support and expertise in the application of GMP and Sanitary design standards across the sites is provided, developing and sharing best practices across the MEU network Work with Cluster, Regional and global teams to align Capital plans across More ❯

responsible for the validation and transfer of novel and established test methods for the analysis of gene therapy products and associated materials used for manufacturing the EU and FDA GMP requirements at both the Meiragtx UK and Ireland sites. The role involves life cycle management of assays, equipment and materials/products. Job Description MajorActivities • Lead the development and validation … qualification/validation projects and associated documentation in support of the analytical activities performed ensuring compliance requirements are maintained. • Ensure all methods are validated and performed in the QC GMP labs in compliance to regulatory standards and adheres to data integrity requirements. Support Validation of Methods for raw Materials testing & sampling booth activities. Responsible for the project management of test … method implementation to required timescales to ensure seamless launch of new products. Responsible for ensuring any external testing activities meet GMP requirements. Maintain the flow of information to key stakeholders, ensure appropriate communications are passed forward and information folders are maintained with most recent versions/communications Ensure the development and rollout of training on new technology/methodology introduced More ❯

Quality Audit and Compliance (SQ A&C) team, supporting the Global Supply Chain globally. The SQ A&C team ensures quality and compliance throughout the product lifecycle by conducting GMP assessments of quality-critical materials and services across GSK's manufacturing network. The Supplier Quality Audit Lead , reporting to SQ A&C Senior Manager, plays a key role in ensuring … GSK's material and service suppliers meet compliance standards with regulatory requirements and GSK expectations. The role involves planning, executing, and documenting GMP and Quality Systems audits for assigned suppliers, managing supplier action plans to address identified gaps, and maintaining audit data in GSK's supplier management systems. Additionally, the auditor may provide expertise on supplier change controls when needed. … In this role you will Performing GMP/Quality System assessments/audits of assigned suppliers; making risk-based recommendation on supplier GMP approval status (including proposals for continued use of suppliers with marginal compliance) and documenting assessments/audits in relevant systems. Agreeing appropriate corrective and preventive action (CAPA) plans with suppliers and following up on the completion of More ❯

as Subject Matter Expert (SME) for lifecycle management of assays, equipment, and materials. Prepare and review qualification and validation documentation. Ensure departmental adherence to regulatory and compliance requirements, including GMP and GDP. Manage the implementation and project lifecycle of new test methods. Collaborate with internal and external stakeholders to support testing and validation needs. Deliver training and development initiatives across … a regulated environment. Strong project management and team leadership skills. Demonstrated ability to work independently and deliver results efficiently. Excellent understanding of EU and FDA regulations and industry standards (GMP, GLP, GCP). Proficient in Microsoft Office and other relevant IT systems. More ❯