20 of 20 Permanent GMP Jobs in London

and embedded analytics for production KPIs. Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable. Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.). Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs. Ability to translate complex operational processes into streamlined SAP-enabled solutions. More ❯

basic understanding of computer system 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 timely and in a RFT state Job Background Minimum of 3 years experience working in More ❯

client based in South West London on a permanent basis. The ideal applicant will have an in depth pharmaceutical background with a strong knowledge of QMS, EU/UK GMP and EU/UK GDP guidelines. Spanish language skills are essential, at a professional level. Responsibilities Include: Ensure Quality Assurance (QA) business and regulatory requirements are met at all times … by all 3rd party suppliers, service providers and customers and Operational activities are compliant with authorised activities and scope detailed in the clients GMP and WDA licences. Co-ordinate the collation and review of supplier licences and certificates. Ensure medicinal products procured, held and distributed are as authorised by WDA of company, storage premises and customers. Manage authorised activities to … of importation performance monitoring. Qualifications: Degree level in a Life Science subject or equivalent in relevant experience. Knowledge of Quality Management system within a pharmaceutical background. Good understanding of GMP/GDP. Good understanding of pharmaceutical regulation and regulators. Good inter-personal and communication skills. Ability to work under pressure and to tight time deadlines. Excellent attention to detail. Ability More ❯

internal stakeholders (IT, Facilities, Engineering, Security, and Real Estate) and external consultants, contractors, and OEMs. Develop and maintain package scope, budget, schedule, and quality requirements. Ensure all systems meet GMP/GxP compliance, cybersecurity standards, and pharmaceutical industry best practices. Lead RFP processes, technical evaluations, and contract negotiations for IT/AV vendors and integrators. Manage interdisciplinary coordination with MEP More ❯

internal stakeholders (IT, Facilities, Engineering, Security, and Real Estate) and external consultants, contractors, and OEMs. Develop and maintain package scope, budget, schedule, and quality requirements. Ensure all systems meet GMP/GxP compliance, cybersecurity standards, and pharmaceutical industry best practices. Lead RFP processes, technical evaluations, and contract negotiations for IT/AV vendors and integrators. Manage interdisciplinary coordination with MEP More ❯

An effective written communicator, able to deliver concise documentation and adapt writing style to audience as appropriate. Educated to degree level or higher. Understanding of EU & UK GDP/GMP legislation. QUALIFICATION, EXPERIENCE & SKILLS DESIRABLE Experience in multiple regulatory and operational jurisdictions. More ❯

You As Senior/Principal Architect Life Sciences you will have experience in delivering projects from concept to detailed design in the life science sector for both laboratories and GMP manufacturing facilities. You will be part of an enthusiastic and committed team of Architects and Technicians who will deliver high quality output on projects. To be successful you will exhibit More ❯

with Python for data processing or image analysis. Background or interest in biology, lab automation, or scientific instrumentation. Experience working with or building distributed systems. Experience with regulated environments (GMP, HIPAA, etc.) Experience with UI/product design processes and tools (wireframes, mockups, looks-like prototypes, etc.). Why You'll Love Working Here Impact : Your work will directly enable … complex problems at the intersection of software, hardware, and biology-you'll constantly learn and develop new skills. Autonomy : You'll have the freedom to shape our approach to GMP readiness, with support from a talented cross-disciplinary team. Team : Work with the best engineers and scientists in a collaborative environment where diverse perspectives drive innovation. Salary and Benefits - Competitive … re building a team that enjoys moving fast, strives for continuous improvement through learning from mistakes, and is passionate about work that contributes to solving real world problems. No GMP experience? No problem! We want someone who is motivated to deliver an innovative product into a regulated space with creative, efficient solutions. If you're excited about solving interesting problems More ❯

clean line sign-off, collection of swabs & water samples Quality checks and then collection of finished product and raw materials for microbiological & nutritional testing Conducting various daily audits (including GMP, Glass & Plastics audits, and ensuring corrective action with the shift manager Conducting internal quality assessment panels (QAS) throughout the shift & raising issues with the senior key-op/shift manager More ❯

Automation Engineer Location: London Our client is a gene therapy company that works with gene therapy discovery, development and GMP manufacturing. They have headquarters in London and the USA and have recently redesigned exciting new labs with cutting edge technology and the ability to work to a higher standard and increase their capacity of production. They are currently seeking an … commissioning protocols, user requirement specifications, acceptance test plans, Functional Specifications. Design Specifications, and drawings and diagrams. Work with site Quality and CSV personnel to ensure automation and control system GMP compliance. Raise and complete Quality Events, change controls, CAPAs, and Deviations for automated GMP systems and equipment into the site QMS system. Support training efforts for new equipment installations Responsible … for ensuring that own work complies with GMP, Data Integrity and GDP and is undertaken in accordance with applicable procedures Skills Required: Bachelor's degree in Engineering from an accredited university in mechanical, chemical, or electrical disciplines with minimum 5 years' experience, supporting or developing automated systems. Strong understanding of automation standards and architecture addressing batch process control, such as More ❯

as a Senior Pensions Data 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 a great chance to work More ❯

Understanding of distributed systems concepts. Experience with Python for data processing or image analysis. Background or interest in biology, lab automation, or scientific instrumentation. Any experience with regulated environments (GMP, HIPAA, etc.) Any experience with UI/product design processes and tools (wireframes, mockups, looks-like prototypes, etc.). Why You'll Love Working Here Impact : Your work will directly … complex problems at the intersection of software, hardware, and biology-you'll constantly learn and develop new skills. Autonomy : You'll have the freedom to shape our approach to GMP readiness, with support from a talented cross-disciplinary team. Team : Work with the best engineers and scientists in a collaborative environment where diverse perspectives drive innovation. Salary and Benefits Competitive … re building a team that enjoys moving fast, strives for continuous improvement through learning from mistakes, and is passionate about work that contributes to solving real world problems. No GMP experience? No problem! We want someone who is motivated to deliver an innovative product into a regulated space with creative, efficient solutions. If you're excited about solving interesting problems More ❯

work environment Self-motivated and proactive with the ability to take ownership of tasks and drive them to completion Desirable: Good Experience in 3rd party tracking & analytics solutions, including GMP and Adobe Previous client-facing media agency experience Knowledge of running Google shopping campaigns Experience on retail media platforms such as Criteo and CitrusAd Benefits: Uncounted holiday & wellbeing (Star) days More ❯

informatics software applications and the 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 with executive-level stakeholders Published More ❯

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 ❯

building and managing cloud-based data pipelines to drive successful business outcomes for large organisations. Your expertise in digital media and marketing platforms, such as Snowflake, Azure, AWS, GCP, GMP, Adobe, and Tealium, enables you to develop scalable data solutions with a customer-centric focus. With a strong technical background and the ability to collaborate effectively with internal and external 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 ❯

and delivers solutions for wide-ranging issues and a varied customer base. Project & Data Solutions delivers the right, cost-effective strategies and solutions for the following: Guaranteed Minimum Pension (GMP) projects Auditing data, benefits and calculations Bulk data rectification and benefit (re-)construction Data cleansing and improving electronic data Supervising the data workstreams for de-risking projects so data is More ❯

media analytics (agency background preferred) Strong knowledge of measurement frameworks incl. attribution and MMM Proficiency in SQL, Python, R, and leading data viz platforms (e.g., Tableau, Looker) Familiarity with GMP, Meta, CDPs/DMPs, ad servers, and tagging solutions Experience with cloud platforms (AWS/Azure) Confident team leadership and stakeholder management Bonus Points: Knowledge of clean rooms, first-party More ❯

media analytics (agency background preferred) Strong knowledge of measurement frameworks incl. attribution and MMM Proficiency in SQL, Python, R, and leading data viz platforms (e.g., Tableau, Looker) Familiarity with GMP, Meta, CDPs/DMPs, ad servers, and tagging solutions Experience with cloud platforms (AWS/Azure) Confident team leadership and stakeholder management Bonus Points: Knowledge of clean rooms, first-party More ❯