76 to 85 of 85 GMP Jobs in the UK

Quality Assurance Officer on a 12-month fixed term contract. This is a great opportunity to join a well-established team and support key QA activities in a regulated, GMP environment. The Role: Support day-to-day QA operations, ensuring compliance with SOPs and GMP Assist with supplier quality management and document control Help implement global quality procedures at site More ❯

site at a pharmaceutical manufacturing facility in Northern Ireland. This is a fantastic opportunity to work on a high-profile project, ensuring the validation of automation systems within a GMP-regulated environment. Key Responsibilities Lead and execute validation activities for automation systems, focusing on DCS/PLC systems within a pharmaceutical manufacturing site. Develop and implement validation documentation including URS … IQ, OQ, PQ, and validation plans. Ensure compliance with regulatory requirements (e.g. GAMP 5, FDA 21 CFR Part 11, EU GMP Annex 11). Perform risk assessments, impact assessments, and deviation investigations. Collaborate with cross-functional teams including automation, quality, and IT departments. Provide support during audits and inspections related to system validation. Required Experience & Skills 4-10 years of … System Validation within the pharmaceutical or life sciences sector. Hands-on experience validating DeltaV systems preferred; other DCS or PLC systems will also be considered. In-depth knowledge of GMP, GAMP 5, and regulatory expectations. Proven ability to author, review, and execute validation protocols and reports. Strong problem-solving, documentation, and communication skills. Ability to work independently on-site in More ❯

to working in a customer-focused service business. Accuracy and attention to detail. Excellent customer service and communication skills. Good written and arithmetic skills to comply with audits and GMP standards. Understanding of GMP/GLP standards. Ability and confidence to work alone on a customer site without supervision and as part of a multi-disciplined team. BSc or equivalent 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 ❯

opportunity to be part of a company that values innovation, collaboration, and the flawless execution of ideas that genuinely improve the world! Key responsibilities: Generate and revise documentation for GMP manufacturing to ensure technical accuracy and GMP compliance. Provide technical support to develop required process documentation in collaboration with internal customers. Independently manage the creation of new documents and revise … GMP documents according to detailed procedures. Use and maintain the Documentation Management System (DMS) according to detailed procedures. Produce and process batch documentation according to standard timelines, coordinate review, approval, and issuance ensuring availability for use in Manufacturing per production schedule. Monitor progress of document creation and communicate with relevant parties to resolve potential issues in a timely manner. Manage … training to others during routine document revision. Understand and align with company policies, departmental practices, regulatory, and statutory requirements. Key requirements: Proven experience as a Technical Writer in a GMP manufacturing environment. Outstanding ability to generate and revise technical documentation with attention to detail. Comprehensive knowledge of DMS and standard methodologies for documentation. Ability to manage multiple tasks and projects 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 ❯

We are currently recruiting for a QA Supervisor based at our Llanidoles site, this will be a 5 day onsite role. The successful candidate will be responsible for leading a small QA team to ensure the efficient and effective operation More ❯

GMP Recruitment are proud to be in partnership with a dynamic and fast-growing Telecommunications company, who are currently recruiting for a Sales Agent to join their nationwide sales team on a 6-month, fixed-term contract. This is a field-based role, requiring travel across Ireland, with a primary focus on the Leinster and South-East regions in Ireland … to travel nationally as required. AN IMMEDIATE START IS AVAILABLE FOR SUCCESSFUL CANDIDATE. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯

GMP Recruitment are proud to be working with a well-known Telecommunications service provider based in Southport.We are recruiting on their behalf for an experienced Telecommunications Engineer to join their team on a rolling contract basis . The desired individual will be supporting hardware installation, fibre cabling, fault finding , and providing hands-on support across multiple data centre sites within … Ciena is a strong advantage AN IMMEDIATE START IS AVAILABLE FOR SUCCESSFUL CANDIDATE. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯

GMP Recruitment are proud to be working with a leading Telecommunications service provider based in Southport. We are recruiting on their behalf for a highly experienced and self-sufficient Telecommunications Engineer to support a high-profile data landing site. The successful candidate will be joining their team on a rolling contract basis . This is not a junior or entry … safety standards, and cabling protocols AN IMMEDIATE START IS AVAILABLE FOR SUCCESSFUL CANDIDATE. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯