51 to 61 of 61 GMP Jobs in England

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 ❯

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 ❯

Learning Lead Huddersfield United Kingdom (GB) Full-time Permanent As a strategic partner to the Site Head, you will lead the Technical Training & Learning function, ensuring compliance in a GMP-regulated environment while delivering impactful learning solutions that build site-wide technical capability. How You Will Make An Impact: Lead the site's Technical and GMP Training strategy, ensuring workforce … competence through structured programs that meet GMP compliance and operational needs. Develop and implement an annual training masterplan based on cross-functional capability analysis to build required technical skills across key site functions. Drive the effectiveness of training for critical roles, improving shop floor execution and boosting long-term technical competencies. Monitor and report on Technical Training KPIs, ensuring data More ❯

We are seeking a Supplier Quality Audit Lead within the Central Supplier Quality Audit and Compliance team, supporting the global supply chain. The role involves planning, executing, and documenting GMP audits, managing supplier action plans, and supporting change controls. Responsibilities Perform GMP and Quality System assessments of suppliers and recommend approval statuses. Agree on CAPA plans and ensure their timely … risks, escalate high-risk issues, and support inspections. Candidate Profile Basic Qualifications & Skills Experience in regulated environments like pharmaceutical manufacturing. Degree in Life Sciences or related fields. Knowledge of GMP requirements and QMS principles. Proficiency in English. Preferred Qualifications & Skills Experience with API, sterile, parenteral, or biopharmaceutical manufacturing. Auditor certification from relevant organizations. Application Details Deadline: Sunday 31st August. Please More ❯

pharmaceutical manufacturer to recruit a QA Officer on a 6-month fixed-term contract (strong chance of going permanent). This role is ideal for someone with experience in GMP environments who can contribute to quality systems, batch review, and regulatory compliance. Key Responsibilities: Review batch documentation to support product release Support generation of Quality System documentation and Product Quality … Reviews Investigate and report on deviations and complaints Liaise with Operations, QC, and NPD to ensure product compliance Support QA Manager in maintaining GMP and quality accreditations (FDA, MHRA, ISO, BRC) Assist with validation of processes and equipment Requirements: Science-based qualification (HNC/HND/Degree or higher) QA experience in a GMP-regulated environment Strong organisational and IT More ❯

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 ❯

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 ❯

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 ❯

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 ❯