21 of 21 GMP Jobs in the UK excluding London

Acting as an internal & external Veeva technical expert with detailed in-depth knowledge of the system configurations and their relationship to ensure compliance with GMP Partnering with OXB Validation department to ensure the Veeva Vault system retains its validated status throughout its lifecycle Owning the solution strategy for the delivery ...

will provide strategic leadership for the IFS product roadmap, ensuring its alignment with organisational objectives, timely and high-quality delivery and adherence to GMP compliance standards where needed, playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Being ...

biology, biomedical sciences) or equivalent. Proven experience in quality assurance within a regulated manufacturing or laboratory environment. Strong knowledge of quality systems, ISO standards, GMP/GDP principles, and regulatory compliance. Skilled in leading audits, managing CAPAs, and interpreting quality metrics. Excellent leadership, communication, and problem-solving abilities. Proficient ...

ensure adherence to specifications and hygiene standards. Compliance & Audits: Ensure full compliance with all relevant food safety authorities and international standards (e.g., HACCP, GMP, BRC, ISO 22000). Prepare for and actively participate in internal, third-party, and regulatory audits. Documentation & Reporting: Maintain accurate and up-to-date quality ...

product direction across cross-functional, multi-region teams. A strategic thinker capable of shaping long-term transformation while executing fast. Comfortable in complex, regulated, GMP-heavy environments. Experience delivering solutions that optimise: Manufacturing performance Supply chain planning Network strategy Quality workflows Data governance & AI compliance Why This Role Matters This ...

with IT, Quality, Operations, and Engineering teams to deliver projects. Generate and execute validation documentation , including Computer System Validation (CSV). Ensure compliance with GMP and regulatory standards. Apply emerging technologies to deliver robust, reliable, and maintainable solutions. What We're Looking For Strong technical experience in Operational Technology architectures ...

conjunction with Production Management To assist with preparation of the site for audits from both internal and external expectation To manage the site GMP audit system and be a member of the site internal auditing team To assist with the recording of all necessary KPI information weekly To manage ...

/Electrical, or Software Engineering. Proven experience in Systems Engineering, specification writing, and validation. Strong organisational, communication, and coordination skills. Familiarity with regulatory standards (GMP, ISO, Medical Devices). Experience with MS Project, MS Office, Visio, and 3D CAD or AutoLab. What you'll get in return Competitive salary ...

industrial applications Desirable: Knowledge of Rockwell Studio 5000/FactoryTalk Experience with isolator or barrier systems Background in pharmaceutical or regulated industries (GAMP, GMP, FDA) Why Join Us? Be part of a global leader in aseptic and containment technology Work in a highly skilled, multidisciplinary engineering team Opportunities for international ...

team fostering a positive, ethical culture aligned with company values. Oversee design, development, and maintenance of software applications and systems. Ensure compliance with SHE, GMP, Data Integrity, and quality standards. Drive technical innovation and continuous improvement within the team. Conduct code reviews, mentor team members, and maintain coding standards. Collaborate ...

completed Collecting micro samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/Fabric audits Temperature checks Quality checks The nature of the role requires a flexible approach to working hours. Core working hours are: Days: Monday ...

solving tools such as Fishbone, 5 Whys etc. Authors, reviews, and approves Controlled Documents in accordance with procedures. Will support in delivering the site GMP training as required. Will conduct the internal audit programme. Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department … investigated and communicated. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experienced in batch review and batch release GMP QA experience is essential! Ideally in a Pharmaceutical setting or similar Experience in CAPA, deviations, change controls, internal auditing (preferred) etc Strong interpersonal skills ...

high standards of sanitation across all areas of the section at all times Support the manufacturing teams to embed quality practices and drive strong GMP compliance. Support the implementation of 5S across the section. Ensure CCP and sPP compliance within the section. Primary accountability around paperwork completion/record management. … e.g. Chemistry, Microbiology, Food Science, Nutrition, Food Technology or related field. Quality auditing skills; HACCP, Sanitation and hygienic design knowledge. Experience at driving strong GMP compliance. Good knowledge of Quality Management Systems, including internal audits and preventative/corrective actions. Experience in root cause analysis and issues resolution. Quality techniques ...

Responsibilities Include: • Lead and drive compliance with ISO and all certified standards. • Own and manage the QMS, processes, and documentation to meet ISO22716 Cosmetic GMP, BRC Consumer Products, RSPO Supply Chain, and Cosmos Organic requirements. • Manage and develop the Quality Team and oversee daily operations. • Chair monthly and annual Quality … Degree in a scientific discipline or extensive manufacturing experience with a strong focus on Quality systems. • Proven track record in Quality systems and GMP compliance, including ISO22716 Cosmetic GMP, BRC Consumer Products, RSPO Supply Chain, and Cosmos/Soil Association Organic. • Experienced leader with a history of managing and developing ...

Review Deviations, CAPAs, Change Controls and Supplier Complaints Review Computer Systems Validation (CSV) documents Identify and lead QMS improvements Monitor and produce metrics for GMP compliance Deliver training on QMS Profile description: We are looking for: A-Level education in (science preferred) or equivalent experience Experience working within a GMP … Knowledge of pharmaceutical regulations and compliance requirements Experience within Quality within a pharmaceuticals environment Hands-on experience using electronic Quality Management Systems (eQMS) to GMP standards. An understanding and awareness of Computer Systems Validation (CSV) An understanding of Quality audits, investigations, and root cause analysis and change Control Processes Proficient ...

ideal for someone with a science or pharmaceutical-related degree and exceptional people management skills, looking to make a meaningful impact in a GMP-licensed facility. Key Responsibilities: Lead and manage a team of QA Officers to ensure product release meets GMP and QMS standards. Support the QA Manager with … Microbiology, Biology, Biomedical Sciences, or equivalent. Pharmacy Technician Level 3 (GPhC registration desirable). Proven experience in Aseptic pharmaceutical manufacturing and working within a GMP-regulated environment. Strong leadership and coaching skills with a track record of team development. Excellent understanding of MHRA regulations, ISO standards, and quality systems. Skilled ...

Managers, Responsible Persons and Qualified Persons with the implementation and maintenance of the Quality Management System in accordance with the GMP and GDP guidelines and GPhC, ISO 9001 and ISO 13485 standards. Supporting the ongoing compliance with relevant standards, legal requirements, regulations and the PSDL documented policies and procedures. Promoting … able to promote a positive Quality culture within the company. Excellent knowledge of Word, Outlook, Excel, PowerPoint, and Teams. Good knowledge of GDP, GMP and GPhC regulations, ISO 9001 and ISO 13485 standards. ...

various stakeholders of the business, line managers and addressing client inquiries whilst delivering exceptional customer service while maintaining compliance with industry standards (BRC/GMP). The Role: Assist with formulation trials, stability testing, and translating R&D products into manufacturing-ready specifications Checking associated labelling/artwork and/… product specifications are accurate. Assisting with continued QMS development Assisting and completing internal auditing (not supplier) Assisting and completing labelling audits Assisting and completing GMP audits Data entry (Word, Excel, SharePoint etc) Deputising for the Technical Manager during annual leave, busier periods and ad-hoc. Maintain a strong presence ...

understanding and competency. The individual is a training professional whose focus is to train and upskill the production teams and wider business within a GMP environment. The role is responsible for the operational technical training, whilst also supporting EHS and GMP training for the production operation. What are we looking … learning tools to support the delivery of training materials using multiple media types. Knowledge and experience of pharmaceutical packaging and manufacturing operations, including GMP knowledge. Good Communication skills across different levels in the organisation (e.g. Ops, OLT). Strong facilitation, coaching and presentation skills. Training qualification (CIPD, City of Guilds ...

Senior Lab Systems Lead, supporting Lab Execution System (LES) deployment. We are seeking highly motivated and organised individuals with previous experience of instrumental methods, GMP testing activities, and data management systems such as Chromatography Data Systems (CDS) or Laboratory Information Management Systems (LIMS). This role is suited to hybrid … Serve as the interface between lab users and IT for system deployments (e.g., LES, LIMS, CDS) Optimise laboratory application usage and ensure compliance with GMP standards Support digital transformation initiatives within regulated environments What We're Looking For Degree in a relevant scientific discipline, for example, Chemistry, Pharmaceutical or Biological ...

GMP Recruitment are proud to be in partnership with a long-established and reputable defence engineering firm based in the Birmingham area. We are currently recruiting on their behalf for an experienced IT Support professional to join their I.T Department on a full-time, permanent basis. This position offers … 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. ...