11 of 11 GMP Jobs in the North of England

required. About You Degree in a Life Science subject (or equivalent experience). At least 3 years' experience in QA/QC within pharmaceutical manufacturing. Strong working knowledge of GMP and QMS processes. Excellent attention to detail and strong organisational skills. A collaborative team player who can also work independently. What's On Offer Competitive salary plus shift allowance and More ❯

with diverse cultures Necessary legal status to work in the UK. Beneficial requirements: The closest relevant experience would be MES/EBR, eQMS, LIMS, ERP or other systems for GMP regulated manufacturers. Experience of different project delivery methodologies including waterfall and agile Experience of client account management Knowledge of Computer System Validation is an advantage. Key Responsibilities: Become an expert More ❯

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive More ❯

Carry out routine quality checks across raw materials, production processes, and finished products. Maintain accurate and compliant documentation in line with industry and company standards. Ensure adherence to HACCP, GMP, and site-specific quality procedures. Support internal and external audits through meticulous record-keeping and process compliance. Investigate non-conformances and assist in implementing corrective actions. Work closely with production 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 ❯

ll devise and deliver best in class data services, develop effective data strategies, and manage technical pension rectification projects. The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team 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 ❯

customers and answering queries and product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder in an auditable state Maintaining quality … limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills and strong written/verbal report 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 ❯