7 of 7 GMP Jobs in the North West

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 ❯

discipline or equivalent experience working in a laboratory environment Proven leadership capabilities with experience managing teams and driving performance Strong understanding of laboratory operations, scientific processes, and compliance within GMP-regulated environments Demonstrated knowledge of health, safety, and environmental standards in laboratory settings Proficiency in Microsoft Office 365 and familiarity with lean methodologies such as Kaizen and Tiered Daily Management More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures 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 ❯