11 of 11 GMP Jobs in the North of England

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 More ❯

and provide sound judgment is highly desired. Understanding of the NPI (New Product Introduction) process and Process Validation is preferred. A thorough understanding of GMP/ISO regulations and validation regulations is preferred. Strong mentoring, coaching and leadership skills are required. Demonstrated project management and project leadership abilities. Rewards & Benefits More ❯

pressurised environment. The ideal candidate for the QA Manager will have: A BSc or equivalent in a Scientific subject Experienced working in a Pharmaceutical GMP environment Excellent leadership and management skills. If you are an experienced QA Manager or QA Head looking for your next challenge then please apply now More ❯

staff. Liaise with production and technical teams to resolve quality issues in real-time. Contribute to continuous improvement initiatives and compliance with HACCP and GMP standards. The Candidate The successful QA Supervisor is someone who is both proactive and detail-driven, with excellent communication skills and a strong grasp of More ❯

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations. Practical knowledge of the Pension Protection Fund (PPF). Circumstances Working hours: Monday to Friday, 37.5 hours per week with additional More ❯

Supply chain planning and optimisation Source: Procurement of externally sourced materials and contract manufacturing Make: Manufacturing and quality release of medicines in a validated (GMP) environment Delivery The role will focus on the definition and governance of enterprise information architectures, strategies, designs, models and consolidating thinking and artefacts across Operations More ❯

fast-paced, ever-changing environment. Strong communication skills. Excellent time management. Desirable skills and experience SQL, R and/or Python coding Experience of GMP rectification and/or equalisation projects Experience working with pension scheme data Knowledge of the journey through Pensions Risk Transfer transactions Experience providing consultancy services More ❯

and converting opportunities into successful outcomes. Consult - give strategic support and guidance to clients, delivering high quality and forward-thinking solutions. Pension Projects - including GMP equalisation, data and administration. Propositions development - influence strategic plans for growth of the Operational Solutions business support. Drive innovation - contribute to new tools and technologies More ❯

dependant on performance), company pension, onsite parking Major Duties and Responsibilities Reviewing Batch records and creating the associated checklists to support batch certification Archiving GMP critical documents in line with company policy Ensuring current versions of controlled documents are available to site personnel Assist in Audits Proactively identifying risks within … release testing in a timely manner The Person Minimum degree in pharmacy, biomedical sciences, or any other scientific degree. 2 years' experience in a GMP/GLP role. Experience in CAPA, OOs, OOt, deviations, change controls etc in a GMP setting Willingness to learn. Strong administrative skills and the ability More ❯

systems at our Holmes Chapel site. You'll provide hardware and software support, resolve breakdowns, implement preventative maintenance, and ensure compliance with GMP (Good Manufacturing Practice), EHS, and company standards. Your role also involves supporting computer system validation, quality improvement initiatives, and training other team members. This is a hands … and coding support to maintain system performance. Resolve equipment breakdowns and conduct root cause analysis. Support engineering CAPEX and improvement projects. Ensure compliance with GMP, EHS, and company standards. Support computer system validation and lifecycle management. Contribute to engineering best practices and project execution. Train team members on equipment, systems More ❯

systems at our Holmes Chapel site. You'll provide hardware and software support, resolve breakdowns, implement preventative maintenance, and ensure compliance with GMP (Good Manufacturing Practice), EHS, and company standards. Your role also involves supporting computer system validation, quality improvement initiatives, and training other team members. This is a hands … and coding support to maintain system performance. Resolve equipment breakdowns and conduct root cause analysis. Support engineering CAPEX and improvement projects Ensure compliance with GMP, EHS, and company standards. Support computer system validation and lifecycle management. Contribute to engineering best practices and project execution. T rain team members on equipment More ❯