17 of 17 GMP Jobs in the UK excluding London

Microsoft 365 Group Policy Software Deployment and Release Management Desirable Experience Experience working within pharmaceutical, biotechnology, life sciences, or other regulated industries. Exposure to GMP, GxP, or validated environments. Experience supporting device refresh, Windows 11 migration, or large-scale workplace transformation programmes. Familiarity with application validation and compliance-driven change ...

contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous ...

development of medicines that improve patients' lives worldwide. Job Responsibilities Main Duties include: Provide data science support as ARD Digital Transformation team partners with GMP-Analytics, Drug Substance (API) and Drug Product (DPA), and Degradation Science and Structural Elucidation (DSSE) teams to digitise laboratory workflows. Partner with Data Science teams ...

would be a plus if you also possess previous experience in: Experience in medical devices or similarly regulated environments, including Good Manufacturing Practices (GMP) and quality systems. Hands-on experience supporting Digital Pathology systems, especially the Aperio GT Platform, Aperio FL, CytoVision/CytoInsight, or VERSA; familiarity with Windows Server ...

collected for testing schedules and testing schedules are met Logging micro samples Accurate carrying out of positive release checks for all finished products GMP audits/Glass and plastic audits, including generation of improvement areas, completing database Ensure close outs of non-conformances Sampling and recording of finished product shelf ...

strategy and methodology across NHSBT. You will ensure that testing processes with Systems Development and Integration department adhere to recognised good practice standards (including GMP, GAMP and GDP) and provide assurance that the quality of testing is appropriate to meet the needs of NHSBT. This includes cascading information about procedures ...

related field 3+ years experience in Control Systems Engineering Hands on experience with DCS systems (ideally Siemens SIMATIC PCS7) Previous work experience in a GMP manufacturing environment (Pharmaceutical experience is desireable) Knowledge of GAMP frameworks Willing to work on customer sites across the Northwest Code: INDENM If you are interested ...

within a QA, Quality Assurance, or Quality Control role. Experience within the food manufacturing industry is essential. Good understanding of HACCP, Food Safety, and GMP standards. Strong attention to detail and excellent record-keeping skills. Confident communication skills and ability to work collaboratively. Ability to work independently and make informed ...

will play a senior,hands-on role within the Quality Assurance team. You will lead compliance with BS EN ISO 22716 Cosmetics Good Manufacturing Practice,Quality Management Systems (QMS),and company standards,working closely with SHE,QC,Production,Process R&D,and Engineering. From raw material to finished product release … approve master records,specifications,and controlled documentation (SOPs,work instructions,policies). Compliance & Standards: Maintain site compliance with BS EN ISO 22716 Cosmetics GMP and QMS standards. Act as a site Subject Matter Expert for QMS processes. QMS Management & Troubleshooting: Lead investigations into deviations,non-conformances,and customer complaints using ...

support the factory QA team, ensuring effective shift coverage, clear responsibilities and opportunities for professional development. Championing food safety: Maintain robust standards across HACCP, GMP, allergen management, hygiene, traceability and product integrity, ensuring compliance with legislation and customer requirements. Driving continuous improvement: Analyse quality performance, investigate complaints and non-conformances … bring: Experience within Quality Assurance or Technical functions in food manufacturing, ideally within chilled food production. A practical understanding of food safety legislation, HACCP, GMP, allergen management and quality risk assessment. Experience of leading, coaching or developing colleagues, with the confidence to provide clear direction and constructive feedback. Knowledge ...

support the achievement of Grade AA BRCGS status. You'll manage non-conformances, customer complaints and corrective actions, drive improvements in good manufacturing practice (GMP), and work closely with production, technical and development teams to embed a strong quality culture. This is an excellent opportunity to influence manufacturing standards, develop ...

standards. Working closely with cross-functional teams, you'll oversee key quality activities, support continuous improvement initiatives, and play a vital role in maintaining GMP compliance across the site. Key responsibilities include: Lead and support the QA team, providing coaching, training and day-to-day guidance. Ensure quality activities … completed in line with GMP, compliance and business requirements. Review batch documentation and support product release activities. Oversee investigations, deviations, CAPAs and change controls, ensuring issues are resolved effectively. Monitor quality performance and drive continuous improvement initiatives. Manage customer and product quality complaints, ensuring thorough investigation and resolution. Deliver ...

Provide technical support, troubleshooting, and ongoing maintenance for QC laboratory electronic systems. Manage and maintain master data to ensure system performance remains compliant with GMP and data integrity requirements. Support system enhancements, software updates, new module deployments, and change control activities. Assist with the qualification, validation, and implementation … this role, you will possess: A degree in a scientific discipline, or equivalent industry experience. Proven experience supporting laboratory electronic systems within a pharmaceutical GMP environment. Strong working knowledge of LIMS and/or CDS platforms, including master data management. Excellent communication skills with the ability to explain technical concepts ...

scale-up and technology transfer activities Leading technical investigations and troubleshooting manufacturing processes Driving process optimisation and continuous improvement projects Supporting validation activities and GMP documentation Working closely with Production, QA, Product Development and Engineering teams Assisting with new equipment evaluation and implementation Providing technical expertise to support business-critical … project management skills Experience with MSAT, process validation, technical transfer or product lifecycle management Ability to work across multiple projects and stakeholders Knowledge of GMP and pharmaceutical manufacturing environments Experience with solid dose products would be a distinct advantage. What we offer Average 36-hour working week (with ...

Specialist will play a key role in supporting site validation activities across a range of projects. This is a great opportunity for someone with GMP validation experience looking to build on their existing knowledge within a supportive and expanding team. Candidates with equipment or process validation experience from pharmaceutical … other GMP-regulated manufacturing environments are encouraged to apply. The role: Plan and execute validation activities in line with site validation plans and project timelines. Author and maintain validation protocols and reports across multiple validation areas such as: Cleaning validation Computerised systems validation Equipment and utilities qualification Process validation Interpret ...

Provide technical support, troubleshooting, and ongoing maintenance for QC laboratory electronic systems. Manage and maintain master data to ensure system performance remains compliant with GMP and data integrity requirements. Support system enhancements, software updates, new module deployments, and change control activities. Assist with the qualification, validation, and implementation … this role, you will possess: A degree in a scientific discipline, or equivalent industry experience. Proven experience supporting laboratory electronic systems within a pharmaceutical GMP environment. Strong working knowledge of LIMS and/or CDS platforms, including master data management. Excellent communication skills with the ability to explain technical concepts ...

function, support and develop the QA team, and make sure products meet customer, legal and internal quality standards. You'll also be involved in GMP, audits, quality control, continuous improvement and working closely with Production to resolve quality issues. As QA Team Leader, you'll work closely with the Operational … quality concerns are identified and reported promptly. Carry out additional quality assessments, including dry matter and hot box testing, where required. Manage the site GMP audit system and participate in internal auditing activities. Support preparation for internal and external audits. Assist with recording and monitoring weekly quality KPIs. Support ...