26 to 50 of 63 GMP Jobs

GMP Recruitment are proud to be in partnership with a highly recognisable, leading manufacturer located in Droitwich. We are currently recruiting on their behalf for someone to join their team as a Service Engineer on a full time, permanent contract. Up to £40,000 + Excellent Benefits + Extensive Worldwide ...

Responsibility QMS Governance & Compliance * Support the QMS Manager in the governance, development and ongoing maintenance of Veeva Quality. * Ensure QMS processes remain aligned with GMP, GDP and applicable global regulatory requirements. * Support periodic review of quality processes and system effectiveness. System Administration * Support configuration change requests through approved change control … technical communicator.Strong stakeholder management. Excellent interpersonal and influencing skills. Data analysis and interpretation. Degree Level Educated or Equivalent experience. Experience with GxP, GMP and/or of working with Veeva Systems and Vaults (desirable). Experience of working in a pharmaceutical environment (desirable, not essential). Additional Information: Occasional global ...

strategy, ensure inspection readiness, maintain licences, and deliver continuous improvement across quality systems and operations. The role is critical in ensuring compliance with GMP/GDP standards, supporting upcoming projects such as implementing an electronic QMS, and driving a culture of collaboration and high performance within the Quality function. … risk-based decision-making. Operational Excellence Support change-control processes and ensure timely resolution of quality issues. Oversee approval and maintenance of SOPs and GMP-related documentation. Always ensure inspection readiness for MHRA and customer audits. Team Development Manage QA and QC teams (approx. 16). Build a nurturing ...

team of technical specialists, overseeing laboratory electronic systems such as LIMS and CDS, introducing new technologies, managing equipment lifecycle plans, and ensuring compliance with GMP and Data Integrity requirements. You will act as the technical lead for key laboratory initiatives, including new product introductions, analytical method transfers, system upgrades, validation … develop a team of QC Technical Specialists, ensuring strong performance and resource planning. Manage laboratory equipment and electronic systems to ensure compliance with GMP and Data Integrity requirements. Deliver technical projects involving equipment procurement, qualification, validation, and implementation. Maintain a long-term equipment replacement strategy to support future laboratory needs. ...

analytics and data What you'll bring: 3+ years' hands-on experience, working at expert level with GA4 — essential Strong GTM knowledge — essential Broader GMP experience: BigQuery, Looker Studio, DV360, SA360 A track record delivering technically complex projects across varied industries Comfort with JavaScript, jQuery, CSS, Python or HTML Experience ...

MSAT Manager Permanent | Darlington | Up to £70,000 About the Role: We are seeking an MSAT Manager to lead technology transfer activities into GMP manufacturing within an advanced biopharmaceutical manufacturing environment. Reporting into the leadership team, this is a highly visible role responsible for bridging the gap between process development … GMP operations, ensuring manufacturing processes are successfully transferred, implemented, and executed within a regulated setting. This role combines technical leadership, people management, and customer engagement, making it ideal for someone who understands both clinical-stage bioprocessing and the practical realities of GMP manufacturing. You'll work closely with Development, Manufacturing ...

biotechnology and/or pharmaceutical industry, including senior Quality leadership roles in regulated manufacturing environments. Strong knowledge of global regulatory authorities including FDA, GMP, GCP and GLP requirements. Proven expertise in Quality Management Systems (QMS), with a particular focus on GMP compliance and data integrity. Demonstrated experience with regulatory inspections ...

providing the required documents and records. Track corrective and preventive actions and ensure they are completed within agreed timescales. Support compliance with relevant ISO, GMP, BRC or other applicable quality standards. REQUIRED EXPERIENCE AND QUALIFICATIONS Previous experience in quality assurance or quality control within a warehouse, logistics, manufacturing or supply … record management. A diploma or degree in Quality, Science, Engineering or a related subject would be beneficial. Quality Management System certification, including ISO, GMP or BRC, would be advantageous. SKILLS REQUIRED Excellent attention to detail. Strong organisational and record-keeping skills. Confident communication and training abilities. Good working knowledge ...

emerging technologies, and support the development of transformation roadmaps that deliver measurable business value. The role requires an individual who has operated within complex GMP-regulated environments and can translate real-world operational experience into strategic advice for pharmaceutical and biotechnology organisations. Responsibilities Act as a trusted advisor to executive … Leverage AI-enabled research and consulting tools to improve the quality, accuracy and relevance of strategic analysis and recommendations. Domain Expertise: Strong knowledge of GMP-regulated pharmaceutical manufacturing. Biopharmaceutical Manufacturing. Pharmaceutical Operations. Engineering & Capital Projects. Manufacturing Strategy. Operational Excellence. Supply Chain Transformation. Digital Manufacturing. Smart Factories. Industrial Automation & Controls. ...

product quality to ensure customer specifications and quality requirements are consistently achieved. Maintain and continuously improve food safety and quality management systems, including HACCP, GMP, and customer-specific standards. Ensure compliance with all food safety, legal, regulatory, and customer requirements. Auditing & Traceability Plan, conduct, and close out internal audits. Maintain … performance. Monitor quality KPIs and drive initiatives that enhance product quality, reduce waste, and improve efficiency. Essential Strong knowledge of food safety systems, HACCP, GMP, quality standards, and audit requirements. Demonstrated experience managing traceability systems and conducting traceback investigations. Strong analytical, problem-solving, and root cause investigation skills. Excellent attention ...

will translate complex processes and investigations into structured, easy-to-follow documentation. This role is critical to ensuring operations remain inspection-ready and GMP/GDP compliant . This is a factory-based role , with time spent both on the production floor and in a dedicated computing/documentation area. … SMEs) to ensure accuracy and relevance Support document updates in line with process changes, audits, and system improvements Compliance & Governance Ensure all documents meet GMP and GDP standards , including version control and traceability Identify gaps or risks in documentation and drive improvements Maintain documentation aligned with site Quality and document ...

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 ...

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 ...

project timing is 16 months (for initial phase with potential extension for subsequent phase). Retrofit of existing warehouse space (~15K sf) into a GMP Packaging Operation (1 Packaging Line only). Admin Area. Packaging Area (CNC) with gowning (packaging line already ordered and FAT planned in Feb '27. Small … cold room for temporary storage. Ambient GMP Warehouse for components storage. Utilities. Packaging line (1 of) - 400 V 3-phase 50.60 Hz and 230 V 1phase 50/60 Hz. Compressed Air 120 psi to support the line + other users. HVAC Units for Admin, CNC space & Ambient Warehouse space ...

patient focus service. The prime function of the unit is the preparation of diagnostic radiopharmaceuticals, in a safe and efficient manner according to Good Manufacturing Practice and National Standards. Main duties of the job Perform duties in Radiopharmacy to aid the safe and efficient preparation of radiopharmaceuticals … radioactive materials oTrained in the Transportation of Dangerous Goods oExperience of using MS packages or similar databases oAn awareness of Good Manufacturing Practice (GMP) and GCP guidelines (Good Clinical Practice) and the EU Clinical Trials Directive Skills Essential oAbility to work within set timeframes working to priorities and deadlines oDemonstrates ...

looking to appoint an experienced Project Engineer - Automation to support the delivery of a major pharmaceutical manufacturing expansion project. Working within a highly regulated GMP environment, you will play a key role in the development, implementation, testing and commissioning of automation systems across process equipment, cleanrooms and critical utilities. This … qualification and validation activities. Review vendor and contractor designs and technical submissions. Participate in design reviews, risk assessments and FMEA workshops. Ensure compliance with GMP, CSV, data integrity and cybersecurity requirements. Maintain accurate project documentation and system handover records. Experience Required Degree qualified in Automation, Control Systems, Electrical Engineering ...

CMMS experience Strong health & safety awareness Ability to work rotating days and nights Desirable Experience Food Manufacturing or FMCG SAP and/or SCADA GMP and Food Safety standards LOTO procedures Permit to Work systems Root Cause Analysis (5 Why, 5W1H) Contractor management Industries Considered Ideal Food Manufacturing FMCG Also … Environment You'll be working in a highly automated, fast-paced food manufacturing facility focused on: Asset reliability Downtime reduction Continuous improvement Health & Safety GMP and Food Safety compliance Equipment You'll Work On Experience with any of the following would be advantageous: Automated production lines PLC-controlled machinery Conveyors ...

Contract | Part-Time | Pirbright, Surrey | Inside IR35 We're looking for a System Administrator with experience supporting validated systems in regulated environments (GxP/GMP) . Key Responsibilities: System administration, maintenance, and patch management Testing and validation activities (CSV/GxP) System implementation and release support Change control and compliance … Computer System Validation (CSV) Change Control & Patch Management Compliance & Audit Readiness System Lifecycle Management CAPA & Risk Management Vendor & Stakeholder Management Project Delivery & Coordination Desirable: GMP, GxP, FDA 21 CFR Part 11, Annex 11 Working Pattern: 2-3 days per week Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting ...

programme. This is an excellent opportunity for an experienced quality professional to take ownership of sponsor-side quality activities, ensuring compliance across GCP and GMP operations while supporting a complex and highly regulated clinical programme. The role offers significant visibility, autonomy, and the opportunity to shape quality systems within … service providers. Ability to influence stakeholders across a matrix organisation. Desirable Experience supporting Phase III or pivotal clinical studies. Audit and regulatory inspection experience. GMP and CMC quality exposure. Knowledge of CSV, GAMP 5, data integrity, and electronic systems compliance. Experience within biologics, advanced therapies, cell therapy, or gene therapy. ...

upgrades. Lead fault finding and implement right-first-time, long-term solutions. Oversee new equipment installations, upgrades and GAP assessments. Ensure equipment meets GMP, safety and regulatory requirements. Develop preventive maintenance strategies and monitor equipment performance, including MTBF. Work closely with engineering teams and third-party suppliers to deliver maintenance … mentorship across the engineering team. Requirements: HNC/HND or equivalent in an engineering discipline. Proven maintenance engineering experience, ideally within pharmaceutical or GMP manufacturing. Strong understanding of pharmaceutical processing equipment and/or GMP infrastructure. Experience in equipment lifecycle management, troubleshooting and continuous improvement. Strong problem-solving, communication ...

integrating advanced and risk-based approaches (e.g., DoE, QbD, stability modeling) Support scale-up and technology transfer to clinical manufacturing, ensuring robust translation into GMP production with internal teams and external partners Playing a leading role in CMC activities, including authoring, reviewing, and shaping documentation for regulatory submissions Drive innovation … data-driven formulation development, applying DoE and QbD principles, with hands-on experience in biophysical and analytical characterization Sound understanding of ICH/GMP requirements and experience preparing CMC documentation for regulatory submissions (e.g., IND, CTA, BLA/MAA) Strong ability to drive scientific decisions, collaborate effectively in cross-functional ...

early • Ensure full supplier approval, including audits, and certification requirements • Support raw material elements of internal, customer, and group audits • Audit compliance with QMS, GMP, and HACCP standards, driving corrective actions to closure • Monitor KPIs, identify trends, and drive continuous improvement initiatives • Communicate customer and business requirements clearly to suppliers … ensure compliance and robustness • Ability to work cross-functionally with Technical, Operations, NPD, and suppliers • Strong audit capability with a clear understanding of GMP and HACCP requirements • Highly organised with excellent attention to detail • Strong communication skills, able to influence at all levels • Proactive mindset with the ability to anticipate ...

early • Ensure full supplier approval, including audits, and certification requirements • Support raw material elements of internal, customer, and group audits • Audit compliance with QMS, GMP, and HACCP standards, driving corrective actions to closure • Monitor KPIs, identify trends, and drive continuous improvement initiatives • Communicate customer and business requirements clearly to suppliers … ensure compliance and robustness • Ability to work cross-functionally with Technical, Operations, NPD, and suppliers • Strong audit capability with a clear understanding of GMP and HACCP requirements • Highly organised with excellent attention to detail • Strong communication skills, able to influence at all levels • Proactive mindset with the ability to anticipate ...

Senior Automation Engineer (PCS7) | Outside IR35 | 6-Month Contract We're currently seeking an experienced Automation Engineer to support a major site upgrade project within a highly regulated manufacturing environment. This is an excellent opportunity ...

Job summary You will be joining NHSBT at a particularly exciting time as we embark on a journey of change, enhancing our current IT service provision. You will lead the systems testing required to ensure ...