51 to 75 of 112 GMP Jobs in England

multi-tenant campus to ensure uptime and regulatory compliance. The role requires experience with BAS, CMMS, and building automation, plus strong knowledge of GMP requirements and safety protocols. A relevant engineering degree and industry certifications are preferred. #J-18808-Ljbffr ...

experience in programmatic advertising, with a deep knowledge of the Google Stack, Google Ads (Display/Video), DSP (e.g. Adform, Tradedesk, DV360, Amazon DSP), GMP and Analytics Strong understanding of the digital advertising ecosystem, including DSPs, DMPs, and ad exchanges Strong analytical skills and ability to provide insights and recommendations ...

experience in programmatic advertising, with a deep knowledge of the Google Stack, Google Ads (Display/Video), DSP (e.g. Adform, Tradedesk, DV360, Amazon DSP), GMP and Analytics Strong understanding of the digital advertising ecosystem, including DSPs, DMPs, and ad exchanges Strong analytical skills and ability to provide insights and recommendations ...

UK. Sitting within our UK Quality function, this role reports directly to the Head of Quality UK and plays a key part in ensuring GMP and regulatory compliance across our network of seven licensed radiopharmacy sites. You will act as a central link between Quality Assurance, Regulatory Affairs, Operations … Quality, Regulatory, or a pharmaceutical discipline. Minimum of 5 years’ regulatory experience, ideally within radiopharmacy, sterile manufacturing or aseptic processing. Proven experience with GMP, MHRA expectations and broader GxP requirements. Experience supporting commercial and IMP product development, including clinical trial supply. Strong understanding of regulatory inspections and authority interactions. Experience ...

implement, and support MES in its production facilities. You will bridge manufacturing and digital systems, focusing on data integrity, efficiency, and regulatory compliance across GMP environments. The role requires 3+ years configuring MES platforms, exposure to SAP integration, and strong SQL skills. Hybrid work in Hook/Speke, UK, with ...

Bespak Limited in the United Kingdom is seeking a Qualification & Validation Specialist to ensure facilities, utilities, equipment, processes and computerised systems are qualified and validated to the highest regulatory and quality standards. You will plan ...

Duties will include: Picking and packing customer orders Receiving deliveries and updating inventory systems Stock control, cycle counts and inventory checks Completing production and GMP paperwork accurately Following standard operating procedures Maintaining high standards of housekeeping and safety Working within ambient, chilled and frozen environments when required Supporting the wider ...

must be eligible Job Purpose The Salesforce Application & Analytics Manager will be responsible for the strategic management, support, development, and continuous improvement of the GMP Application and associated analyti click apply for full job details ...

join the Cost & Commercial Management team, supporting the post-contract commercial management of a major hyperscale data centre programme. You will work on GMP development, contract administration, change control, valuations, forecasting and final accounts with site-based teams and client representatives. The role requires strong post-contract experience, ability ...

programme in the North East. This site-based role focuses on post-contract cost management across Civil, Structural and Architectural packages. You will influence GMP procurement, FIDIC contract administration, change control, valuations and final accounts, working alongside the site leadership, contractors and design teams to drive robust commercial #J ...

Baxter Healthcare Ltd. in Thetford is seeking a Multi-skilled Automation Bias Maintenance Engineer to join the Operational Maintenance Engineering team. You will perform plant-wide reactive and proactive maintenance and support new installations across ...

join a site-based commercial team in Newcastle, supporting a major hyperscale data centre programme in North East England. The role focuses on GMP procurement, contract administration and post-contract cost control, including valuations, forecasts and final accounts, working with contractors, consultants and client representatives to ensure robust cost governance ...

delivering a major hyperscale data centre programme in North East England. You will support commercial delivery, cost control, and governance across large packages, including GMP conversions, with strong collaboration among contractors, consultants, and client representatives. This role emphasizes data-driven insights and proactive risk management. #J-18808-Ljbffr ...

Limited is seeking a skilled data engineer to design, develop and operate scalable ETL/ELT pipelines across structured and unstructured data in a GMP-like cloud environment. You will build batch and real-time processing solutions using BigQuery, Dataflow, Cloud Storage, Pub/Sub and related GCP services, while ...

Conveyor Systems and Thermal processing equipment. 3. City & Guilds 2382 (minimum of 18th Edition Regulations) 4. Familiar with the requirements of working within a GMP facility. 5. Excellent internal and external communications skills 6. Experience of working an on-call maintenance system. ...

Responsibilities: Under general direction, provides support on Quality systems to ensure compliance with company standards and GMP regulatory guidelines Develops, maintains and improves GMP-related quality control systems including standard operating procedures (SOPs) Participates in project teams to provide review and approval of project Validationdocumentation according to applicable approval matrix ...

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 ...

issues and opportunities for improvement. Calibration: Take responsibility for the calibration and control of quality equipment, ensuring records are accurate and up to date. GMP Auditing: Conduct and coordinate GMP audits, ensuring standards are maintained and actions are followed through. Internal Audits: Assist with internal audits and support the site … ideally have: Previous experience working in a QA/Quality role, preferably within food manufacturing, FMCG or fresh produce A good understanding of GMP, HACCP, food safety and quality systems. Experience with non-conformance, CAPA and Root Cause Analysis. Experience supporting or completing audits. Strong attention to detail and excellent ...

transfer of novel and established test methods for the analysis of gene therapy products and associated materials used for manufacturing the EU and FDA GMP requirements. Job Description Major Activities To support the development and validation of established and novel analytical test methods for the current and newly developed gene … support of the method transfer and validation activities performed ensuring compliance requirements are maintained. Ensure all methods are validated and transferred to QC GMP labs in compliance with regulatory standards and adhere to data integrity requirements. Generate method SOPs are developed and implemented to support all validated methods. Ensure these ...

dedicated Quality Analyst to support the digital transformation journey of a manufacturing site, focusing on implementing and maintaining IT systems that align with GMP regulations. This role will primarily involve working with Quality Systems such as LIMS, CDS, and other QC equipment applications, while also supporting broader manufacturing IT needs. … have the right to work in this location or hold an EU passport. Responsibilities Implement and maintain IT systems and processes in line with GMP regulations, focusing on Quality Systems (e.g., LIMS, CDS, QC equipment applications). Provide day‐to‐day IT support, including issue resolution, system changes, and service ...

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 ...

Oversee swabbing and sampling programmes, ensuring all activities are completed on time and any out-of-specification results are addressed. Lead the site's GMP audit programme and support customer and third-party audits. Ensure completion of actions arising from internal and external audits. Promote a culture of continuous improvement … Quality Assurance or Technical role within the food manufacturing industry. Experience conducting internal audits. Strong knowledge of food safety, quality systems, and GMP standards. Excellent communication and stakeholder management skills. The ability to make informed decisions quickly in relation to food safety, legality, and quality. Strong organisational skills ...

Multi-Skilled Engineer, you will play a key role in maintaining site equipment, ensuring production efficiency and upholding high standards of food safety, GMP and Health & Safety. Key responsibilities include: Championing and maintaining Good Manufacturing Practice (GMP) standards across the site Fault finding and troubleshooting across electrical, mechanical and control ...

deliver efficient, scalable solutions. Key Responsibilities: Lead process improvement and automation initiatives Develop and implement technical solutions for manufacturing challenges Ensure compliance with GMP and other regulatory requirements Utilise ERP systems for planning and reporting Collaborate with cross-functional teams to deliver projects on time and within scope About … experience in high-end manufacturing environments such as pharma, electronics, or cleanroom operations. Knowledge of automation systems and ERP platforms is essential, and GMP experience is highly desirable. You will ideally have: Degree in Engineering or related discipline Proven experience in Lead Process Engineering and automation ERP system proficiency Understanding ...

must be eligible Job Purpose The Salesforce Application & Analytics Manager will be responsible for the strategic management, support, development, and continuous improvement of the GMP Application and associated analytics capabilities. The role will ensure the effective operation of the Salesforce platform, delivery of the application roadmap, and development of high … driving innovation and data-driven decision-making. Key Responsibilities Salesforce Application Management Own the day-to-day administration, maintenance, support, and enhancement of the GMP Application hosted on the Salesforce platform. Act as the primary subject matter expert for the application, ensuring stability, performance, and user satisfaction. Develop and maintain ...