26 to 50 of 85 GMP Jobs in the UK

internal stakeholders (IT, Facilities, Engineering, Security, and Real Estate) and external consultants, contractors, and OEMs. Develop and maintain package scope, budget, schedule, and quality requirements. Ensure all systems meet GMP/GxP compliance, cybersecurity standards, and pharmaceutical industry best practices. Lead RFP processes, technical evaluations, and contract negotiations for IT/AV vendors and integrators. Manage interdisciplinary coordination with MEP More ❯

sufficient for an individual to meet the requirements of the role. Required Skills/Experience Process Automation : Experience in automation within the biopharmaceutical or pharmaceutical industry or another industry. GMP experience required. Good understanding of the biopharmaceutical/pharmaceutical development process. Expertise in commissioning and validation of automation systems. Understanding of device networking and communication protocols. Experience in installing and More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

Overseeing a liquid manufacturing facility, the Technical Operations Manager will lead 10 direct reports across various departments. This position holds overall responsibility for ensuring site compliance with MHRA and GMP guidelines. The role involves leading continuous improvement and change management initiatives, as well as acting as the site lead on CAPA projects. Job Details: Pay: £50,000 per annum Hours … Friday, 8am - 4.30pm Duration: Permanent Essential Skills & Experience: Previously held a Senior Technical Manager, Manufacturing Manager or similar role in a regulated industry Sound knowledge of Good Manufacturing Practices (GMP), regulatory compliance, and pharmaceutical manufacturing Background in chemical manufacturing, pharma, or other highly regulated industries Desired Skills & Experience: Experience in oral dosage production Previous involvement in pharmaceutical manufacturing Essential Qualifications More ❯

continuous improvement. You will lead a skilled team of operators, technicians, and supervisors, overseeing day-to-day plant operations while ensuring production targets, quality standards, and regulatory compliance (MHRA, GMP, Home Office) are consistently met. This is a hands-on leadership role, requiring a balance of strategic insight, technical expertise, and operational execution. Key Responsibilities Lead the operations of a … pharmaceutical manufacturing facility. Drive continuous improvement, process optimisation, and operational excellence. Ensure GMP compliance and uphold the highest quality standards. Provide hands-on technical support and troubleshoot production issues. Collaborate cross-functionally with Quality, R&D, Supply Chain, and Engineering. Champion Lean principles and eliminate waste through process improvement. Lead investigations, CAPAs, and Change Control processes. Mentor and develop team … What We're Looking For We're seeking someone with experience in a senior technical or operational management role within pharmaceutical manufacturing. You'll have a deep understanding of GMP, regulatory compliance, and dosage form production. Essential: Proven leadership within a pharmaceutical manufacturing setting. Strong knowledge of GMP, MHRA regulations, and pharmaceutical manufacturing. Track record of process improvements, cost control More ❯

meet quality and regulatory standards. Ensure consistency in automation design and execution between all Sanofi facilities, adhering to a uniform approach. Identify and manage risks proactively, ensuring compliance with GMP and minimizing disruptions to project timelines and costs. About you Experience : Proven track record in managing complex manufacturing systems involving automation, robotics, and advanced technologies, in the pharmaceutical sector. Technical More ❯

systems, HVAC, process utilities, power distribution, and BMS. Oversee multidisciplinary engineering teams from pre-construction through to commissioning and handover. Ensure design compliance with UK building regulations, industry standards (GMP, ISO, IEC), and client specifications. Drive innovation in delivery methods, digital engineering (BIM), and energy efficiency. Support bid and tender processes with technical insight, resource planning, and value engineering. Collaborate More ❯

team in Milton Keynes. As a senior contributor, you'll lead the design and implementation of cutting-edge process control systems-PLC, DCS, HMI, SCADA-for a high-performance, GMP-regulated manufacturing environment. This is an exciting opportunity to make a direct impact on the setup and development of a new facility, work on high-value capital projects, and support More ❯

team in Milton Keynes. As a senior contributor, you'll lead the design and implementation of cutting-edge process control systems-PLC, DCS, HMI, SCADA-for a high-performance, GMP-regulated manufacturing environment. This is an exciting opportunity to make a direct impact on the setup and development of a new facility, work on high-value capital projects, and support More ❯

be responsible for the delivery of technical administration projects The types of projects you may be asked to work on will include, but is not limited to, the following: GMP reconciliation projects; benefit analysis and rectification work; De-risking activity including projects relating to insurance transactions; individual technical or high priority cases data work; .CETV Top Up Exercises and No … related activities and pension administration processes. What we're looking for Demonstrable experience of delivering administration services to Defined Benefit pension schemes. Experience of working on bulk projects including GMP, Data Rectification of De-risking. Strong analytical and problem-solving skills, with a keen eye for detail. Excellent communication and interpersonal skills, with the ability to build and maintain effective More ❯

of quality excellence across the business. Conducting supplier audits, internal inspections, and management reviews. Key Requirements: Proven experience in a GMDP or similar regulated environment. Strong knowledge of GDP, GMP, ISO 9001, and ISO 13485 standards. Excellent organizational, communication, and stakeholder management skills. A positive attitude toward promoting quality across all departments. Proficiency in MS Office applications (Word, Excel, PowerPoint More ❯

An effective written communicator, able to deliver concise documentation and adapt writing style to audience as appropriate. Educated to degree level or higher. Understanding of EU & UK GDP/GMP legislation. QUALIFICATION, EXPERIENCE & SKILLS DESIRABLE Experience in multiple regulatory and operational jurisdictions. More ❯

used in implant and instrument manufacturing Good understanding of the design process and tools used Experience in DFMEA, PFMEA, 6 sigma and Lean Experience of working with GMP(Good Manufacturing Practice). Experience in project management and problem solving Knowledge of quality systems, regulatory requirements and related standards, with demonstrated understanding of the practical application of these requirements Excellent planning More ❯

policies and procedures Ensuring samples are 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 life Carryout of routine More ❯

policies and procedures Ensuring samples are 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 life Carryout of routine More ❯

Customer Complaint and Foreign Body handling. Working hours:4 days on, 4 days off. Hours based on business and production requirements. Pay: £29,092 per annum Main Responsibilities Conduct GMP audits with production and address any issues. Verify traceability documents have been completed correctly and challenge any mistakes Log complaints and Foreign Bodies conduct investigations and work with production to More ❯

extensive and successful work with RNA manipulation, RNA constructs and a good understanding of transcriptomics and/or viral genomics is essential. Experience in RNA-related biopharma methodologies or GMP is also desirable. The role also requires 2-3 years of prior managerial experience overseeing experimental work of junior team members. We encourage the successful candidate to liaise with senior … QC data and sequencing data to support sample prep methodologies as they are developed and investigated Working with relevant partners to deliver methodologies congruent with Q-line and regulatory GMP practices What We're Looking For We will expect you to have a PhD and postdoctoral experience (or equivalent experience) in a molecular biology/biotechnology-based field, and/ More ❯

extensive and successful work with RNA manipulation, RNA constructs and a good understanding of transcriptomics and/or viral genomics is essential. Experience in RNA-related biopharma methodologies or GMP is also desirable. The role also requires 2-3 years of prior managerial experience overseeing experimental work of junior team members. We encourage the successful candidate to liaise with senior … QC data and sequencing data to support sample prep methodologies as they are developed and investigated Working with relevant partners to deliver methodologies congruent with Q-line and regulatory GMP practices What We're Looking For We will expect you to have a PhD and postdoctoral experience (or equivalent experience) in a molecular biology/biotechnology-based field, and/ More ❯

to working in a customer-focused service business. Accuracy and attention to detail. Excellent customer service and communication skills. Good written and arithmetic skills to comply with audits and GMP standards. Understanding of GMP/GLP standards. Ability and confidence to work alone on a customer site without supervision and as part of a multi-disciplined team. BSc or equivalent More ❯

You As Senior/Principal Architect Life Sciences you will have experience in delivering projects from concept to detailed design in the life science sector for both laboratories and GMP manufacturing facilities. You will be part of an enthusiastic and committed team of Architects and Technicians who will deliver high quality output on projects. To be successful you will exhibit More ❯

ensuring efficient, compliant, and high-quality production. This senior leadership role involves overseeing daily operations, driving continuous improvement, and managing cross-functional teams. The ideal candidate will have strong GMP knowledge, proven leadership in regulated manufacturing, and a focus on process optimisation and regulatory compliance. Technical Operations Manager Job Responsibilities: Oversee daily manufacturing operations to ensure production runs efficiently, safely … standards. Lead, support, and develop a skilled team while promoting a culture of accountability, collaboration, and continuous improvement. Implement process enhancements, resolve technical challenges, and maintain full compliance with GMP and regulatory requirements. Work cross-functionally with key departments to coordinate seamless operations, manage new product launches, and uphold safety and quality standards. Champion Lean initiatives, lead root cause investigations More ❯

a QA role within a manufacturing environment. Strong leadership and people management skills. In-depth knowledge of QA processes (QC experience desirable but not essential). Familiarity with ISO, GMP, or similar standards. Excellent communication, organisation, and problem-solving skills. Ability to manage multiple tasks and priorities in a fast-paced setting. What's on Offer: An attractive salary of More ❯

with Python for data processing or image analysis. Background or interest in biology, lab automation, or scientific instrumentation. Experience working with or building distributed systems. Experience with regulated environments (GMP, HIPAA, etc.) Experience with UI/product design processes and tools (wireframes, mockups, looks-like prototypes, etc.). Why You'll Love Working Here Impact : Your work will directly enable … complex problems at the intersection of software, hardware, and biology-you'll constantly learn and develop new skills. Autonomy : You'll have the freedom to shape our approach to GMP readiness, with support from a talented cross-disciplinary team. Team : Work with the best engineers and scientists in a collaborative environment where diverse perspectives drive innovation. Salary and Benefits - Competitive … re building a team that enjoys moving fast, strives for continuous improvement through learning from mistakes, and is passionate about work that contributes to solving real world problems. No GMP experience? No problem! We want someone who is motivated to deliver an innovative product into a regulated space with creative, efficient solutions. If you're excited about solving interesting problems More ❯

as Studio5000 & FactoryTalk Software especially FT View SE, FT Batch). Knowledge of Batch Process Control, ISA-S88 standard programming. Knowledge of GAMP, 21 CFR Part 11, ASTM E2500, GMP, etc Knowledge of Virtualisation technology. What We Offer: Comprehensive mindfulness programs with a premium membership to Calm Volunteer Paid Time off available after 6 months of employment for eligible employees More ❯

and waste. supporting deployment and lifecycle management of automation tools and digital assets within a validated environment. ensuring data accuracy, integrity, and accessibility in compliance with regulatory requirements including GMP, CFR Part 11 Compliance, SDLC and DI. collaborating closely with Robotic Automation teams, IT, Supply chain and method development organizations to assist in implementation of data automation across the network. More ❯