26 to 50 of 71 GMP Jobs in England

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 ❯

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 ❯

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 ❯

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 ❯

clean line sign-off, collection of swabs & water samples Quality checks and then collection of finished product and raw materials for microbiological & nutritional testing Conducting various daily audits (including GMP, Glass & Plastics audits, and ensuring corrective action with the shift manager Conducting internal quality assessment panels (QAS) throughout the shift & raising issues with the senior key-op/shift manager More ❯

Ability to work independently and manage multiple priorities Solid organizational and record-keeping skills Qualifications Experience in customer technical support, ideally in the diagnostics or healthcare industry Knowledge of GMP, ISO, and other relevant quality standards Proficiency with Microsoft Office and customer support tools Education Bachelor's degree in Life Sciences, Biomedical Engineering, Medical Technology, or a related field What More ❯

Automation Engineer Location: London Our client is a gene therapy company that works with gene therapy discovery, development and GMP manufacturing. They have headquarters in London and the USA and have recently redesigned exciting new labs with cutting edge technology and the ability to work to a higher standard and increase their capacity of production. They are currently seeking an … commissioning protocols, user requirement specifications, acceptance test plans, Functional Specifications. Design Specifications, and drawings and diagrams. Work with site Quality and CSV personnel to ensure automation and control system GMP compliance. Raise and complete Quality Events, change controls, CAPAs, and Deviations for automated GMP systems and equipment into the site QMS system. Support training efforts for new equipment installations Responsible … for ensuring that own work complies with GMP, Data Integrity and GDP and is undertaken in accordance with applicable procedures Skills Required: Bachelor's degree in Engineering from an accredited university in mechanical, chemical, or electrical disciplines with minimum 5 years' experience, supporting or developing automated systems. Strong understanding of automation standards and architecture addressing batch process control, such as More ❯

as a Senior Pensions Data Specialist to deliver data services to our clients, which include data and benefit audits, preparing data strategies and plans, undertaking various pension rectifications including GMP rectification and equalisation. While we continue to help clients meet their GMP objectives, the data challenges our clients face are becoming more diverse, giving you a great chance to work More ❯

for example). Working collaboratively with all operations teams within the business, such as Quality and Health and Safety to uphold the stringent protocols necessary along with adhering to GMP and Data Integrity at all times. Your background: BSc or equivalent in a Life Science discipline. Demonstrable experience in a business development role, from within the Biologics or Pharmaceutical Manufacturing More ❯

detail. Excellent computer skills (MS Office, particularly Excel and Word). Strong communication and interpersonal skills to work with cross-functional teams. Ability to work independently Experience in a GMP-regulated manufacturing environment. Basic knowledge of maintenance trades (mechanical, electrical, utilities). Experience in generating reports and dashboards using CMMS or BI tools. Benefits Holiday 24 days plus 8 stat More ❯

development life cycle methodologies, 21 CFR Part 11, and GAMP. Development of detailed specification, engineering documents, SOP and operating standards. Ownership and administration of process control automation in a GMP regulated manufacturing setting. Lead technical root cause analysis, incident investigations, and troubleshooting on process control issues related to electrical, instrumentation and control systems. Design and test of newly installed and More ❯

with this role involving standing 60% to 100% of the time and lifting heavy weights. Knowledge and experience using computer software including ERP system. and possibly Experience in a GMP environment would be advantageous. Certified to handle and ship Dangerous Goods or willingness and ability to be trained immediately. Supplier account management. Working with couriers, customs and brokers. Experience delivering More ❯

in a fast-moving environment 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 hours as and when required. More ❯

technical and mathematical skills. Desirable knowledge and skills Possess a strong knowledge of Google Marketing Platform, including Google Tag Manager (GTM). Able to perform high-level analysis within GMP platforms such as GA4 and Floodlight to extract insights and support marketing efforts. Utilise programming languages (e.g., Python, R) and database management tools (e.g., SQL) Awareness of customer data SaaS More ❯