26 to 50 of 93 GMP Jobs

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 ❯

EudraLex Volume 4 Annex 11. Experience in developing and executing validation test plans, test scripts, and test cases. Excellent problem-solving, analytical, and risk-assessment skills. Experience within a GMP production environment. Fluency in written and spoken English; Dutch language skills are a plus. Skills: Critical evaluation and interpretation of data. Strong knowledge of pharmaceutical manufacturing processes and quality systems. More ❯

standards set nationally and by our grocery retailer partners. Full training on internal quality processes is provided to the successful candidate. 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 ❯

standards set nationally and by our grocery retailer partners. Full training on internal quality processes is provided to the successful candidate. 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 ❯

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 ❯

This position will be responsible for providing control system engineering support to troubleshoot, maintain and improvement projects of Automation and Controls systems for the Automated Equipment in a dynamic GMP regulated environment, requiring minimal downtime of the machinery. Responsibilities include fast response for troubleshooting to sustain machinery uptime when unscheduled downtime occurs, identification of improvements, PLC programming (modifications/configuration … problems, risks and technical conflicts and develop the necessary contingency plans to improve business continuity. Performs troubleshooting and modifications to the automated equipment adhering to Pharmaceutical and Medical Devices GMP change control standards and policies. Creates and modifies system specifications and standard operating procedures for the systems supported. Trains users and peers on systems. Supports software life cycle efforts. Contributes More ❯

annual bonus 24 days' holiday plus bank holidays Company pension scheme What you'll be doing: You will play a pivotal role in maintaining and improving the QMS, ensuring GMP and BRCGS/BRC compliance. As a senior member of the team, you will take ownership of critical QA activities, manage customer-facing tasks, and mentor junior team members. What 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 ❯

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 ❯

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 ❯

associated to Lean process creation Identify opportunities during process development to improve process capability, machine performance and uptime Adhere to legal, corporate and site legislation, and procedures Compliance with GMP requirements and uphold these standards Compliance with EHS requirements and uphold these standards Seek and deliver CI opportunities through project development Key requirements include: Relevant work experience as automation/ 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 ❯

where we continue to deliver value to their manufacturing operations. About the Role - End-to-end digital production demand management right from project initiation to project closure. Experience in GMP Environment critical to the role ,Pharma, life science, Medical device background required Responsibilities Work will be in the EST Time zone Digital Production Demand Management & Planning Coordinating with the Development More ❯

with global sterilisation vendors to plan and manage process transfers. Write protocols, oversee vendor testing, and analyse data. Lead design reviews and recommend optimal sterilisation procedures. Ensure compliance with GMP practices and regulatory standards. Support regulatory documentation and submission processes. The start date is for ASAP. The initial contract length is for 12 months, with options to extend after. The More ❯

Main requirements: In-depth knowledge of cGMPs: 21 CFR Parts 11, 210, 211; EU Directives 75/319/EEC, 2003/94/EC; Annex 11, and related GMP guidelines. Proficiency with GAMP guidelines (particularly GAMP 5): risk-based validation approaches for GxP systems. Experience in software development, testing, and validation processes. Strong quality audit and software quality metrics More ❯