101 to 124 of 124 Permanent GMP Jobs

. Manage contractors to ensure work is carried out safely, efficiently, to the highest quality standards with minimal disruption to the process. Support and expertise in the application of GMP and Sanitary design standards across the sites is provided, developing and sharing best practices across the MEU network Work with Cluster, Regional and global teams to align Capital plans across … . Manage contractors to ensure work is carried out safely, efficiently, to the highest quality standards with minimal disruption to the process. Support and expertise in the application of GMP and Sanitary design standards across the sites is provided, developing and sharing best practices across the MEU network Work with Cluster, Regional and global teams to align Capital plans across More ❯

as Subject Matter Expert (SME) for lifecycle management of assays, equipment, and materials. Prepare and review qualification and validation documentation. Ensure departmental adherence to regulatory and compliance requirements, including GMP and GDP. Manage the implementation and project lifecycle of new test methods. Collaborate with internal and external stakeholders to support testing and validation needs. Deliver training and development initiatives across … a regulated environment. Strong project management and team leadership skills. Demonstrated ability to work independently and deliver results efficiently. Excellent understanding of EU and FDA regulations and industry standards (GMP, GLP, GCP). Proficient in Microsoft Office and other relevant IT systems. 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, light 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 ❯

brands & act accordingly to report any evidence of unsafe or out of specification product, equipment, packaging or raw materials to the Technical Manager. Responsible for undertaking Good Manufacturing Practice (GMP) audits, start up checks and draw attention to the Technical Manager of any potential food safety hazards/risks or infringements of Health & Safety Legislation. Responsible for the identification, segregation More ❯

basic understanding of computer system validation in the pharmaceutical sector Experience and knowledge of working in a regulated environment, specifically with regards to record retention Knowledge of GCP and GMP with regards to QMS activities Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures Responsible … for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions are closed timely and in a RFT state Job Background Minimum of 3 years experience working in More ❯

at East Suffolk and North Essex NHS Foundation. You will be based at Colchester Hospital, however you will be required to work across at Ipswich Hospital. You will have GMP experience within a pharmaceutical manufacturing facility. You will be a team player, joining an established department with a multi-disciplinary team. Our team have various professional scientific backgrounds, including different … licence, performing Quality Control analysis on raw materials and manufactured products, and maintaining Quality Assurance functions within Pharmacy Technical Services in line with Standard Operating Procedures and current Good Manufacturing Practice (cGMP) requirements. You will be expected to support the Pharmacy Quality Assurance team in ensuring that the regulatory requirements and standards set by the Medicines and Healthcare products Regulatory … Job description Job responsibilities For full details of the responsibilities and duties of this role please see the attached job description. Person Specification Experience Essential Previous experience of pharmaceutical GMP in NHS manufacturing unit or pharmaceutical industry as required by MHRA guidance for specials manufactures for batch release Demonstrated experience of multi- disciplinary working Handling of high risk medicines Desirable More ❯

client's biotechnology start-up facility in North East England. This role offers the opportunity to be part of a high-performing automation team delivering critical systems in a GMP-regulated environment. Responsibilities: Executing FAT/SAT/IOQ protocols including generation of protocols and reports. Design, configure, and support Emerson DeltaV PCS and/or BMS platforms for bioprocessing … qualification, and validation of automation systems in collaboration with CQV and Operations teams. Participate in the development, testing, and deployment of automation changes, and maintain documentation in compliance with GMP requirements. Provide technical input during design reviews, FATs, SATs, and system walkdowns. Qualifications & Experience: Bachelor's degree in Automation Engineering, Software Engineering, or a related field. Prior experience in a More ❯

Learning Lead Huddersfield United Kingdom (GB) Full-time Permanent As a strategic partner to the Site Head, you will lead the Technical Training & Learning function, ensuring compliance in a GMP-regulated environment while delivering impactful learning solutions that build site-wide technical capability. How You Will Make An Impact: Lead the site's Technical and GMP Training strategy, ensuring workforce … competence through structured programs that meet GMP compliance and operational needs. Develop and implement an annual training masterplan based on cross-functional capability analysis to build required technical skills across key site functions. Drive the effectiveness of training for critical roles, improving shop floor execution and boosting long-term technical competencies. Monitor and report on Technical Training KPIs, ensuring data More ❯

practice etc ). In support of this develop process standards, SOP's and work instructions for key maintenance activities to ensure compliance to standard and ongoing maintenance of our GMP compliance and standard. - Track/Monitor and report upon utility costs and consumption data for R&D site ensuring that all invoicing, payment and consumption tracking is maintained accurately in … background and knowledge of mechanical & electrical systems is essential. - Strong knowledge of evaluating and vendor selection based on quality, compliance and cost effectiveness and the ability to meet specific GMP requirements. - Experience in systems and building management, around certification in Legionella & Asbestos Management - Knowledge of Pharmaceutical manufacturing processes and understanding of GMP requirements is advantageous. - Extensive work-based experience with More ❯

pharmaceutical manufacturer to recruit a QA Officer on a 6-month fixed-term contract (strong chance of going permanent). This role is ideal for someone with experience in GMP environments who can contribute to quality systems, batch review, and regulatory compliance. Key Responsibilities: Review batch documentation to support product release Support generation of Quality System documentation and Product Quality … Reviews Investigate and report on deviations and complaints Liaise with Operations, QC, and NPD to ensure product compliance Support QA Manager in maintaining GMP and quality accreditations (FDA, MHRA, ISO, BRC) Assist with validation of processes and equipment Requirements: Science-based qualification (HNC/HND/Degree or higher) QA experience in a GMP-regulated environment Strong organisational and IT More ❯

working with a global name in the pharmaceutical industry to help them find a QA Specialist to join their team. If you have Quality Assurance (QA) experience from a GMP environment then this could be a great next step for you. The company offer an excellent benefits package and scope for growth and development. The Role: Perform batch reviews within … required timelines Author and review SOPs Document and report all work in adherence with GMP and departmental procedures Review change controls and provide feedback/corrections to authors and escalate concerns to the Quality Manager/Head of Quality where necessary Raise, approve and review CAPAs Represent the QA team for improvement projects and with clients and internal teams Assist … with technical support to the audit team and responding to requests for documentation and information Conducts self-inspections/audits to ensure compliance with Quality Management System procedures and GMP regulations Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management Carries out site internal audits and identifies areas of GMP improvement More ❯

Quality Assurance Officer on a 12-month fixed term contract. This is a great opportunity to join a well-established team and support key QA activities in a regulated, GMP environment. The Role: Support day-to-day QA operations, ensuring compliance with SOPs and GMP Assist with supplier quality management and document control Help implement global quality procedures at site More ❯

site at a pharmaceutical manufacturing facility in Northern Ireland. This is a fantastic opportunity to work on a high-profile project, ensuring the validation of automation systems within a GMP-regulated environment. Key Responsibilities Lead and execute validation activities for automation systems, focusing on DCS/PLC systems within a pharmaceutical manufacturing site. Develop and implement validation documentation including URS … IQ, OQ, PQ, and validation plans. Ensure compliance with regulatory requirements (e.g. GAMP 5, FDA 21 CFR Part 11, EU GMP Annex 11). Perform risk assessments, impact assessments, and deviation investigations. Collaborate with cross-functional teams including automation, quality, and IT departments. Provide support during audits and inspections related to system validation. Required Experience & Skills 4-10 years of … System Validation within the pharmaceutical or life sciences sector. Hands-on experience validating DeltaV systems preferred; other DCS or PLC systems will also be considered. In-depth knowledge of GMP, GAMP 5, and regulatory expectations. Proven ability to author, review, and execute validation protocols and reports. Strong problem-solving, documentation, and communication skills. Ability to work independently on-site in 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 ❯

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 ❯

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 ❯

high-quality, complex projects that drive scientific discovery and technological advancement. Our Client: This company specialises in the design and delivery of highly regulated environments, focusing on laboratories and GMP manufacturing facilities. They pride themselves on understanding the unique challenges of each project, creating efficient workflows that emphasise user safety and well-being. With a commitment to flexibility and adaptability … ensure that their designs meet the evolving needs of their clients from day one. Senior/Principal Architect Responsibilities: Deliver projects from concept to detailed design for laboratories and GMP manufacturing facilities, ensuring adherence to life science standards. Develop layouts for various laboratory classifications and environments, including clean rooms. Communicate complex ideas clearly and effectively to stakeholders, simplifying technical details … Requirements: Registered Architect (RIBA/ARB) with demonstrable experience in the Life Sciences sector. Proven track record of delivering projects from concept to detailed design for both laboratories and GMP manufacturing facilities. Strong understanding of life science standards and facility classifications. Excellent communication and presentation skills, with the ability to convey complex ideas succinctly. Proficient in Autodesk Revit and AutoCAD More ❯

opportunity to be part of a company that values innovation, collaboration, and the flawless execution of ideas that genuinely improve the world! Key responsibilities: Generate and revise documentation for GMP manufacturing to ensure technical accuracy and GMP compliance. Provide technical support to develop required process documentation in collaboration with internal customers. Independently manage the creation of new documents and revise … GMP documents according to detailed procedures. Use and maintain the Documentation Management System (DMS) according to detailed procedures. Produce and process batch documentation according to standard timelines, coordinate review, approval, and issuance ensuring availability for use in Manufacturing per production schedule. Monitor progress of document creation and communicate with relevant parties to resolve potential issues in a timely manner. Manage … training to others during routine document revision. Understand and align with company policies, departmental practices, regulatory, and statutory requirements. Key requirements: Proven experience as a Technical Writer in a GMP manufacturing environment. Outstanding ability to generate and revise technical documentation with attention to detail. Comprehensive knowledge of DMS and standard methodologies for documentation. Ability to manage multiple tasks and projects More ❯

recruit an Associate Expert Bioprocess DSP (m/f/d) to join the Pilot Plant Downstream Process team starting at the next possible date at our Research and GMP Production Site in Heidelberg. Associate Expert Bioprocess DSP (m/f/d) What's the best thing about working with us? A permanent position in full-time (40 hrs. … development and process transfer from laboratory to pilot scale Planning and execution of DSP unit operations at pilot scale in technical and clinical campaigns (cleanroom class D + C, GMP regulated environment) Development and implementation of new process technologies within the framework of process optimization Creation of process risk analyses, control strategies, process mappings, batch protocols, development plans, and reports More ❯

Understanding of distributed systems concepts. Experience with Python for data processing or image analysis. Background or interest in biology, lab automation, or scientific instrumentation. Any experience with regulated environments (GMP, HIPAA, etc.) Any 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 … 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 ❯

We are currently recruiting for a QA Supervisor based at our Llanidoles site, this will be a 5 day onsite role. The successful candidate will be responsible for leading a small QA team to ensure the efficient and effective operation More ❯

systems function reliably and effectively. Required Skills Proven experience with the design and development of control systems e.g. PLC, SCADA, DCS, MES, etc. Ideally person would be from a GMP environment (e.g. Pharma, Food, FMCG, Chem, etc.), but not essential. Control System experience is ideally with Siemens products. Preferred Skills Experience in a GMP environment. Familiarity with Siemens products. More ❯

GMP Recruitment are proud to be working with a well-known Telecommunications service provider based in Southport.We are recruiting on their behalf for an experienced Telecommunications Engineer to join their team on a rolling contract basis . The desired individual will be supporting hardware installation, fibre cabling, fault finding , and providing hands-on support across multiple data centre sites within … Ciena is a strong advantage AN IMMEDIATE START IS AVAILABLE FOR SUCCESSFUL CANDIDATE. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯

GMP Recruitment are proud to be working with a leading Telecommunications service provider based in Southport. We are recruiting on their behalf for a highly experienced and self-sufficient Telecommunications Engineer to support a high-profile data landing site. The successful candidate will be joining their team on a rolling contract basis . This is not a junior or entry … safety standards, and cabling protocols AN IMMEDIATE START IS AVAILABLE FOR SUCCESSFUL CANDIDATE. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. More ❯