1 to 25 of 96 Permanent GMP Jobs in England

user requirements gathering, risk assessments, validation planning and test execution. Maintain documentation including SOPs, validation records, configuration specifications and change records. Ensure compliance with GMP, GAMP 5, Annex 11, 21 CFR Part 11 and company quality procedures. Support internal audits, external audits and regulatory inspections. Project and Vendor Management Work ...

endpoint management solutions Experience working within a pharmaceutical, biotechnology, medical device or similarly regulated environment would be highly desirable An understanding of GxP, GMP, GAMP 5, Annex 11 and 21 CFR Part 11 would be advantageous Strong understanding of IT service management and ITIL principles Excellent analytical and troubleshooting skills ...

Understanding of relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes Knowledge of ISO 13485and 14971, FDA21CFR Part 803, 820, 822, 806, EU GMP Annex 11 Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability ...

teams needs, challenges and requirements. Develop strategies to leverage Salesforce Media Cloud for centralizing and monetizing ad inventory across platforms like Google Marketing Platform (GMP); Meta Ads; Criteo and LinkedIn and more. Provide expert advice on best practices for ad operations, inventory optimization, and revenue growth. Implementation and Configuration Lead ...

Investigational Medicinal Product (IMP) manufacturing and associated Quality Management Systems at MedPharm. The role is responsible for supporting compliance with Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), applicable regulatory requirements and internal quality procedures through the review of quality documentation, management of quality systems … analytical methods, sampling instructions and protocols. Support review of analytical investigations including OOS, OOT and atypical results. Review laboratory documentation to ensure compliance with GMP, GLP and internal procedures. Support QA oversight of reference standards, retained samples and stability documentation where applicable. Materials Management Perform QA review and disposition ...

time. To manage internal taste panel and shelf-life sample assessments. Assist in the management and completion of internal audits including CCP, GMP, fabrication, hygiene, plastic, and system audits. Skills and Experience Required Relevant certification - HACCP Level 3 Basic Food Hygiene Attention to detail and able to prioritise workload. Organised ...

site is audit-ready at all times. Maintain accurate quality records & contribute to the reporting of site quality KPIs. Manage the site's GMP auditing programme & actively participate in the internal audit team. Drive continuous improvement initiatives that enhance product quality, food safety and operational performance. Ensure Health & Safety, Hygiene ...

root cause analysis. Support supplier approval processes and supplier questionnaires. Ensure quality control equipment is calibrated and maintained. Promote continuous improvement, quality culture and GMP standards. Deliver quality-related training across site where required. Essential Skills & Experience Previous experience within a manufacturing environment. Knowledge of quality systems and food safety ...

Oriented Programming Git version control Basic electrical, mechanical and pneumatic knowledge Robotics Machine Vision SCADA/MES systems Pharmaceutical or regulated manufacturing environments GAMP, GMP, 21 CFR Part 11 or EU Annex 11 Industrial communication protocols including EtherCAT, Profinet, CAN, Ethernet/IP and Serial communications .NET ...

Experience with industrial automation systems and OT architecture, including integration with IT systems Familiarity with regulated environments and standards such as GxP (including GMP and GAMP5) and IEC 61508/61511 Understanding of cyber security risk assessments, controls, and system documentation Experience in system lifecycle management, including validation, change control ...

records, maintenance schedules, equipment hierarchies, and work order data remain accurate and up to date. Record, monitor, and close maintenance activities in line with GMP and regulatory requirements. Develop, maintain, and optimise preventative maintenance programmes to support site compliance and asset performance. Manage the maintenance service desk, ensuring maintenance requests ...

execute commissioning, qualification, and SAT protocols. Prepare system impact assessments, qualification documentation, and validation reports. Review project documentation for technical accuracy, compliance, and GMP requirements. Ensure systems are safe and ready for start-up, testing, and qualification activities. Perform installation verification, system start-up, and functional testing. Monitor progress, coordinate ...

execute commissioning, qualification, and SAT protocols. Prepare system impact assessments, qualification documentation, and validation reports. Review project documentation for technical accuracy, compliance, and GMP requirements. Ensure systems are safe and ready for start-up, testing, and qualification activities. Perform installation verification, system start-up and functional testing. Monitor progress, coordinate ...

maintenance activities are completed in line with approved work procedures, engineering standards are applicable statutory and regulatory requirements. Participate in health and safety reviews, GMP audits, and improvement initiatives as required. Consult and negotiate with engineering and facility suppliers, in line with IPL polices, to agree service requirements and contractual ...

faulty material. When required support sorting activity. Conduct where appropriate, testing of raw material. Carry out internal audits to the standards - Monitor and maintain GMP/BBQ. G&P, Internal audit performance. Publish results, raise and manage non-conformances. Oversee and conduct quality inspection rounds during the designated shifts. Monitor ...

quality systems are adhered to, support investigations, conduct audits and help drive continuous improvement initiatives across the site. Key Responsibilities Conduct internal audits covering GMP, hygiene, traceability, product quality, documentation and manufacturing processes, ensuring corrective actions are completed effectively. Investigate quality, food safety and compliance issues, including customer complaints ...

Oriented Programming Git version control Basic electrical, mechanical and pneumatic knowledge Robotics Machine Vision SCADA/MES systems Pharmaceutical or regulated manufacturing environments GAMP, GMP, 21 CFR Part 11 or EU Annex 11 Industrial communication protocols including EtherCAT, Profinet, CAN, Ethernet/IP and Serial communications .NET ...

62443Experience with industrial automation systems and OT architecture, including integration with IT systemsFamiliarity with regulated environments and standards such as GxP (including GMP and GAMP5) and IEC 61508/61511Understanding of cyber security risk assessments, controls, and system documentationExperience in system lifecycle management, including validation, change control, and documentation practicesKnowledge ...

seeking an experienced Technical Architect to support a large-scale enterprise device migration and workplace transformation programme, within a highly regulated pharmaceutical GMP environment. The role will define, guide, and assure the end-to-end architecture across infrastructure, identity, networking, and security domains within a complex enterprise environment. The successful ...

areas and uses these to develop options for project progression (e.g. technical, process, plan or system). Demonstrates understanding of clinical study designs and GMP documentation. Articulate in both verbal and written communication. A strong presenter that can deliver messages within the internal organization and externally with our partners. Excellent ...

responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site. This role ensures ongoing compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, GAMP5 principles, and applicable global regulatory requirements. The position provides technical oversight of electronic systems, manages validation activities, assesses system … validated state. Identify and close existing CSV gaps to ensure compliance with Annex 11 and data integrity requirements. EudraLex Volume 4 Good Manufacturing Practice (GMP) guidelines, laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/ ...

control. Produce weekly stock expenditure reports highlighting asset management costs and repeat product failures. Promote and support continuous improvement initiatives such as 5S, GMP, and TPM pillars. Demonstrate safe working behaviors and conform to site safety standards and procedures. Identify personal skills gaps and contribute to training and development plans. ...

fault finding activities across warehouse systems and processes where appropriate. Work confidently around high-speed machinery, automated warehouse processes and manufacturing plant. Maintain GMP, hygiene, quality and audit standards within the warehouse, supporting checks, audits and follow-up actions as required. Share technical and systems knowledge with team members ...

environment Desirable 1. Experience with catheter-based or similarly complex diagnostic/therapeutic devices 2. Experience managing US FDA regulatory interactions or GLP/GMP study programmes 3. Prior experience in a Series A-B medical device company What's on Offer A pivotal, high-impact role in a well ...

. Experience with process control and automated systems for production lines. Familiarilty with PID tuning for production lines. Familiarity with industry-specific regulations (HACCP, GMP, etc.) and food safety standards. Knowledge of instrumentation and process equipment . Knowledge of Java, Python, C++ and VB Scripting Familiarity with Flow Charts ...