16 of 16 GMP Jobs in England

will provide strategic leadership for the IFS product roadmap, ensuring its alignment with organisational objectives, timely and high-quality delivery and adherence to GMP compliance standards where needed, playing a key part in advancing our mission and making a real difference. Please note, this is a hybrid opportunity based ...

weekend work (In addition to a normal 37 hour, 5 day shift operation) - Be comfortable working in a highly regulated environment (existing knowledge of GMP practices beneficial but not essential) - Have experience using Microsoft Office suite - Have an analytical mind with acute attention to detail - Have good problem-solving abilities ...

monitor standards, provide coaching where needed, and escalate any risks to ensure corrective actions are taken promptly. Key Responsibilities Carry out process audits including GMP, fabrication, foreign body, CCP, glass & hard plastic audits Verify and audit production paperwork for accuracy and completion Coach and support production staff to ensure correct ...

monitor standards, provide coaching where needed, and escalate any risks to ensure corrective actions are taken promptly. Key Responsibilities Carry out process audits including GMP, fabrication, foreign body, CCP, glass & hard plastic audits Verify and audit production paperwork for accuracy and completion Coach and support production staff to ensure correct ...

ideal candidate is a seasoned, commercially-minded analytics expert with hands-on experience across the Google Cloud and Google Marketing platforms (BigQuery, Looker, GA4, GMP). They must have a proven track record in client consulting, the ability to advise senior stakeholders and experience of building an analytics practice centered ...

work directly with clients to analyse, cleanse and migrate data, design and test Pension calculations, and support key industry programmes such as GMP rectification and equalisation. Key Responsibilities Analyse complex Pensions data using SQL and Excel Deliver data mapping, migration and cleanse activities Produce and test calculation specifications based ...

completed Collecting micro samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/Fabric audits Temperature checks Quality checks The nature of the role requires a flexible approach to working hours. Core working hours are: Nights: Monday ...

Data Consulting Manager - must have GMP expertise A growing data and digital consultancy is looking for an experienced Digital Consulting Manager to join its London-based team. This role is ideal for someone who enjoys leading complex client projects, building trusted senior relationships, and developing high-performing teams. The Role ...

Services, Senior Pharmacists, technical leads and other external service providers/contractors, to develop and maintain the aseptic service provision, and Good Manufacturing Practice (GMP) regulatory requirements for unlicensed activity. Responsible for the provision of technical support and advice on medicines quality/quality assurance matters to all areas … with clear career pathways and access to further education. Key Duties Quality Assurance To lead and maintain systems based on quality assurance requirements for GMP activities under the Medicines Act 1968 Section 10 exemption for unlicensed activity and for GDP activities under the MHRA WDA(H) licence. Ensure efficient ...

product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder … Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills ...

both technical and stakeholder-facing teams. You will play a key role in delivering high-profile transformation projects such as data cleanses, benefit rectification, GMP reconciliation/equalisation, and system implementations. Key Responsibilities: Lead the technical delivery of complex pension data and calculation projects. Define technical approaches and delivery strategies … individual member calculations. Proven experience delivering bulk pension data and/or calculation projects. Experience leading or heavily influencing pensions transformation projects (e.g. GMP reconciliation, GMP equalisation, benefit rectification, risk settlement data cleanse, system implementation). Advanced Excel skills, including building and reviewing calculation models. Strong problem-solving and analytical ...

Respectful . Were currently recruiting for a Manufacturing Equipment & Systems Specialist to join our Manufacturing Team . In this role, you willensure compliance of GMP Equipment & Systems within the manufacturing department enabling efficient batch delivery against production schedule in line with GMP, safety and environmental requirements, playing a key part … Systems We are Looking For: A-Level, preferably science based with previous industrial experience Graduate in STEM subject (preferred) Experience working in a GMP environment Experience working with of Cell & Gene therapy manufacturing equipment and systems. e.g. bioreactors, chromatography, clean rooms etc. Ability to travel across all Oxfordshire sites Willingness ...

Program Manager will lead planning, execution, and validation of upgrades across validated lab PCs, instrument workstations, and OT endpoints, ensuring compliance with GxP/GMP/CSV requirements and minimal disruption to critical lab operations. Key Responsibilities: Lead the global roll-out of Windows 11 upgrades for validated … manage timelines, costs, and expectations. Skills & Experience: Proven experience managing Windows migrations in validated lab or OT environments. Strong understanding of GxP/GMP/CSV requirements and lab system validation. Excellent project management and stakeholder communication skills. Experience coordinating multi-country, cross-functional programs. Detail-oriented and able ...

Gold data layers with Data Engineers Document business rules, data mappings, and de-duplication logic Conduct data quality checks and validation for GDPR/GMP compliance Develop analytical models and curated views for business use cases Build and maintain Power BI dashboards from certified data sources Collaborate with stakeholders … Familiarity with dbt or ELT tools (desirable) Knowledge of data modelling (star schema, slowly changing dimensions) Awareness of data governance and compliance (GDPR/GMP) Manufacturing or regulated industry experience is an advantage Ability to translate business requirements into reliable datasets ...

Gold data layers with Data Engineers Document business rules, data mappings, and de-duplication logic Conduct data quality checks and validation for GDPR/GMP compliance Develop analytical models and curated views for business use cases Build and maintain Power BI dashboards from certified data sources Collaborate with stakeholders … Familiarity with dbt or ELT tools (desirable) Knowledge of data modelling (star schema, slowly changing dimensions) Awareness of data governance and compliance (GDPR/GMP) Manufacturing or regulated industry experience is an advantage Ability to translate business requirements into reliable datasets ...

knowledge of relevant electronic systems, including SAP. * Complete electronic batch documentation, equipment logbooks and other documentation relevant all stages of production. * Understand and follow GMP requirements and defined procedures to maintain the requirements of quality standards in the packaging environment. * Work safely in packaging environment, understanding personal responsibility for Health … risk management. * Understand and comply with procedures relevant to COSHH. * Participate in internal audits. Essential: * Experience of packaging and labelling environment in a GMP environment, preferably within clinical trials. * Working knowledge in SAP * Basic knowledge of clinical trial operations Click Apply now/contact Lianne to be considered ...