11 of 11 GxP Jobs in the UK

Group Policy Software Deployment and Release Management Desirable Experience Experience working within pharmaceutical, biotechnology, life sciences, or other regulated industries. Exposure to GMP, GxP, or validated environments. Experience supporting device refresh, Windows 11 migration, or large-scale workplace transformation programmes. Familiarity with application validation and compliance-driven change controls. ITIL ...

degree in computer science, Engineering, or related technical field. PREFERRED QUALIFICATIONS Familiarity with Generative AI infrastructure, evaluation frameworks, and integration patterns. Knowledge of GxP/regulated environments and qualification processes. Proven Track record of driving platform adoption and mentoring engineering teams. Experience in pharmaceutical, healthcare, or other highly regulated industries. ...

then appropriately evaluate, new tools and technologies 4. Experience testing randomization schemas 5. Knowledge of drug management 6. Familiarity with industry regulatory requirements (GxP) 7. Must possess a strong technical background in software and object-oriented systems development and testing, and be able to apply this knowledge to designing test ...

manufacturing initiatives including MES, electronic batch records, paperless production, laboratory digitisation, analytics, AI, integration, cloud, and edge technologies. Ensure architecture decisions align with GMP, GxP, CSV/CSA, data integrity, cybersecurity, validation, and operational resilience requirements. Develop and maintain architecture artefacts including capability maps, data flows, system landscapes, integration diagrams … Strong understanding of pharmaceutical manufacturing technologies and processes. Proven experience defining architecture roadmaps, standards, governance frameworks, integration strategies, and platform lifecycle plans. Experience supporting GxP-regulated environments, including validation, data integrity, change control, audit readiness, and inspection support. Knowledge of manufacturing systems including: ERP MES LIMS ...

Title: IT Automation Project Execution Specialist (Pharma/GxP Manufacturing) Start Date: asap Location: Milton Keynes Duration: 6 Months Contract Type: Full Time Remote Role: No, onsite 5 days a week in Milton Keynes £31-53 PAYE PH or umbrella equivalent Description: This is a position for IT/… critical automation and infrastructure projects within a regulated pharmaceutical manufacturing environment. The role focuses on implementing and upgrading validated systems, ensuring compliance with GxP standards, and supporting the full system lifecycle (SDLC). You will work at the interface between IT and Operational Technology (OT), supporting manufacturing systems that ...

critical automation and infrastructure projects within a regulated pharmaceutical manufacturing environment. The role focuses on implementing and upgrading validated systems, ensuring compliance with GxP standards, and supporting the full system lifecycle (SDLC). You will work at the interface between IT and Operational Technology (OT), supporting manufacturing systems that … systems Administer and support Windows Server environments (2022 or later) Support and integrate automated systems used in pharmaceutical manufacturing Ensure systems comply with GxP regulations, including validation and documentation Create and maintain GxP documentation (IQ/OQ/PQ, SOPs, risk assessments, validation plans) Participate in and support the Software ...

record leading clinical technology migrations, integrations, or large-scale data transfer programmes Strong understanding of clinical trial systems, data governance, validation, regulatory compliance, and GxP requirements Experience working with platforms such as Veeva Vault, CTMS, eTMF, Siebel CTMS, or related clinical development systems (Inform, Rave, etc) Ability to engage … confidential discussion on your career. Keywords: Clinical, Technology, Systems, CTMS, eTMF, Veeva, Siebel, Migration, Data, Transfer, Integration, Validation, Compliance, Pharmaceutical, Biotechnology, Trials, Governance, Quality, GxP, Operations, Vendor, CRO, Transformation, Analytics, Inspection, Audit, Development, Programme, Strategy, Lifecycle TPBN1_UKTJ ...

record leading clinical technology migrations, integrations, or large-scale data transfer programmes Strong understanding of clinical trial systems, data governance, validation, regulatory compliance, and GxP requirements Experience working with platforms such as Veeva Vault, CTMS, eTMF, Siebel CTMS, or related clinical development systems (Inform, Rave, etc) Ability to engage … confidential discussion on your career. Keywords: Clinical, Technology, Systems, CTMS, eTMF, Veeva, Siebel, Migration, Data, Transfer, Integration, Validation, Compliance, Pharmaceutical, Biotechnology, Trials, Governance, Quality, GxP, Operations, Vendor, CRO, Transformation, Analytics, Inspection, Audit, Development, Programme, Strategy, Lifecycle ...

record leading clinical technology migrations, integrations, or large-scale data transfer programmes Strong understanding of clinical trial systems, data governance, validation, regulatory compliance, and GxP requirements Experience working with platforms such as Veeva Vault, CTMS, eTMF, Siebel CTMS, or related clinical development systems (Inform, Rave, etc) Ability to engage … confidential discussion on your career. Keywords: Clinical, Technology, Systems, CTMS, eTMF, Veeva, Siebel, Migration, Data, Transfer, Integration, Validation, Compliance, Pharmaceutical, Biotechnology, Trials, Governance, Quality, GxP, Operations, Vendor, CRO, Transformation, Analytics, Inspection, Audit, Development, Programme, Strategy, Lifecycle ...

powered analytics) and Snowflake Write-Back to bridge analytical and operational workflows. enterprise data intelligence: build end-to-end cataloging, data lineage, and GxP-compliant governance policies using Collibra Data Intelligence Cloud . devops & metadata integration: connect Collibra with GitHub to parse technical lineage (dbt, LookML) and develop custom … Back. collibra practitioner: deep experience setting up Collibra cataloging, data quality, lineage, and repository integrations (e.g., GitHub). pharma domain specialist: strong understanding of GxP, data integrity, and regulatory compliance standards in life sciences. consulting mindset: comfortable leading conversations, challenging assumptions, and advising C-suite client leaders. tech stack & preferred ...

AWS Cloud Architect | Hybrid | £110,000 About the Role: We're partnering with a growing business to hire a Platform Architect to own the design, security, reliability, and operational management of their AWS platform. This ...