26 to 37 of 37 GxP Jobs in the UK excluding London

templates, assessments, remediation plans and change controls for key or critical systems. - Review and approve key validation and project lifecycle documentation, including validation plans, GxP assessments, data migration plans, functional risk assessments, UAT/PQ test reports, validation reports, data migration reports and go/no-go decisions where appropriate. … quality, compliance, IT, systems or business-related discipline, or equivalent practical experience overseeing computerised systems in a regulated or compliance-led environment. - Experience in GxP, ERES, pharmaceutical, chemical, manufacturing, life sciences or another highly regulated environment. - Experience of Computer Systems Validation, system lifecycle documentation, change control and periodic review ...

cloud-based and regulated environments Driving audit readiness, compliance programs and evidence-based assurance across frameworks such as ISO 27001, GDPR, SOC 2 and GxP Providing leadership on risk management, governance and security strategy Partnering with customers, auditors and key stakeholders on security reviews, assurance activities and regulatory compliance Supporting … several of the following areas: Security leadership, governance, risk and compliance (GRC) Cloud security architecture and security strategy ISO 27001, GDPR, SOC 2, GxP, 21 CFR Part 11 or similar regulated frameworks Audit leadership, customer assurance and certification programs Healthcare technology, pharmaceutical, biotechnology or regulated SaaS environments Customer-facing security ...

effective IT service desk and provide hands‐on technical support. Develop cybersecurity, data protection and information security frameworks. Support UK GDPR, ISO 27001, GxP and other relevant regulatory requirements. Lead business continuity, disaster recovery, patching and vulnerability management. Select and implement systems such as ERP, CRM, HR and collaboration platforms. … explain technical subjects clearly to non‐technical stakeholders. A practical, commercially aware and solutions‐focused approach. Experience with LIMS, ELN platforms, laboratory systems, GxP, MHRA guidance or FDA 21 CFR Part 11 would be particularly valuable. What’s next? If you are an experienced IT leader who enjoys combining strategy ...

environment, supporting mission‐critical applications that enable research, clinical processes. The role has a direct impact on compliance with global regulatory standards (e.g., GxP/CSV), ensuring system reliability, and uninterrupted delivery of ongoing innovation initiatives. You will work on complex, integrated platforms leveraging modern engineering practices and tools (e.g. … system integrations, ensuring timely issue resolution. Drive end-to-end compliance activities including validation documentation, audit readiness, and adherence to regulatory standards (CSV/GxP). Oversee multiple concurrent workstreams with competing priorities in resource-constrained environments, ensuring optimal delivery outcomes. Proactively manage risks, issues, and schedule pressures, implementing mitigation ...

applicable regulations, and internal quality standards. Lead the implementation, improvement and validation of new processes, procedures, and IT systems (e.g., eQMS, eTMF) to support GxP compliance and operational excellence. Oversee internal and external audits, including regulatory inspections, ensuring findings are addressed promptly and effectively. Partner with Clinical Operations, IT, Engineering … Science Teams to integrate quality and regulatory requirements into digital platforms, AI-enabled solutions, and GxP-relevant systems. Embed a culture of quality awareness through training, workshops, and mentoring, ensuring all staff are competent and compliant with GCP, ISO standards, and internal policies. Support the Quality Manager in maintaining ...

preparation and delivery of user training, management of technical documentation, enhancement of system capabilities, and collaboration with cross-functional teams. Responsibilities include supporting GxP -compliant system validation activities, user acceptance testing, and participation in regulatory inspections and internal audits as needed. The Associate Director will work directly with business stakeholders … development support. Oversee system lifecycle activities including requirements gathering, design, testing, validation, deployment, and ongoing support. Ensure delivery of high-quality solutions that meet GxP , regulatory, security, and data integrity requirements. Partner with Quality and Validation teams to support system validation, audit readiness, and inspection activities. Drive continuous improvement initiatives ...

System Administrator (GxP Systems) 3-Month Contract | Part-Time | Pirbright, Surrey | Inside IR35 We're looking for a System Administrator with experience supporting validated systems in regulated environments (GxP/GMP) . Key Responsibilities: System administration, maintenance, and patch management Testing and validation activities (CSV/GxP) System implementation … control and compliance activities Audit readiness and documentation Root cause analysis and issue resolution Collaborate with Engineering, Manufacturing, Quality, and external vendors Required Experience: GxP System Validation/Computer System Validation (CSV) Change Control & Patch Management Compliance & Audit Readiness System Lifecycle Management CAPA & Risk Management Vendor & Stakeholder Management Project Delivery ...

point for the Regulatory organisation, resolving issues quickly and minimising disruption Ensure platforms meet regulatory, data integrity, security, and inspection-readiness requirements in validated GxP environments Oversee vendor-provided technologies and outsourced application management support Drive lifecycle management of platforms upgrades, enhancements, cloud evolution, and reduction of technical debt Establish … experience with Veeva Vault Regulatory systems Working knowledge of regulatory operations, submissions and publishing, and the technology that supports them Strong experience operating within GxP settings, including system validation, inspection readiness, and data integrity Proven ability to partner with senior leadership to deliver technology solutions PV/safety experience would ...

leadership responsibility within IT in biotech, pharmaceutical, or other regulated environments Demonstrable experience in leading IT services, operating models, governance, policies, and procedures in GxP or similarly controlled settings Experience partnering with senior stakeholders across Quality, Regulatory, TechOps, Supply Chain, PV, Finance, HR, and other business functions Strong experience … plans Strong understanding of enterprise architecture principles, systems integration, and application lifecycle management in complex business environments Experience supporting compliance activities including CSV, SOX, GxP, ITGC, privacy, and audit‐related requirements Demonstrated ability to lead through influence across matrixed organisations and third‐party service models Kyowa Kirin International ...

Competitive + great benefits An experienced senior IT leader is required for our pharmaceutical manufacturing client to take ownership of Manufacturing IT Services and GxP-regulated Business Systems across its EMEA manufacturing hub. This is a senior leadership role responsible for digital strategy, operational resilience, compliance, business continuity and technology … transformation within a regulated pharmaceutical environment. Key responsibilities: Leading Manufacturing IT Services and Business Systems. Driving digital transformation and site technology strategy. Ensuring GxP compliance, validation, data integrity and audit readiness. Managing technology portfolios, vendors and key stakeholders. Building and developing high-performing teams. Experience required: Proven IT leadership experience ...

LIMS implementation within a highly regulated life sciences environment. This role requires someone who has successfully delivered LIMS projects and can operate effectively in GxP and GMP-regulated environments , where data integrity, compliance, and patient safety are central to the programme's success. Key Requirements Proven experience delivering LIMS implementation … projects Experience with LabVantage LIMS Strong understanding of GxP and GMP regulations Experience managing complex stakeholder groups across business and technical teams Track record of delivering projects in highly regulated environments Contract Details 6-month initial contract Outside IR35 Potential for a multi-year engagement , with further European ...

responsibility, respecting CBL lab SOPs, sexed production planning and CBL lab production standards (details on following points below). - Ensure the CBL lab GxP on the flow cytometers operation and the sorting lab working area are observed and maintained. - Ensure the CBL Lab GxP on media preparation, processing of semen ...