26 to 42 of 42 GxP Jobs in the UK excluding London

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and ...

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and ...

MedPharm Ltd in Guildford is seeking a CSV Specialist to govern and manage validated computerised systems (GxP) across the site, ensuring compliance with EU GMP Annex 11 and MHRA guidance. You will oversee the validation lifecycle (URS, IQ/OQ/PQ, reports), assess updates, perform risk assessments, and support ...

hour PAYE The Role We are looking for an experienced IT/OT Automation Engineer with a strong background in pharmaceutical manufacturing and GxP-regulated environments. You will support the delivery, upgrade and lifecycle management of validated automation and infrastructure systems, working at the interface between IT and Operational Technology … environments. Administer and support Windows Server 2022 or later environments. Support and integrate automated systems used within pharmaceutical manufacturing. Ensure systems comply with GxP requirements, including validation and documentation standards. Create and maintain GxP documentation, including IQ/OQ/PQ, SOPs, risk assessments and validation plans. Support the Software ...

appropriate, timely validation/revalidation is maintained Conducts internal audits and assists with 3rd party quality audit; plans and implements continuous improvement projects Supports GxP health authority inspections by serving as subject matter expert forcomputerized systems topics Provides guidance on quality and regulatory requirements to project teams, internal stakeholders … other teams on GxP compliance relating to computerized systems Collaborates to resolve technical issues, provide quality training and communicate best practices Qualifications: Bachelor degree in Engineering or a relevant scientific discipline (Chemistry, Biology, Microbiology, IT etc.) or equivalent experience 5+ years' quality systems experience in pharmaceutical manufacturing/cGMP regulated ...

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 ...

main point of contact for the Head of Product Management, surfacing technical constraints, feasibility, and delivery risk that should inform prioritisation and roadmap decisions. GxP-aware delivery. Ensure requirements and backlog items affecting GxP-relevant systems are documented and validated in line with Qureight's ISMS and Management of Software … requirements into implementation but not core to the role. Experience working on products used in clinical trials, healthcare, or another regulated environment. Familiarity with GxP, ISO 27001, or computerised system validation (CSV) concepts. Even better if A software engineering or development background, or other hands-on technical experience. What ...

We'rebuilding a connected, end-to-end Enterprise AI engine - uniting data foundations, AI technology, process reinvention, and business-facing AI to accelerate results across the whole value chain. Success depends on being exceptional connectors ...

Join us as a Senior IT Quality & CSV Specialist. As Senior IT Quality & CSV Specialist you will provide independent quality and validation oversight for GxP computerised systems and complex global IT projects within a pharmaceutical environment. You will work with project teams, system owners, IT teams and regulated business functions … ensure computer system validation activities are risk-based, compliant with global regulatory requirements, and inspection-ready. What you'll do: Provide quality oversight of GxP computerised systems throughout the full validation lifecycle. Review validation documentation including Validation Plans, Validation Reports, requirements, traceability matrices, design documentation, test plans, test reports, testing ...

experience working across Quality, Regulatory, Finance, and operational business teams Understanding of IT governance, change control, documentation, validation-aligned processes, and compliance expectations across GxP and non-GxP systems Kyowa Kirin International is an equal opportunities employer. No agencies please. #J-18808-Ljbffr ...

Finance teams spend less time on manual processes and can focus on their core work. As several of these systems hold or track GxP-relevant records, i.e. trial imaging in Box and validated change history in JIRA, this is not "citizen developer" tinkering. Every automation that touches a regulated system … maintain integrations across Box, JIRA, HiBob and other platforms, including MCP-based and Claude Code-driven automations to remove manual handoffs between teams. GxP-aware delivery. Ensure every automation touching a validated or GxP-relevant system is version-controlled, peer-reviewed, documented, and validated in line with Qureight's ISMS ...

force multiplier, aligning stakeholders across technical and non-technical teams Bringing discipline to delivery across both fast-moving AI/ML development and regulated, GxP-adjacent processes What you'll bring: An original background as an engineer or scientist, with a career since built in programme or delivery management Proven … Technical Programme Manager | OKR | OKRs | Objectives and Key Results | Delivery Lead | Product Delivery | AI | Artificial Intelligence | Machine Learning | ML | Techbio | Life Sciences | Clinical Trials | GxP | Scale-up | Cross-functional Leadership | Stakeholder Management | PMO | Agile ...

Data Flow Documents Data Integrity Risk Assessments UAT Scripts & Execution Documentation Release Notes Business Communications Participate in system validation, periodic reviews, CAPAs, deviations and GxP compliance activities Collaborate with global stakeholders to continuously improve safety processes and supporting technologies What We're Looking For 5+ years' experience supporting Pharmacovigilance/… Drug Safety systems Strong knowledge of pharmacovigilance processes and operations Experience working within GxP-regulated environments Experience supporting validated computer systems Excellent business analysis skills with the ability to translate operational requirements into system solutions Strong stakeholder management and communication skills Experience supporting system implementations, upgrades, releases and change management ...

extend Box, Zendesk, JIRA, HiBob, and Pipedrive across Clinical Operations, Quality & Regulatory Affairs, People, and Finance teams. You will design scalable automation, ensure GxP-aware delivery, and work with AI/LLM tooling to improve efficiency. Strong scripting, SaaS integration experience, and secure delivery workflows are essential. #J-18808-Ljbffr ...

formats, and data quality challenges Ability to work effectively and cross-functionally with data science, data engineering, legal, commercial, and product teams Familiarity with GxP/regulatory software environments Healthcare, biotech, medtech, or techbio experience is advantageous Experience in high-growth startups or scaleups is advantageousFamiliarity with technology transfer offices … Relationship Building Risk Tracking Industry Keywords Healthcare Biotech Medtech Techbio Clinical Trials AI/Machine Learning Research Collaboration Agreements Technology Transfer Offices Tools & Technologies GxP Software Environments Data Annotation Workflows #J-18808-Ljbffr ...

Engineering & Facilities Team. You will perform planned and reactive calibration, maintenance and fault diagnosis across site instrumentation and control systems, ensuring safety, accuracy and GxP compliance. You will work with CMMS systems, support HVAC, reactor systems and cold rooms, and contribute to qualification activities for new or modified instrumentation while ...

Milton Keynes. The role focuses on delivering, upgrading and lifecycle management of validated automation systems, interfacing IT and OT, with a strong emphasis on GxP compliance and documentation in a regulated pharma environment. 6-month contract, ASAP start, full-time. #J-18808-Ljbffr ...