51 to 75 of 75 GxP Jobs in the UK excluding London

another regulated environment. Familiarity with document management or OCR tools. Experience using Jira and Confluence. Awareness of clinical governance or quality frameworks (for example GxP, ISO 13485, DCB0129/0160). What success looks like in the first 6 months Full ownership of e-sign configuration and first-line troubleshooting ...

intersection of Digital Technology, science, engineering, and business operations, ensuring that systems meet the highest standards of cybersecurity, data integrity, operational resilience, and GxP compliance. Who you'll work withYou will work closely with CMC Development Sciences scientists, Functional System Owners, business stakeholders, vendors, and Digital Technology colleagues to deliver … define implementation roadmapsLead solution design and coordinate implementation, integration, qualification, validation, testing, and transition into operation for new and existing systemsEnsure systems comply with GxP, cybersecurity, quality, regulatory, and service management requirements while maintaining data integrity, resilience, and business continuityCollaborate with vendors, DT teams, and service component owners to resolve ...

across DNA/RNA isolation, qPCR, ddPCR, RNA sequencing, MSD, ELISA and immunoblotting, establishing internal and partner bioanalytical capabilities while aligning with GLP and GxP expectations. #J-18808-Ljbffr ...

Technology Product Owner for Finance, leading Design Authority sessions, maintaining system roadmaps aligned with SAP S/4 standards, and ensuring full compliance with GXP/Quality Framework requirements.Solution Architecture & Strategy: Drive design conversations and business cases with senior stakeholders, providing functional direction to internal teams and 3rd-party delivery … inter-company transactions, banking connectivity, and regulatory requirements (LFR/IFRS).Preferred Qualifications & Background:Experience in Pharmaceuticals or highly regulated manufacturing/CPG environments (GXP exposure).Experience with connected finance systems (Esker, Concur) and cross-ERP knowledge (Oracle EBS).SAP Certification or Agile/Project Management delivery qualifications.Background in management ...

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 ...

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 ...

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 Ability to engage and influence business, quality … 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 ...

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 ...

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 ...

performance, including obsolescence management and application of functional and safety standardsDevelop and maintain procedures for integration of IT and IACS systems in both GxP and non-GxP environmentsSupport development of OT architecture, standards, and governance, and collaborate with global and local stakeholdersDrive communication and change management within engineering teams … 2700x and IEC 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 ...

Regulatory. Design and build scalable, full-stack solutions across front-end and back-end technologies, embedding security, privacy, data protection, and regulatory compliance (GxP, GDPR) into every digital solution. Partner with Product Owners, Product Managers, and Designers to shape the product backlog, validate feature feasibility, and translate business requirements into … culture, including CI/CD, Test-Driven Development (TDD), and Kubernetes-based deployment. Background in data engineering (Oracle, SQL, ETL) with an understanding of GxP and GDPR data governance, combined with strong communication skills across technical and business stakeholders in complex, regulated environments. What will give you a competitive edge ...

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 ...

extended its flexible, scalable solutions to the IDBS Polar and PIMS cloud platforms to help scientists make smarter decisions with assured confidence in both GxP and non GxP environments. The Principal Software Engineer (AI) will provide technical leadership in the design and delivery of production‐grade, GenAI‐enabled capabilities across … driving delivery in complex environments. Desirable (but not essential) Experience applying GenAI solutions in life sciences/biopharma contexts, including scientific, clinical, or regulated (GxP‐aligned) environments. Familiarity with building AI capabilities that support knowledge extraction, decision support, and workflow automation across enterprise data ecosystems, including cloud‐based platforms such ...

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 ...

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 ...