126 to 150 of 156 GxP Jobs in the UK

outcomes, evidence, risk and enterprise value.• Communicate complex concepts clearly and influence without direct authority.8. Regulated Environment, Quality & Controls• Ensure solution designs support applicable GxP, SOX, privacy, cybersecurity and medical device quality requirements.• Apply risk-based thinking to validated systems, electronic records, audit trails, access controls and data integrity.• Partner … governance.• Excellent business process analysis, communication, facilitation and stakeholder influencing skills.Desirable• Experience in medical device, life sciences, pharmaceutical or similarly regulated environments.• Knowledge of GxP, computer system validation, SOX controls and data integrity.• Experience with Salesforce integrations and customer-facing platforms.• Knowledge of SAP Integration Suite, SAP Build, SAP Datasphere ...

pharmaceutical manufacturing sites. This individual will play a key role in PAS-X solution design, integration, process standardization, testing, and deployment within a regulated GxP environment. The successful candidate will bring strong expertise in Werum PAS-X , pharmaceutical manufacturing processes, SAP integration, and Electronic Batch Record (EBR) solutions. Key Responsibilities … with Crystal Reports and/or Jaspersoft is highly desirable. Industry Experience Pharmaceutical, Biotechnology, or Life Sciences industry background. Strong understanding of: ISA-95 GxP Computer System Validation (CSV) Preferred Qualifications Experience supporting global template deployments and multi-site rollouts. Strong communication and stakeholder management skills. Ability to work effectively ...

About TetraScience TetraScience is the Scientific Data and AI Company building Tetra OS, the operating system for scientific intelligence. We help the world’s leading life sciences firms turn fragmented scientific data into AI-native ...

Senior IT Project Manager - OT Security & Secure File Transfer in Pharma Full-time Transforming Life Science Consulting Worldwide. Fusion Consulting is a globally leading Business and IT boutique consultancy specialized in the Life Sciences industry ...

Intelance, a UK-based technology, AI and cyber assurance firm, is seeking a freelance due diligence reviewer to assess GxP validated software used in drug development. You will work remotely in the UK, with occasional London meetings, delivering findings for client reports. The role requires deep experience in computerised system ...

Architecture, Data Governance, Information Security and Quality & Compliance. You will turn business needs into production-grade solutions that are secure, traceable and, where required, GxP-compliant - taking my client step by step from AI assistants to supervised and orchestrated agents. Essential Technical Skills Experience: At least 4 years in software … through REST APIs. Engineering practices: Git, CI/CD, containerisation (Docker), cloud services (AWS) and observability (logging, tracing, metrics). Regulated environments: Understanding of GxP, computer system validation, data privacy and reproducibility for AI in a regulated industry. Communication: Explains complex technical choices in plain language to non-technical stakeholders ...

portfolio, resourcing, and operational metrics. Shared Foundations: Build and govern a centralized library of reusable AI skills, connectors, and evaluation benchmarks across the organization. GxP & Trust by Design: Partner with Quality & Compliance to establish validation pathways, deterministic guardrails, human-in-the-loop controls, and audit trails. Technical Leadership & MLOps: Establish … deployment. Visualization: Solid experience with R Shiny or Shiny for Python. Governance & Mindset: Working knowledge of validation, auditability, data privacy, and security (GxP/regulated environment awareness) with strong cross-functional communication skills. Preferred Qualifications The following qualifications are advantageous: Advanced degree (Master's or Ph.D.) in Computer Science ...

portfolio, resourcing, and operational metrics. Shared Foundations: Build and govern a centralized library of reusable AI skills, connectors, and evaluation benchmarks across the organization. GxP & Trust by Design: Partner with Quality & Compliance to establish validation pathways, deterministic guardrails, human-in-the-loop controls, and audit trails. Technical Leadership & MLOps: Establish … deployment. Visualization: Solid experience with R Shiny or Shiny for Python. Governance & Mindset: Working knowledge of validation, auditability, data privacy, and security (GxP/regulated environment awareness) with strong cross-functional communication skills. Preferred Qualifications The following qualifications are advantageous: Advanced degree (Master's or Ph.D.) in Computer Science ...

features across asset teams; contracting vendors on outcomes and holding teams to account for quality, pace and measurable value. Embed quality, risk and compliance - GxP, privacy and AI governance - from the outset, ensuring transparent, auditable platforms and good hygiene in core systems of record. Build trusted partnerships and influence … building high-performing product teams. Experience delivering AI, data and analytics-enabled products on modern data platforms and cloud technologies. Experience operating in a GxP/validated-systems context, with strong data integrity, quality and compliance judgement. Preferred Qualifications If you have the following characteristics, it would be a plus ...

Resources is seeking a Validation Tester to support a global programme delivering Computer System Validation (CSV), Computer Software Assurance (CSA) and risk management across GxP-regulated systems in the Life Sciences sector. The role is fully remote in the United Kingdom, with exposure to regulated environments and collaboration with cross ...

Global Resources seeks a Validation Tester to support a global programme delivering Computer System Validation (CSV), Computer Software Assurance (CSA) and risk management across GxP-regulated systems in Life Sciences. This role is remote, challenging, and highly regulated, offering opportunities to contribute to enterprise IT validation efforts. You will design ...

supporting business- critical production systems. Develop target-state architectures and migration strategies for large-scale technology modernisation initiatives. Ensure solutions comply with GMP/GxP requirements, validation standards, cybersecurity frameworks, and industry best practices. Experience required Extensive experience as a Solutions Architect, Enterprise Architect, or Technical Architect within regulated manufacturing … including industrial systems, plant infrastructure, and manufacturing technology. Proven experience delivering complex IT infrastructure transformation and migration programmes. Significant cybersecurity experience within GMP/GxP-regulated environments. #J-18808-Ljbffr ...

Foundation Creation: Establish and govern a library of reusable AI components, promoting efficiency across the organisation. Regulatory Compliance: Collaborate with Quality & Compliance to ensure GxP compliance and validation for AI applications. Operational Evaluation: Define metrics for performance, monitor quality, and maintain comprehensive documentation and runbooks. Technical Leadership: Set standards … APIs, SQL, Snowflake, and REST APIs. Engineering Practises: Skilled in Git, CI/CD, Docker, AWS, and observability tools. Regulatory Knowledge: Familiarity with GxP, data privacy, and reproducibility in regulated environments. Communication Skills: Ability to articulate complex technical concepts to non-technical stakeholders and translate business requirements into clear technical ...

help Data Scientists move code from notebooks into tested workflows Make sure pipelines support the traceability and change control expected in a regulated, GxP environment What we need Proven experience as a Data Engineer or clinical data programmer, ideally working closely with data scientists, analysts or researchers Hands‐on experience … environments e.g. Docker, Kubernetes Experience with medical imaging data e.g. CT or MRI in DICOM format or clinical trial data Experience working in regulated, GxP or ISO 13485 environments Experience in respiratory or interstitial lung disease trials What can you expect from us A comprehensive benefits package that includesan annual ...

help Data Scientists move code from notebooks into tested workflows Make sure pipelines support the traceability and change control expected in a regulated, GxP environment What we need Proven experience as a Data Engineer or clinical data programmer, ideally working closely with data scientists, analysts or researchers Hands‐on experience … environments e.g. Docker, Kubernetes Experience with medical imaging data e.g. CT or MRI in DICOM format or clinical trial data Experience working in regulated, GxP or ISO 13485 environments Experience in respiratory or interstitial lung disease trials What can you expect from us A comprehensive benefits package that includesan annual ...

MedPharm Ltd in the United Kingdom seeks a Computer System Validation (CSV) Specialist to govern validation of GxP‐relevant computerised systems on site, ensuring compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, and GAMP5 principles. The role provides technical oversight of electronic systems, manages validation activities, and closes ...

Norgine is seeking a Computer Systems Validation Engineer in Hengoed for a 12-month fixed-term contract. You will guide validation of GxP-regulated computerised systems, ensuring data integrity and regulatory compliance across the system lifecycle. You will develop validation plans, perform testing, support audits and collaborate with Quality, Manufacturing ...

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 ...

controlled software or configuration changes to decouple equipment, documenting all updates under approved change control Execute automation and control system decommissioning pre‐requisites for GxP and non‐GxP equipment, ensuring data integrity and regulatory compliance Manage decommissioning of pharmaceutical production equipment, ancillary support systems, and facility plants (excluding HVAC/ ...

Build natural-language interfaces and dashboards over business data for actionable insights. Shared Foundation: Create and govern reusable AI components for cross-team use. GxP Compliance: Collaborate with Quality & Compliance teams to ensure regulated AI use cases meet validation requirements. Evaluation & Operations: Define test sets, monitor solution performance, and maintain … integration with enterprise systems (e.g., Snowflake, REST APIs). Familiarity with Git, CI/CD, Docker, AWS, and observability tools. Regulated Environments: Understanding of GxP, computer system validation, and data privacy in regulated industries. Communication: Ability to explain technical concepts to non-technical stakeholders and translate business needs into technical ...

Corporate Functions. Drive modernisation and rationalisation where it improves speed, resilience, cost or user experience. Risk, Compliance and Resilience Embed security, privacy, resilience, GxP and regulatory compliance into technology design without slowing delivery unnecessarily. Make balanced risk decisions that support innovation in a regulated environment. Leadership and Culture Build … outcomes Desirable Pharmaceutical, life sciences, healthcare or regulated‐industry experience Experience in a digital‐native, product‐led or platform‐led technology organisation Knowledge of GxP, clinical systems, R&D, manufacturing or commercial technology landscapes MBA, advanced technical degree or equivalent experience Skills and Capabilities Strategic technology leadership Product mindset ...

fully aligned, informed, and motivated to achieve world-class results Requirements Extensive program leadership experience (7+ years) delivering enterprise-scale R&D or GxP technology programs in Pharma (Clinical, Regulatory, or Safety) Deep understanding of Pharmaceutical R&D functions such as Clinical Operations, Regulatory Affairs, Safety, Quality, or Manufacturing Proven … Veeva Vault implementation (e.g., Clinical, RIM, Quality, Safety) Previous experience with large-scale Software as a Service (SaaS) implementations in the highly regulated GxP environment Interviewing with Veeva We value your time and believe in a transparent hiring process. Here is the process you can expect. Within 3 days ...

standards, including Human‐in‐the‐Loop design, ethical AI principles, and the use of approved technology only. Maintain strong awareness of data privacy and GxP requirements given the sensitivity of working within a pharma R&D environment, ensuring solutions are compliant, auditable, and safe to scale. Secure & Compliant Working Practices … responsible AI concepts such as Human‐in‐the‐Loop design, ethical AI, and data privacy, with an appreciation for why these matter in a GxP/pharma R&D setting. Technical Skill Requirement Programming Foundations: Working proficiency in at least one language commonly used in data/automation work (e.g. ...

standards, including Human-in-the-Loop design, ethical AI principles, and the use of approved technology only. Maintain strong awareness of data privacy and GxP requirements given the sensitivity of working within a pharma R&D environment, ensuring solutions are compliant, auditable, and safe to scale.* **Secure & Compliant Working Practices … responsible AI concepts such as Human-in-the-Loop design, ethical AI, and data privacy, with an appreciation for why these matter in a GxP/pharma R&D setting. **Technical Skill Requirement*** **Programming Foundations:** Working proficiency in at least one language commonly used in data/automation work (e.g. ...

Replimune is seeking a Laboratory GxP Systems Administrator to own the administration, validation and compliance of laboratory systems in a regulated environment. This role is based at Milton Park with a five‐day on‐site expectation. You will manage access controls, inventories, change controls, audits, data integrity, cybersecurity and vendor ...