25 of 25 Remote/Hybrid GxP Jobs in the UK

configure and customise an ELN (Benchling preferable) or comparable laboratory informatics platform, including schemas, modules and custom workflows. Understanding of regulatory standards including GxP, ALCOA+ principles, and 21 CFR Part 11 requirements. Desirable: Knowledge and understanding of the cell and gene therapy industry. Experience designing and implementing system integrations using ...

primary business owner for the platformPartner with Biometrics, Data Science, IT, Quality, and external vendors to ensure platform reliability, compliance, and business value.Ensure GxP compliance, validation, inspection readiness, and data integrity requirements.Translate clinical analysis and reporting requirements into scalable platform capabilities supporting regulatory submissions and evidence generation.Drive adoption of modern ...

single platform or technology. Experience working in complex, cross-functional enterprise environments. Experience with cloud-based data and integration architectures. Experience with regulated/GxP environments preferred. Skills/Specialist Knowledge Strong knowledge of enterprise data architecture and solution architecture principles. Advanced data modeling skills, including conceptual, logical, dimensional ...

with infrastructure considerations (networking, hosting, security, etc.) in enabling on-premise and cloud IT solutions. Knowledge of data integrity and compliance standards within a GxP-regulated environment (e.g., 21 CFR Part 11). Solution architecture certifications for Microsoft Azure or Google Cloud Platform. Experience working in a product operating model ...

Engineering or a related field. Significant’ experience in a Systems Analysis, Business Analysis or related analytical role. Experience of software delivery activities within a GxP/pharmaceutical/other regulated environment. Demonstrable experience of leading, supervising or line-managing a team of analysts or related professionals. A record of being ...

Annex 11 Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability to quickly understand business requirements and design creative solutions Excellent verbal and written communication skills Experience in the Life Sciences Quality, Manufacturing, or Healthcare spaces ...

software implementation Excellent verbal and written communication skills and the ability to engage with senior/executive‐level stakeholders Good understanding of SaaS and GxP principles Ability to travel 25-50%; easy access to an airport Must be legally authorized to be employed in the EU. Veeva Systems does ...

type of person who loves experimenting, learning new frameworks, or building side projects in your spare time. (Bonus: Experience or familiarity with GxP/GDPR or the Pharmaceutical industry is a nice-to-have, but certainly not a dealbreaker!) What we offer in return Flexible benefits package Opportunities for learning ...

Pharmaceutical or Life Sciences industryFunctional knowledge of Clinical, Regulatory, Quality, or Safety business processesPrevious Project Management exposure for complex enterprise software implementationsFamiliarity with GxP and software validation regulationsDeep understanding of the migration verification and reconciliation processCoding experience, particularly with Java or PythonInterviewing with VeevaWe value your time and believe ...

Strong interpersonal skills with the confidence to articulate technical concepts, present ideas, and engage directly with senior business leaders.(Bonus: Experience or familiarity with GxP/GDPR or the Pharmaceutical industry is a nice-to-have, but certainly not a dealbreaker!)**What we offer in return**Flexible benefits packageBuilding ...

systems. The role is remote with an initial 6-month contract for a high-impact life sciences programme, requiring extensive experience in GMP/GxP and cybersecurity within #J-18808-Ljbffr ...

enhancements and new implementations. You will be responsible for generating validation documentation and ensuring systems are maintained in a validated state, compliant with GxP and data integrity requirements.Stakeholder Collaboration: Work closely with Manufacturing Operations, Quality Assurance, and Process Science teams to gather system requirements and provide updates on technical activities.User … Emerson Syncade, POMSnet).Manufacturing Environment Experience: Experience working directly in a manufacturing environment, preferably within the pharmaceutical, biologics, animal health, or another GxP-regulated industry.Regulatory Knowledge: A working knowledge of GxP (Good Manufacturing Practices) and familiarity with computer system validation (CSV) principles.Process Control Understanding: Familiarity with industrial automation concepts, including ...

trails, electronic signatures, role-based access, segregation of duties, data integrity, master data, time synchronisation and lifecycle controls . Ensure architectural decisions support GMP, GxP, data integrity, patient safety, product quality and inspection readiness . Partner with Engineering, Automation, Manufacturing, Quality, Validation, Cybersecurity, Infrastructure, Data, Applications and senior site stakeholders. … have: Strong experience designing OT/IT architectures within pharmaceutical, life sciences, chemical, food & beverage or similarly regulated manufacturing environments . Strong understanding of GxP/GMP regulated environments and the implications these have on technology architecture. Experience with IT/OT convergence and industrial control environments . Strong understanding ...

computerised-system lifecycle in Stevenage. You will partner with Quality, Manufacturing, Engineering and IT to deliver compliant CSV solutions across GxP operations in CAR‐T cell therapy manufacturing. The role requires 5+ years in validation, strong GAMP5 knowledge, data integrity and regulatory-inspection experience, plus excellent technical writing and cross ...

regulatory requirements into practical, compliant solutions that support innovation Quality Management & Digital (QM&D) is responsible for the Innovative Medicine Quality Management System (IMQS), GxP ownership, and global Quality Management processes. Within QM&D, the Process & Data Management (PDM) team works with partners across Therapeutic Areas, Global Development, Global Regulatory … solutions that support business needs throughout the development lifecycle.In this role, you will contribute to improvement and compliance programs that require expertise across the GxP Quality Management System. Activities include Adopting Regulatory Requirements (ARR), Quality Framework integration, and strategic R&D Quality initiatives. The position evaluates, compares, maps, and integrates ...

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 ...

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 ...

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 ...

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 ...

datasets. Quality & AI-Driven Compliance: Lead Test-Driven Development (TDD) and Behavior-Driven Development (BDD) initiatives. Use AI test generators to produce HIPAA/GxP-compliant synthetic clinical trial datasets for automated validation. Leverage AI tools to auto-draft validation artifacts, data lineage manifests, and audit documentation required under GxP … quality checks. Domain & Regulatory Awareness: Strong foundational understanding of clinical trial data workflows (e.g., EDC architectures), healthcare data models, and life science compliance standards (GxP, HIPAA, GDPR), with the ability to apply AI/ML tools for schema mapping and zero-loss data integrity verification . Base ...

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 ...

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 ...

will work closely with cross-functional global teams to provide GCP support for Veeva products in varying Services areas by promoting GCP compliance, authoring GxP documents and records, reviewing project implementation deliverables, incident management review, and performing occasional supplier assessments. What You'll Do Verify compliance to applicable policies, procedures … work instructions and regulations in GCP project implementations Perform GxP/Quality review of various records, including project implementation deliverables Document audit findings and supports remediation efforts to project audit observations Promote GCP compliance by authoring records (e.g., project audit reports) Perform process improvement activities and incident/CAPA investigations ...

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 Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. As an equal opportunity ...