26 to 50 of 70 GxP Jobs in England

degree in computer science, Engineering, or related technical field. PREFERRED QUALIFICATIONS Familiarity with Generative AI infrastructure, evaluation frameworks, and integration patterns. Knowledge of GxP/regulated environments and qualification processes. Proven Track record of driving platform adoption and mentoring engineering teams. Experience in pharmaceutical, healthcare, or other highly regulated industries. ...

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 ...

Management), Modular Content, MLR review,and European regulatory requirements (e.g., ABPI, ANSM, AIFA) Understanding of life sciences compliance and computer systems validation requirements (e.g., GxP, GcP) Project management certification (e.g., PRINCE2, PMP) Veeva certification Experience with product pre‐sales, solution consulting, or engagement management Interviewing with Veeva We value your ...

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 ...

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 ...

then appropriately evaluate, new tools and technologies 4. Experience testing randomization schemas 5. Knowledge of drug management 6. Familiarity with industry regulatory requirements (GxP) 7. Must possess a strong technical background in software and object-oriented systems development and testing, and be able to apply this knowledge to designing test ...

standards, and be the person others come to when infrastructure decisions matter. Bonus You've operated under formal security or compliance regimes (SOC2, HIPAA, GxP, or similar) and know how to make controls a strength rather than a tax Experience with Argo CD, EKS, or Terragrunt specifically What ...

improvement of the Company’s IT infrastructure. The IT Analyst role ensures the availability, reliability, security and compliance of IT systems supporting business and GxP activities. Working within a regulated environment, the position contributes to computer system validation, cybersecurity, data integrity, audit readiness and regulatory compliance. Your Responsibilities Infrastructure & Network … requests, problems and changes using ITIL principles. Maintain SLA performance and perform root cause analysis for recurring issues. Maintain IT asset and configuration records. GxP Compliance and Validation Responsibilities Support validated and regulated computer systems throughout their lifecycle. Participate in user requirements gathering, risk assessments, validation planning and test execution. ...

will bring a strong background in IT infrastructure, Windows Server, AD/GP, and virtualization (VMware/Hyper-V), with experience in regulated environments (GxP) being a plus. Expect 36-hour weeks and an on-site presence in Haverhill. #J-18808-Ljbffr ...

Kafka, develop backend services in Java or Scala on AWS, and apply AI-assisted tooling for schema mapping, testing, and validation, while ensuring GxP, HIPAA and GDPR compliance. #J-18808-Ljbffr ...

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 ...

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 … 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. ...

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 ...

Data Engineering team to align with common standards and best practices. The role focuses on developing end-to-end data infrastructure in a regulated, GxP environment, leveraging #J-18808-Ljbffr ...

with Data Engineers and Data Scientists, implement CDISC SDTM/ADaM, and apply best practices in data quality, versioning and regulatory compliance within a GxP environment. #J-18808-Ljbffr ...

with Data Engineers and Data Scientists, implement CDISC SDTM/ADaM, and apply best practices in data quality, versioning and regulatory compliance within a GxP environment. #J-18808-Ljbffr ...

pharmaceutical industry? Are you ready to challenge yourself in a highly-regulated and fast-paced environment? Are you experienced in IT Validation for GxP and enterprise systems and ready to work fully remote? You could be the perfect candidate for this opportunity! Don't hesitate, apply today! Job Description … seeking a Validation Tester to support a global programme delivering Computer System Validation (CSV), Computer Software Assurance (CSA) and risk management activities across GxP-regulated systems within the Life Sciences sector. Key Responsibilities 1. Requirements Analysis and Testability Assessment Review URS, FRS, Design Specifications and related documentation to assess completeness ...

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 ...

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 ...

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 (Inform, Rave, etc) Ability to engage … 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 ...

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 (Inform, Rave, etc) Ability to engage … 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 ...

Architect and develop API integrations (REST, GraphQL, JSON) connecting the ELN platform with upstream and downstream systems across R&D, Manufacturing and Regulatory, ensuring GxP and GDPR governance is respected across all data flows. Partner with the Product Manager and Principal Engineer to shape and size the product backlog, define … informatics platforms (e.g. Revvity Signals, Benchling, LabVantage) in a life sciences or pharmaceutical environment, including system integration and workflow automation. Understanding of GxP, data integrity and computer system validation requirements. Experience integrating AI and agentic workflows into custom software solutions. Working knowledge of data foundations and integration into downstream data ...

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 ...

maintain platform‐specific engineering principles, golden paths, coding/configuration standards, quality gates and reusable patterns. Embed secure‐by‐design, regulatory, privacy, resilience and GxP‐aware controls into engineering practices where applicable. Define guardrails for the appropriate use of AI‐assisted engineering tools, ensuring code, configuration, documentation and operational outputs … ITIL, TOGAF, cloud provider certifications, DevOps/DevSecOps, cyber security, reliability engineering or quality management where relevant to the platform domain. For regulated or GxP‐impacting platforms, awareness of applicable quality, validation and compliance expectations. Expert level enterprise networking certification, such as CCIE or JNCIE. Experience with Network/infrastructure ...