1 to 25 of 37 Permanent GxP Jobs in the UK excluding London

storage and endpoint management solutions Experience working within a pharmaceutical, biotechnology, medical device or similarly regulated environment would be highly desirable An understanding of GxP, GMP, GAMP 5, Annex 11 and 21 CFR Part 11 would be advantageous Strong understanding of IT service management and ITIL principles Excellent analytical ...

engineering discipline, or relevant product and AI certifications (e.g. Pragmatic Institute, Certified Scrum Product Owner, cloud/ML platform certifications). Working knowledge of GxP computerised system validation principles (e.g. GAMP 5) as applied to automated content-generation and reporting tools. Familiarity with CMC regulatory report types and submission formats ...

IMechE, IChemE and other professional bodies) Access to healthcare and wellbeing programs Employee recognition programs Skills Asset Life Cycle Management, Data Integrity, Digital Fluency, GxP Regulations, Lean Management, Manufacturing Technologies, Pharmaceutical Manufacturing, Problem Solving, Risk Awareness, Standards Compliance Why GSK? Unifying science, technology and talent to get ahead of disease ...

IMechE, IChemE and other professional bodies) Access to healthcare and wellbeing programs Employee recognition programs Skills Asset Life Cycle Management Data Integrity Digital Fluency GxP Regulations Lean Management Manufacturing Technologies Pharmaceutical Manufacturing Problem Solving Risk Awareness Standards Compliance Why GSK? Uniting science, technology and talent to get ahead of disease ...

careers/orion-as-an-employer/. We are seeking an individual with experience in pharma or industrial environments, including an understanding of GxP compliance and IT support in regulated environments. Skills & Qualifications: Technical Proficiency: Windows, macOS, Microsoft 365, Active Directory, VPN, remote desktop tools, and enterprise applications. Customer ...

resolving complex cloud infrastructure issues. Excellent communication and stakeholder management skills, able to explain technical trade‐offs to non‐technical audiences. Familiarity with GxP and GAMP5 frameworks, and experience supporting regulated (validated) cloud systems. **Preferred Qualifications:** Experience with multi‐cloud strategies and hybrid cloud architectures Knowledge of Kubernetes and container ...

testable requirements and operational evidence; contribute to threat modeling and risk assessment using leading frameworks; support risk-tiered controls across research, business, regulated and GxP-relevant use cases; document residual risk, control limitations, exceptions and approvals to enable defensible decisions; engage vendors and peers to evaluate capabilities and shape adoption ...

Finance and integrated processes. You will guide delivery teams and AMS partners, manage complex changes, and support new entity setups, with a focus on GXP/Quality compliance and global scalability. Hybrid work in Cambridge or London. #J-18808-Ljbffr ...

strategic and hands-on levels in a fast-moving, international business. Preferred Experience Experience supporting operations across both the UK and US. Knowledge of GxP, clinical trial systems, health data, sponsor audits or regulated research operations. Experience establishing AI governance, enterprise data standards or analytics platforms. CISSP, CISM, CRISC ...

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 ...

tooling (for example, Azure/AWS, Databricks, Snowflake, data quality and lineage tools). Background in highly regulated industries and privacy regimes (for example, GxP, HIPAA, GDPR) and their application to data access, retention and disposal. Service design and product analytics experience to measure adoption, usability and value realisation. FinOps ...

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 ...

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 ...

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 ...

opportunity for a Computer Systems Validation Engineer to join Norgine in Hengoed. The Role: In this role, you will help ensure that Norgine's GxP-regulated computerised systems, equipment, validation documentation and associated processes meet applicable quality and regulatory requirements. You will provide practical validation expertise throughout the system lifecycle … effectiveness. This is a 12-month fixed-term contract (FTC) role Key Responsibilities: Plan, coordinate and carry out validation activities for new and existing GxP-regulated computerised systems. Develop, review and maintain validation plans, risk assessments, protocols, test scripts, reports and traceability matrices. Perform system testing and verification to confirm ...

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. ...

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 ...

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 (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 ...

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 ...