25 of 25 Permanent GxP Jobs in London

integration patterns. Document application behavior, technical designs, and operational procedures. Ensure solutions align with healthcare privacy, security, and regulatory expectations including HIPAA, GDPR, and GxP-aligned practices where applicable. Mentor other engineers and contribute to engineering standards, code quality, and technical best practices. Required Knowledge, Skills and Abilities Strong proficiency ...

across IT and the wider business. Fluent English. Desirable experience Experience in biopharma, life sciences, healthcare, R&D or another regulated environment. Familiarity with GxP, GLP, GDPR, validated systems, data integrity, research collaborations or contractual partner obligations. Experience with recognised cybersecurity frameworks and standards such as NIST ...

4HANA Finance and Controlling (FI, CO, Product Costing, Profitability Analysis & Project Systems). Map life sciences business processes into SAP while ensuring alignment with GxP, SOX compliance needs. Deep expertise in Universal Journal (ACDOCA), New GL, Asset Accounting, Material Ledger & Actual Costing, Transfer Pricing (multiple valuation), Margin Analysis ...

implementation and scaling of AI solutions across GPS, ensuring solutions are fit‐for‐purpose and deliver measurable value Ensure AI‐enabled solutions comply with GxP, validation, data integrity, privacy, and regulatory requirements Partner with key technology teams (e.g., GD IT, Cloud, Dev Ops, AI & Digital, Compliance) to ensure technology alignment ...

implementation and scaling of AI solutions across GPS, ensuring solutions are fit-for-purpose and deliver measurable value Ensure AI-enabled solutions comply with GxP, validation, data integrity, privacy and regulatory requirements Partner with key technology teams (e.g., GD IT, Cloud, Dev Ops, AI & Digital, Compliance) to ensure technology alignment ...

governance, portfolio management, planning, risk and dependency management capability. Desirable Experience within Life Sciences, Consumer Healthcare, Pharmaceuticals or Medical Devices sectors. Experience operating within GxP-regulated environments. Experience supporting technology delivery for manufacturing operations and global manufacturing sites. Understanding of ERP platforms and associated infrastructure landscapes. Knowledge of technology delivery ...

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 ...

industry role Experience working with one or more R&D operational roles (clinical operations, regulatory, safety or similar discipline) either in industry or consulting GxP System Implementation and Validation experience Desired Requirements: Experience supporting implementations of cloud-based enterprise software such as Veeva Vault, Oracle, Medidata or OpenText At Syneos ...

industry role Experience working with one or more R&D operational roles (clinical operations, regulatory, safety or similar discipline) either in industry or consulting GxP System Implementation and Validation experience Desired Requirements: Experience supporting implementations of cloud-based enterprise software such as Veeva Vault, Oracle, Medidata or OpenText Why Syneos ...

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) Experience with product pre-sales, solution consulting, or engagement management Fluency in Italian, French, or German SaaS/ ...

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 Veeva’s headquarters is located ...

Experience managing third-party/vendor risk for SaaS and AI tooling. Nice to have Exposure to life sciences or pharma, and awareness of GxP, GDP, or healthcare data considerations (e.g., HIPAA for US-facing work). Experience establishing data-protection or data-risk practices. Experience supporting ...

Recursion is seeking a platform engineer to build, scale, and operate a validated data platform in London. You will be responsible for handling massive datasets, ensuring data integrity, and mentoring across teams. The role is ...

Title: QA/GxP Lead Job Type: Full-time, permanent Location: London, UK - Hybrid Remuneration: Up to £90,000 Cpl Life Sciences is partnering with an innovative biotech company to appoint a QA/GxP Lead to support a late-stage clinical development programme. This is an excellent opportunity … supplier management activities. Ensure compliant management of investigational products throughout the clinical supply chain. Computerised Systems & Data Integrity Support validation and oversight of GxP-relevant computerised systems. Ensure compliance with data integrity requirements and electronic records regulations. Contribute to quality risk assessments relating to digital platforms and emerging technologies. Inspection ...

Strong understanding of healthcare and life sciences workflows (e.g., drug discovery, clinical trials, regulatory submissions, market access) Familiarity with data privacy and compliance (HIPAA, GxP) Demonstrated ability to design and execute complex deal and partnership strategies You might thrive in this role if you: Are customer-centric and can translate ...

skills: End User Computing/Desktop Support Active Directory & Windows environments Hardware, software & network troubleshooting IP networking, subnetting & OSI model IT/OT environments GxP/regulated laboratory environments ServiceNow Endpoint security & device imaging You'll support laboratory systems, onboard and secure new devices, troubleshoot scientific equipment connectivity, manage incidents ...

role Certified auditor Minimum 10 years auditing experience. At least 30 audits in one or more of these areas: Computer System Validation (CSV), IT GxP compliance, AI GxP compliance, electronic data integrity. Minimum 15 years in Pharma/Med Device industry Fluent in English and ideally one other EU language … applications. Experience in validation of multiple system delivery models including SaaS, PaaS, IaaS, and On Prem. Basic understanding of AI use cases and emerging GxP compliance requirements Experience in authoring policies and procedures (SOPs). Experience conducting audits and gap assessments. Experience managing internal personnel, contract resources, and projects. Expert ...

role Certified auditor Minimum 10 years auditing experience. At least 30 audits in one or more of these areas: Computer System Validation (CSV), IT GxP compliance, AI GxP compliance, electronic data integrity. Minimum 15 years in Pharma/Med Device industry Fluent in English and ideally one other EU language … applications. Experience in validation of multiple system delivery models including SaaS, PaaS, IaaS, and On Prem. Basic understanding of AI use cases and emerging GxP compliance requirements Experience in authoring policies and procedures (SOPs). Experience conducting audits and gap assessments. Experience managing internal personnel, contract resources, and projects. Expert ...

Ipsen in the United Kingdom is seeking a Senior GCP/GCLP Quality Auditor to lead audits across GxP environments. You will manage audit planning, execution, reporting and CAPA oversight, acting as a trusted SME to advise stakeholders and support regulatory inspections. The role requires the Lead Auditor certification ...

applicable regulations, and internal quality standards. Lead the implementation, improvement and validation of new processes, procedures, and IT systems (e.g., eQMS, eTMF) to support GxP compliance and operational excellence. Oversee internal and external audits, including regulatory inspections, ensuring findings are addressed promptly and effectively Cross-Functional Collaboration & Leadership Partner with … Clinical Operations, IT, Engineering, and Science Teams to integrate quality and regulatory requirements into digital platforms, AI-enabled solutions, and GxP-relevant systems. Embed a culture of quality awareness through training, workshops, and mentoring, ensuring all staff are competent and compliant with GCP, ISO standards, and internal policies. Support ...

Consulting in the UK seeks an experienced Pharma Quality Specialist Consultant to join its Life Sciences team. You will design and transform GxP QMS, advise on GMP, GDP, GCP and GLP compliance, and lead quality transformations across R&D, manufacturing and distribution. You will oversee CSV activities, supplier quality, regulatory ...

drug development. Key Requirements: 10+ years' experience within biopharma, clinical trials, healthcare technology. Strong experience supporting Clinical Trial Applications (CTAs), drug development programmes, or GxP-regulated clinical environments. Experience leading senior discussions around business strategy for developing products and taking these products to health authorities. Confident in leading … engineering best practices. Experience collaborating with cross-functional teams across Engineering, Data Science, Product, and Quality. Strong knowledge of QMS, Computer System Validation (CSV), GxP, GAMP 5, ICH-GCP, and 21 CFR Part 11. Familiarity with evolving AI regulations, including the EU AI Act and FDA/EMA guidance ...

experience Knowledge of SaaS products and landscape Strong business process analysis and design experience Hands-on product design/digital product experience Experience with GxP-regulated applications/products Workshop facilitation to help harmonize divergent business processes into one target design Rapid wireframing/prototyping (Figma or similar) to validate … experience in business analysis, process design, product design, or business transformation roles. Understanding of pharmaceutical R&D and supply chain processes in a regulated (GxP) environment. Proven ability to translate business requirements into solution designs and product features. Key qualities Strong collaboration and influencing skills across functions and levels. Ability ...

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 ...

Business Analyst — LabWare LIMS (Pharma) 📍 London (Hybrid, 3 days on-site/week) ⏳ 3-month contract intiially (extendable) 💷 £300-340/day, Inside IR35 A pharmaceutical client is looking for a LabWare LIMS Business Analyst ...