26 to 50 of 118 GxP Jobs in the UK

with organisations operating in highly regulated and complex environments. Your experience in any of the following would be advantageous: Life SciencesPharmaceuticalsBiotechnologyMedical DevicesRegulated ManufacturingExperience with: GxP environments21 CFR Part 11 and EU Annex 11 complianceElectronic records and audit requirementsContract Manufacturing (CMO/CDMO)Batch manufacturing and lot genealogyQuality and release managementCold ...

with organisations operating in highly regulated and complex environments. Your experience in any of the following would be advantageous: Life SciencesPharmaceuticalsBiotechnologyMedical DevicesRegulated ManufacturingExperience with: GxP environments21 CFR Part 11 and EU Annex 11 complianceElectronic records and audit requirementsContract Manufacturing (CMO/CDMO)Batch manufacturing and lot genealogyQuality and release managementCold ...

with organisations operating in highly regulated and complex environments. Your experience in any of the following would be advantageous: Life SciencesPharmaceuticalsBiotechnologyMedical DevicesRegulated ManufacturingExperience with: GxP environments21 CFR Part 11 and EU Annex 11 complianceElectronic records and audit requirementsContract Manufacturing (CMO/CDMO)Batch manufacturing and lot genealogyQuality and release managementCold ...

with organisations operating in highly regulated and complex environments. Your experience in any of the following would be advantageous: Life SciencesPharmaceuticalsBiotechnologyMedical DevicesRegulated ManufacturingExperience with: GxP environments21 CFR Part 11 and EU Annex 11 complianceElectronic records and audit requirementsContract Manufacturing (CMO/CDMO)Batch manufacturing and lot genealogyQuality and release managementCold ...

with organisations operating in highly regulated and complex environments. Your experience in any of the following would be advantageous: Life SciencesPharmaceuticalsBiotechnologyMedical DevicesRegulated ManufacturingExperience with: GxP environments21 CFR Part 11 and EU Annex 11 complianceElectronic records and audit requirementsContract Manufacturing (CMO/CDMO)Batch manufacturing and lot genealogyQuality and release managementCold ...

with organisations operating in highly regulated and complex environments. Your experience in any of the following would be advantageous: Life SciencesPharmaceuticalsBiotechnologyMedical DevicesRegulated ManufacturingExperience with: GxP environments21 CFR Part 11 and EU Annex 11 complianceElectronic records and audit requirementsContract Manufacturing (CMO/CDMO)Batch manufacturing and lot genealogyQuality and release managementCold ...

skills. Experience managing suppliers or third-party service providers. Experience within regulated industries such as life sciences, pharmaceuticals, biotechnology, or clinical research. Knowledge of GxP, ISO 27001, or similar compliance frameworks. Relevant Microsoft, Citrix, VMware, or security certifications. Personal Attributes Collaborative and approachable leadership style. Able to balance strategic thinking ...

Data Protection Act**: Ensure all IT practices comply with data privacy regulations in the EU and UK.* **Pharma-Specific Regulations**: Familiarity with GxP (Good Practices) and other quality standards commonly required in the pharmaceutical industry. #J-18808-Ljbffr ...

leadership, and the front door through which site requirements are captured, shaped, and routed into the correct cross-functional platform backlog.Operating within highly regulated GxP and SOX environments, this role remains accountable for operational excellence, financial stewardship, and risk management across a complex laboratory technology landscape, including ownership ...

with both scientific and business audiences Familiarity with European data privacy and health data frameworks, including GDPR, the EU Health Data Space (EHDS) regulation, GxP requirements, and EMA guidance on AI/data‐driven technologies The annual compensation range for this role is listed below. For sales roles, the range ...

teams (e.g., bioinformatics, wet lab, clinical research) Experience designing systems that manage laboratory or bioinformatics data (e.g., LIMS, sequencing pipelines, assay metadata) Familiarity with GxP practices and regulatory reporting requirements in clinical studies is a plus Prior experience working in biotech, diagnostics, or life sciences companies Experience supporting sample tracking ...

credibly with both scientific and business audiencesFamiliarity with European data privacy and health data frameworks, including GDPR, the EU Health Data Space (EHDS) regulation, GxP requirements, and EMA guidance on AI/data-driven technologiesThe annual compensation range for this role is listed below. For sales roles, the range provided ...

mindset, make resource trade-offs, and drive measurable commercial outcomes. Navigate the tension between speed-to-market and regulatory compliance (GxP, 21 CFR Part 11, GDPR, HIPAA). Cultivate strategic partnerships with data providers and standards bodies (CDISC, HL7 FHIR) to accelerate Evinova's product capabilities. Champion a culture ...

reporting. Strong knowledge of GCLP/GLP guidelines preferred and requirements for phase‐appropriate validation for clinical trial biomarker/endpoints; familiarity with GxP/MHRA/GCLP/ICH expectations and inspection readiness. Proficiency with library prep (amplicon, hybrid capture, poly(A)/RNA workflows), nucleic acid extraction from ...

Data & Compliance Mastery: Experience navigating security frameworks (ISO 27001, ISO 42001) or strict data privacy and validation standards common in health tech or pharma (GxP, FDA, EU AI Act).Advanced Coding & DevSecOps Mastery: Proficiency in Python or Go, alongside deep expertise in automated CI/CD security tooling, Terraform ...

core ML backends.Regulated Environments: Prior exposure to BioTech, Pharma, and/or Deep Tech industries where data integrity, intellectual property protection, and regulatory compliance (GxP) are paramount.Education & Background: BSc, MSc, or PhD in Computer Science, Machine Learning, Cybersecurity, or a related quantitative field.Advanced Certifications: Relevant security or cloud credentials (e.g. ...

comparable regulatory systems experience will be considered. Strong requirements gathering, process mapping and stakeholder management skills. Agile experience, including user stories and backlog management. GxP/FDA or Computer System Validation experience would be advantageous. This is an excellent opportunity for a strong Regulatory Business Analyst to join a global ...

comparable regulatory systems experience will be considered. Strong requirements gathering, process mapping and stakeholder management skills. Agile experience, including user stories and backlog management. GxP/FDA or Computer System Validation experience would be advantageous. This is an excellent opportunity for a strong Regulatory Business Analyst to join a global ...

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 ...

Annex 11Proven ability to work both independently and in teams in a dynamic, fast-moving environmentGood understanding of SaaS and GxP principlesAbility to quickly understand business requirements and design creative solutionsExcellent verbal and written communication skillsExperience in the Life Sciences Quality, Manufacturing, or Healthcare spacesExperience with Data or Content Management ...

within regulated industries , such as Life Sciences, Pharmaceuticals, Chemicals or Manufacturing PRINCE2, PMP, APM PMQ or equivalent project management qualification Desirable Experience Knowledge of GxP validation or validated system implementations Experience delivering global software rollouts across multiple sites Strong commercial awareness, including experience managing project financials, budgets and contract scope ...

projects within regulated industries, such as Life Sciences, Pharmaceuticals, Chemicals or ManufacturingPRINCE2, PMP, APM PMQ or equivalent project management qualification Desirable Experience Knowledge of GxP validation or validated system implementationsExperience delivering global software rollouts across multiple sitesStrong commercial awareness, including experience managing project financials, budgets and contract scope The Company ...

projects. Familiarity with common enterprise services (Directory Services, Information Assurance, Identity and Access Management, etc.), products (i.e., Oracle, SAP) and frameworks (ITIL, Zachman, TOGAF, GxP, HIPAA, etc.) Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions ...

twins, simulation environments, and human-in-the-loop workflows.Develop production readiness criteria for AI systems operating in Development environments.Support technical validation activities required for GxP-relevant and regulated AI systems.Ensure AI systems are tested under realistic operating conditions and supported by objective validation evidence.Reliability, Monitoring & PerformanceDefine how AI system reliability ...