1 to 25 of 118 GxP Jobs in the UK

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 ...

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 APIs ...

required. Monitoring project performance and ensuring expected business benefits are realised. Collaborating with third-party suppliers to support project delivery. Working within regulated and GxP-compliant environments. About You You will have a degree in Computer Science, Information Technology, or a related discipline, or equivalent industry experience, alongside: 5+ years ...

archival strategies Familiarity with equipment qualification and validation processes (IQ/OQ/PQ) and how IT systems support thes Knowledge of regulatory requirements (GxP, 21 CFR Part 11, ISO standards) and their impact on research technology Familiarity with global IT service management practices (ITIL) and support models Location & Mobility ...

archival strategies Familiarity with equipment qualification and validation processes (IQ/OQ/PQ) and how IT systems support thes Knowledge of regulatory requirements (GxP, 21 CFR Part 11, ISO standards) and their impact on research technology Familiarity with global IT service management practices (ITIL) and support models Location & Mobility ...

making systems better for the people who use them, we want to hear from you. 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 ...

experience in enterprise data platforms, with a proven track record in regulated or fast-moving industries (e.g., Consumer Goods, Pharmaceuticals, Medical Devices) operating within GxP-compliant frameworks.Stakeholder Management: Exceptional communication skills with a proven ability to align regional/global workstream leaders, data engineering teams, and executive leadership.Preferred QualificationsA Bachelor ...

experience in enterprise data platforms, with a proven track record in regulated or fast-moving industries (e.g., Consumer Goods, Pharmaceuticals, Medical Devices) operating within GxP-compliant frameworks. Stakeholder Management: Exceptional communication skills with a proven ability to align regional/global workstream leaders, data engineering teams, and executive leadership. Preferred ...

particularly Emerson DeltaV, and HMI/SCADA platforms.Strong knowledge of process instrumentation principles, calibration techniques, troubleshooting methodologies, and industrial communication protocols.Experience working in a GxP/cGMP regulated environment, with knowledge of computerized system validation (CSV) principles.Ability to interpret P&IDs, electrical schematics, and technical documentation, with excellent problem-solving ...

business.Manage and develop the IT Support team, prioritising workloads and ensuring timely resolution of incidents, requests and user issues.Ensure IT operations remain compliant with GxP, Data Integrity, Information Security, validation and change control requirements.Own and continuously improve ITSM processes, including Incident, Request, Problem, Knowledge and Major Incident Management.Oversee IT hardware ...

develop the IT Support team, prioritising workloads and ensuring timely resolution of incidents, requests and user issues. Ensure IT operations remain compliant with GxP, Data Integrity, Information Security, validation and change control requirements. Own and continuously improve ITSM processes, including Incident, Request, Problem, Knowledge and Major Incident Management. Oversee ...

skills and strong communication are essential. Key Responsibilities: Working within a controlled ISO 13485 and ISO 9001 laboratory quality system and in accordance with GxP procedures. Design, plan and execute Physical Testing in support of R&D activities and base business projects in accordance with applicable procedures and guidelines. Development ...

Azure integration technologies and reporting tools. Desirable: familiarity with healthcare, pharmaceutical or other regulated industries, and compliance frameworks such as GDPR, Cyber Essentials Plus, GxP and ALCOA+ principles. On offer Salary up to £105,000 DOE Enhanced annual leave package increasing with Length of Service (25 days + bank holidays ...

Platform, Azure integration technologies and reporting tools.Desirable: familiarity with healthcare, pharmaceutical or other regulated industries, and compliance frameworks such as GDPR, Cyber Essentials Plus, GxP and ALCOA+ principles.On offer Salary up to 105,000 DOEEnhanced annual leave package increasing with Length of Service (25 days + bank holidays, increasing ...

adaptable approach in fast-paced delivery environments. Particularly valuable experience The following experience would be highly beneficial: Pharmaceutical, life sciences or healthcare programme delivery. GxP, 21 CFR Part 11 and regulated validation environments. Computer System Validation (CSV), equipment validation and IQ/OQ/PQ approaches. Performance testing and automation ...

Provide pathology oversight of assay performance, result review and reporting practices in an accredited environment supporting clinical and biomarker development. - CAP/CLIA and GxP Compliance: Act in a role aligned to CAP/CLIA expectations; ensure testing and reporting practices meet regulatory and professional standards, including ...

hypotheses fast; contracting vendors on outcomes and holding internal and external teams to account for quality, speed and value. Embed quality and compliance , applying GxP, privacy and AI-governance considerations from the start, maintaining good hygiene in core systems of record, and closing risks and issues in a timely manner. ...

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 ...

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 ...