business needs with data, AI, and Oracle platform opportunities. Data Strategy & Architecture: Ensures adherence to data governance frameworks, FAIR principles (Findable, Accessible, Interoperable, Reusable), and pharma regulatory standards (e.g., GxP). Change Management: Champions a culture of data and AI adoption across the business, ensuring teams are empowered to use new tools and insights effectively. Vendor & Partner Management: Manages relationships More ❯
business needs with data, AI, and Oracle platform opportunities. Data Strategy & Architecture: Ensures adherence to data governance frameworks, FAIR principles (Findable, Accessible, Interoperable, Reusable), and pharma regulatory standards (e.g., GxP). Change Management: Champions a culture of data and AI adoption across the business, ensuring teams are empowered to use new tools and insights effectively. Vendor & Partner Management: Manages relationships More ❯
business needs with data, AI, and Oracle platform opportunities. Data Strategy & Architecture: Ensures adherence to data governance frameworks, FAIR principles (Findable, Accessible, Interoperable, Reusable), and pharma regulatory standards (e.g., GxP). Change Management: Champions a culture of data and AI adoption across the business, ensuring teams are empowered to use new tools and insights effectively. Vendor & Partner Management: Manages relationships More ❯
business needs with data, AI, and Oracle platform opportunities. Data Strategy & Architecture: Ensures adherence to data governance frameworks, FAIR principles (Findable, Accessible, Interoperable, Reusable), and pharma regulatory standards (e.g., GxP). Change Management: Champions a culture of data and AI adoption across the business, ensuring teams are empowered to use new tools and insights effectively. Vendor & Partner Management: Manages relationships More ❯
london (city of london), south east england, united kingdom
La Fosse
business needs with data, AI, and Oracle platform opportunities. Data Strategy & Architecture: Ensures adherence to data governance frameworks, FAIR principles (Findable, Accessible, Interoperable, Reusable), and pharma regulatory standards (e.g., GxP). Change Management: Champions a culture of data and AI adoption across the business, ensuring teams are empowered to use new tools and insights effectively. Vendor & Partner Management: Manages relationships More ❯
OPC UA, MQTT, REST/SOAP APIs, SQL, Python, etc. Familiarity with lab automation platforms (e.g., Tecan, Hamilton, Agilent, Beckman, Sartorius) and related data workflows. A good understanding of GxP, 21 CFR Part 11, data integrity principles, and validated environments is a plus. Every day, Lonza's products and services have a positive impact on millions of people. For us More ❯
OPC UA, MQTT, REST/SOAP APIs, SQL, Python, etc. Familiarity with lab automation platforms (e.g., Tecan, Hamilton, Agilent, Beckman, Sartorius) and related data workflows. A good understanding of GxP, 21 CFR Part 11, data integrity principles, and validated environments is a plus. Every day, Lonzas products and services have a positive impact on millions of people. For us, this More ❯
levels. Results-driven with a focus on innovation and continuous improvement. Proficiency in business intelligence and analytics tools (e.g., Tableau, Power BI). Knowledge of regulatory frameworks such as GxP, GDPR, SOX, or other compliance standards. Expertise in enterprise architecture, system integration, and process optimization. Deep understanding of financial management, supply chain, and other core ERP-supported business processes. Proficiency More ❯
exposure to clinical trials. Clinical, pharmacological, and therapeutic knowledge in neuroscience. Good understanding of clinical study design principles and basic familiarity working with clinical data in a clinical trial (GxP) setting. Strong knowledge and understanding of (multivariate implementations of) statistical methods such as time to event analysis, machine learning, meta-analysis, mixed effect modelling, longitudinal modelling, Bayesian methods, variable selection More ❯
alignment with business objectives and IT roadmaps. Establish testing policies, standards, and best practices in collaboration with process experts to ensure consistency, quality, and compliance with regulatory requirements (e.g., GXP, GDPR, and other pharmaceutical industry standards). Define key performance indicators (KPIs) and metrics to measure testing effectiveness, leveraging input from process teams to assess system reliability and defect resolution More ❯
Hatfield, England, United Kingdom Hybrid / WFH Options
Planet Pharma
Electronic Batch Record systems. Collaborate with cross-functional teams and external vendors to deliver impactful solutions. Mentor apprentices and contribute to team development. What You’ll Bring: Experience in GxP environments and understanding of GAMP 5. Hands-on experience with MES, SAP ERP, and system integration. Strong problem-solving, communication, and stakeholder engagement skills. Bonus: Experience with Tulip platform, ServiceNow More ❯
hatfield, east anglia, united kingdom Hybrid / WFH Options
Planet Pharma
Electronic Batch Record systems. Collaborate with cross-functional teams and external vendors to deliver impactful solutions. Mentor apprentices and contribute to team development. What You’ll Bring: Experience in GxP environments and understanding of GAMP 5. Hands-on experience with MES, SAP ERP, and system integration. Strong problem-solving, communication, and stakeholder engagement skills. Bonus: Experience with Tulip platform, ServiceNow More ❯
watford, hertfordshire, east anglia, united kingdom Hybrid / WFH Options
Planet Pharma
Electronic Batch Record systems. Collaborate with cross-functional teams and external vendors to deliver impactful solutions. Mentor apprentices and contribute to team development. What You’ll Bring: Experience in GxP environments and understanding of GAMP 5. Hands-on experience with MES, SAP ERP, and system integration. Strong problem-solving, communication, and stakeholder engagement skills. Bonus: Experience with Tulip platform, ServiceNow More ❯
NIST, AI Governance, CIS etc. • Good compliance understanding of industry domains such as BFSI – (SOX, FFIEC, PCI-DSS, BASEL, MAS etc.), Healthcare & Life-sciences – (HIPAA, Hi-Trust, FDA CFR, GxP Compliance), Telecom, Retail, Data Privacy (GDPR, CCPA) Energy & Utilities (NERC, FERC) Information Security (ISO 27000, NIST, CIS) TPRM • Business Resiliency & Cyber Recovery, ZTA • GRC Project & Program Management • Excellent written and More ❯
NIST, AI Governance, CIS etc. • Good compliance understanding of industry domains such as BFSI – (SOX, FFIEC, PCI-DSS, BASEL, MAS etc.), Healthcare & Life-sciences – (HIPAA, Hi-Trust, FDA CFR, GxP Compliance), Telecom, Retail, Data Privacy (GDPR, CCPA) Energy & Utilities (NERC, FERC) Information Security (ISO 27000, NIST, CIS) TPRM • Business Resiliency & Cyber Recovery, ZTA • GRC Project & Program Management • Excellent written and More ❯
NIST, AI Governance, CIS etc. • Good compliance understanding of industry domains such as BFSI – (SOX, FFIEC, PCI-DSS, BASEL, MAS etc.), Healthcare & Life-sciences – (HIPAA, Hi-Trust, FDA CFR, GxP Compliance), Telecom, Retail, Data Privacy (GDPR, CCPA) Energy & Utilities (NERC, FERC) Information Security (ISO 27000, NIST, CIS) TPRM • Business Resiliency & Cyber Recovery, ZTA • GRC Project & Program Management • Excellent written and More ❯
london (city of london), south east england, united kingdom
HCLTech
NIST, AI Governance, CIS etc. • Good compliance understanding of industry domains such as BFSI – (SOX, FFIEC, PCI-DSS, BASEL, MAS etc.), Healthcare & Life-sciences – (HIPAA, Hi-Trust, FDA CFR, GxP Compliance), Telecom, Retail, Data Privacy (GDPR, CCPA) Energy & Utilities (NERC, FERC) Information Security (ISO 27000, NIST, CIS) TPRM • Business Resiliency & Cyber Recovery, ZTA • GRC Project & Program Management • Excellent written and More ❯
NIST, AI Governance, CIS etc. • Good compliance understanding of industry domains such as BFSI – (SOX, FFIEC, PCI-DSS, BASEL, MAS etc.), Healthcare & Life-sciences – (HIPAA, Hi-Trust, FDA CFR, GxP Compliance), Telecom, Retail, Data Privacy (GDPR, CCPA) Energy & Utilities (NERC, FERC) Information Security (ISO 27000, NIST, CIS) TPRM • Business Resiliency & Cyber Recovery, ZTA • GRC Project & Program Management • Excellent written and More ❯
Hatfield, England, United Kingdom Hybrid / WFH Options
Cpl Life Sciences
a strong emphasis on stakeholder management and effective communication with senior managers and directors. What are we looking for? Experience delivering business changes or IT business system projects to GxP environment, either in a pharma site or equivalent a must have Demonstrated experience in IT Project Management. Demonstrated experience in stakeholder management and presenting to senior managers and directors. Experience More ❯
meet regulatory standards and align with architectural best practices. Key Responsibilities: Build and optimise scalable data pipelines using Databricks and Apache Spark (PySpark). Ensure performance, scalability, and compliance (GxP and other standards). Collaborate on requirements, design, and backlog refinement. Promote engineering best practices including CI/CD, code reviews, and testing. Research and introduce new tools, technologies, and More ❯
meet regulatory standards and align with architectural best practices. Key Responsibilities: Build and optimise scalable data pipelines using Databricks and Apache Spark (PySpark). Ensure performance, scalability, and compliance (GxP and other standards). Collaborate on requirements, design, and backlog refinement. Promote engineering best practices including CI/CD, code reviews, and testing. Research and introduce new tools, technologies, and More ❯
for an exciting capital project involving a new production line. This role is critical in ensuring that all computerised systems are validated, compliant, and operate reliably in accordance with GxP and industry regulations. You will be working with a variety of systems, including Sartorius and SAP alongside other GxP-regulated systems within a manufacturing environment. Key Responsibilities Validation Protocols: Develop More ❯
for an exciting capital project involving a new production line. This role is critical in ensuring that all computerised systems are validated, compliant, and operate reliably in accordance with GxP and industry regulations. You will be working with a variety of systems, including Sartorius and SAP alongside other GxP-regulated systems within a manufacturing environment. Key Responsibilities Validation Protocols: Develop More ❯
align with Orchard's strategic goals. The role focuses on process improvement, digital transformation, and cross-functional collaboration, ensuring seamless integration of ERP and patient orchestration platforms within a GxP-regulated environment. Key Responsibilities Business Process Optimization: Analyze, design, and improve SCM business processes across logistics, distribution, manufacturing, and warehousing. Lead process improvement projects, ensuring alignment with operational goals. Define … knowledge of SCM ERP modules (procurement, logistics, manufacturing, warehousing). Experience with patient orchestration platforms for Cell and Gene Therapy. Proficient in business process mapping, Lean Six Sigma, and GxP compliance. Familiar with IT and quality change control processes. Skills & Competencies Certified Business Analysis Professional (CBAP) or equivalent preferred. Strong leadership, problem-solving, and project management skills. Excellent communication, organizational More ❯
compliance with GAMP 5 guidelines and global regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11), while also supporting a company-wide risk stratification initiative for all GxP-relevant systems. As a CSV Specialist your responsibilities will include, although not limited to: Leading and executing validation activities for new and existing computerised systems, including both bespoke and COTS … solutions, in accordance with GAMP 5 principles. Performing risk assessments to define the appropriate validation strategy and documentation scope, aligned with the organisation’s overall GxP risk stratification framework. Preparing and maintaining validation documentation, including User Requirements Specifications (URS), Functional Specifications (FS), validation plans, protocols, reports, and traceability matrices. Working collaboratively with IT, QA, system owners, and vendors to ensure … compliant manner. Providing support during audits and regulatory inspections, addressing data integrity and CSV-related queries. Ensuring all system lifecycle documentation is maintained in accordance with internal SOPs and GxP standards. Assisting in developing implementing and testing disaster recovery plans for key computerised systems in collaboration with business departments. Contributing to the continuous improvement of CSV procedures, templates, and best More ❯