126 to 150 of 192 GxP Jobs in the UK

We're Looking For Experience leading teams and driving technology initiatives Deep understanding of software architecture, development, and design methodologies Strong vendor management, compliance (GxP, HIPAA, SOX), and financial acumen Broad IT knowledge and ability to translate business needs into technology solutions Excellent communication skills and ability to engage with More ❯

platforms (e.g., Veeva Vault, OpenText Documentum), migration tools, SQL, XML, scripting languages, and cloud/on-premise solutions. Strong understanding of life sciences regulations, GxP validation, and compliance. Proven leadership in managing technical teams and complex projects. #J-18808-Ljbffr More ❯

Vault, OpenText Documentum), migration tools, SQL, XML, scripting languages, and cloud/on-prem solutions. Strong understanding of life sciences regulations, validation processes, and GxP compliance. Proven leadership skills and project management experience. #J-18808-Ljbffr More ❯

Veeva Vault, OpenText Documentum), migration tools, SQL, XML, scripting languages, and cloud/on-prem solutions. Strong understanding of life sciences regulations, validation, and GxP requirements. Proven leadership in managing technical teams and complex projects. #J-18808-Ljbffr More ❯

demonstrated through industry experience. Significant experience in pharmaceutical R&D technology support. Knowledge of business processes in RA and PV. Demonstrated operational support background. GxP and SDLC fluency. A track record of partnering cross-functionally with a wide range of stakeholders and cross-functional teams. A passion for communication with More ❯

advisory roles, with significant exposure to the medical, life sciences, or pharmaceutical industry. Demonstrated knowledge of regulatory processes, medical content lifecycle, and compliance frameworks (GxP, HIPAA, ABPI, etc.). Proven experience working with or consulting on: Veeva Vault Medical Suite Salesforce (Health Cloud or Life Sciences verticals) Adobe Experience tools More ❯

advisory roles, with significant exposure to the medical, life sciences, or pharmaceutical industry. Demonstrated knowledge of regulatory processes, medical content lifecycle, and compliance frameworks (GxP, HIPAA, ABPI, etc.). Proven experience working with or consulting on: Veeva Vault Medical Suite Salesforce (Health Cloud or Life Sciences verticals) Adobe Experience tools More ❯

partnering with other Gilead information technology groups to enhance and improve R&D systems and related technical infrastructure. Good Practice quality guidelines and regulations (GxP) systems validation and user acceptance testing is also a specific responsibility of R&D Information Systems. R&D Information Systems may also provide technical support More ❯

supplier issues. Inventory Management: Monitor stock levels, prevent shortages, track usage, and maintain accurate procurement records. Compliance & Documentation: Ensure adherence to industry regulations (FDA, GxP), manage procurement documentation, and stay updated on best practices. Budget & Cost Control: Align purchases with financial plans, track spending, analyze trends, and recommend cost-saving More ❯

job include: Cloud-native development of multi-tenant SaaS architecture using IAC and with cost optimisation in mind, ideally in regulated environments such as GxP Event-driven and distributed systems, using messaging systems like Kafka, AWS SNS/SQS and languages such as Java and Python Data Centric architectures, including More ❯

area and the relevant business processes, solutions, and external environment. Compliance: Appropriately document, maintain, and provide evidence for product compliance across applicable regulatory controls (GxP, SOx, InfoSec, Privacy). Agile Methodologies: Knowledge and practical experience in applying SCRUM/Agile methodologies for teamwork, progress measurement, and collaboration. Vendor Management: Where More ❯

area and the relevant business processes, solutions, and external environment.* Compliance: Appropriately document, maintain, and provide evidence for product compliance across applicable regulatory controls (GxP, SOx, InfoSec, Privacy).* Agile Methodologies:Knowledge and practical experience in applying SCRUM/Agile methodologies for teamwork, progress measurement, and collaboration.* Vendor Management:Where More ❯

Quality System documents and procedures relevant to all employees (local and Convatec corporate e.g. Code of Ethics and Business Conduct, Quality Policy, Complaints, relevant GxP documents), including regular re-training when required. Quality System documents and procedures relevant to job performance. Principal Contacts & Purpose of Contact: Internal: Global T&I More ❯

Quality System documents and procedures relevant to all employees (local and Convatec corporate e.g. Code of Ethics and Business Conduct, Quality Policy, Complaints, relevant GxP documents), including regular re-training when required Quality System documents and procedures relevant to job performance Principal Contacts & Purpose of Contact Internal – All Michalovce plant More ❯

life sciences industry. Extensive experience with ECM platforms like Veeva Vault, OpenText Documentum, Generis CARA, and migration tools. Strong understanding of life sciences regulations, GxP validation, and compliance requirements. Proven leadership skills and experience managing complex projects and technical teams. #J-18808-Ljbffr More ❯

engagement and communication skills Experience in process improvement and implementation Interest in automation and productivity solutions (e.g., AI, S/4HANA, RPA) Awareness of GxP regulations If interested, please apply. All applicants must be eligible to work in the specified country. Whitehall Resources is an equal opportunities employer committed to More ❯

Generis CARA; experience with migration tools, SQL, XML, scripting, and cloud/on-premise solutions. Strong knowledge of life sciences regulations, validation processes, and GxP compliance. Proven leadership skills and experience managing complex projects and technical teams. #J-18808-Ljbffr More ❯

Documentum, Generis CARA), migration tools, SQL, XML, scripting languages, and cloud/on-premise solutions. Strong understanding of life sciences regulations, validation processes, and GxP compliance. Proven leadership in managing technical teams and complex projects. #J-18808-Ljbffr More ❯

exposure to the medical, life sciences, or pharmaceutical industry. They must demonstrate knowledge of regulatory processes, the medical content lifecycle, and compliance frameworks including GxP, HIPAA, and ABPI. Proven experience working with or consulting on Veeva Vault Medical Suite, Salesforce Health Cloud or Life Sciences verticals, Adobe Experience tools for More ❯

demonstrated through industry experience Significant experience in pharmaceutical R&D technology support Knowledge of business processes in RA and PV Demonstrated operational support background GxP and SDLC fluency A track record of partnering cross-functionally with a wide range of stakeholders and cross-functional teams A passion for communication with More ❯

On-Demand sector to ensure compliance with regulatory, customer and other relevant standards as applicable. Provide guidance and support the business to ensure existing GxP regulations are adhered to throughout the project for example, supporting change management and periodic reviews. Support the delivery of the Uniphar On-Demand sector quality More ❯

operational technology, OT-IT integration and relevant protocols. Strong technical expertise in OT environments with practical knowledge of operational processes and infrastructure. Familiarity with GxP requirements and regulations for OT systems. Proven leadership qualities, empathy and a solutions and teamwork centered approach. The role requires hands-on experience with OT More ❯

Risk & Compliance: Support operational technology compliance with internal security and risk management policies and practices, as well as external regulatory and statutory requirements e.g. GxP and that Tech continuity plans are in place for all critical areas. People Management: Collaborate with internal owners of security technologies such as antivirus, IDS More ❯

implement and troubleshoot end-to-end solutions, supporting a robust and scalable environment. Compliance and Regulatory Adherence Ensure all processes adhere to industry standards, GxP regulations, FDA 21 CFR Part 11, and internal governance frameworks. Monitor system performance and integration functionalities to support audit readiness and risk mitigation. Qualifications & Experience … demonstrated ability to translate complex business requirements into efficient, integrated SAP solutions. Experience working within pharmaceutical, biotech, or similarly regulated manufacturing environments. Familiarity with GxP protocols, FDA regulatory compliance, ISO standards, and other pertinent quality assurance standards. Bachelor's degree in Information Technology, Engineering, Business, or a related field. SAP More ❯

software engineering expertise with architectural ownership across digital quality systems. Key Responsibilities: Lead technical configuration and validation of laboratory and EHS systems in a GxP environment. Oversee authoring and review of system lifecycle documents including system configurations, SOPs, risk assessments, and test protocols. Act as a digital administrator and technical More ❯