10 of 10 Permanent Validation Jobs in Oxford

e.g., AWS, Azure, GCP, etc). Contribute to the design of tools that enhance product scalability, improve efficiency and reduce manual effort in data validation, reporting, and visualization. Support the update and forecasting process for GTS and GCT. Stay informed on industry and technological trends to propose innovative product enhancements More ❯

a capability supporting developments across the full product life cycle. The team integrates real products, models and synthetic environments to provide visualisations, demonstrations, verification & validation as well as training capability and support. What we're looking for from you: A Lead Software Engineer who is adaptable and creative in their More ❯

degree in a relevant field Previous product management training (Pragmatic Marketing, Design Thinking, etc.) Preferred: Experience in API-based data exchange, data mapping, and validation rules Experience with clinical research or EDC systems Knowledge of regulatory requirements for clinical trials (GCP, 21 CFR Part 11) Familiarity with Agile development methodologies More ❯

degree in a relevant field Previous product management training (Pragmatic Marketing, Design Thinking, etc.) Preferred: Experience in API-based data exchange, data mapping, and validation rules Experience with clinical research or EDC systems Knowledge of regulatory requirements for clinical trials (GCP, 21 CFR Part 11) Familiarity with Agile development methodologies More ❯

invisible root cause of the disease. Multiple patents underpinning CaRi-Heart technologies have been granted in major jurisdictions around the world. In addition, exceptional validation results showing CaRi-Heart's ability to aid the prediction of heart attacks have been published in leading medical journals including the Lancet , JACC , European More ❯

evaluate and refine these systems will be critical to ensuring high performance integration with our quantum hardware. Hands-on experience with simulation, fabrication and validation will be essential. You should be comfortable using commercial tools for optical modelling, managing the outsourcing and fabrication of custom optical components and implementing rigorous More ❯

Manage capital investment projects from concept to completion, including specifying, justifying, and procuring equipment to enhance manufacturing capabilities. Equipment Implementation: Oversee installation, commissioning, and validation of new equipment, ensuring alignment with operational goals, safety standards, and production timelines. Factory Acceptance Testing (FAT): Witness and validate factory acceptance tests (FAT) at More ❯

Digital Design Engineer to join and complement our engineering design team within our R&D Department. Responsibilities: Take charge of the design, development and validation of digital electronic instrumentation and support equipment Work within a multi-disciplinary team on design projects, working from initial concept through to production release Support More ❯

Digital Design Engineer to join and complement our engineering design team within our R&D Department. Responsibilities: Take charge of the design, development and validation of digital electronic instrumentation and support equipment Work within a multi-disciplinary team on design projects, working from initial concept through to production release Support More ❯

reagents and assays. Experience of working in an MDSAP-compliant environment. Experience of leading ISO 13485 certification audits. Detailed understanding of risk management, process validation, clinical validation and IVD performance evaluation requirements. Experience of working in an IVD environment along with practical experience in working to applicable management standards (i.e. … of management of (and consequent future prevention of) recalls or other challenging health authority interactions is highly desired. Understanding or experience of computer systems validation is desirable (e.g. GAMP5). Knowledge/Skills/Abilities Essential: Detailed working knowledge of ISO13485, MDSAP requirements and the IVDR are essential. Demonstrable experience More ❯