26 to 29 of 29 Validation Jobs in Oxfordshire

Experimental Data Engineer - Advanced Engineering Start-Up - Oxfordshire We have an incredible opportunity for an Experimental Data Engineer to join one of the UK's most exciting venture-backed deep-tech start-ups. This fast growing company is redefining the More ❯

technology. Key Responsibilities for the Contract Hardware Design Engineer: - Design and develop high-speed digital hardware components. - Implement and optimise DDR, PCIe, and Ethernet interfaces. - Conduct thorough testing and validation of hardware designs. - Collaborate with cross-functional teams to ensure seamless integration. - Troubleshoot and resolve design issues promptly. Essential Skills and Experience for the Contract Hardware Design Engineer: - Proven experience … in high-speed digital design. - In-depth knowledge of DDR, PCIe, and Ethernet technologies. - Experience in complete board bring-up, from initial hardware validation to full system readiness. - Strong analytical and problem-solving skills. - Proficiency in using industry-standard design and simulation tools. - Excellent communication and teamwork abilities. If you are a driven and skilled Contract Hardware Design Engineer ready More ❯

and reviewing of periodic Asset documentation including audit trails, Asset Folders, and User Access levels Maintaining access control for manufacturing and ensuring trained personnel and host access to support Validation/Engineering activities Supporting in progressing of Validation Lifecycle documents and activities for assets (URS, DQ, RQ, VRRs, CST etc) Generating and updating of asset documentation e.g. equipment logbooks, SOPs … Providing technical support and point of contact for queries/data from internal departments e.g. Validation and support QMS, and Audits and Client requests Liaising with Equipment & Systems vendors to resolve any technical issues that are identified Executing NPI actions which relate to equipment introduction or modification Supporting the implementation and review of HAZOPs Acting as the subject matter expert More ❯

Senior Quality Systems Officer to join our QA team. In this role, you will be responsible for maintaining the Quality Management Systems (QMS) and Compliance (including CSV - Computerised System validation) at Oxford Biomedica and will promote ongoing continuous improvement to meet business needs. Your responsibilities in this role would be: Leading improvements to the Quality Management System (QMS), driving projects … root cause analysis, and change control. Experience managing electronic Quality Management Systems and document/records management in a regulated environment. In-depth knowledge of data integrity, computer systems validation (CSV), and software development lifecycle concepts. Strong IT skills, including advanced use of Microsoft Office (Word, Excel, and related tools). Ability to identify, prioritise, and drive continuous improvements in More ❯