Verification and Validation Jobs in County Antrim

2 of 2 Verification and Validation Jobs in County Antrim

QA Engineer

Newtownabbey, County Antrim, United Kingdom
Xirgo Technologies
Xirgo Technologies offers a complete portfolio of proprietary supply chain monitoring and management technology to convert IoT data from information to insights - enabling the smartest telematics data analytics solutions. About the role Xirgo Technologies is recruiting a Quality Assurance Engineer to join us in creating the next generation of Smart Fleet Logistics products and solutions. Xirgo is the future of … Smart Fleet Logistics - fleet management and logistics made smarter, safer and more productive. We lead the way with world-class technology, unparalleled expertise and unwavering partnership in everything we do, so our customers can move the world forward with confidence and peace of mind. As a QA Engineer at Xirgo, you will play a pivotal role in ensuring the integrity … and performance of complex systems through rigorous verification and validation processes. You'll collaborate with cross-functional teams-including hardware, firmware, and systems engineers -to develop and execute test plans, identify issues, and ensure system requirements are met. This position demands a strong analytical mindset, attention to detail, and a solid foundation in engineering principles to help deliver high-quality More ❯
Employment Type: Permanent
Salary: GBP Annual
Posted:

Lead R&D Engineer

Northern Ireland, Belfast
Hybrid / WFH Options
Real Staffing
drive the development of next-generation catheter-based medical devices. This role is ideal for an experienced engineer with a biomedical or mechanical background, strong knowledge of design controls, and a track record in global medtech environments. Key Responsibilities: Lead end-to-end R&D activities for catheter systems, from concept through to design transfer. Ensure compliance with ISO … and FDA 21 CFR Part 820 design control requirements. Develop and review technical drawings and documentation using AutoCAD. Collaborate with cross-functional teams (Quality, Regulatory, Manufacturing). Conduct design verification and validation (V&V) activities. Support risk management processes including FMEA and hazard analysis. Mentor junior engineers and contribute to technical leadership. Requirements: Degree in Biomedical Engineering, Mechanical Engineering, or … related field. 6-8+ years of R&D experience in the medical device industry, ideally with large global manufacturers. Proven experience in catheter design and development. Proficiency in AutoCAD. Strong understanding of design controls and regulatory compliance. Excellent communication and leadership skills. Contract Details: Duration: 12 months (with potential for extension) Work Model: 3 days onsite/2 days More ❯
Employment Type: Contract
Rate: £47 - £60
Posted: