Software Engineer, Quality, IEC 62304, ISO 13485, Medical Devices, COR7184
A rare and exciting opportunity has arisen for a Software Engineer with experience working with software as a medical device and IEC 62304 standards, to join a pioneering scientific R&D company specialising in the development of medical devices.
The Role
The Software Engineer will take ownership of ensuring software quality and compliance for innovative In Vitro Diagnostic products. Working alongside a highly skilled team, you’ll be responsible for implementing and maintaining SDLC processes, software risk management, and compliance with ISO 13485, IEC 62304, and 21 CFR Part 820. This is a fantastic opportunity to make a significant impact in a fast-growing company at the forefront of medical technology.
The Company
The Software Engineer will join an innovative organisation leading the way in medical device development. This company is revolutionising diagnostics, and as they continue to grow, they are looking for a passionate Quality Engineer to enhance their software quality and risk management processes.
What’s Required of the Software Engineer?
What Next?
If you’re a Software Quality Engineer looking to work on meaningful products that will have a massive impact in the medical field, apply today to learn more!
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.