Role responsibilities
The role involves designing and implementing quality software applications integrated with hardware for FDA-regulated medical devices. Responsibilities include PC and microprocessor-based development, system validation, and customer interaction.
Requirements
Candidates must have a BS in Computer Science or Electrical Engineering and at least 5 years of experience. Proficiency in C#, WPF, and web technologies is required, with a need to learn FDA and IEC 62304 regulations.
Key skills
C#, WPF, SQL, XML, HTML, JavaScript, ASP.Net, Graphical User Interfaces, Serial Communications, TCP/IP, Software/Hardware Integration, System Verification and Validation
Keywords
Software Engineering, Medical Devices, FDA 21 CFR Part 820, IEC 62304, C#, WPF, SQL, XML, HTML, JavaScript, ASP.Net, GUI, Serial Communications, TCP/IP, Microprocessor, System Verification, System Validation, Quality System Regulation, Software Development Lifecycle