Collaborate cross‑functionally with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management
Contribute across the full product lifecycle—from concept, design, and development through verification, validation, and launch
Design, develop, modify, and verify medical device software components
Translate user, clinical, market, and Voice of Customer inputs into design requirements
Conduct advanced prototyping, testing, research, and problem solving
Participate in code reviews
Generate, review, and maintain comprehensive engineering documentation
Mentor others on R&D procedures, design controls, risk management, and regulatory standards

Bachelor’s degree in Software Engineering, Computer Science or a related discipline
Minimum of 4+ years of professional software engineering experience
Strong hands-on experience developing Windows-based applications using C#, C++, and .NET
Deep proficiency in WPF and Windows Services
Experience designing, developing, and integrating APIs, including REST, SOAP, WCF, and gRPC.
Strong knowledge of Ethernet and IP networking, including AV‑over‑IP protocols
Networking certifications such as CCNA or equivalent preferred
Knowledge of FPGAs
Experience in research and development of Video and Communication system/workflow design
Familiarity with US FDA and ISO standards like IEC 62304, IEC 60601, 21CRF 820 is a plus.

Staff Software Engineer

Key skills