Software Developer II R&D

Under general supervision, contributes to the design, development, testing, and maintenance of software systems supporting regulated medical devices and healthcare solutions. Works as part of a cross-functional software engineering team, implementing well-defined components and features while following established architectural, quality, and regulatory guidelines.

Collaborates with senior engineers, technical leads, Quality, and Regulatory teams to ensure software solutions meet functional, performance, and compliance requirements. Demonstrates growing independence, strong technical fundamentals, and a commitment to quality and continuous improvement within the medical device software development lifecycle (SDLC).

Essential Functions