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Mid-level requirement at a known employer but niche embedded/regulatory skillset limits broad applicant competition.
Embedded firmware for regulated medical devices is highly domain-specific, limiting cross-industry transferability.
Explicit 5–7 years, degree requirement, and embedded/regulatory domain needs create stringent shortlisting filters.
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Design and develop embedded software components aligning with regulatory and design requirements, including conducting prototyping and bench testing.
Lead code reviews and estimate coding time/resources to support project planning and execution.
Collaborate cross-functionally with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams to ensure project success and compliance with industry standards.
Bachelor's degree in Software Engineering, Computer Science, or related discipline.
5 to 7 years of relevant work experience in embedded or firmware software engineering.
Onsite work required.
Exposure to programming and design of components applying design concepts and patterns.
Experienced in Software Development Life Cycle (SDLC) processes including regulatory and compliance standards.
Skilled with integrated development environments (IDEs) and software analysis tools (static/dynamic analysis, memory management, code coverage).
Able to independently manage complex problems with minimal supervision and lead technical practices such as code reviews.