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Job Description
Structured overview of role & requirementsAbout This Role
Own and govern the complete software architecture for regulated medical devices in Sleep & Respiratory Care products, ensuring safety, compliance, and sustainability.
Lead complex technical design decisions, risk assessments, and architecture documentation adhering to medical device standards (IEC 62304, ISO 13485, ISO 14971, EU MDR, FDA).
Mentor engineers and collaborate cross-functionally to drive technical feasibility, release planning, secure SDLC adoption, and continuous product modernization.
Minimum Requirements
Bachelor's or Master's degree in Computer Science, Electronics, Electrical Engineering or related discipline.
10+ years of embedded software development, with at least 5 years as an architect or lead architect.
Proven experience architecting embedded software for regulated domains; medical device experience strongly preferred.
Office-based role with minimum 3 days per week attendance requirement in India.
Ideal Candidate Profile
Deep expertise in C++/C and embedded real-time software design for microcontroller/SoC platforms, including communications and security protocols.
Experience owning product/platform architecture through full lifecycle including risk management, verification, and regulatory compliance.
Strong technical leadership skills demonstrated by influencing cross-functional teams and mentoring engineers in a regulated engineering environment.