Principal Software or Systems Engineer
15 hours ago
Location: Greater Boston, MA (5 days onsite - relocation offered)
Employment Type: Full-Time/Direct (W2)
Visa: US Citizen or Green Card only (No sponsorship)
Domain: Class III Medical Device - Electronic
Experience Required: 10-25 years (exception: 6+ years if candidate meets all requirements)
Interview Process: 2 Teams meetings + onsite interview (client pays travel expenses)
Position Overview
We are seeking a Principal Systems Software Engineer to lead the design, development, and integration of advanced embedded systems for Class III medical devices. The ideal candidate will have strong experience with bare-metal and RTOS-based embedded C development, combined with an electrical engineering background. This role requires ownership from concept through final integration, working in a safety-critical, regulated environment.
Key Responsibilities
- Lead the architecture, design, and development of embedded software for Class III medical devices.
- Work closely with Electrical Engineers and Systems Engineers on hardware-software integration.
- Perform bare-metal and RTOS-based real-time embedded C programming.
- Manage full system integration, including sensor integration and hardware-software interfacing.
- Ensure compliance with medical device regulations and safety-critical design standards.
- Collaborate on system verification, validation, and testing processes.
- Document design decisions, system architecture, and technical specifications.
- Experience: 10-25 years (minimum 6+ years if meeting all core requirements).
- Technical Skills:
- Embedded C (bare-metal and RTOS-based development)
- Real-time embedded systems
- Hardware-software interfacing
- Sensor integration
- Domain Knowledge: Class III medical devices and safety-critical systems.
- Integration Experience: Collaborating with EE and Systems teams for board bring-up and hardware debugging.
- Strong understanding of embedded systems architecture and low-level firmware development.
- Experience in electronic medical device product development.
- Knowledge of FDA Class III regulatory requirements and documentation.
- Board bring-up experience.
- Familiarity with medical device communication protocols and diagnostic tools.
- Master's or Ph.D. in Electrical Engineering, Biomedical Engineering, Computer Engineering, or a related technical field.
- Advanced coursework or research in embedded systems, real-time systems, or medical device development preferred.
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