Principal Firmware Engineer
Boston, Massachusetts
Hybrid
Full Time
$165k - $180k
Our client is a premier consulting firm specializing in the design, development, and manufacturing of cutting-edge medical devices. With a commitment to excellence and innovation, they collaborate closely with leading medical device companies to deliver high-quality solutions that improve patient outcomes globally. They're seeking a Principal Firmware Engineer to join their team!
As a Principal Firmware Engineer, you will lead the development of embedded firmware solutions for medical devices, playing a pivotal role in ensuring compliance, performance, and reliability. You will lead a team of skilled engineers, guiding them through all phases of firmware development while adhering to regulatory standards and best practices. This position offers a unique opportunity to contribute to groundbreaking medical technologies and advance your career in a dynamic consulting environment.
As a Principal Firmware Engineer, you will lead the development of embedded firmware solutions for medical devices, playing a pivotal role in ensuring compliance, performance, and reliability. You will lead a team of skilled engineers, guiding them through all phases of firmware development while adhering to regulatory standards and best practices. This position offers a unique opportunity to contribute to groundbreaking medical technologies and advance your career in a dynamic consulting environment.
Requirements:
- Bachelor’s degree in Electrical Engineering, Computer Engineering, or a related field. Master’s degree preferred.
- Proven experience (8+ years) in embedded firmware development, preferably within the medical device industry or other regulated environments.
- Expertise in programming languages such as C/C++ for embedded systems.
- Strong understanding of real-time operating systems (RTOS), device drivers, and hardware/software integration.
- Demonstrated leadership experience, including leading teams, making technical decisions, and driving projects to successful completion.
- Knowledge of regulatory standards and guidelines applicable to medical devices (e.g., ISO 13485, IEC 62304, FDA regulations).
- Excellent communication skills and the ability to collaborate effectively in a team-oriented environment.
- Ability to travel occasionally to client sites as needed.