Principal Embedded Software Engineer
$150k/y-$180k/y
Cirtec Medicala day ago
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OnsiteFull-timeSenior
Summary
Cirtec Medical is seeking a Principal Embedded Software Engineer to join their team in Brooklyn Park, MN. The role involves software development for Class II and III medical devices, focusing on advanced implantable systems.
About the Role
As a Principal Embedded Software Engineer, you will lead the development of embedded software for active implantable medical devices. Your responsibilities will include architecting and implementing software for ARM-based microcontrollers, mentoring engineers, ensuring compliance with IEC standards, and collaborating with cross-functional teams to bring innovative medical solutions to market.
About You
Required:
- Bachelor’s degree in a STEM engineering discipline (or equivalent experience) and 10+ years of embedded software development.
- Deep expertise in C++ and object-oriented design for embedded systems.
- Experience leading technical teams on complex, multidisciplinary projects.
- Strong background in hardware–software integration and use of diagnostic tools.
- Experience with Human Interface Devices (HIDs).
- Familiarity with IEC 60601 and IEC 62304.
- Excellent communication skills and the ability to collaborate with customers and internal teams.
Preferred:
- Experience with active or passive implantable medical devices, especially Class III.
- Hands-on work with NXP, TI, Nordic, or Zarlink microcontrollers; DSP; SPI.
- Experience with MICS-band and/or BLE communication.
- Exposure to MBSE, SysML, or UML.
- Background in neuromodulation, BCI, active orthopedics, or other advanced implantable systems.
Benefits
- Training and career development.
- Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs.
- Paid Time Off.
- 401(k) retirement savings with a company match.
Cirtec Medical
Whether you’re a cutting-edge startup or a leading Class II or III medical device manufacturer, Cirtec is here to help bring life-enhancing therapies to market – quickly and cost-effectively. Our staff of engineers and manufacturing experts can help you succeed at any or every stage of your product development cycle, including design, development, pilot and clinical build, manufacturing and finished device assembly. Cirtec brings over three decades of experience in developing medical devices fabricated under 21 CFR 820 and ISO 13485 quality standards. Our dedicated program management experts are here to help you bring your product from concept through commercialization – on time, on budget and as seamlessly as possible.
Santa Clara, CA