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Senior Embedded Software EngineerKaav Inc.United States

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Senior Embedded Software Engineer

Kaav Inc.
  • US
    United States
  • US
    United States

Über

Job Title:
Senior Embedded Software Engineer (Medical Devices)
Location:
~15 miles North of Boston, MA (3 Days Onsite, 2 Day WFH) Employment Type:
Full-Time, Direct Hire (W2 Only - No Relocation, Locals Only) Salary Range:
Salary + 10-15% Bonus Interview Process:
Virtual (Microsoft Teams) followed by Onsite Interview Visa Status:
US Citizens or Green Card Holders only (No sponsorship available) Job Summary:
We are seeking an experienced
Senior Embedded Software Engineer
with 8-15 years of hands-on experience in
embedded C/C++ development
for
Class II/III medical devices . This role involves the full software development lifecycle in FDA-regulated environments and requires close collaboration with cross-functional teams, including systems, hardware, and quality engineering. Ideal candidates will have a deep understanding of real-time operating systems (RTOS), regulatory standards, and a passion for innovation in the medical technology sector. Key Responsibilities: Design, develop, test, and document
embedded software
for medical devices, primarily in
C/C++ . Develop on
RTOS-based platforms , optimizing for performance, reliability, and safety. Contribute to
architecture, requirements analysis , software design, and risk assessments. Ensure compliance with
FDA regulations
and medical device software development standards (IEC 62304, ISO 13485, etc.). Collaborate with hardware engineers, QA, systems engineers, and regulatory teams throughout the development lifecycle. Support verification and validation activities including unit testing and integration testing. Participate in code reviews, debugging, and performance tuning of software. Maintain detailed
software documentation
in accordance with internal SOPs and regulatory requirements. Required Qualifications: 8-15 years
of experience in
embedded software development
using
C and C++ . Experience developing software for
Class II/III FDA-regulated medical devices . Strong background in
real-time operating systems (RTOS) . Proven knowledge of the
medical device development lifecycle
and documentation standards. Familiarity with
hardware interfaces
(I2C, SPI, UART, CAN, USB, etc.). Strong understanding of
software risk analysis , FMEA, and design for safety-critical systems. Excellent problem-solving, communication, and cross-functional collaboration skills. Bachelor's or Master's degree in
Electrical Engineering, Computer Engineering , or related field. Preferred Qualifications: Experience with
Bluetooth, BLE, wireless communication , or battery-powered devices. Exposure to
unit testing frameworks , automated testing, and static code analysis tools. Familiarity with
Python, shell scripting , or other auxiliary languages for test automation. Experience working in
Agile or hybrid SDLC environments .
  • United States

Sprachkenntnisse

  • English
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