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QA Analyst I

  2025-06-05     Motion Recruitment Partners LLC     Providence,RI  
Description:

Our client, an innovative and rapidly growing medical device company, is seeking a Senior Embedded Software Engineer to join their dynamic R&D team. This organization is at the forefront of developing cutting-edge, life-saving technologies that are reshaping the future of patient care.

The ideal candidate will have a strong background in embedded systems, a passion for working on mission-critical software, and a proven track record of developing robust, reliable code in regulated environments. This is a high-impact role where your contributions will directly support the design and development of Class II/III medical devices that improve and save lives.

Key Responsibilities:
  1. Design, develop, and optimize embedded software for next-generation medical devices.
  2. Collaborate with cross-functional teams including hardware, systems, and QA engineers to define software architecture and requirements.
  3. Implement and test firmware using C/C++ on RTOS-based or bare-metal platforms.
  4. Participate in code reviews, risk analysis, and software verification and validation in compliance with FDA, IEC 62304, and ISO 13485 standards.
  5. Support root cause analysis and continuous improvement efforts during product development and post-market phases.
  6. Document software designs, architecture decisions, and development processes clearly and thoroughly for regulatory compliance.
Qualifications:
  1. Bachelors or Masters degree in Computer Engineering, Electrical Engineering, Computer Science, or a related field.
  2. 5+ years of experience in embedded software development, ideally within the medical device, aerospace, automotive, or other safety-critical industries.
  3. Strong proficiency in C/C++, with a solid understanding of real-time operating systems, microcontrollers (e.g., ARM Cortex), and low-level hardware interactions.
  4. Experience with development tools such as Git, JIRA, and version control systems.
  5. Familiarity with FDA regulations, IEC 62304, and ISO 13485 is strongly preferred.
  6. Excellent analytical, problem-solving, and communication skills.
  7. Passion for working on impactful technology in a highly collaborative environment.

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