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Embedded Software Engineer

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Company
Lumicity
Job location
Houston, TX, US
Salary
Undisclosed
Posted
Hosted by
Adzuna

Job details

Senior Software Engineer – C++ / RTOS – Regulated Industry Robotics A pioneering surgical robotics company is looking to add a Senior Software Engineer to its growing R&D team. This company is developing a next-generation flexible robotic system designed for minimally invasive procedures and is backed by strong partnerships across the global medical ecosystem. Why This Role Stands Out: You’ll be working on a highly regulated robotic platform (IEC-62304 Class B/C), building production-level embedded software for real-time surgical systems. The software stack includes a mix of real-time embedded systems and GUI work, with approximately 80% of your focus on low-level C++ development. You’ll collaborate directly with a global engineering team and cross-functional partners in hardware, controls, and systems. Key Responsibilities: Design, develop, and test real-time embedded software in C++ for a surgical robotic platform. Work across the software lifecycle, from requirements to verification, in a regulated (medical/aerospace/automotive) environment. Contribute to both robotic core functionality and GUI development (approx. 20%). Collaborate with global team members, including regular interaction with the engineering team in Korea. Participate in code reviews, design discussions, and documentation aligned with regulated industry standards. Required Experience: Strong proficiency in modern C++ (C++11 or later) and Object-Oriented Programming. Hands-on experience with RTOS (e.g., QNX) and multi-threaded software design. Background working with safety-critical or regulated industries (medical, aerospace, automotive, etc.). Familiarity with embedded systems development and integration with hardware components. Experience with version control tools like Git and testing frameworks such as G-Test or Parasoft. Strong communication skills and willingness to work in a distributed international team. Nice to Have: Prior experience developing software for FDA-regulated medical devices. Knowledge of standards like ISO 13485, IEC 62304, or FDA 21 CFR 820. Exposure to graphics/UI programming, robotics kinematics/dynamics, or data encryption.
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