Roles and Responsibilities

• Design, implement, debug, and test embedded software for regulated medical devices (Class B/C).
• Deliver robust, maintainable, and testable code aligned with system requirements and safety standards.
• Conduct thorough unit testing, static analysis, code reviews, and integration testing to ensure software quality.
• Collaborate with electrical, mechanical, systems, and software engineering teams to define interfaces and system behaviors.
• Support hardware/software integration, including board bring-up and hardware co-design activities.
• Contribute to Agile-V model software development processes including sprint planning, backlog grooming, reviews, and retrospectives.
• Author and maintain high-quality software documentation in compliance with FDA regulations and IEC 62304.
• Operate effectively in a dynamic, fast-paced environment both independently and as part of a collaborative team.

Required Qualifications

• Bachelor's or Master's degree in Computer Science, Electrical Engineering, or a related field.
• 8+ years of experience developing embedded software in C/C++ for safety-critical or regulated systems.
• Proficiency with Python for scripting, automation, or test development.
• Strong knowledge of embedded system architecture, real-time operating systems (RTOS), and microcontroller programming.
• Experience in medical device software development and knowledge of FDA and IEC 62304 requirements.
• Skilled in software verification techniques including unit testing, integration testing, and code reviews.
• Experience with hybrid Agile-V development methodologies.
• Excellent problem-solving, documentation, and communication skills.

Posted By