Software Development, Software Testing, Software Engineer

Search Leaders, LLC – Minneapolis, Minnesota, United States. Contact: j

Our client is a pioneering medical technology organization focused on advancing minimally invasive cardiac procedures through innovative MRI compatible solutions that eliminate radiation exposure and improve patient outcomes.

• Design, develop, and maintain Java based application software supporting capital medical equipment products.
• Develop application and system level software that enables real time navigation, device control, and clinical workflows.
• Collaborate cross functionally with engineering, clinical, regulatory, quality, and manufacturing teams to define and refine product requirements.
• Build reliable, scalable, and safety compliant software aligned with IEC 62304 and FDA Class II and III medical device standards.
• Develop and execute automated, unit, and integration testing while supporting formal Verification and Validation activities.
• Support product lifecycle activities including design transfer, manufacturing integration, software releases, and post market updates.
• Analyze user feedback, field data, and defect trends to improve product performance and reliability.
• Create and maintain software requirements, architecture documentation, design specifications, traceability, and risk assessments.
• Ensure adherence to Quality Management System and Design Control processes throughout software development.
• Partner with operations and marketing teams to support manufacturability and customer focused product enhancements.
• Mentor software engineers on development best practices, testing methodologies, and software quality.

• Bachelor's degree in Computer Science, Software Engineering, or related technical field.
• Five or more years of software development experience within the medical device industry.
• Strong Java software development experience building commercial or medical device applications.
• Experience developing application or system level software rather than exclusively embedded firmware.
• Experience working within FDA regulated environments including Design Controls, IEC 62304, software traceability, and software lifecycle documentation.
• Experience supporting FDA 510(k), PMA, or EU MDR regulatory submissions.
• Experience developing automated tests, unit tests, integration tests, and supporting Verification and Validation.
• Experience collaborating across engineering, quality, regulatory, manufacturing, and clinical teams.
• Strong analytical, problem solving, communication, and cross functional collaboration skills.

• Experience with C or C++ for device communication or supporting embedded software.
• Experience with embedded systems, RTOS, or microcontrollers.
• Experience using Azure Dev Ops, static code analysis tools, and modern software development practices.
• Advanced degree in a related technical field.
• Experience with cybersecurity standards and post market surveillance practices.
• Previous experience in a startup or high growth environment.
• Experience mentoring or providing technical leadership to software engineering teams.

• Competitive salary plus a comprehensive benefits package.
• Health coverage, retirement plans, and other company-sponsored perks.
• Generous paid time off, including holidays, to support work‑life balance.
• Flexible schedules and work life balance.
• Strong focus on employee development with on‑the‑job training and career growth.
• A positive company culture that values diversity and collaboration.

The pay range for this role is: 110, USD per year (Minneapolis, MN)