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Principal Medical Device Software Engineer (Python/C++)

Medtronic

$148,000 - $222,000
Jan 2, 2026
Newton, MA, US
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Medtronic is seeking a Principal Software Engineer to design and develop intuitive, user-friendly interfaces for advanced medical devices, specifically the Affera Mapping and Ablation System, to enhance usability and functionality, and make a tangible difference in patients' lives.

Requirements

  • Expert-level proficiency in Python and C++
  • Deep understanding of software engineering principles, including architecture, data structures and algorithms
  • Experience with embedded systems
  • Solid understanding of network communication protocols and technologies
  • Experience with software version control systems, such as Git
  • Experience with Agile development methodologies
  • Experience with cloud-based platforms and services (e.g., AWS, Azure)

Responsibilities

  • Lead the design, development, and maintenance of complex software systems, ensuring high performance, scalability, and reliability
  • Develop and debug software for embedded systems, ensuring seamless integration with hardware components
  • Collaborate with cross-functional teams, including hardware engineers, product managers, and quality assurance, to define software requirements and deliver high-quality solutions
  • Optimize software performance, ensuring low latency, high reliability, and scalability
  • Conduct code reviews and provide constructive feedback to ensure code quality and adherence to best practices
  • Mentor and guide junior software engineers, fostering a culture of continuous learning and professional growth
  • Implement and maintain robust software testing strategies, including unit, integration, and automated testing to ensure high-quality code

Other

  • Bachelor's degree and 7 years of relevant experience, OR Master's degree with 5 years of relevant experience, OR PhD with 3 years relevant experience
  • Strong communication and collaboration skills, with the ability to work effectively in a team environment
  • Ability to work a minimum of 4 days a week onsite
  • Ability to attend and participate in pre-clinical in-vivo system evaluations and laboratory demonstrations for internal stakeholders and clinicians
  • Ability to work in a fast-paced environment with multiple priorities and deadlines