Description:

What You’ll Work On
As the Software Engineer, you’ll provide technical contributions within a vibrant, high-performing R&D team that is redefining the treatment of structural heart disease. You will lead and/or support key software workstreams including software development, software testing, non-product software testing, documentation, and other as directed.

Job Responsibilities
• Develop and maintain unit tests for C++, QML, and C codebases.
• Write and maintain comprehensive code documentation for Qt-based applications.
• Assist in building and customizing Linux distributions using Yocto Project.
• Manage Qt application dependencies and deployment strategies across platforms.
• Participate in UI/UX development using the Qt Framework, with a focus on usability and performance.
• Perform static and dynamic code analysis to ensure code quality and security.
• Conduct feature testing for NFC/BLE daemons and other embedded components, including:
• Capturing and analyzing logs.
• Identifying and reporting issues or anomalies.
• Collaborating with development teams to resolve concerns.

Required Qualifications
• Bachelor’s degree in Computer Science, Software Engineering, Electrical Engineering or similar.
• Experience in C, C++ family of coding languages.
• Ability to work with software developers and produce concise, unambiguous software design/test documentation.
• Flexibility to adapt workstreams to support business priorities.
• Self-motivated with ability to collaborate across multiple disciplines (e.g., electrical, software, systems) to meet program milestones.
• High motivation, technical curiosity and inclination to find creative ways forward when faced with challenges.Preferred Qualifications
• Advanced degree (Master’s or PhD) in Computer Science, Computer Engineering or similar.
• Linux experience, including secure boot, kernel, LUKS configuration.
• Experience in developing and/or implementing UI/UX designs within Qt framework
• Experience in non-product software validation compliant with FDA 21 CFR Part 820, EU-MDR regulations, and ISO 13485.
• Familiarity with implementation of static and dynamic unit test tools, such as CodeSonar, Veracode, etc.
• Familiarity with cybersecurity principles and implementation of cybersecurity control measures.
• Familiarity with common code repositories and maintenance thereof (e.g., GIT, BitBucket).
• Experienced in the sequential phases of the medical device development from early feasibility and VOC through development, test, commercial launch, and post-market support.
• Experience in first-in-human and pivotal clinical trials.
• Experience and/or familiarity with cardiac anatomy and interventional cardiology.

• Years Experience: 0-3 yrs.

This position works out of our Plymouth, MN location in the SH division.