Senior Software Engineer -CRDN

Medtronic•Minneapolis, MN

2d•$124,800 - $187,200•Onsite

About The Position

Medtronic Coronary & Renal Denervation (CRDN) business is looking for a Senior Software Engineer to be part of a high-performing team that is revolutionizing the design and development of energy-based therapeutic medical devices to treat hypertension. In this role, you will leverage both your technical breadth and business acumen to support the newly approved therapy medical device software and participate in the design and development of next generation medical devices. This position is in Mounds View, MN. within the Coronary and Renal Denervation (CRDN) unit. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We are working on-site 4 days per week as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects. We believe that when people from different cultures, genders, and points of view come together, innovation is the result —and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive. This role requires strong technical skills to support the full software development lifecycle of innovative new medical device products with embedded software within the CRDN Group. The Senior Software Engineer will apply advanced technical principles, theories, and concepts in working on complex technical problems, and will provide technical leadership of projects from concept generation through development and market release.

Requirements

Experienced in C/C++ programming and at least one scripting language such as Python
Demonstrated ability to troubleshoot and resolve issues in embedded software
Experience with an embedded Linux Environment
Bachelor’s degree in computer engineering, software engineering, computer science, electrical engineering, or a related technical discipline and minimum of 4 years of work experience OR advanced degree in computer engineering, software engineering, computer science, electrical engineering, or a related technical discipline with 2 years of work experience.

Nice To Haves

Demonstrated knowledge of software design, development, debug and test practices
Experience using unit test frameworks, such as Google Test / Mock and following a Test-Driven Development software practice
Familiar with using static analysis tools, such as Coverity
Experience using Git for source control and experience in a pull-request based workflow
Experience with Docker containerization, including creating, managing, and optimizing Docker containers and images.
Familiarity with CI/CD tools such as Jenkins, GitLab CI/CD, or Travis CI to automate the build, test, and deploy software products.
Experience in designing and developing Graphical User Interface, preferably in QT
Experience with medical device design controls (e.g. ISO 13485), risk analysis (e.g. ISO 14971), and IEC62304 and SDLC
Demonstrated experience in the following: embedded processors, microcontrollers, and development tools such as emulators, logic analyzers, and oscilloscopes
Proficiency in embedded communications protocols such as SPI, I2C

Responsibilities

Design, develop, test, and maintain high-quality medical device embedded software solutions as part of the software team in accordance with Agile principles and Scrum methodologies.
Collaborate with cross-functional team members to understand the product needs and capabilities and to provide guidance on potential solutions.
Write clean, efficient, and well-documented code, following best practices and coding standards.
Write unit tests, integration tests, and automated acceptance tests to ensure software quality and functionality.
Integrate code frequently into version control repositories, ensuring a consistent and reliable CI/CD pipeline that automates testing, builds, and deployments.
Collaborate with QA engineers to perform manual and automated testing, participating in bug triaging and resolution.
Work with different stakeholders and Cross-function team to prioritize team work according to business needs.
Participate in Risk Assessment and requirements development.
Cross-function collaboration with manufacturing and production.
Participate in the documentation of the software including architecture and design detail, unit testing, defect tracking and reports.
Cross function team collaboration with HW and systems partners, including integration team, testing team, Quality, System V&V…etc.
Follow Medical device regulations (IEC 62304, IEC 82304, FDA…etc.)
Provide leadership in solving engineering problems and fostering creativity and innovation in design and problem solutions.