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# Sr Software Engineer

- **Company:** Medtronic Inc.
- **Location:** Minneapolis, MN, United States
- **Experience:** Expert
- **Salary:** $124,800.0 - $187,200.0
- **Contract:** Temporary contract
- **Skills:** Adobe InDesign, Software Applications, Systems Engineering, Automation of Tests, Unit Testing, Bluetooth Low Energy (Bluetooth), C++ (Programming Language), Communications Protocols, Software Debugging, Device Drivers, Embedded Software, Firmware, Integrated Development Environments, Interoperability, Regression Testing, Software Engineering, Test Data, Test Scripts, Peripherals
- **Published:** August 14, 2026
- **Apply:** https://www.minneapoliscareersite.com/job.asp?id=3353310803&tx=FL838FFQ&pt=1&aff=0B19D771-A501-4A5E-8338-2A822B784D54&utm_source=Job%20Feed&utm_medium=textkernel&utm_campaign=DE&utm_term=0B19D771-A501-4A5E-8338-2A822B784D54

## About the Role

Sponsorship: This position is not eligible for immigration sponsorship. Applicants must be authorized to work in the country of employment without sponsorship., * Bachelor's degree with 4 years of relevant experience OR Masters degree with 2 years of relevant experience OR PhD, * 3 years of experience developing embedded software using C and C++.

 * Strong knowledge of embedded systems design, low-level firmware development, device drivers, peripherals, and communication protocols.
 * Experience developing software for medical devices or other regulated products, with a solid understanding of applicable software development processes and quality standards.
 * Experience developing and debugging Bluetooth Low Energy (BLE) embedded firmware, including wireless communication protocols, device connectivity, power optimization, and interoperability across mobile and embedded platforms.
 * Experience partnering with Systems Engineering, Verification & Validation, Human Factors, Quality, and other cross-functional stakeholders throughout the product development lifecycle.
 * Experience authoring software requirements and translating them into comprehensive verification strategies, test designs, and test cases.
 * Experience participating in the complete software development lifecycle, from planning and design through implementation, verification, and product release.
 * Familiarity with regulated software development environments and industry standards for medical device software.
 * Knowledge of Medtronic Neuro devices, programs, and associated software applications is preferred.
 * Strong written and verbal communication skills, with the ability to effectively collaborate across cross-functional teams.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

## Description

As a Sr. Software Engineer, you will design, develop, and verify embedded software for implantable medical devices that advance Pelvic Health Therapies. Working in a highly regulated medical device environment, you will contribute to the full software development lifecycle - from requirements and architecture through implementation, testing, verification, and product release. You'll collaborate with cross-functional teams, including Systems, Electrical Engineering, Security, and Quality, to deliver safe, reliable, and innovative therapy solutions while ensuring compliance with medical device regulations and quality standards., * Own firmware features for implantable neurostimulator systems.

 * Design, develop, and maintain embedded software using Bluetooth Low Energy (BLE) and proprietary communication protocols.
 * Develop embedded software utilizing various BLE stacks.
 * Contribute to firmware requirements, architecture, traceability, scope management, software hazard analysis, and design documentation.
 * Design, implement, debug, and optimize embedded firmware while executing unit and integration testing.
 * Develop test designs, test scripts, and formal technical reports to support verification activities.
 * Perform regression testing, failure analysis, and debugging of embedded software and automated test scripts.
 * Analyze test data, document findings, and recommend design or process improvements.
 * Collaborate with cross-functional teams to support overall system design and product development.
 * Participate in design reviews, development milestones, and product release activities.
 * Ensure compliance with medical device regulations, software development processes, and quality system requirements while driving continuous improvement.


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