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# Software Systems Engineer II

- **Company:** Medtronic Inc.
- **Location:** Saint Paul, MN, United States
- **Salary:** $93,600.0 - $140,400.0
- **Contract:** Temporary contract
- **Skills:** Application Programming Interfaces (APIs), Agile Methodology, C Sharp (Programming Language), C++ (Programming Language), Computer Programming, Firmware, Failure Mode Effects Analysis, Hardware Interface Design, Python (Programming Language), Software Architecture, Systems Development Life Cycle, Software Engineering, Software Requirements Analysis, Software Systems, Systems Modeling Language, Systems Architecture, Git, Hardware Infrastructure, Software Version Control, Programming Languages
- **Published:** October 14, 2026
- **Apply:** https://www.techcareers.com/job.asp?id=3445763264&tx=CT3331TTV&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

Medtronic is seeking a motivated and detail-oriented Software Systems Engineer II to join our Affera Mapping and Ablation System team, supporting the design and development of advanced software-enabled capital systems for the cardiac electrophysiology lab., * Bachelor's degree with a minimum of 2 years of experience, or master's degree plus 0 years related experience.

 * Knowledge of Medical Product development, IEC-62304, ISO 13485, and FDA guidance in a technical discipline, preferably software related, or relevant regulated industries
 * Proficient in programming languages such as Python, C++/C# or similar languages
 * Experience with requirements-driven development and traceability.
 * Familiarity with MBSE concepts and SysML.
 * Strong understanding of good documentation practices

Preferred Qualifications

 * Model-Based Systems Engineering (MBSE) and system architecture modeling
 * SysML v1/v2 proficiency and associated modeling tools
 * Requirements development and bidirectional V-model traceability
 * Software and hardware interface definition, allocation, and risk identification
 * Regulated medical-device software development, including IEC 62304, ISO 13485, and FDA guidance
 * Software risk management and FMEA
 * Programming proficiency in Python, C++, C#, or similar languages
 * Technical documentation and report writing
 * Cross-functional collaboration and clear written and verbal communication
 * Agile development, Git-based version control, and process/tooling improvement

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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

* Develop and maintain system and software architecture models using SysML (v1/v2).
 * Apply MBSE principles to connect system intent to software services, APIs, schemas, modules, and firmware.
 * Define interface contracts and allocations between system functions, software, and hardware components.
 * Support V-model traceability across requirements, design, implementation, and verification
 * Author and review software system requirements with full bidirectional traceability.
 * Perform risk analysis activities including FMEA and interface risk identification.
 * Contribute to process and tooling improvements for MBSE adoption and trace automation.
 * Apply the appropriate standards, processes, procedures, and tools throughout the system development life cycle.