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# Sr. Software Systems Engineer

- **Company:** Medtronic Inc.
- **Location:** Minneapolis, MN, United States
- **Experience:** Expert
- **Salary:** $120,800.0 - $181,200.0
- **Contract:** Temporary contract
- **Skills:** Adobe InDesign, Agile Methodology, Artificial Intelligence, Data Analysis, Systems Engineering, Software Quality, Computer Engineering, Iterative and Incremental Development, Software Architecture, Software Engineering, Software Requirements Analysis, Software Systems, Verification and Validation (Software), Systems Architecture, Integration Tests
- **Published:** August 8, 2026
- **Apply:** https://www.minneapoliscareersite.com/job.asp?id=3347476028&tx=VT6762TYD&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

The ideal candidate combines strong systems engineering and software development knowledge with experience in design controls, risk management, verification and validation, and regulatory expectations for medical device development., * Bachelor's degree in Software Engineering, Computer Engineering, Electrical Engineering, Systems Engineering, or a related technical field and minimum of 4 years of relevant experience OR Master's degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience.

 * Demonstrated experience with design controls, software development lifecycle activities, and verification/validation.
 * Strong understanding of risk management principles, design failure analysis concepts, and traceability across requirements, design, and testing.
 * Experience supporting cross-functional product development teamss, * Strong written and verbal communication skills with the ability to influence and collaborate effectively.
 * Ability to manage multiple priorities in a fast-paced environment.
 * Experience in software engineering, systems engineering, design assurance, reliability, or quality engineering in a regulated industry.
 * Experience in the medical device industry or another highly regulated environment.
 * Knowledge of IEC 62304, ISO 14971, ISO 13485, FDA design control expectations, and related standards.
 * Familiarity with agile development environments and how quality practices integrate into iterative development.
 * Experience with AI used in process development and embedded in products
 * Experience with software architecture reviews, cybersecurity considerations, or usability/human factors support.
 * Advanced degree in engineering or a related discipline.

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

Across our global Neuroscience organization, we advance care for some of medicine's most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey.

The Senior Software Systems Engineer on the Neuromodulation and Pelvic Health Pre-Market Design Quality team will partner with cross-functional development teams to ensure software and system-level design activities are planned, executed, and documented in compliance with applicable quality and regulatory requirements.

This role supports new product development by providing quality oversight and technical guidance throughout the design control lifecycle, with a focus on software-intensive medical device systems., * Provide design quality support for software and software-enabled medical device development programs from concept through transfer to manufacturing.

 * Ensure compliance with applicable design control, software lifecycle, and risk management requirements.
 * Review and contribute to system requirements, software requirements, architecture, and design documentation.
 * Support development of verification and validation strategies for software, system, and integration testing.
 * Partner with engineering, product development, regulatory, clinical, manufacturing, and quality teams to resolve design quality issues.
 * Evaluate software development deliverables for completeness, traceability, and regulatory readiness.
 * Support risk management activities, including hazard analysis, software-related risk evaluation, and mitigation verification.
 * Participate in design reviews and provide constructive feedback to improve product quality, safety, and compliance.
 * Assist in root cause analysis and corrective action activities related to design or software quality issues.
 * Mentor less experienced engineers on design quality practices, documentation expectations, and compliance requirements.
 * Contribute to continuous improvement initiatives for design quality processes, tools, and templates.


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