Senior Software Engineer

SkyWater Search Partners; Lakeville (MN); On-site; USD 110,000 - 150,000; Full time

Job summary

SkyWater Search Partners is seeking a Senior Software Engineer for a Twin Cities medical technology company to develop advanced software for medical procedures. This hands-on role demands ownership of requirements, design, testing, and regulatory compliance.

You will design, debug, and integrate software with embedded systems, contribute to documentation and audits, and mentor peers while collaborating with QA and engineering teams to support product releases.

Qualifications

• 5+ years of software engineering experience.
• Experience in a regulated environment, ideally medical devices.
• Strong experience with C#, Python.
• Experience with complex, integrated software/hardware systems.
• Strong debugging and problem-solving skills.
• Ability to translate technical concepts into clear documentation.
• Excellent communication and cross-functional collaboration skills.

Responsibilities

• Design, develop, debug, and support software features across complex integrated systems.
• Translate technical requirements into clear, testable software requirements.
• Create and maintain software design and architecture documentation.
• Support verification, traceability, and risk-management activities.
• Partner with QA and engineering teams to support product releases.
• Participate in code reviews, design discussions, and complex troubleshooting.
• Help improve software development and documentation processes.
• Mentor engineers on requirements, traceability, and compliant development practices.

Skills

Software engineering

Regulated environment experience

C#

Python

Debugging

Documentation

Cross-functional collaboration

Communication

Job description

A Twin Cities medical technology company is seeking a Senior Software Engineer to join a team developing sophisticated software used in advanced medical procedures.

This is a hands‑on engineering role for someone who enjoys building and debugging complex systems while also taking ownership of software requirements, design documentation, testing, and regulatory compliance.

Responsibilities

• Design, develop, debug, and support software features across complex integrated systems
• Translate technical requirements into clear, testable software requirements
• Create and maintain software design and architecture documentation
• Support verification, traceability, and risk‑management activities
• Partner with QA and engineering teams to support product releases
• Participate in code reviews, design discussions, and complex troubleshooting
• Help improve software development and documentation processes
• Mentor engineers on requirements, traceability, and compliant development practices

Qualifications

• 5+ years of software engineering experience
• Experience in a regulated environment, ideally medical devices
• Strong experience with C#, Python
• Experience with complex, integrated software/hardware systems
• Strong debugging and problem‑solving skills
• Ability to translate technical concepts into clear documentation
• Strong communication and cross‑functional collaboration skills

Preferred: Experience with IEC 62304, ISO 14971, requirements traceability, SDS/SAD, FMEA, DVT, verification/validation, or regulatory audits.