Senior Software Engineer (Minnesota-Only)

SkyWater Search Partners; Lakeville (NY); On-site; USD 108,000 - 132,000; Full time

Job summary

SkyWater Search Partners is seeking a Senior Software Engineer to join a Twin Cities medical technology team developing sophisticated software used in advanced medical procedures. This hands-on role requires ownership of software requirements, design documentation, testing, and regulatory compliance.

Responsibilities include designing and debugging features across complex systems, translating requirements into testable software, maintaining architecture docs, and supporting verification and

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

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.
• Mentor engineers on requirements, traceability, and compliant development practices.

Skills

C#

Python

Regulated environment experience

Job description

• Salary: $120,000

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 processesMentor 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.