Senior Software Engineer

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 for a Twin Cities medical technology company. You will develop and maintain software used in advanced medical procedures, owning requirements, design, testing and regulatory compliance.

The role requires hands-on engineering, strong debugging skills, and collaboration with cross-functional teams to deliver safe, compliant software across complex systems.

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.

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

C#

Python

Job description

• Job Tag:
• Posted: September 09,2026
• 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 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.