Software Verification Engineer I

Location: St. Paul, MN (Onsite)
Duration: 6-month contract with possibility for extension
Schedule: Monday–Friday, 8:00 AM–5:00 PM
Employment Type: W2 Contract 

About the Role

We are seeking a motivated and detail-oriented Software Verification Engineer I to join a collaborative software verification team supporting innovative medical device technologies. This is an excellent opportunity for recent graduates or early-career engineers looking to develop hands-on experience in software testing, verification, and quality processes within a regulated environment.

The ideal candidate is a strong communicator, eager to learn, and passionate about ensuring software quality through thorough testing and documentation.

Key Responsibilities

• Develop, execute, and maintain software verification test cases and test protocols.
• Analyze software requirements and design effective verification strategies.
• Create new test suites to support product enhancements and new functionality.
• Perform verification activities, including dry runs and formal testing.
• Set up and configure test equipment and test environments.
• Document test results and maintain accurate records in accordance with quality standards.
• Identify, document, and support resolution of software defects.
• Participate in requirements, design, and test reviews.
• Collaborate with cross-functional teams including software development, systems engineering, and quality teams.

Required Qualifications

• Bachelor’s degree
• Understanding of software testing principles and methodologies.
• Strong written and verbal communication skills.
• Excellent attention to detail and organizational skills.
• Ability to work independently and within a team environment.
• Strong analytical and problem-solving capabilities.
• Demonstrated project, internship, or academic experience that showcases technical aptitude.

Preferred Qualifications

• Exposure to software verification, validation, or testing activities.
• Internship, academic project, or professional experience in medical devices, healthcare technology, or regulated industries.
• Familiarity with software development lifecycle (SDLC) concepts.
• Knowledge of FDA-regulated or ISO-compliant environments.
• Exposure to electrophysiology (EP), cardiac mapping, or medical device systems.

What We're Looking For

• Team-oriented and collaborative mindset.
• Strong willingness to learn and grow in a technical environment.
• Patient, dependable, and proactive approach to problem solving.
• Ability to effectively communicate technical information to diverse audiences.