Software Verification Engineer I

Software Verification Engineer I

Location: St. Paul, MN (On‑site)

Duration: 6‑month contract (extensions and conversion possible)

Experience Level: Entry Level

A global medical device organization is seeking a Software Verification Engineer I to join its Software Verification team supporting a real‑time cardiac mapping and ablation system. This role focuses on ensuring software performs safely, accurately, and reliably in a highly regulated medical device environment.

This is an excellent entry‑level opportunity for recent graduates or early‑career engineers looking to gain hands‑on experience in medical device software verification. The role includes structured onboarding, mentorship, and strong potential for contract extension and full‑time conversion based on performance and business needs.

• Plan, write, execute, and document manual software test cases in compliance with internal procedures and FDA/ISO standards
• Analyze system and software requirements to design effective test strategies and test suites
• Execute dry runs and formal Verification & Validation (V&V) activities
• Identify, document, track, and support resolution of software defects
• Configure and maintain test equipment and environments (mapping systems, monitors, amplifiers, RF generators)
• Participate in requirements, design, and test reviews to ensure traceability and quality
• Collaborate cross‑functionally with software, systems, and quality teams

• First 4 weeks: Structured training, self‑paced learning, and shadowing
• By 90 days: Strong understanding of the application and independent test execution
• Longer term exposure to test development and automation as the team evolves

• Bachelor’s degree in Computer Science, Computer Engineering, Electrical Engineering, Biomedical Engineering, or equivalent (required)
• 0–2 years of experience (recent graduates encouraged to apply)
• Foundational understanding of software testing principles and methodologies
• Strong attention to detail, documentation, and problem‑solving skills
• Excellent written and verbal communication skills
• Willingness to learn and adapt in a regulated environment

• Python coursework or 1–2 years of hands‑on experience
• Exposure to medical device or regulated software environments

• On‑site, collaborative engineering environment
• Regulated medical device development setting
• One‑on‑one mentorship with senior team members
• Highly collaborative culture across engineering, quality, and regulatory teams

• Hands‑on experience supporting life‑critical medical device software
• Structured training and strong mentorship
• Opportunity to grow technical and regulatory skills
• High potential for contract extension and full‑time conversion

This is a Contract position based out of St Paul, MN.

The pay range for this position is $25.00 - $30.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in St Paul,MN.

This position is anticipated to close on Apr 17, 2026.

We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

We’re a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We’re a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We’re strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We’re building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.