Software Verification Engineer I
Location: Little Canada, Minnesota 55117
Schedule: Monday–Friday, 8:00 AM–5:00 PM (local time)
Work Authorization: Contract, W2
Work Arrangement: Onsite
Pay: $36-38/hr
About the Role
We’re looking for a Software Verification Engineer I to join a fast?paced verification team focused on delivering high?quality releases in a regulated environment. You’ll contribute across the verification lifecycle, requirements analysis, test design, execution, defect tracking, and closure, while collaborating closely with engineering and quality teams. This role is ideal for a detail?oriented tester with strong documentation skills who thrives in structured FDA/ISO practices.
What You’ll Do
- Plan, author, and execute test cases aligned to internal quality practices and FDA/ISO standard procedures.
- Design new test suites for features and enhancements; perform dry runs and formal verification & validation (V&V) activities.
- Set up and configure test equipment, environments, and data sets to enable repeatable testing.
- Log, track, and close defects discovered during V&V; partner with developers to drive resolution.
- Conduct requirements, design, and test reviews; ensure traceability and coverage.
- Produce clear, decision?ready documentation (test plans, procedures, results, deviation records).
What You’ll Bring
- Bachelor’s degree in Computer Science, Computer/Electrical Engineering, or Biomedical Engineering.
- Knowledge of software testing methods (functional, regression, negative, boundary, etc.).
- Familiarity with SDLC tooling (e.g., test case/defect management, requirements management, CI artifacts).
- Organized, on?time, quick learner, and detail?oriented.
- Excellent documentation and communication skills concise test evidence, status reporting, and stakeholder updates.
- Demonstrated quantitative/analytical ability, strong follow?up, and relationship building across teams.
- Proactive, self?starter with an energized attitude.
Nice to Have
- Exposure to medical?device or other regulated domains (FDA, ISO 13485)
- Experience with test automation scripting (e.g., Python/Matlab), data analysis tools (Excel/Minitab), or Linux test environments
- Familiarity with verification traceability (requirements ? tests ? defects)
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