Senior Systems Verification Engineer

Senior Systems Verification Engineer – Medical Devices

Location: Plymouth, MN (100% Onsite)

Pay Rate: $50/hr W2

Contract Duration: 12 Months

Start Date: November 16, 2026

End Date: November 14, 2027

Employment Type: Contract

We are seeking an experienced Senior Systems Verification & Validation (V&V) Engineer to support the development, testing, and validation of complex medical devices and electromechanical systems.

This is a hands‑on engineering role focused on ensuring medical devices perform safely, reliably, and according to product requirements. The ideal candidate will have experience developing test strategies, executing system‑level and hardware verification tests, analyzing performance data, and investigating product failures.

• Develop, execute, and document system‑level and hardware‑level verification and validation testing for complex medical devices.
• Create and maintain test plans, verification protocols, technical reports, requirements traceability matrices, and risk assessments.
• Perform hands‑on testing of electromechanical systems integrating hardware, software, sensors, and mechanical components.
• Apply statistical methods such as Design of Experiments (DOE), ANOVA, capability analysis, and sample-size determination to evaluate product performance.
• Investigate test failures, perform root cause analysis, and collaborate with engineering teams to resolve product defects.
• Develop and validate test methods to ensure accurate, repeatable, and reliable testing results.
• Support requirements verification, risk‑based testing, and regulatory compliance.
• Identify opportunities to improve testing efficiency through automation, simulation, and alternative verification approaches.
• Collaborate with cross‑functional engineering, quality, and product development teams.

• Bachelor's degree in Engineering with 4+ years of relevant experience OR an advanced Engineering degree with 2+ years of relevant experience.
• Ability to work 100% onsite in Plymouth, MN.

• Experience with medical device verification and validation in a regulated environment.
• Hands‑on experience testing complex electromechanical or software‑controlled systems
  .
• Experience developing and executing system‑level test protocols and verification plans.
• Knowledge of statistical analysis, including DOE, ANOVA, capability analysis, and sampling methodologies.
• Experience with requirements management tools such as DOORS, Jama Connect, Polarion, Codebeamer, or Open Text ALM.
• Proficiency with Minitab, MATLAB, Python, R, or similar data analysis tools.
• Experience with requirements traceability, risk assessments, and test method validation.
• Strong troubleshooting, root cause analysis, and technical documentation skills.
• Familiarity with Agile product development and continuous improvement initiatives.

The ideal candidate has a strong background in systems verification, medical device testing, and electromechanical systems
. They are comfortable independently developing testing strategies, conducting hands‑on verification activities, interpreting statistical data, and collaborating with engineering teams to ensure product quality and reliability.

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