Job Description Job Title: Sr Test Engineer
Client: Medical Device Manufacturing Company
Duration: 12 Months Contract
Location: Lafayette, CO 80026
Job Summary
Lead system verification and validation (V&V) activities for Interventional medical device products. Responsible for verification planning, test method development/validation, test execution, technical analysis, and regulatory-ready documentation while working with cross-functional R&D teams.
Show more Key Responsibilities
Develop verification plans, protocols, sample-size justifications, and acceptance criteria. Lead design-input verification for sterilized disposable instruments. Develop and validate test methods, plans, and validation reports. Execute system-level verification testing and document results. Prepare regulatory submission-ready engineering reports. Support design validation using real users in simulated or actual-use environments. Support design reviews, risk management, and system-level validation. Collaborate with Systems, Mechanical, Electrical, Quality, Manufacturing, Marketing, Human Factors, and Regulatory teams. Perform minimally invasive therapy/product testing in soft tissue according to applicable standards. Analyze test results and communicate findings, conclusions, and recommendations. Provide technical leadership to engineers and external development partners. Support V&V activities throughout the product development lifecycle. Numbers & Facts Location Lafayette, CO Job Type Contractor Salary $50–$55 Per Hour
Qualifications Required Qualifications
Bachelor’s degree in Engineering/Science + 6+ years technical testing or engineering experience; OR Advanced degree + 4+ years relevant experience. Experience leading system-level verification and validation planning, execution, and documentation. Experience with ex-vivo tissue testing. Basic mechanical and electrical engineering knowledge. Experience with test equipment such as Instron and multimeters. Ability to work independently and cross-functionally. Strong organization, prioritization, communication, and technical reporting skills. Preferred Qualifications
Medical device, aerospace, defense, or other regulated industry experience. Knowledge of IEC 60601, electrical safety, and EMC testing. Design for Reliability/Manufacturability and Six Sigma knowledge. Experience tracing system design inputs through test results. Experience with systems combining mechanical, electrical, and software components. Experience owning systems-engineering execution across the full V-model lifecycle. Top 3 Technical Skills
V&V Strategy & Leadership Test Method Development & Validation Test Execution & Regulatory Documentation About Company Medical Device Manufacturing Company
Skills
Cross-Functionalunmatched
Documentationunmatched
Manufacturingunmatched
Medical Equipmentunmatched
Medical Productsunmatched
Quality Assurance Methodologyunmatched
Regulationsunmatched
Research & Development (R&D)unmatched
System Validationunmatched
Technical Analysisunmatched
Test Plan/Scheduleunmatched
Testingunmatched
Validation Testingunmatched
Verification Plansunmatched
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