Verification & Validation Test Engineer. (1159880)

The Judge Group; Marlborough (MA); On-site; USD 75,000 - 90,000; Full time

Job summary

The Judge Group seeks a Verification & Validation Test Engineer in Marlborough, MA to design, build, and validate test methods for medical devices in an ISO 13485 and FDA QSR environment. You will execute V&V for electromechanical devices and disposables, develop test methods, document protocols and data, and ensure compliance with ISO 13485, FDA 21 CFR Part 820, and ISO 14971.

This is a full-time permanent role with benefits like 401k, dental, vision, etc.

Qualifications

• Bachelor’s degree in Mechanical, Electrical, Biomedical, or Quality Engineering.
• 1–3 years of engineering experience within the medical device or regulated industry.
• Working knowledge of ISO 13485, FDA QSR, and ISO 14971 risk management standards.
• Direct experience in planning and/or execution of Verification and Validation for complex electrotechnical devices.

Responsibilities

• Medical Device Testing: Execute Design Verification and Validation activities for complex electromechanical devices and single-use disposables.
• Test Method Development: Design, develop, validate and execute test methods to inform design decisions and verify system functionality.
• Documentation: Author test protocols, data sheets, and final reports. Author/assist manufacturing procedures, machine instructions.
• Quality Compliance: Ensure all activities align with ISO 13485, FDA 21 CFR Part 820, and risk management standards.
• Data Analysis: Apply statistical techniques like ANOVA, Gage R&R, and capability analysis to test datasets.
• Communication: Present test findings to relevant stakeholders, communicate risk and countermeasure insights as applicable.

Education

Bachelor’s degree in Mechanical, Electrical, Biomedical, or Quality Engineering

Job description

Location: Marlborough, MA

Salary: $75,000.00 USD Annually - $90,000.00 USD Annually

Description: Our client is currently seeking a Verification & Validation Test Engineer.

The Verification and Validation Test Engineer designs, builds, and validates test methods for verification and validation testing for medical devices and disposables in an ISO 13485 and FDA QSR compliant environment.

This is a full time permanent role with benefits like 401k, dental, vision etc.

Key Responsibilities

• Medical Device Testing: Execute Design Verification and Validation activities for complex electromechanical devices and single-use disposables.
• Test Method Development: Design, develop, validate and execute test methods to inform design decisions and verify system functionality.
• Documentation: Author test protocols, data sheets, and final reports. Author/assist manufacturing procedures, machine instructions.
• Quality Compliance: Ensure all activities align with ISO 13485, FDA 21 CFR Part 820, and risk management standards.
• Data Analysis: Apply statistical techniques like ANOVA, Gage R&R, and capability analysis to test datasets.
• Communication: Present test findings to relevant stakeholders, communicate risk and countermeasure insights as applicable.

Required Qualifications

• Education: Bachelor’s degree in Mechanical, Electrical, Biomedical, or Quality Engineering
• Experience: 1–3 years of engineering experience within the medical device or regulated industry.
• Regulations: Working knowledge of ISO 13485, FDA QSR, and ISO 14971 risk management standards.
• Verification & Validation: Direct experience in planning and/or execution of Verification and Validation for complex electrotechnical devices.

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