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Verification & Validation Test Engineer.

Judge Group, Inc.

Marlborough, Massachusetts • Today

Full-time

USD 75,000.00 - 90,000.00 per year

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Full-time

Senior Verification Engineer

Analog Devices, Inc.

Wilmington, Massachusetts • Today

Full-time

USD 110,385.00 - 151,808.00 per year

Senior Software Verification & Validation Engineer

Draper

Cambridge, Massachusetts • Today

Full-time

USD 75,000.00 per year

Judge Group, Inc.

Job Details

Skills

Mergers and Acquisitions
Testing
Electromechanics
Test Methods
Documentation
Manufacturing
Regulatory Compliance
Data Analysis
Analysis Of Variance
Communication
Mechanical Engineering
Electrical Engineering
Biomedicine
Quality Assurance
Medical Devices
ISO 13485
ISO 9000
Risk Management
Management
Verification And Validation
Privacy
Marketing

Summary

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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Contact:
This job and many more are available through The Judge Group. Please apply with us today!

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: cxjudgpa
Position Id: 1159880
Posted 1 day ago

Company Info

About Judge Group, Inc.

The Judge Group, is a leading professional services firm specializing in talent, technology, and learning solutions. We consult, staff, train, and solve. Through our work we make people and organizations better.

Our services are successfully delivered through a network of more than 30 offices across the United States, Canada, and India. The Judge Group is proud to partner with the best and brightest companies in business today, including over 60 of the Fortune 100. We serve organizations in financial services, healthcare, life sciences, insurance, government (including aerospace and defense), manufacturing, and technology and telecommunications.

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Judge Group, Inc.

Job Details

Skills

Mergers and Acquisitions
Testing
Electromechanics
Test Methods
Documentation
Manufacturing
Regulatory Compliance
Data Analysis
Analysis Of Variance
Communication
Mechanical Engineering
Electrical Engineering
Biomedicine
Quality Assurance
Medical Devices
ISO 13485
ISO 9000
Risk Management
Management
Verification And Validation
Privacy
Marketing

Summary

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.

Dice Id: cxjudgpa
Position Id: 1159880
Posted 1 day ago

Company Info

About Judge Group, Inc.

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

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