Verification & Validation Test Engineer.

Marlborough, MA, US • Posted 1 day ago • Updated 51 minutes ago
Full Time
On-site
USD $75,000.00 - 90,000.00 per year
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Fitment

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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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