V&V Test Engineer

Irvine, CA, US • Posted 1 day ago • Updated 1 day ago
Full Time
No Travel Required
On-site
$100,000 - $110,000/yr
Fitment

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Job Details

Skills

  • Medical Devices
  • IQ
  • OQ
  • Veritas
  • Testing
  • Performance Testing
  • ISO 13485
  • PQ

Summary

Job Description
Must Have Technical/Functional Skills
•  5+ years of hands-on testing experience in medical device or regulated industry 
• Strong experience in: Executing IQ/OQ/PQ protocols, Protocol reading and step-by-step execution, Test data recording and documentation
• Familiarity with: Lab instruments (multimeters, oscilloscopes, sensors, etc.), Equipment validation processes
• Understanding of GxP and validation practices
• Experience with Veritas Console or similar medical equipment
• Exposure to equipment validation in manufacturing or R&D labs 
 
Roles & Responsibilities
We are looking for a hands-on V&V Test Engineer responsible for executing validation protocols on medical device equipment (Veritas Console). The role primarily involves protocol-based testing, data recording, and documentation to ensure equipment meets defined performance and regulatory requirements.
 
Key Responsibilities
Protocol Execution
• Execute pre-approved validation protocols (IQ/OQ/PQ) for medical equipment such as Veritas Console.
• Follow detailed step-by-step test procedures and ensure strict adherence to instructions.
• Set up test environments, instruments, and equipment as per protocol requirements.
Testing Activities
• Perform functional, operational, and performance testing of equipment.
• Conduct tests under various conditions and scenarios defined in protocols.
• Capture accurate test results, observations, and evidence during execution.
Documentation & Reporting
• Record test results in protocol documents, logbooks, and validation reports.
• Document any deviations, anomalies, or failures observed during testing.
• Ensure completeness and compliance of executed protocols per quality standards.
Defect & Issue Handling
• Identify and report defects or non-conformances.
• Work closely with engineering and quality teams for issue resolution.
• Retest equipment after fixes as required.
Compliance & Quality
• Ensure all activities comply with: 
o GxP guidelines
o FDA 21 CFR Part 820 / 11
o ISO 13485
• Maintain proper traceability and document control.
Equipment Handling
• Operate and handle medical equipment, test setups, and measurement instruments safely.
• Ensure calibration status of instruments before testing.
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: 91172467
  • Position Id: 9006095
  • Posted 1 day ago
Contact the job poster
DK

Dinesh Kumar

Recruiter @ TATA Consultancy Services Limited
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