LT
Design Verification Engineer
Accepting applicationsL&T Technology Services · Houston, TX
Contract Entry
Posted
1d ago
Category
Verification
Experience
Entry
Country
United States
We are looking for a Design Verification Engineer with experience in Class II or Class III medical devices to join a leading medical device project in Houston, TX. If you have a strong background in design verification, product testing, and regulatory compliance, we'd love to hear from you!
Key Responsibilities:
Plan and execute design verification activities for medical devices.
Develop verification protocols, test plans, and reports.
Perform functional, electrical, mechanical, and system-level testing.
Analyze test results, troubleshoot issues, and document findings.
Maintain Design History File (DHF) documentation and requirements traceability.
Collaborate with R&D, Quality, Regulatory, and Manufacturing teams.
Ensure compliance with FDA regulations, ISO 13485, IEC 60601, and other applicable standards.
Required Qualifications:
Bachelor's degree in Electrical Engineering or Biomedical Engineering.
3–5 years of Design Verification experience.
Hands-on experience with Class II or Class III medical devices.
Strong knowledge of verification testing, documentation, and medical device regulations.
Excellent analytical, problem-solving, and communication skills.
Ability to work onsite in Houston, TX.
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Key Responsibilities:
Plan and execute design verification activities for medical devices.
Develop verification protocols, test plans, and reports.
Perform functional, electrical, mechanical, and system-level testing.
Analyze test results, troubleshoot issues, and document findings.
Maintain Design History File (DHF) documentation and requirements traceability.
Collaborate with R&D, Quality, Regulatory, and Manufacturing teams.
Ensure compliance with FDA regulations, ISO 13485, IEC 60601, and other applicable standards.
Required Qualifications:
Bachelor's degree in Electrical Engineering or Biomedical Engineering.
3–5 years of Design Verification experience.
Hands-on experience with Class II or Class III medical devices.
Strong knowledge of verification testing, documentation, and medical device regulations.
Excellent analytical, problem-solving, and communication skills.
Ability to work onsite in Houston, TX.
Show more Show less