Position Details
About this role
This role involves supporting quality engineering activities for medical devices, including design verification, validation, risk management, and reliability testing to ensure compliance and product quality.
Key Responsibilities
- Support design verification
- Conduct validation testing
- Lead risk management activities
- Perform FMEA sessions
- Ensure documentation control
Technical Overview
Focus on quality engineering, design verification and validation, risk management, FMEA, statistical testing, and regulatory compliance within medical device development.
Ideal Candidate
The ideal candidate is a mid-level quality engineer with 3+ years supporting design verification, validation, and risk management in medical device development. They are familiar with FMEA, statistical testing, and regulatory standards.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of experience in medical device quality engineering, No experience with design verification or validation, Inability to support risk management and FMEA
Get matched to jobs like this
Luna finds roles that fit your skills and career goals — no endless scrolling required.
Create a Free Profile