Position Details
About this role
Leads quality assurance activities including design verification, process validation, and risk management for medical devices.
Key Responsibilities
- Coordinate quality assurance activities
- Develop and execute validation protocols
- Lead risk management efforts
- Ensure compliance with regulations
- Support product lifecycle quality
Technical Overview
Focuses on quality systems, validation protocols, and regulatory compliance within healthcare product development.
Ideal Candidate
The ideal candidate is a senior quality engineer with extensive experience in medical device quality assurance, design verification, and process validation, capable of leading quality activities in a healthcare environment.
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 assurance, No background in validation or verification, Unwilling to work in Irvine
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