QA Engineer - Medical Devices, ISO
Listed on 2026-10-07
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Prismatik in Irvine, CA is seeking a Quality Assurance Engineer to integrate quality into every stage of medical device development and manufacturing. You will own quality engineering, risk management, CAPA, validation, and QMS activities, collaborating across functions to ensure safety, performance, and regulatory compliance.
You will drive investigations, root cause analyses, design verification, and continuous improvement across processes and products, with an onsite role that emphasizes high
The QA Engineer
- Medical Devices, ISO 13485 role at Prismatik is now open for applications in Irvine, CA, United States.
This is a great role to take on the QA Engineer
- Medical Devices, ISO 13485 role at Prismatik.
As a QA Engineer
- Medical Devices, ISO 13485, you will play an important part at Prismatik in Irvine, CA, United States.
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