Regulatory Affairs Specialist, Medical Devices
Listed on 2026-10-15
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Healthcare
Healthcare Compliance, Healthcare Management
Pro-Dex, Inc. in Irvine, CA is seeking a Regulatory and Compliance Specialist to support product development with regulatory inputs, strategies, and design control deliverables. The role ensures compliance with local, state, federal and international requirements for medical devices.
Responsibilities include preparing submissions, reports, and supporting audits, while maintaining procedures and supporting 510(k)/CE documentation. Travel is occasional; in-office position in Irvine.
The following role is for a Regulatory Affairs Specialist, Medical Devices – Irvine with Pro-Dex, Inc.
This posting is for the Regulatory Affairs Specialist, Medical Devices – Irvine role at Pro-Dex, Inc., based in Irvine, CA, United States.
We are looking to fill the Regulatory Affairs Specialist, Medical Devices – Irvine position at Pro-Dex, Inc. in Irvine, CA, United States.
The Regulatory Affairs Specialist, Medical Devices – Irvine role at Pro-Dex, Inc. is now open for applications in Irvine, CA, United States.
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