About the role

Advanced Sterilization Products, Fortive family, seeks a senior Quality Engineer to lead risk management, design control, and verification/validation across new product introductions and lifecycle management. You will investigate complex issues, coordinate cross-functional teams, and ensure compliance with FDA QSR 21 CFR 820 and ISO 13485. The role includes audits support and process improvements. The ideal candidate has 4+ years in quality engineering within regulated industries, strong

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JOB OVERVIEW

Experience level

Senior

Location

Irvine, CA

Occupation

Validation Engineers

Industry

Surgical Appliance and Supplies Manufacturing

Posted

yesterday

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