Senior Regulatory Affairs Specialist - Onsite

What you’d do

Serve as regulatory data subject matter expert for the Neurovascular portfolio, managing data governance, UDI coordination, standards gap assessments, and regulatory change evaluations. Full-time onsite role in Irvine, California. Found on the employer's careers page on Oct 20, 2026. Apply through the link.

You’ll need

• Bachelor's degree and 4+ years regulatory affairs, quality, standards, or medical device experience,
• Experience managing projects or processes with multiple stakeholders
• Regulatory data governance and data quality experience
• UDI and device registration experience
• Onsite in Irvine, California