Regulatory Affairs Specialist

The Regulatory Affairs Specialist at Masimo is responsible for obtaining domestic and internal regulatory clearances for medical device products to ensure compliance with pre-market requirements. This on-site role in Irvine, CA, supports the regulatory team by managing filings, coordinating product changes, and assisting with communications regarding health authority inquiries. The position reports to the Director of Regulatory Affairs and contributes to the company's mission of innovating patient care technologies.