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© All Rights Reserved. ApplyBlast.com
masimo
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 regulatory requirements. This on-site role in Irvine, CA, supports the regulatory team in managing international and domestic filings, coordinating product changes, and communicating with health authorities worldwide. The position reports to the Director of Regulatory Affairs and contributes to the company's mission of innovating patient care technologies.
Headquarters
Irvine, California, United States
Company Size
1001-5000 employees
Founded
1989
Masimo is a global medical technology company headquartered in Irvine, California, that develops noninvasive patient monitoring technologies and systems for hospitals, clinics, and home care. Best known for its SET pulse oximetry and Rainbow™ platform—designed to measure multiple blood parameters noninvasively—Masimo offers bedside and wearable monitors, sensors, connectivity platforms, and telehealth solutions to support clinical decision-making and remote care. Founded by Joe Kiani, the company focuses on innovation in patient safety, continuous monitoring, and interoperability with health‑care IT, and its products are used worldwide across acute and ambulatory settings.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for masimo.