Senior Global Regulatory Affairs Specialist
Masimo Corporation
Masimo Corporation in Irvine, CA is seeking an Sr Regulatory Affairs Specialist to oversee international and domestic registrations and lead regulatory submissions for medical device products. The role interfaces with Sales, Marketing, QA, and Engineering to ensure pre-market clearances and ongoing compliance across regions. The candidate should have 3+ years in a Class II/III medical device environment, strong FDA/International regulation knowledge, ISO 13485 experience, and proven ability to #J-18808-Ljbffr Masimo Corporation
Vacancy posted 2 days ago
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