Senior Medical Device Regulatory Lead

Viltis is seeking a Senior Regulatory Affairs Specialist to support a leading medical device organization in San Diego, CA. The ideal candidate brings 7+ years of Medical Device Regulatory Affairs experience, with strong expertise in regulatory change assessments and U.S. submissions. You will partner with Quality, Engineering, Manufacturing, R&D and Marketing to ensure timely approvals, maintain regulatory compliance for marketed products, and assess impact of changes across the product