Senior Medical Device Regulatory Lead
viltisBrooklyn (NY)
About the role
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
Before you apply
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Your profile is current
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Two examples you can talk through
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A number in mind
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Your notice period
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Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.
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