Route 92 Medical is seeking a Senior Regulatory Affairs Specialist to lead international submissions and regulatory lifecycle activities for UK, LATAM, and Japan from our San Mateo option or West Jordan, UT in a hybrid working environment. The role requires a minimum of 5 years in medical device regulatory affairs, plus strong writing and communication skills to collaborate with cross-functional teams and regulatory authorities.

Also on the board Same function, level within a rung

Level

Manager

Location

San Mateo, CA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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