Regulatory Product Strategy Lead – SaMD & Digital Health

A global health technology company in San Diego is seeking a Regulatory Affairs professional to provide regulatory guidance for software-driven and digital health solutions. Responsibilities include authoring FDA submissions, evaluating regulatory impact, and ensuring compliance with global regulations. Ideal candidates will have a minimum of 3 years in regulatory affairs, experience with Software as a Medical Device (SaMD), and strong communication skills. Join a diverse culture focused on innovation and excellence. #J-18808-Ljbffr