Senior SaMD Regulatory Lead

A leading global information services company is seeking a Senior Regulatory Affairs Specialist. In this role, you will guide product teams through regulatory requirements for Software as a Medical Device (SaMD), ensuring compliance with global standards. Ideal candidates will have over 5 years of regulatory affairs experience, excellence in leading significant medical device submissions, and a strong understanding of SaMD regulations. This hybrid position allows flexibility with in-office requirements for 8 days a month, promoting a healthy work-life balance.