Eko is seeking a Director of Regulatory Affairs to lead global strategy for SaMD and hardware. You will own FDA/CE/Health Canada submissions, shape regulatory pathways, and partner with R&D, Quality, and Commercial teams to accelerate compliant market access.
You will build and mentor a small team, embed intelligence on EU MDR and AI regulation, and drive submission excellence while aligning with business goals. Based in Emeryville, CA.
#J-18808-LjbffrGlobal Regulatory Affairs Director — AI MedTech in emeryville at Unknown Company
This position is listed as full time and onsite.