
Global Regulatory Lead for AI/ML SaMD – Remote-Eligible
Cleerly, Denver, CO, United States
A healthcare technology company is seeking a Principal Regulatory Affairs Specialist to guide regulatory strategies for AI/ML-enabled medical devices. This role involves preparing submissions for global authorities and providing regulatory guidance throughout product development. The ideal candidate will have extensive experience in regulatory affairs within the medical device sector and a strong background in AI/ML technologies. Join us in playing a critical role in helping innovative technologies reach patients worldwide.
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