iRhythm Technologies, Inc. is seeking a Senior Regulatory Affairs Specialist to lead global regulatory strategies for medical devices and SaMD. This remote US role partners with cross-functional teams to prepare submissions, align labeling, and navigate regulatory approvals.
You will interact with authorities, ensure lifecycle compliance, and contribute to post-market surveillance. 3 years of experience and knowledge of major regulations are required; travel up to 10% may be needed.
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