Strategic Regulatory Labeling Lead – MedTech
Listed on 2026-10-06
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Healthcare
Healthcare Compliance, AI Business & Operations
PROCEPT Bio Robotics Corporation is seeking a Senior Regulatory Affairs Labeling Specialist in San Jose, CA. You will lead regulatory labeling activities for global submissions and author content for user manuals and labeling, ensuring compliance with 21 CFR and EU MDR guidelines.
The role requires 5+ years in medical device regulatory affairs, strong documentation skills, and experience coordinating with engineering, manufacturing, and legal teams.
This opportunity is for the Strategic Regulatory Labeling Lead – Med Tech role at PROCEPT Bio Robotics Corporation.
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This posting is for the Strategic Regulatory Labeling Lead – Med Tech role at PROCEPT Bio Robotics Corporation, based in Northern, KY, United States.
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