MDR Regulatory Reporting Specialist

Medline Industries, Inc.

Medline Industries, LP is seeking a Regulatory Reporting Specialist to review and correlate product complaints for MDR reportability under FDA regulations and 21 CFR 803. This role ensures complete data collection and accurate regulatory decisions across Quality, Regulatory Affairs, and R&D teams. The candidate will prepare MDR submissions via the FDA eMDR portal and coordinate with international regulatory partners to meet global reporting obligations. #J-18808-Ljbffr Medline Industries, Inc.

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Vacancy posted 4 days ago

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