Regulatory Affairs Associate, IVD Medical Devices

Viltis

Viltis, a global diagnostics organization, seeks a detail-oriented Regulatory Affairs Specialist I to support regulatory submissions, product registrations, and quality management for IVD products in South Portland, Maine. The role focuses on domestic and international submissions within the Infectious Disease unit and requires strong organizational skills and a scientific background. Ideal candidates have 0–2 years in regulatory affairs, familiarity with FDA regulations, and the ability to #J-18808-Ljbffr Viltis

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Vacancy posted 2 days ago

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