Global Regulatory Affairs Specialist - Medical Devices

A leading technology company located in Chantilly, Virginia, seeks a Regulatory Affairs Specialist to support regulatory submissions and compliance activities for Class I ELISA instruments and consumables. The ideal candidate will hold a Bachelor's degree in a scientific field with 2–3 years of relevant experience in regulatory affairs. Key responsibilities include maintaining device registrations and supporting updates to global product technical files.

This role requires excellent communication and technical writing skills, along with a strong understanding of regulatory requirements.
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