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FDA-Focused Principal Regulatory Lead - Medical Devices
Edgewater, MDMarch 20th, 2026
A specialized medical device consulting firm is seeking a Principal Consultant to develop regulatory strategies for Class II and III devices. The ideal candidate should have 4-5 years of experience at the FDA or equivalent, and possess strong technical writing and regulatory compliance skills. Responsibilities include leading FDA submissions and serving as a primary liaison with the FDA to support innovative medical device companies. This role offers a chance to work with a talented team and contribute to long-term partnerships.
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