Remote Principal Regulatory Consultant: Hands-On FDA/EU MDR

A consulting firm specializing in regulatory affairs is seeking a Principal Regulatory Consultant to lead global regulatory strategies for medical devices and biologics. The role involves preparing and submitting regulatory filings, driving compliance activities with FDA and EU standards, and performing quality engineering. Ideal candidates have over 15 years of experience in regulatory affairs, with strong regulatory communication skills. This position offers an opportunity to work on meaningful engagements that make a significant impact in the regulatory landscape.