
Senior Principal Regulatory Affairs Lead, Medical Devices
Werfen North America, norcross, ga, United States
A leading medical device company seeks a Senior Principal Regulatory Affairs Specialist in Norcross, GA. This role involves managing regulatory submissions and ensuring compliance with FDA and international regulations. Candidates should have at least eight years of regulatory experience in the medical device industry, a Bachelor’s degree in a related field, and preferably RAPS certification. The position supports quality compliance and includes mentoring junior team members, contributing to product lifecycle projects. Occasional travel (10%) may be required.
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