Regulatory Affairs Expert Drug/Device (Hybrid)
Systems Plus
Systems Plus, Inc. is seeking a Regulatory Affairs Subject Matter Expert in Frederick, Maryland. This full-time, hybrid role focuses on directing regulatory strategy across drugs, biologics, medical devices and related medical solutions to support military and federal agency products. You will develop submissions, interact with FDA and other agencies, mentor team members, and collaborate with R&D, manufacturing, and clinical teams to ensure regulatory compliance throughout the product lifecycle. #J-18808-Ljbffr Systems Plus
Vacancy posted 1 day ago
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