Hybrid Regulatory Associate - eCTD & FDA Submissions

A pharmaceutical company in New Jersey seeks a Regulatory Affairs Associate to support regulatory submissions and document management, ensuring compliance with FDA standards. Candidates should have a Bachelor's degree, 5+ years of relevant experience in Regulatory Affairs, and proficiency in eCTD publishing tools. This role requires strong attention to detail and communication skills, with a hybrid work environment expected. #J-18808-Ljbffr