Regulatory Affairs Associate, CMC & PMA Submissions

A pharmaceutical manufacturing company located in Miami, FL is seeking a Regulatory Affairs Associate to manage CMC dossiers and ensure compliance with FDA regulations for Class III implantable medical devices. The ideal candidate will have a BA/BS in Chemical or Biological Sciences and 4+ years of relevant experience. Responsibilities include preparing regulatory submissions, collaborating with project teams, and ensuring the accuracy and thoroughness of submissions. This role is a contract position at the mid-senior level with strong project management and communication skills required. #J-18808-Ljbffr