Regulatory Affairs Associate - CMC & PMA Submissions Lead

A life sciences firm in Miami is seeking a Regulatory Affairs professional to manage projects focused on Compliance Management Change (CMC) processes. The ideal candidate will have a minimum of 4 years in the pharmaceutical industry, strong project management skills, and familiarity with regulations for Class III implantable medical devices. This role requires detail-oriented individuals with excellent communication abilities to collaborate across various teams and ensure successful authoring and submission of necessary regulatory documents. #J-18808-Ljbffr