Regulatory Affairs Specialist - FDA Submissions & Strategy

A leading global engineering and sciences firm is seeking a Regulatory Affairs Specialist in St. Louis, MO. This role involves managing FDA applications, compiling and submitting necessary documents in eCTD format, and overseeing regulatory impacts of changes. Ideal candidates should have at least 3 years of experience in regulatory affairs within the pharmaceutical sector and a strong understanding of CMC processes. The position offers competitive pay rates and various benefits, requiring full onsite work in St. Louis. #J-18808-Ljbffr