CMC Regulatory Affairs Associate II — Submission Expert

A pharmaceutical company located in Jersey City is seeking an experienced professional to manage and compile chemistry, manufacturing, and control (CMC) sections for marketed product variations. The role requires a Bachelor's degree in science and 4 years of relevant pharmaceutical experience. The candidate should possess strong project management skills and the ability to collaborate across multiple teams, ensuring timely and accurate regulatory submissions. This position is critical for supporting submission documents and regulatory filings. #J-18808-Ljbffr