Sandoz Inc in Princeton, NJ, is looking for an Associate Director of Regulatory Affairs – Biosimilars to lead U.S. regulatory strategy for biosimilar development. This pivotal role involves overseeing regulatory submission processes and ensuring compliance with FDA regulations while collaborating cross-functionally for timely approvals.
The ideal candidate will have at least 7 years of experience in regulatory affairs with a strong focus on biosimilar programs, supported by a relevant academic background. The position offers a competitive salary along with a hybrid work environment.
#J-18808-LjbffrU.S. Biosimilars Regulatory Lead — Hybrid Work in princeton at Unknown Company
This position is listed as full time and hybrid.