U.S. Biosimilars Regulatory Lead — Hybrid Work (Princeton)

Full-time

U023 (FCRS = US023) Sandoz Inc

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.

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Vacancy posted 2 hours ago

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