Senior Manager Regulatory Affairs
Sandoz
Sandoz, located in Princeton, NJ, seeks a Regulatory Affairs professional to support the US biosimilar regulatory program and lifecycle management for products in development and on the market. You will prepare US eCTD documents, manage regulatory archives, and coordinate Health Authority interactions across cross‑functional teams in a hybrid work model with remote options. Requirements include a Bachelor in science, 3–5 years of regulatory affairs experience (biosimilars preferred), and fluent #J-18808-Ljbffr
Vacancy posted 12 hours ago
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