Biosimilars Regulatory Lead; US): Submissions & Strategy
Listed on 2026-10-07
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Business
Regulatory Compliance Specialist
Sandoz invites experienced Regulatory Affairs professionals to join our Princeton, NJ headquarters in a hybrid role that supports US regulatory strategy for biosimilar programs and guides submissions and lifecycle activities.
You will lead preparation and submission of INDs, BLAs, and supplements, coordinate FDA interactions, and ensure compliant strategies enabling timely approvals and ongoing post‑market compliance.
We are seeking a motivated Biosimilars Regulatory Lead (US):
Submissions & Strategy to join Sandoz US in Princeton, NJ, United States.
We have an opening for a Biosimilars Regulatory Lead (US):
Submissions & Strategy in Princeton, NJ, United States within Legal, Management & Operations.
This role, Biosimilars Regulatory Lead (US):
Submissions & Strategy at Sandoz US, could be your next career step.
Are you ready to take on the Biosimilars Regulatory Lead (US):
Submissions & Strategy role at Sandoz US?
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