Regulatory Affairs Specialist: FDA Submissions & DMFs
Listed on 2026-10-03
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Healthcare
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Quality Assurance - QA/QC
Sandoz in Princeton, NJ seeks a Regulatory Specialist, Regulatory Affairs CMC, to prepare and manage regulatory submissions, DMFs, and FDA communications across lifecycle of generic products. You will partner with cross-functional teams to ensure compliance and timely filings.
This role requires coordinating with FDA, sustaining regulatory records, and prioritizing workloads in a hybrid environment with some US office-based work, up to 50% remote.
For the Regulatory Affairs Specialist: FDA Submissions & DMFs position at Sandoz, we are reviewing applications now.
We would love to welcome a new Regulatory Affairs Specialist: FDA Submissions & DMFs to our team in AL, United States.
Step into the Regulatory Affairs Specialist: FDA Submissions & DMFs role at Sandoz in AL, United States and grow with us.
Please review the full job details above before applying.
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