Senior CMC Regulatory Lead - Molecule
Listed on 2026-10-09
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Healthcare
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Management
Travere Therapeutics in the United States is seeking an Associate Director, CMC Regulatory Affairs to lead global regulatory strategies for small molecule products, focusing on oral solid dosage forms and lifecycle management.
The role serves as the primary CMC regulatory lead on cross-functional teams, collaborating with Regulatory Operations, Manufacturing, Quality, and Clinical Development to drive submissions with global authorities including FDA, EMA, GCC, and PMDA.
We are looking to fill the Senior CMC Regulatory Lead - Small Molecule position at Travere Therapeutics in Boston, MA, United States.
The position is based in Boston, MA, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 150..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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