Global CMC Regulatory Lead – Molecule Drugs

PTC Therapeutics, Inc. is seeking an Associate Director, Regulatory Affairs – CMC to lead global CMC strategy for small molecule development and registration.

You will coordinate cross-functionally with Technical Operations, Quality, and Regulatory Affairs to ensure timely, high-quality submissions and lifecycle changes. Experience in IND/CTA, NDA/MAA submissions, eCTDs and post-approval changes is required.

This is a great role to take on the Global CMC Regulatory Lead – Small Molecule Drugs role at PTC Therapeutics, Inc.

The Global CMC Regulatory Lead – Small Molecule Drugs role at PTC Therapeutics, Inc. is now open for applications in NJ, United States.

Join us at PTC Therapeutics, Inc. as our next Global CMC Regulatory Lead – Small Molecule Drugs in NJ, United States.

We are currently recruiting a Global CMC Regulatory Lead – Small Molecule Drugs for our team in NJ, United States.