Global CMC Regulatory Lead, Molecules

PTC Therapeutics, Inc. is seeking an Associate Director, Regulatory Affairs – CMC to lead global regulatory strategy for product development and registration. This role ensures documentation meets quality standards for small molecule submissions. Qualified candidates will have 7-8 years of experience in Regulatory Affairs or CMC technical writing within a biopharmaceutical setting.

With strong analytical skills, you will manage cross-functional communications and ensure compliance with regulatory requirements. This position offers a competitive base salary and additional incentives.