CMC Regulatory Affairs Lead – Submissions & Strategy

A leading pharmaceutical company located in Florham Park, NJ, is seeking an Associate Director of Regulatory Affairs to manage regulatory submissions and strategies for product approvals. The role requires a Bachelor's degree and 8+ years of pharmaceutical experience, including leadership in regulatory affairs. Candidates should have strong analytical and communication skills, and the ability to work in a complex environment. A comprehensive benefits package is offered, contributing to a supportive work culture. #J-18808-Ljbffr