Director Regulatory Site CMC — Hybrid, Global Post‑Approval

A leading pharmaceutical company in Boston seeks a Director Regulatory Site CMC to manage regulatory change control and post-approval activities. The role requires a solid background in global HA requirements, strong communication skills, and 10+ years of relevant experience. Key responsibilities include leading post-approval change management, collaborating with partners, and leveraging automation to improve efficiency. This position offers a hybrid work model and competitive compensation, reinforcing the company's commitment to employee growth and well-being. #J-18808-Ljbffr