Description
Vertex is hiring a Manufacturing Process & Technical Quality Associate Director to provide end-to-end quality oversight for cell and gene therapy programs across clinical development, commercialization, product launch, and post-approval lifecycle management. The role leads QA reviews, quality and compliance frameworks, investigations, change controls, CMC governance, manufacturing quality oversight, and the use of digital manufacturing, analytics, and AI tools. It requires a bachelor’s degree in a scientific or allied health field, 8+ years of regulated pharmaceutical experience, and offers a hybrid or on-site work arrangement with a base salary of $156,600–$234,800 plus bonus and equity opportunities.
