Lilly is seeking an experienced GMP manufacturing project manager to lead the planning and execution of non-viral drug product manufacturing with multiple external CDMOs and Lilly sites. You will drive technology transfer, manufacturing readiness, materials, analytics, quality, and delivery in a complex cGMP environment.
You will connect internal teams with manufacturing-site staff, identify dependencies and risks, facilitate critical decisions, and drive mitigation and recovery plans to ensure
#J-18808-LjbffrSenior GMP Program Director – Multi-CDMO Operations in watertown at Unknown Company
This position is listed as full time and onsite.