Lilly in Watertown, MA is seeking an experienced GMP manufacturing project manager to lead cross‑site drug product manufacturing programs with external CDMOs. You will develop integrated plans spanning tech transfer, manufacturing readiness, analytics, release, and delivery.
You will partner with CMC, Manufacturing, QA, Regulatory, and Supply Chain, manage risks, and drive milestones in a fast‑paced, cGMP environment. A strong track record in multi‑vendor programs and leadership is required.
#J-18808-LjbffrSenior GMP Program Director – Multi‑Site Ops in watertown at Unknown Company
This position is listed as full time and onsite.