This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
Lilly in Indianapolis, IN, seeks a Director of GRA-CMCD Lifecycle Innovation to lead post-approval regulatory activities for parenteral products. You will shape global lifecycle strategies, manage data packages, and drive timely submissions across sites and CMOs, partnering with cross-functional teams to ensure high-quality lifecycle outcomes.
Requirements include a STEM degree and 10+ years in regulatory CMC for biologics or parenteral products; advanced degrees preferred.
#J-18808-Ljbffr
Worksite address
indianapolis, IN, 46262, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.