Director, Global Regulatory CMC – Peptides & Oligos

Lilly in Indianapolis seeks a senior Regulatory CMC leader to guide development and manufacturing for synthetic peptides and oligonucleotides. The role spans regulatory strategy, global submissions, and lifecycle management, combining deep technical expertise with broad regulatory know-how. You will lead cross-functional teams, influence decision-making across geographies, and ensure high-quality CMC documentation for clinical trials, registrations, and post-approval activities.