Senior Director, Global Parenteral Drug Product Technical Services (MSAT)

Role: Senior leader overseeing global technical stewardship of parenteral drug product manufacturing within Lilly's MSAT organization. Objectives include ensuring process robustness, compliance, and continuous improvement across internal and external manufacturing sites. Responsibilities: direct and develop a high-performing team of global product stewards; set technical strategy for lifecycle management, process transfer, and optimization; serve as the escalation point for complex technical issues; influence process improvement, regulatory interactions, and site readiness; foster cross-site collaboration and a culture of safety and excellence. Requirements: Bachelor's degree or higher in sciences or engineering; 15+ years in pharmaceutical manufacturing, with 10+ years specifically in parenteral drug products and technical roles such as process support or manufacturing science; extensive leadership experience across global manufacturing networks. Preferences: experience leading network expansion, technology transfer, and working with regulatory agencies like FDA or EMA; strong communication skills, influence, and stakeholder management. HighValue: parenteral (injectable) drug products, manufacturing science, lifecycle management, process validation, regulatory interactions, global network leadership, cGMP environment. Work setup: on-site with some flexibility (up to 4 days remote/month), requiring domestic and international travel (~25%).