Associate Director - Joint Process Team Lead

Role: LP2-EM Joint Process Team Leader overseeing the startup of Lilly's advanced Gene Therapy manufacturing facility in Lebanon, Indiana. Responsibilities: lead cross-functional Lilly/contract manufacturer teams to develop and execute Quality and Supply Plans, ensure regulatory and cGMP compliance, manage production schedules and supply chain performance metrics, resolve operational issues, facilitate meetings, and foster strong internal and external partnerships. Qualifications: Bachelor's in Chemical, Mechanical, Chemistry, Biochemistry or related science; 5+ years in pharmaceutical manufacturing, quality assurance, or technical support. Preferred skills include leadership, stakeholder management, cGMP compliance, experience with third-party contract manufacturing, and proficiency in project management tools and Lilly systems. High-value: focus on biologics, gene therapy modalities, manufacturing start-up, external supply chain management, compliance oversight, and cross-functional collaboration. Work setup involves travel (~20%) in a startup environment for a pioneering biologics manufacturing site.