Lilly is seeking a qualified professional for Analytical GMP Laboratories (AGL) in Lebanon/Indianapolis to lead deviation investigations and drive CAPA planning. You will author critical reports, collaborate with QA, SMEs, and cross-functional teams, and ensure ALCOA+ data integrity across investigations.
The role emphasizes mentoring, regulatory writing, and risk-based CAPA prioritization within a GMP manufacturing and analytical testing environment.
#J-18808-LjbffrLead Deviation & CAPA Scientist, GMP Quality in lebanon at Unknown Company
This position is listed as full time and onsite.