QA - Stat Sort Specialist

Role: QA Specialist – Stat Sort, responsible for manual visual inspection of 100% final inspection of Parenteral products at Lilly's new Concord facility. Objectives: ensure defect classification accuracy, support final product quality, and maintain GMP compliance. Responsibilities: perform visual sorting aligned with production schedules, document defect data, manage sample sampling and delivery to QC labs, and support technician training and defect investigations. Requirements: High School Diploma or GED, authorized to work full-time in the U.S., strong attention to detail, and prior experience in pharmaceutical QA/QC or GMP environments preferred. High-Value: manufacturing focus on Parenteral (parenteral), GMP standards, visual inspection, final product defect classification, support for sterile injectable production, and cross-functional collaboration with Operations and QC labs. Additional details include potential off-shift work, site mobility, and physical ability to differentiate colors and perform light manual tasks.