Minimum 5 years of production, master planning, or supply chain planning experience in a GMP-regulated pharmaceutical, biotechnology, medical device, or CDMO manufacturing environment, including scheduling, capacity planning, ERP or MRP system use, and coordination of production, quality testing, and batch release activities. This role coordinates across Operations, Supply Chain, Quality, Analytical Services, Manufacturing, Project Management, and Customer Program Teams to support on-time delivery, resource utilization, and GMP-compliant operations.