Role Purpose To lead and manage end-to-end production planning and scheduling for ophthalmic formulation manufacturing (sterile liquids/ointments), ensuring compliance with global regulatory requirements, optimal capacity utilization, and on-time delivery through data-driven, digitized planning systems.Key Responsibilities Prepare and execute monthly, weekly, and daily production plans in line with forecasts, customer demand, regulatory commitments, and plant capacity. Coordinate with Manufacturing, QA, QC, Microbiology,
Engineering, Warehouse, and Supply Chain for smooth sterile manufacturing operations.Ensure optimal inventory management of raw materials, packaging materials, WIP, and finished goods by balancing
service levels, shelf‑life constraints, and working capital. Monitor line performance, changeovers, campaign planning, and sterile manufacturing constraints; proactively resolve bottlenecks.Ensure compliance with GMP, aseptic processing norms, validation requirements, and batch release timelines. Drive automation, digitization, and continuous improvement through ERP optimization, dashboards, and analytics. Support global regulatory inspections including USFDA, EU, WHO, and other regulated markets.Planning&Technology Strong working knowledge of ERP/MRP systems. High level of tech savviness with proven experience in automation and digitization. Advanced skills in Excel, Power BI, macros, dashboards, and planning analytics tools. Behavioral&Cognitive Traits Highly detail-oriented with strong analytical capability. Ability to understand complex planning problems and implement effective solutions. Strong ownership, accountability, and cross-functional communication skills. Qualifications&Experience MBA/M.Pharm preferred or Bachelor of Technology. 8–12 years of experience in pharmaceutical production planning (ophthalmic). Experience supplying global and regulated markets is strongly preferred. Strong understanding of GMP, aseptic controls, and regulatory supply commitments.