Year: 2025
Type: article
Abstract: Pharmaceutical manufacturing is one of the most critical and highly regulated industries worldwide. The complexity of production processes, coupled with stringent regulatory requirements, necessitates a focus on quality, efficiency, and cost optimization. Lean Six Sigma (LSS) combines Lean principles for eliminating waste and Six Sigma methodologies for reducing variability, ensuring both quality and efficiency. This document explores the comprehensive application of LSS across pharmaceutical processes, including API synthesis, granulation, tablet production, capsule filling, coating, and packaging. The implementation is illustrated through case studies, step-by- step methodology, tables, charts, value stream maps, SIPOC diagrams, FMEA analyses, 5S/Kaizen practices, ROI calculations, and regulatory compliance frameworks. This document is designed to serve as a full reference for pharma professionals looking to implement LSS in manufacturing, ensuring measurable improvements in defect reduction, cycle time, yield, and cost savings..
Authors: Shravani Pawar, Priyanka Patil, Megha Hange, Pravin Sable
Language: English
Subfield: Management Information Systems
Domain: Social Sciences
Open Access status: diamond
OpenAlex ID: W4413311399