I am a Pharma 4.0-driven Pharmaceutical Project & Operations Leader with over 19 years of global experience in GMP-compliant facility design, technology transfer, and manufacturing excellence.
My career spans end-to-end project execution — from concept design to commercial production — across multiple regulated markets under US FDA, EU GMP, and WHO standards. I specialize in automation integration, digital transformation, and Pharma 4.0 implementation to achieve data-driven efficiency and sustainable quality.
As a recognized Keynote Speaker, I have represented Bangladesh in international pharmaceutical conferences held in the USA, Germany, and Singapore, sharing insights on Pharma 4.0, smart manufacturing, and the future of operational excellence. These global platforms have enriched my understanding of emerging technologies and global regulatory convergence.
My leadership philosophy is grounded in collaboration, innovation, and continuous improvement. I have successfully led multi-million-dollar projects, built cross-functional teams, and driven GMP and digital transformation initiatives aligned with global best practices.
I am open to global opportunities across North America and Europe, where I can contribute my expertise to build next-generation pharmaceutical operations powered by Pharma 4.0 principles and data integrity excellence.
Case Study
Tuesday, March 24
10:00 am - 10:30 am
Live in Everett
Less Details
This session explores the journey from concept to commercial production in large-scale pharmaceutical operations, leveraging Pharma 4.0 principles to enhance efficiency, compliance, and sustainable quality. Drawing on extensive global experience in GMP-compliant facility design, technology transfer, and manufacturing operations, the presentation highlights practical strategies for implementing automation, digital transformation, and data-driven manufacturing excellence across multiple dosage forms and regulated markets. Participants will gain insights into designing, executing, and optimizing next-generation pharmaceutical operations—from initial facility planning to high-volume production—while ensuring data integrity, regulatory compliance, and operational resilience. In this session, participants will learn how to: