Accomplished Professor of Pharmaceutics and Pharmaceutical Technology with over 20 years of combined experience in academic leadership, industrial R&D, and quality assurance. Proven expertise in drug formulation, technology transfer, cGMP/GLP compliance, Quality by Design (QbD), and scale-up operations. Author and co-author of over 60 peer-reviewed scientific publications in high-impact international journals and supervisor of numerous Ph.D. and Master's thesis projects in drug delivery systems and industrial pharmacy. CORE COMPETENCIES & EXPERTISE • Industrial Pharmacy & R&D: Generic Drug Development (Solid, Semi-solid, Liquid dosage forms), Technology Transfer, Process Validation, Scale-up (High Shear Granulator to FBD). • Quality & Regulatory Affairs: cGMP, GLP, ICH Guidelines, Quality by Design (QbD), Process Analytical Technology (PAT), Cleaning Validation. • Formulation & Research: Controlled Release Systems, Bioavailability/Bioequivalence, Novel Drug Delivery Systems (Nanoemulgels, Microneedles, Mucoadhesive Tablets), Natural & Organic Skincare/Cosmetics. • Academic Leadership: Curriculum Development, Master’s & PharmD Program Management, Laboratory Establishment, Faculty Governance.