Pooja Deshpande

WORK HISTORY

EDUCATION

ABOUT POOJA DESHPANDE

Seasoned pharmaceutical professional with over [17] years of progressive experience across Regulatory Affairs, Quality Assurance, Analytical and R&D. Currently serving as a Director, bring a strategic and cross-functional approach to ensuring regulatory compliance, product development and innovation in drug categories.My background spans the full product lifecycle—initiation to collaborations of partnerships, from concept to formulation and clinical /Bioequivalent development to regulatory submissions and post-marketing compliance. Have successfully led global regulatory strategies, overseen complex quality systems, and collaborated with cross-border teams to bring safe, effective, and compliant therapies to market.Key Strengths:Regulatory strategy & global submissions (ICH, FDA, EMA, etc.)GMP, GCP, and QA audits & complianceLeadership: formulation, analytical, tech transfer, regulatory, partnering with manufacturersCross-functional team leadership and strategic planningRisk management and regulatory intelligenceDriven by science, compliance, and patient safety, I thrive in dynamic, high-stakes environments where quality and innovation intersect. Always open to collaboration, knowledge exchange, and opportunities that push boundaries in healthcare and pharmaceutical excellence.