Dynamic and results-driven Analytical Leader with over 20 years of extensive experience in pharmaceutical analytical research, method development, validation, regulatory submissions, and quality systems. Expertise includes aligning laboratory operations with GMP, GLP, OQM, HSE, ISEC, and Quality Guidelines while fostering a culture of compliance, safety, and continuous improvement. Proven track record in building and mentoring high-performing teams, streamlining processes, and delivering innovative analytical solutions that expedite product development and regulatory approvals. Comprehensive hands-on proficiency spans analytical testing across various formulations, including Active Pharmaceutical Ingredients (APIs), Solid Oral Dosage Forms (OSDs), and Parenteral Liquid Injections (LIVI), complemented by a strong foundation in stability studies, technology transfers, compliance, audit readiness, CAPA management, documentation optimization, and team leadership.