
Pharmaceutical R&D and Formulation Development Specialist with over 5 years of experience in solid oral dosage forms, sterile formulations (ophthalmic, injectable, parenteral), and veterinary pharmaceutical products. Skilled in formulation optimization, pre-formulation studies, excipient compatibility, technology transfer, pilot and exhibit batch production, and troubleshooting. Strong background in CTD dossier preparation, BMR drafting, stability studies, and compliance with cGMP, ICH, QbD, and regulatory standards. Leadership experience as R&D Section Head, managing multidisciplinary teams and driving successful tech transfers for both human and veterinary medicines.