Dynamic seasoned professional, with in-depth scientific, regulatory, and Bioequivalence knowledge in leading Generic R&D (Formulations). Development and submission of over 150+ products (including simple generics and complex /novel non-infringing / modified release formulations, 505(b)2, First time-Generics, FTFs, NCE-1). Rich experience and expertise in Technology Transfer from lab to commercial (including scale up and validation) and global product transfers from one site to another for complex dosage forms. Well versed with IPR and ability to design around.