A biopharmaceutical research professional with 12 years of academic and industrial expertise in the technical and scientific affairs of drug development spanning areas such as R&D, technology assessment, technical writing, competitive intelligence, program management, global drug regulations for product in-licensing and technology transfer related activities with future goals in global drug regulatory sciences to support the techno-commercial activities, portfolio execution and integrated development for biologicals.
- Technical expertise in the integrated sciences of biological/biosimilar drug development, with area of specialization in Mammalian Cell Culture R&D and Upstream Bioprocess...