Our leadership team brings decades of experience across pharmaceutical R&D, manufacturing, regulatory affairs, and busines development — united by a commitment to scientific excellence.
SP
30+ years in biopharmaceutical process R&D. Specializes in fermentation, metabolic engineering, and API manufacturing. Former roles at Biocon and Shanta Biotech.
MG
30+ years across regulatory, quality and operations. Successfully managed inspections by MHRA, TGA, ANVISA, and NAFDAC. Leads manufacturing at multiple Bioplus facilities.
RA
24 years in pharmaceutical development. Ph.D. in Pharmaceutical Sciences. Led 10+ IND/NDA and 80+ ANDA programs for USA, Europe, and China. Former roles at Dr. Reddy's, Glenmark, Hetero.
SK
22+ years in analytical development and quality control. Ph.D. in Pharmacy. Expert in IND, NDA, and ANDA submissions for USFDA, MHRA and TGA. Former roles at Kemwell (Recipharm), Micro Labs.
JS
27+ years in pharmaceutical manufacturing. Specialist in UK MHRA, EU GMP, TGA, Health Canada, and PMDA Japan certifications. Former roles at Medreich, Caplin Point, Micro Labs.
SM
Age 51 · MS Environmental Science, PhD Molecular Genetics — Ohio State University, USA (Post-doc, Weill Cornell Medical College, USA) · Prior: Pfizer, Intas, Abchem, Anthem
AP
Age 48 · M.Sc & PhD Organic Chemistry — Karnatak University, India · Prior: Pharmed, Bioplus
MM
Age 46 · M.Sc Molecular Biology & Genetic Engineering, PhD Molecular Biology & Genetics — JNCASR, Bangalore, India · Prior: Cancyte Tech, Bhat Biotech
NR
Age 55 · M.Sc, Nagarjuna University, AP, India; PhD Organic Chemistry — Oxford University, UK (Post-doc, Oxford University, UK) · Prior: Dr. Reddy's, Glenmark, Lupin, Hetero Drugs, Aragen Life Sciences
SS
30+ years in pharmaceutical manufacturing. Handled multiple regulatory audits including US FDA, UK MHRA, EU GMP, TGA Australia, Health Canada, and PMDA Japan. Previously worked with Dr. Reddy's Laboratories, Hetero Drugs, Aurobindo Pharma, and AMRI.
JN
A Medical and Clinical Affairs professional with 4+ years of experience in scientific engagement, KOL management, medical communication and cross-functional collaboration to support medical strategy, product lifecycle management, and compliant scientific exchange. Previously served as a Medical Advisor at Boehringer Ingelheim.
SS
15+ years across clinical practice, medical affairs and clinical research. Expertise in medical strategy, clinical development, KOL engagement & publications. Former roles at Novo Nordisk, Viatris, Boehringer Ingelheim and Manipal Hospitals, Bangalore.