Qa/Regulatory Affairs/Research
Taux horaire: membres seulement
Disponibilité: membres seulement
Disponibilité à voyager: Partout dans le monde
Statut professionnel: Pigiste
Dernière mise à jour: 28 juil. 2025
Expérience de travail totale: 8 année(s)
Connaissances linguistiques: Anglais, Hindi,
Sommaire professionel
I have over 13 years of experience in pharmaceutical manufacturing, formulation development, and regulatory compliance. Currently, as a Process Engineering Specialist II at Teva Pharmaceuticals, I lead product improvement and validation initiatives, focusing on nanotechnology and regulatory compliance. Previously, as an Assistant Manager at AET Laboratories, I directed technology transfers, scale-up processes, and formulation development for various drug products. My expertise includes pre-formulation, process engineering, nanotechnology, quality systems, and technology transfer. I also have experience in regulatory filings (ANDA, 505(b)(2)), scientific publications, and patents related to drug formulations. Additionally, completed my MSc in Regulatory Affairs at Northeastern University, strengthening my expertise in eCTD submissions and compliance. Education: Masters in Other
Connaissances linguistiques
Anglais
Fluide
Hindi
Fluide