Chetan Argade

Regulatory Affairs Specialist | Pharmaceuticals | CMC Scientist | eCTD | Life cycle Management | CMC Post Approval | Generic Drugs | Quality Assurance | Validation| APQR | IPQA | Documentation| M.Pharm |

Role
Lead Associate at Genpact
Location
Mumbai, MH, IN
LinkedIn followers
500 followers
General Business & ManagementView LinkedIn profile

Experience

  1. Lead Associate

    Genpact

    Sep 2021 — Present · Mumbai, IN

Skills

  • Quality Assurance
  • Good Laboratory Practice (Glp)
  • Pharmaceutical Industry
  • Sop
  • Standard Operating Procedure (Sop)
  • Quality System
  • U.s. Food and Drug Administration (Fda)
  • Technology Transfer
  • Regulatory Affairs
  • Cleaning Validation
  • Corrective and Preventive Action (Capa)
  • High-Performance Liquid Chromatography (Hplc)
  • Gmp
  • Verification and Validation (V&V)
  • Pharmaceutics
  • Validation

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Chetan Argade — Lead Associate at Genpact in Mumbai, MH, IN | Unifers