Naimesh Rao

Naimesh Rao

Associate Director, CQA, CPGP, CMDA, CFSQA (ASQ Certified); Lead Auditor (IRCA)

Role
Associate Director at Merck
Location
New York, NY, US
LinkedIn followers
500 followers

About Naimesh Rao

Result oriented and experienced GMP compliance professional with the accomplished ability…

Experience

  1. Associate Director

    Merck

    May 2017 — Present · New York, NY, US

Skills

  • Microsoft Excel
  • Iso 13485
  • Uv/Vis
  • Glp
  • Quality Assurance
  • Technology Transfer
  • Dissolution
  • Auditing
  • Vaccines
  • Deviations
  • Computer System Validation
  • Pharmaceutics
  • Process Improvement
  • Cleaning Validation
  • Microsoft Office
  • Fda Gmp
  • Lims
  • Contract Manufacturing
  • Regulatory Affairs
  • Analytical Chemistry
  • 21 Cfr Part 11
  • Medical Devices
  • Capa
  • Hplc
  • Quality System
  • V&V
  • Quality Control
  • Gmp
  • Biotechnology
  • Gxp
  • Quality Auditing
  • Aseptic Processing
  • Project Management
  • Strategic Planning
  • Management
  • Clinical Development
  • Chromatography
  • Regulatory Requirements
  • Change Control
  • Drug Development

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