GM/ Sr. GM - Regulatory Affairs

Konnect HR
  • Ahmedabad
  • Confidential
  • 15-20 years
  • 18 May 2015

  • Compliance/ Regulatory

  • Pharmaceuticals/ Life Sciences/ Clinical Research
Job Description

Sound knowledge of compiling registration dossier , Reviewing & filling of dossier of E-CTD Projects for Europe , US & ROW market for solid oral dosage, Parenteral preparations and sterile dosage form etc.
Min 10 to 15 yrs for Regulatory ( EU , US & ROW Market)
Must have deal USFDA, WHO/ European Regulatory Bodies.
Exp. of filing DMFs for approval in US/ Europe
Willing to work in Ahmedabad region

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Konnect HR