GM / Sr. GM - Regulatory Affairs

Konnect HR
  • Ahmedabad
  • 20-35 lakh
  • 15-20 years
  • 06 Jul 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

Competencies/Skill sets for this job

Regulatory Affairs Regulatory Dosage Parenteral Oral Dosage Projects

Job Posted By

About Organisation

Konnect HR