Job Description:

  • Validation and Ensuring Compliance with Regulatory Authorities, of all the Development Documents
  • Preparing/Compiling of CTD Dossiers for Europe/Australia/Canada and Other Emerging Market, and Responding/Resolving to their Queries
  • Review of Dossiers for Registration
Qualification: M.Pharma/M.Sc
Experience: 2-4 Yrs
Salary: Negotiable
Contact Details:
Mr. Sekhar S
aravinda.p@medreich.com, sekhar.s@medreich.com

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