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Job Details:

  • Position: Sr. Executive in Regulatory Affairs
  • Location: Navi Mumbai
  • Experience Required: 8+ Years
  • Qualifications: B.Pharma / M.Pharma

Job Role:

  • Prepare and review dossiers.
  • Knowledge in preparing CTD/ACTD and country-specific dossiers.
  • Handle DMF/API & SF.
  • Prepare dossiers for tablets, capsules, creams, ointments, etc.
  • Familiarity with FDA requirements, including checking PVSS data and application of COPP/FSC.

Application Details:

For further information on clinical courses and clinical research courses, you can explore additional resources and training programs.

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