Executive/Asst Manager | Regulatory Affairs | Emcure Pharma | Ahmedabad

Job Description

  • Compilation of dossiers in CTD, eCTD & national formats
  • Compilation and submission of queries and variations.
  • Review of documents, artworks
  • Review of change controls
  • Gap analysis for new product filing
  • Maintaining product Life cycle

Candidates having experience in the Europe market and ready to work for Australia New Zealand/Brazil/China markets with eCTD can also apply.

Qualification: B.Pharma, M.Pharma

Location