- 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