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