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Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Brief Job Description:

  1. Review Data and Documents:
    • Review all data and documents related to product registrations for various health authorities.
  2. Compile Registration Dossiers:
    • Compile registration dossiers for submission to various health authorities including US-FDA, Health Canada, Europe, Australia/New Zealand, Japan, and Israel.
  3. Prepare Responses:
    • Prepare responses to deficiency letters received from various agencies.
    • Maintain life-cycle/post-approval changes for drug product registration dossiers.
  4. Regulatory Support:
    • Provide regulatory support to cross-functional departments.
  5. Scientific Advice Preparation:
    • Prepare and submit scientific advice to various health authorities.
  6. eCTD Compilation:
    • Compile, verify, and submit eCTD through electronic gateway.

How to Apply:

Send your resume to: Hr.tandalja@sunpharma.com

Join our team at Sun Pharma and contribute to our mission of providing high-quality healthcare solutions globally!

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