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Manager - 2

SUN PHARMA

tandalja, gujarat, India Full-time June 14, 2026
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Found Description

Executive and Sr. Executive

  • Review all data and documents related to product registrations for various health authorities.
  • Compile registration dossiers for submission to various health authorities like – China , Canada, Europe, Australia/New Zealand, Japan and Israel.
  • Prepare responses to deficiency letters received from various agencies.
  • Maintain life-cycle / post approval changes for drug product registration dossiers.
  • Provide regulatory support to cross functional departments.
  • Prepare and submit scientific advice to various health authorities.
  • eCTD compilation, verification and submission through electronic gateway

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    Found Details

    Locationtandalja, gujarat
    CountryIndia
    TypeFull-time
    CategoryOther-General
    PostedJune 14, 2026

    About SUN PHARMA

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    SUN PHARMA

    tandalja, India

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