RA Executive

1 day ago


Vapi, Gujarat, India Mangalam Drugs & Organics Full time
  1. To prepare documents Technology Transfer Document, Product scale up report, Product development report, Chemistry manufacturing & control, Polymorphism study etc.

  2. To collect necessary information from all concerned Department.

  3. To prepare DMF (Drug Master File) for Regulatory Market.

  4. To ensure that manufacturing procedure and specification of materials are in accordance with the submitted DMF.


  • RA Executive

    4 days ago


    Vapi, Gujarat, India Mangalam Drugs & Organics Full time

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