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    Job · 21136963

    MUMBAI · FULLTIME

    Cipla - Regional RA - Vikhroli

    Cipla

    Cipla

    Mumbai · onsite · Posted 6d ago

    Sourced fromNaukri
    Undisclosed2–7 yrsfulltimeMumbai

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    Section · 01

    About this role

    Key Accountabilities


    Achieve timely submission of dossier/DMF and deficiency responses to regulatory authority by reviewing, collating, and compiling documents in order to ensure approvals for launch in stipulated time

    • Co-ordinate with cross-functional teams and external stake-holders for query response discussion and distribute updated work plan

    • *Create DMF master in LOA software & issue LOAs/CEPs

    • Verify pre-approved documents

    • Leverage product gap analysis #Preparation compilation and submission of the dossier documents I deficiency responses to agency as per the region specific requirements(for Para-IV -US) Preparation of MI documents, and collate the dossier/ deficiency responses package/DMF received from CDT and submit to the regulatory authority/customer

    • Submit online audit dossier/DMF dong with queries

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    Section · 02

    Skills

    DossierRegulatory AffairsSubmissionCTDDMFDrug Regulatory AffairsDeficiency responses

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