Preparation of dossiers for Europe, Australia, Current Zealand, and Canada (EANC).
Responding to queries from regulatory agencies of EANC advanced markets and customers.
Liaising with R&D;, manufacturing plants, clinical teams, and respective EANC offices/BD teams.
Assisting in the life cycle management of EANC-registered products by obtaining variation approvals.
Maintenance of departmental databases.
Regular study of regulatory guidelines and electronic Common Technical Document (eCTD).
Work Experience - 2-3years
Education B. Pharma
Competencies
Customer CentricityDeveloping TalentCollaborationStrategic AgilityProcess ExcellenceStakeholder ManagementInnovation & CreativityResult Orientation
📌 Sr Executive Ra Navi Mumbai (India)
🏢 LUPIN
📍 India