- 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 Centricity
Developing Talent
Collaboration
Strategic Agility
Process Excellence
Stakeholder Management
Innovation & Creativity
Result Orientation
📌 Sr. Executive - RA (Mumbai)
🏢 Important Business
📍 Mumbai
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