1. Preparation of dossiers for Europe, Australia, New Zealand and Canada EANC.
2. Response to Queries of Regulatory agencies of EANC Advanced markets and customers.
3. Liaise with R&D, manufacturing plants, clinical team, respective EANC offices/BD teams.
4. Helping in life cycle of EANC registered products by achieving variation approvals.
5. Maintenance of Department data bases.
6. Regular study of Regulatory guidelines and Electronic etc.
B) Relevant work experience - 1 to 2 Years.
C) Education Qualification - B. Pharma
