Manager - RA

A) Job description:-
1. Review and guide the team for dossiers for Europe, Australia, NZ and Canada (EANC).
2. Review and guide the team to respond to Queries of agencies of EANC region 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.
7. Maintenance and submission of GMP applications.

B) Relevant work experience - 10 to 12 Years.
 
C) Education Qualification - M. Pharma / B. Pharma.