Mumbai; B.Pharma/ M.Pharma, Executive/Sr Executive-Regulatory Affairs, Intas Pharmaceuticals

1.preparation of registration dossiers for semi regulated and regulated markets.

2.Compilation and review of plant and R&D documents

3.Response to letters from various health authorities

4.Checking/reviewing of documents as per regulatory requirements

5.guide site for regulatory filing documentation

6.maintenance of lists/documents/records

7.co-ordinate with QA/production

Send resume to:
hrd@usv.co.in