Manager - Regulatory Affairs - Healthcare

1. Will handle regulatory tasks for Health Care Business products.

2. Working on Indian Regulatory affairs domain.

3. Working on Regulatory affairs of drugs or medical devices or other healthcare related products.

4. Participation in regulatory committees

5. Preparing and submitting the documents to the regulatory authorities & follow up for the grant of specific licenses / documents.

6. Meeting relevant authorities to know the status of applications, identifying road blocks and determining ways to correct them.

7. To interact with Department of Pharmaceuticals, NPPA, Government organisations and other regulatory agencies for matters pertaining to the Company s health care products.

8. To participate and represent the Company in Industry forum meetings and various BIS Committees.