Drug Regulatory Affairs

1) Compile and maintain regulatory documentation databases or systems.

2) Coordinate efforts associated with the preparation of regulatory documents or submissions.

3) Analyze product complaints and make recommendations regarding their reportability.

4) Develop or conduct employee regulatory training.

5) Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review.

6) Escort government inspectors during inspections and provide post-inspection follow-up information as requested.

7) Coordinate, prepare, or review regulatory submissions for domestic or international projects.

8) Interpret regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures.

**Salary**: ₹167,150.67 - ₹3,000,000.00 per year

Schedule:

- Day shift

**Experience**:

- total work: 3 years (preferred)