Sun Pharma hiring Executive for the location Baroda.
Job Summary
Regulatory submissions of drugs and medical devices in India.
Responsibility Area
- Evaluation of regulatory strategies for products to be registered in India.
- Evaluation and submission of application on online portal for getting domestic manufacturing and marketing permission from DCGI.
- Evaluation and submission of applications on online portal for import registration/import license of drugs and medical devices in India.
- Evaluation of the documents that need to be submitted with the applications and coordinating with the respective team for finalization.
- Evaluation and submission of application for getting BE permission for export registration.
- Evaluation and submission of application for getting permission to manufacture drugs for examination, test or analysis in Form CT-10/12/13.
Eligibility
Educational Requirement
Education in M.Pharm
Experience
2 to 10 years experience required in Regulatory Affairs for India Market
Location
Tandalja- Baroda
