Check Disclaimer, Privacy policy for use this dataAmneal India Gujarat jobs for Regulatory Affairs apply now
🔶 Reference - Industrial Guide Always write reference for better attention.
Interview Data Loading ...We at Amneal Pharma looking for Regulatory Affairs professionals. Request to find below the required details:
Experience: 08-13 YearsPosition: ManagerJob Location: Ahmedabad[ads id="ads1"] Job Role:
1. Ensuring submission to DCGI, LFDA in compliance with current regulatory guidelines.2. Performing Indian Regulatory legal activities (DCGI and LFDA).Prepare, review, compile Manufacturing & Marketing application and submit online on SUGAM portal.3. Prepare, review and compile BE & CT NOC application and submit online on SUGAM portal. [ads id="ads1"] 4. Prepare and Review Form 29 NOC (CT 10, CT 12, and CT 13), Form 29, Form 10 (import license), LFDA, CDTL NOC, CDTL report.5. Review data integratory for all submitted documents.6. Ensuring all regulatory compliance for submission of application.7. To evaluate queries raised by Regulatory Authority and preparing, reviewing and submitting the Query Response.[ads id="ads1"] 8. Review all the technical documents required for post approval changes.
Interested candidates may share their updated CV at kavitriy@amnealindia.com
Check Disclaimer, Privacy policy for use this data
Amneal India Gujarat jobs for Regulatory Affairs apply now
🔶 Reference - Industrial Guide Always write reference for better attention.
Interview Data Loading ...
We at Amneal Pharma looking for Regulatory Affairs professionals. Request to find below the required details:
Experience: 08-13 Years
Position: Manager
Job Location: Ahmedabad
[ads id="ads1"]
Job Role:
1. Ensuring submission to DCGI, LFDA in compliance with current regulatory guidelines.
2. Performing Indian Regulatory legal activities (DCGI and LFDA).
Prepare, review, compile Manufacturing & Marketing application and submit online on SUGAM portal.
3. Prepare, review and compile BE & CT NOC application and submit online on SUGAM portal.
[ads id="ads1"]
4. Prepare and Review Form 29 NOC (CT 10, CT 12, and CT 13), Form 29, Form 10 (import license), LFDA, CDTL NOC, CDTL report.
5. Review data integratory for all submitted documents.
6. Ensuring all regulatory compliance for submission of application.
7. To evaluate queries raised by Regulatory Authority and preparing, reviewing and submitting the Query Response.
[ads id="ads1"]
8. Review all the technical documents required for post approval changes.
Interested candidates may share their updated CV at kavitriy@amnealindia.com