a. Manage end-to-end regulatory projects related to drugs and
healthcare products.
b. Coordinate preparation, review, and submission of regulatory
documents.
c. Track application status on CDSCO portals and maintain
project trackers.
d. Ensure timely completion of assigned regulatory activities.
e. Handle regulatory activities related to:
CDSCO Drug Import License
Manufacturing License Coordination
Current Drug Approval Support
Regulatory Submissions and Compliance Requirements
Other pharmaceutical regulatory approvals
f. Review client-provided documents and prepare regulatory
checklists.
g. Identify documentation gaps and coordinate with clients for
required information, communicate project status and timelines.
h. Maintain proper records of regulatory documents and project
files.
i. Coordinate with Regulatory Affairs, Documentation, Legal, and
Business Development teams.
j. Stay updated with CDSCO notifications, regulatory changes,
and compliance requirements.

📌 Drug Regulatory Affairs Executive New Delhi (India)
🏢 ELT Corporate
📍 India