Role & responsibilities 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 Officer (New Delhi)
🏢 ELT Corporate Private
📍 New Delhi