Company

Siza Internationals Pvt. Ltd.

Location

Lahore, Pakistan (On-site)

Employment Type

Full-Time, Morning Shift

Job Summary

Responsible for managing regulatory activities including new plant licensing, product registrations, regulatory submissions, correspondence with DRAP, approvals, and renewals. Work closely with internal teams to prepare and submit documentation and ensure compliance with DRAP regulations and pharmaceutical legislation.

Responsibilities

• Prepare and submit applications for new plant licensing.
• Compile and manage documentation for new product and new molecule registrations.
• Prepare regulatory submissions, dossiers, and licensing documents.
• Correspond and follow up with DRAP for submissions, approvals, renewals, and regulatory queries.
• Ensure compliance with DRAP regulations and pharmaceutical legislation.
• Maintain accurate...