Job Description

Company: Siza Internationals Pvt. Ltd.

Location: Lahore, Pakistan (On-site)

Employment Type: Full-Time

Shift: Morning Shift

Role Summary

• Manage licensing and product registration activities for pharmaceutical products.
• Prepare and maintain regulatory documentation for registrations, renewals, and regulatory filings.
• Prepare and submit registrations for new products and new molecular entities.
• Manage new plant licensing processes and prepare required submissions.
• Correspond with DRAP for submissions, approvals, renewals, queries, and other regulatory matters.
• Ensure compliance with DRAP regulations and applicable pharmaceutical legislation.
• Produce regulatory writing and technical documents with accuracy and clarity.

Job Specification

• 5 to 7 years of regulatory affairs experience in the...