Job Description
Siza Internationals Pvt. Ltd., a pharmaceutical company based in Lahore, is seeking an experienced Regulatory Affairs Professional to manage regulatory compliance and product lifecycle activities.
Key Responsibilities
- Prepare and manage submissions for new plant licensing and new product registrations.
- Compile, review, and maintain regulatory documentation for new molecule registrations, renewals, and variations.
- Draft clear regulatory correspondence and responses for DRAP queries and inspections.
- Monitor and interpret DRAP regulations and pharmaceutical legislation to ensure company compliance.
- Coordinate with cross-functional teams (QA, Production, R&D) to gather required dossiers and technical information.
- Track submission timelines, follow up on approvals, and maintain accurate records of regulatory activities.
Job Specification