Manager Regulatory Affairs

Job details

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: Must-have: • 5 to 7 years of regulatory affairs experience in the pharmaceutical industry. • Strong knowledge of DRAP regulations and pharmaceutical legislation in Pakistan. • Experience in new plant licensing and product registration processes. • Regulatory writing, documentation, and submission preparation skills. • Ability to manage correspondence and interactions with regulatory authorities (DRAP). • Attention to detail and ability to maintain regulatory records and timelines.Job Rewards and Benefits: Incentive Bonus