1. Manufacturing process validation, product development records, dossiers, BMR, BPR, stability data analysis etc.2. Food and Drug Administration (FDA) related work, Loan License Documentation, Certificate of Pharma Products (COPP) registrations, etc.3. Department coordination to manufacturing for QA / QC, R&D, Legal, etc.4. Preparing & reviewing art works, labels, pack inserts, etc.5. Response to various queries from various departments, etc.