Officer /Executive

Job Description

Key Responsibilities: Conduct Literature Search, Pharmacopoeia & Patent Search, and document findings Apply for NOC, Test License, Manufacturing & Import Licenses Perform Reference Product Characterization, Reverse Engineering & Prototype Development Conduct Preformulation studies & bench-scale trials Prepare & manage stability batches Optimize manufacturing process, scale-up & submission batches Develop Bill of Material (BOM) & Master Formula Record (MFR) for submission batches Prepare Product Development Reports for regulatory filing Ensure compliance with EU/UK/Canada regulatory requirements Apply QbD & DOE principles in formulation & process development Coordinate with DQA, Clinicals, Regulatory, Technology Transfer & Production teams Work on IR/MR solid oral dosage forms