Description
Position Description :
Position ensures that the products provided to the market are tested as per customer specifications and in compliance with applicable pharmacopoeias as well cGMP/GLP/ICH/USFDA/ISO guidelines.
Key Responsibilities:
Analysis of Finished products / raw materials/ in process & stability samples (Wet & Instrumental analysis). Preparing stability trend and then sharing with all stake holders. Conducting LSC to update all stake holders on stability status. Calibration of HPLCs as per defined procedure and schedule. Method validations as per applicable guidelines. Inventory management of reagents/columns spares etc. required for Premix analysis. Mobile phase preparation and their record keeping. Printing and preparation of record of analysis. Log books management for various activities. Preparation/Revision of method of an...