Key Responsibilities:
Perform analysis of Raw Materials, In-Process, Finished Products, and Stability Samples using HPLC.
Operate and maintain HPLC instruments as per SOP.
Preparation and standardization of reagents, volumetric solutions, and mobile phases.
Documentation of analytical records as per GMP/GLP guidelines.
Calibration and routine maintenance of laboratory instruments.
Ensure compliance with regulatory requirements and quality standards.
Handling of OOS, OOT, and deviations related to laboratory activities.
Coordination with QA and Production departments for quality-related activities.
Required Skills:
Hands-on experience in HPLC analysis.
Knowledge of GMP, GLP, and pharmaceutical documentation.
Valuable understanding of analytical testing procedures.
Ability to work independently and in a team workplace.