To perform calibration of the analytical instruments as per calibration schedule
Follow the standard practices cGLP during lab experiments
Cleaning verification method development and validation
API method evaluation and verification
API solubility study assessment
Working standard qualification
Method Development for drug product formulation
Routine analysis of development samples and lab stability samples
Method verification of different analytical methods
Reporting of analytical data and submit for review and release
ARF release of raw material and packaging material
Preparation of test procedures for routine development analysis
Follow in-house compliance system
Maintain hygienic condition in respective department
Recording audit trails.
TRF entries in common portal for tracking management
Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements.
Follow GxP (GMP, GDP, GLP) for all processes.
