Executive Quality Control

Sampling

Sampling of Raw Material, intermediate andFinish Product as per the relevant SOP's
Ensure proper storage as per Storageconditions for Raw Material, intermediate,
stability samples and Finish Product as per therelevant SOP's.

Analysis:

Analysis of Raw Materials, stability samples,finished goods as per the requiredspecifications in time.
Ensure cGLP in the laboratory activities.Carry out instrumental analysis of stabilitysamples, Raw materials, Finished Goods suchas Karl Fischer,IR spectrophotometer, RamanAnalyzer, Dissolution tester, Disintegrationtester, Viscometer, Tap density apparatus,Microscope, UV-Vis Spectrophotometer,
Conductivity meter, pH Meter, Sieve shaker,Melting point ,HPLC ,GC etc.

Documentation:

Prepare and maintain raw data and analyticalrecords in compliance with the currentregulatory requirements.

Maintain the raw data as per regulatory requirements.Scanning and Proper Storage of Raw Material ATR in documentation store.Filling and documentation of ILI/Deviations at site.Review of logbooks, Calibration records, Qualification documents etc.Review and revise the specifications and test procedures based on the pharmacopeia.Raising Deviation, ILI, Change control and implementation of CAPAs through QualiPSO.Carry out result recording, Review of data, Sampling instruction transactions in SAP ATHENA.

Qualification/Calibration/Validation:

To perform Calibration and PM of instrumentsas per SOP and maintain recordsPerform qualifications of instruments.