Cadila Pharma

•	Follow cGMP and GMP PRACTICES.
•	Responsible for charging the stability sample of Finished Product as per SOP.
•	To follow and maintain stability study schedule.
•	Pulling out samples from chambers as per the schedule
•	Maintain all stability chambers daily temperature and humidity monitoring.
•	To follow safety Procedure in QC department.
•	Responsible for withdraw the stability sample for analysis as per schedule. 
•	To maintain stability study log book of stability sample.
•	Responsible for preparation of stability study protocol and maintain all relevant records.
•	Ensure working of all the stability chambers as per the condition and in case of any problems take the correction action.
•	Ensure cleanliness of stability chamber.
•	Preparation of stability samples monthly planner.
•	Analysis of Stability Samples as per schedule
•	Maintain all stability chambers daily temperature and humidity monitoring.
•	Preparation of stability summary of all the products.
•	To do any other Work assign by HOD.

•	Follow cGMP and GLP practices in Quality Control Lab.
•	To analyze the Sample of stability on non-chromatographic instrument such as FTIR, UV, Dissolution, DT, Hardness etc by following test procedure.
•	Analysis of Stability Samples as per schedule
•	To attend the training as per schedule.
•	To follow safety procedure in QC department.
•	To receive the samples for analysis and making entry in Inward register.
•	To maintain the Instruments log books related to sample analysis.
•	To analyze the sample and compilation of documents.
•	Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS. 
•	Responsible for cleaning & monitoring of laboratory.
•	Responsible for online documentation. 
•	To do any other Work assign by HOD.

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