Analyze Commercial stability/Finish samples allotted for testing using HPLC, GC, UV instruments, etc. as per Stability Protocols and standard test procedures.
Ensure standardisation of working standards and conduct calibration of laboratory instruments.
Document analytical data and calculate results.
Enter analytical data in Stability Software and generate Stability Reports.
Ensure compliance to cGMP requirements and laboratory procedures.
Submit samples for destruction after completion of analysis.
Ensure integrity, accuracy and adequacy of the analysis performed.
Compliance of electronic systems like DCM and LMS in the laboratory.
Review of specification in stability software (Novatek).
Review of Analytical Raw data.
Analysis of Exhibit/Commercial stability samples.
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