Responsible for assure the quality of Sun’s products manufactured at Sun Pharmaceutical Industries Ltd for the domestic market as well as export to emerging markets.
Responsible for system up-gradation as per CQ and regulatory guidelines
To analyze and report the stability sample & FG sample if needed.
Monitoring of gowning and sanitation practices in area of operation.
Monitoring of compliance of standard operation procedure for operation of analytical instrument.
To operate the analytical equipment in quality control as per the allotment works in shift.
To follow the procedure of good documentation and recording of result as per SOP on GDP and good execution of laboratories practices.
To support the internal audit/Regulatory/FDA audit with best of practices
Following all regulations of cGMPs as per schedule M.
To maintain the safety procedure in handling analytical equipment and hazards.
Completing the training assigned as per the training need identified by participating in trainings organized or self-reading.
To calibrate the analytical equipment’s as per the calibration procedure for assigned responsibility of calibration.
To maintain the analytical equipment’s and laboratories in good state of operation
To follow procedure for non-conforming result as it is applicable in SOP of OOT, Lab Incident & OOS.
To follow the administrative procedure of compliance with respect to term and condition for attendance, leave and other benefits .
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