Officer - Quality Control

7 hours ago


Paonta Sahib Himachal Pradesh, India Sun Pharmaceutical Industries Full time

1 Analysis of RM FG PM validation samples allotted for testing using analytical instruments like IR Dissolution UV and other instrument as per STP and approved protocol 2 Documentation of analytical data and calculation of results 3 Responsible for samples receiving and perform the sample description test 4 Ensure compliance to cGMP requirements and laboratory procedures 5 Ensure integrity accuracy and adequacy of the analysis performed



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