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.