•Follow cGMP and GLP practices in Quality Control Lab. •To analyze the Sample of RM, In process validation, FP, Stability ,GLP on GC instrument by following test procedure. •To follow safety Procedure in QC department. •To attend the training as per schedule. •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.
