Job Description
"
•Follow cGMP and GLP practices in Quality Control Lab.
•To follow safety procedure in qc department.
•To analyze the Sample of in process validation and finish product on instrument such HPLC, GC, UV, FTIR etc. by following test procedure.
•To attend the training as per schedule.
•To follow safety procedure in QC department.
•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 online documentation.
•To do any other Work assign by HOD."