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.