Senior Executive

• 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.

Cadila Pharmaceuticals