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Cadila Pharma

Assistant Manager

Posted Updated
Discussion
  • Follow cGMP and GLP practices in Quality Control Lab.
  • To analyze the Sample of stability on instrument such HPLC, UV, FTIR etc. by following test procedure.
  • Analysis of Stability Samples as per schedule
  • 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 online documentation.
  • To do any other Work assign by HOD.
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