Posted:2 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • Follow cGMP and GLP practices in Quality Control Lab.
  • To analyze the Sample of stability on non-chromatographic instrument such as FTIR, UV, Dissolution, DT, Hardness etc by following test procedure.
  • Analysis of Stability Samples as per schedule
  • 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 cleaning & monitoring of laboratory.
  • Responsible for online documentation.
  • To do any other Work assign by HOD.
  • 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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Cadila Pharmaceuticals Limited logo
Cadila Pharmaceuticals Limited

Pharmaceuticals

Ahmedabad

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