via Career pages·2d ago

Technical Supervisor

Cadila Pharmaceuticals

Full-timeOn-sitecgmp complianceglp practiceshplc operationsample analysisftir analysisuv spectroscopygc analysislcms operationpolarimeter usagekf titrationlims documentationautotitrator operationsafety proceduresdocumentation skillstraining attendance

Location:Dholka, IndiaType:Full-timePosted:2d ago

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Follow cGMP and GLP practices in Quality Control Lab.

To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator 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.

Follow cGMP and GLP practices in Quality Control Lab.
To analyze the Sample of Raw Material on instrument such HPLC, GC, LCMS 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.