via Career pages·Yesterday
Technical Supervisor
Cadila Pharmaceuticals
Full-timeOn-sitecgmp complianceglp practicesftir analysisuv spectroscopyhplc operationgc analysissample analysislims usagedocumentation skillssafety procedurestraining attendancelaboratory monitoringrecord keepingteam collaborationanalytical documentation
Location:Dholka, IndiaType:Full-timePosted:Yesterday
- Follow cGMP and GLP practices in Quality Control Lab.
- To analyze the Sample of In process validation and finish product on non-chromatographic instrument such as FTIR, UV, Dissolution, DT , Hardness 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 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 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.
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