via Career pages·Yesterday
Technical Supervisor
Cadila Pharmaceuticals
Full-timeOn-sitecgmpglplimsquality controlsapsample managementrecord of analysiscontinuation sheetlaboratory cleaninginward registermaster preparationcalibrationsafety proceduresteam supervision
Location:Dholka, IndiaType:Full-timePosted:Yesterday
- Follow cGMP and GLP practices in Quality Control Lab.
- 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 prepare the master & COA in lims & SAP.
- Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS.
- Responsible for cleaning & monitoring of laboratory.
- Sample management & make entry in LIMS.
- To prepare Masters in Caliber LIMS & Record of analysis (ROA).
- To do any other Work assign by HOD.
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