Technical Supervisor
Posted Updated
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.
Support equipment qualification, process validation, cleaning validation, and validation activities.
Participate in protocol execution and review of validation documents as assigned.
Ensure validation activities are conducted according to approved protocols.