• 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.
📌 Technical Supervisor (India)
🏢 Cadila Pharmaceuticals
📍 India
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