Talentmate
India
11th September 2026
2609-6430-505
• 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.
| Role Level: | Associate | Work Type: | Full-Time |
|---|---|---|---|
| Country: | India | City: | Dholka ,Madhya Pradesh |
| Company Website: | https://www.cadilapharma.com/ | Job Function: | Information Technology (IT) |
| Company Industry/ Sector: |
Pharmaceutical Manufacturing | ||
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