Talentmate
India
2nd September 2026
2609-6430-395
• Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of stability on instrument such HPLC, UV, FTIR etc. by following test procedure. • Analysis of Stability Samples as per schedule • To follow safety procedure in QC department. • To attend the training as per schedule. • 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: | General Management |
| Company Industry/ Sector: |
Pharmaceutical Manufacturing | ||
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