12 Aug
|
Cadila Pharmaceuticals
|
Dholka
12 Aug
Cadila Pharmaceuticals
Dholka
- 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.
📌 Senior Executive (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka