Talentmate
India
19th August 2026
2608-6430-140
Maintain GLP in the laboratory as per regulatory requirement. Analytical method development as per ICH Guidelines. To perform In-process, routine and stability sample analysis. Perform the analytical method verification / validation as per protocol. Analytical method transfer to QC Laboratory. Documentation as per the GLP requirement. Trouble shooting during day to day analysis with proper instrument care. Perform dissolution development, multimedia dissolution and CDP activity. Working standard preparation as per SOP.
| Role Level: | Associate | Work Type: | Full-Time |
|---|---|---|---|
| Country: | India | City: | Dholka ,Madhya Pradesh |
| Company Website: | https://www.cadilapharma.com/ | Job Function: | Clinical & Lab Research |
| Company Industry/ Sector: |
Pharmaceutical Manufacturing | ||
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