Job Description
1) Method development and report preparation. 2) Routine F&D and stability sample analysis. 3) Method development and report preparation 4) Analytical method verification of assigned products. 5) To perform the forced degradation studies. 6) To develop and validate the cleaning method. 7) To Perform partial method validation for new develop method. 8) Characterization and analysis of reference product. 9) To perform the multimedia dissolution and preparation of CDP report. 10) Preparation of working standard as per SOP. 11) Analytical method transfer to QC Lab. 12) Cleaning and maintenance of laboratory equipment.
Job Details
| Role Level: | Entry-Level | 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 | ||
What We Offer
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