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Job Description
- Documentation of method of analysis of each product
- Documentation of formulation trials of each product
- Performing calculations of accelerated and long term stability studies of each product.
- Preparing the final stability report submitted to MOH
- Preparation of CTD Files
- Revision of Method Validation,NODCAR files , Stability Studies , comparative dissolution studies , Analytical COAs and record of Analysis.
Job Requirements
- B.Sc of pharmaceutical science or science
- 1-5 years practical experience in related job.