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Job Description
- Creation and Development of Assay and Dissolution methods, as well as Method development reports for new Drug Products.
- Validation of Assay and Dissolution methods of finished drug products.
- Analysis of stability samples including their related substances and In-use stability studies, and creation of stability study files.
- Making Bio-waiver and comparative dissolution Studies according to FDA Guidance.
- Internal calibration and performance Qualification of instruments according to work instructions.
- Handling all Documentation and Reports for the performed analysis.
- Ensuring and controlling GMP in Analytical Research laboratories.
Job Requirements
- Job qualification : Pharmacist or Chemist
- Job experience : 3-5 experience on the same position