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Job Description
- Follow-up development of method of analysis of new drug molecules suitable for routine work of QC.
- Development of stability indicating assay of pharmaceutical products.
- The validation of all the developed methods of analysis.
- Solving any problems encountered in all the developed methods of analysis.
- Performing analysis in the accelerated stability testing of R & D batches.
- Documentation of MOA
- Analysis of formulation trials performed in Formulation section.
- Responsible for compliance with quality integrated system for quality, environment, health and safety in relation with his job and duties
Additional Information:
- Salary will be negotiable based on experience
Job Requirements
- Minimum education: Bachelor Degree in Pharmaceutical Sciences or Science
- Ideal experience: Technical: 1-5 years practical experience in related job
- Knowledge of analysis equipment such as HPLC, GC UV, and FT- IR is a MUST
- Languages: Fluent English & Arabic written, read and spoken
- Computer: Microsoft office & internet browsing
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