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. 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
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