飦禤reparation of SMF,VMP,Quality Manual, EMP,CVMP,Biosafety manual, Master formula of Vaccine
飦禤erform Process simulation study (Media fill) for Vaccine manufacturing, Sterile, Cephalosporins.
飦禫endor Approval and Disqualification System, qualification od visual inspector
飦� Quality Risk Analysis
飦禤erticipation in performance qualification of different equipments involved in Vaccine manufacturing, Solid doses, Sterile, LVP area.
飦禦esponsible for assuring that manufacturing operations are performed in compliance with cGMP as well as with company standards.
飦禝mplementing and maintaining the quality system conducting personnel training, controlling product design, controlling ...
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