| Job Location | Saudi Arabia |
| Education | Graduate |
| Salary | Not Mentioned |
| Industry | Pharmacy / Lab / HealthCare Quality / Testing |
| Functional Area | Not Mentioned |
Analysis of Finish Products as per the schedule with emphasis on first pass analysis.Inventory of Lab requirements including Glassware/ StationaryWork in another department whenever required like AMD (due to unavailability of instrument in QC)To provide training to trainees on the analytical techniques used for the Finish Goods analysis.To learn incorporation of data and other functions related to SAP.cGMP / GLP Compliance in QC Laboratory. Maintain good documentation practices.To maintain reference standards, chemicals, reagents, and solvents.Raise OOS and fill LIR in given time Frame.Perform testing of market complaint samples whenever required.To look for logbooks for proper entries.Maintenance & Daily checks of Analytical Balance, pH Meters.Support in procurement procedure related to instruments/Reagents/StandardsTo prepare User requirement for the CAPEX approved instrumentsCarryout Analytical Method transfer between the two labs.Qualifications:Bachelor?s or Master?s degree in Chemistry .5 to 6 years? experience in Pharmaceuticals Quality ControlBasic fire safety Awareness .Knowledge of Pharmaceutical products.Data analysis and good observation capabilities .Familiarized with cGMP and SFDA regulatory compliance.You will be redirected to the company website to apply for this position
Keyskills :
experience in Pharmaceuticals Quality Control
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