الرئيسية / الوظائف / 9040 مشاهدة28 مارس 2020


Quality control analyst,GSK - STJEGYPT



Quality control analyst,GSK - STJEGYPT

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Work Type : Full Time
Experience : 0-3 Years




Gender : male and female
Salary: Not mentioned
Salary Type : Net Salary
Location: Cairo, EG
Job Purpose


Ensure working in a safe environment. Test and analyze lab samples, and operate lab equipment and instruments, to ensure the quality of products and materials in compliance with GSK standard, specification, local requirements and GMP working with our values and expectations.


Key Responsibilities


Proceed an examination of the product before analysis.
Analyze and test Raw and Packaging materials, RM re-testing and intermediates as well as finished products according to approved protocols and specifications.
Operate & Calibrate departmental section equipment and instruments according to approved SOPs e.g. HPLC, GC, UV/Vis, IR and Atomic Absorption Spectrophotometer, balances and other analytical equipment.
Implement and maintain GMP, GLP and ISO requirements relevant to his/ her job.
Responsible for keeping the retained samples of materials and products and their disposal, according to the approved SOPs.
Prepare, standardize and maintain availability of reference standard, volumetric solutions, glassware, and reagents and ensure their good handling and storage according to the approved SOPS.
Perform environmental analysis cleaning validation analysis, water analysis and other monitoring lab tests under the supervision of the section head.
Ensure that EHS requirements are fulfilled during work.
Out of Specification handling: Contribution in investigation using root cause analysis.
CAPA management: Set corrective actions and preventives action plans for L1 audit points and required action for improvement and follow up for progress.
Change control system: Contribution in implementation of change control system for any process or equipment.
Apply the GSK production system “GPS” basic elements in the analytical lab to reach zero accident, zero waste & zero defect.
Additional non-routine tasks related to section or individuals development plan may be assigned.
Ensure that the data integrity requirements are fulfilled during work.
Handle of supplier complains.




Knowledge/ Education / Previous Experience Require


University bachelors Degree in Pharmaceutical sciences.
At least 2 years of experience in similar role.
Good command of English Language,
Good level of computer skills.
Excellent communication skills
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