Site Name: Egypt - Giza - Giza
Posted Date: Aug 2 2022
Are you excited by the opportunity to develop your career within the Quality Control team of one of the leading pharmaceutical companies worldwide? If so, then this opportunity is the one for you to consider As a Raw Materials Analyst, you will be responsible to 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, with our values and expectations in mind. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:

• Physical 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 SOP's 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 SOP's.
• Prepare, standardize and maintain availability of reference standard, volumetric solutions, glassware, and reagents and ensure their good handling and storage according to the approved SOP's.
• 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.
• Applying 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 individual’s development plan may be assigned.
• Ensure that the data integrity requirements are fulfilled during work.
• Handle supplier complaints.

Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:

• Bachelor’s Degree
• 1 year of experience in a similar role is preferable
• Energy and Resilience
• Communication Skills
• English Language
• Computer Skills

Why GSK? At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Health, strengthening our leadership, and transforming our commercial execution. Now, we’re making the biggest changes we’ve made to our business in over 20 years. We’re on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands.
With new ambition comes new purpose. For New GSK, this is to unite science, talent and technology to get ahead of disease together – all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive.
Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients – so we deliver what matters better and faster; accountable for impact – with clear ownership of goals and support to succeed; and where we do the right thing. So, if you’re ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together.
Contact information:
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