Senior QC Raw and Packaging Analyst

Job description

Site Name: Egypt – Giza
Are you a Senior QC Raw and Packaging Analyst who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this Senior QC Raw and Packaging Analyst role is the one for you to explore.

As a Senior QC Raw and Packaging 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. Working with our values and expectations in mind.

In this role you will…

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.
Handling of supplier complaints and Root cause analysis.
Perform second person check, review analysis raw data and release materials for use in production.
Stock management for QC lab consumables and chemicals.
Training and coaching for newly hired QC analysts.
Act as Raw materials section head delegate during his/her absence.

Qualifications:

Bachelor’s Degree of Pharmaceutical sciences.

3-5 year of experience at similar role is a must.

Pharma manufacturing experience is highly preferred through multinational companies.

Excellent Communication Skills

Good command of English.