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Job Description
Roles & Responsibilities
You will carry out analytical testing and stability sample management to help ensure product quality and regulatory compliance. You will work closely with laboratory colleagues, quality and production teams. We value accuracy, curiosity, and a willingness to learn and coach others. This role offers growth through hands-on technical work, exposure to stability programs, and clear opportunities to develop your laboratory and leadership skills while contributing to GSK s mission of uniting science, technology and talent to get ahead of disease together.
Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Perform routine analytical testing of raw materials, packaging, intermediates, finished products and stability samples using validated methods and approved protocols.
- Operate and maintain laboratory instruments such as HPLC, GC, UV/Vis, IR, balances and other analytical equipment following standard operating procedures.
- Manage stability sample handling, inventory, storage conditions and documentation to meet study timelines and regulatory requirements.
- Record, review and report accurate and complete laboratory data, ensuring data integrity and adherence to quality systems.
- Support laboratory investigations, troubleshooting of methods and instruments, and contribute to corrective actions.
- Train and coach new analysts on methods, systems and good laboratory practices to build team capability.
Desired Candidate Profile
Basic Qualifications:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelor s degree in Pharmaceutical Sciences, Chemistry, Biology or related science field.
- 0 to 3 years laboratory experience in analytical testing, preferably in pharmaceutical or regulated industry
- Practical experience with instrumental techniques and laboratory equipment handling.- Working knowledge of good laboratory practice (GLP) and good manufacturing practice (GMP) requirements.
- Good computer skills and ability to use laboratory information systems or electronic records.
- Effective communication skills in English and ability to work collaboratively in diverse teams.
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
- 2 or more years experience in operational quality, production quality or quality assurance.
- Experience with stability programs and stability sample management.
- Experience with HPLC, GC method operation and basic method troubleshooting.
- Knowledge of Quality Management Systems and experience following SOPs and protocols.
- Experience in preparing reagents, reference standards and solution standardization.
- Strong attention to detail and a commitment to data integrity.
- Previous experience in a multinational or regulated environment
Company Industry
- Pharma
- Biotech
- Clinical Research
Department / Functional Area
- Quality
- Testing
- QA
- QC
- Inspector
Keywords
- QC/Stability Analyst
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GlaxoSmithKline
https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Egypt---Cairo/QC-Stability-Analyst_432141
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