QC/Stability Analyst

Site Name: Egypt - Cairo
Posted Date: Dec 17 2025

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

QC/Stability Analst

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.

Why you?

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

Working arrangement

This position is on-site in Egypt. You will work from our laboratory location and collaborate regularly with cross-functional colleagues.

What we offer

You will join a team that cares about patient impact and your development. You will have opportunities to learn new techniques, grow your technical skills and take on broader responsibilities. We welcome candidates from different backgrounds and encourage people who are curious, reliable and ready to contribute.

Ready to apply?

If this role speaks to you, we encourage you to apply. Tell us how your experience and attitude will help the team deliver high-quality results. We look forward to learning about you.

Why GSK?
Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Contact information:
You may apply for this position online by selecting the Apply now button.

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