QC Analyst

659 Glaxo Saudi Arabia Limited; Jeddah; On-site; SAR 45,000 - 60,000; Full time

Job summary

A global biopharma company in Saudi Arabia is seeking a QC Analyst to perform analytical testing in their quality control laboratory. The ideal candidate will have a Bachelor's degree in a related science and at least 2 years of laboratory experience. Responsibilities include conducting rigorous testing, maintaining detailed records, and ensuring compliance with GMP and GLP standards. The role offers opportunities for professional growth within a supportive environment focused on innovation and patient care.

Qualifications

• Minimum 2 years of laboratory experience in QC, analytical testing or a similar role.
• Working knowledge of GMP, GLP and laboratory safety (EHS) requirements.
• Good written and spoken English for accurate documentation and team communication.

Responsibilities

• Perform routine chemical and microbiological testing of raw materials and products.
• Prepare reagents, maintain laboratory records and complete test documentation.
• Assist with investigations for out-of-specification results and document findings.

Skills

Attention to detail

Clear communication

Problem solving

Technical skills

Education

Bachelor’s degree in Chemistry, Biochemistry, Pharmacy, Microbiology or related science

Tools

Laboratory equipment

Analytical techniques

Basic computer tools (Word, Excel)

Job description

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 Analyst

You will perform and support analytical testing in our quality control laboratory in Saudi Arabia. You will work closely with laboratory colleagues, technical teams and quality partners to deliver reliable test results. We value attention to detail, clear communication and a practical approach to problem solving. This role gives you space to grow your technical skills and to contribute to work that supports 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 chemical and microbiological testing of raw materials, in-process samples and finished products using approved methods and instruments.
• Prepare reagents, maintain laboratory records and complete test documentation according to procedures.
• Follow and support data integrity, quality management and good manufacturing practice requirements.
• Carry out equipment checks, basic maintenance and participate in calibration and validation activities.
• Assist with investigations for out-of-specification results and document findings clearly.
• Support training of new analysts and share practical knowledge to help the team deliver accurate results.

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Pharmacy, Microbiology or related science.
• Minimum 2 years of laboratory experience in QC, analytical testing or a similar role.
• Working knowledge of GMP, GLP and laboratory safety (EHS) requirements.
• Practical experience using common laboratory equipment and analytical techniques.
• Good written and spoken English for accurate documentation and team communication.
• Proficiency with basic computer tools such as Word and Excel.

Preferred Qualifications

• Experience with stability testing, method transfer or validation activities.
• Familiarity with a quality management system and risk-based laboratory practices.
• Experience with laboratory instrument troubleshooting and maintenance.
• Prior exposure to microbiological testing alongside chemical analysis.
• Training or experience in data integrity practices and record keeping.
• Strong problem solving and time management skills.

Working arrangements

This position is on-site at our Saudi Arabia facility. Regular laboratory presence is required.

How to apply

We welcome applicants who want to grow their technical skills and help deliver high quality results. If this role fits your experience and ambitions, please apply and tell us about a time you solved a lab problem or improved a test process. We look forward to hearing from 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.

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