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QC Analyst

GSK

Jeddah

On-site

SAR 200,000 - 300,000

Full time

Today
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Job summary

A global biopharma company is seeking a QC Analyst in Jeddah, Saudi Arabia to perform routine testing of raw materials and finished products. You will support data integrity and quality management, requiring a Bachelor's degree in a relevant field and at least 2 years of laboratory experience. The role demands a working knowledge of GMP, GLP, and lab safety, along with practical skills in laboratory equipment. This position is on-site, necessitating regular laboratory presence.

Qualifications

  • Bachelor’s degree in Chemistry, Biochemistry, Pharmacy, Microbiology or related science.
  • Minimum 2 years of laboratory experience in QC or related role.
  • Working knowledge of GMP, GLP and laboratory safety requirements.
  • Practical experience using common laboratory equipment.

Responsibilities

  • Perform routine testing of raw materials and finished products.
  • Prepare reagents and maintain laboratory records.
  • Support data integrity and quality management requirements.
  • Assist with investigations for out-of-specification results.

Skills

Laboratory testing
Analytical techniques
Good Manufacturing Practices (GMP)
Good Laboratory Practices (GLP)
Problem solving
Time management

Education

Bachelor’s degree in Chemistry or related field

Tools

Laboratory equipment
Word
Excel
Job description
Overview

Site Name: Saudi Arabia - Jeddah

Posted Date: Feb 2 2026

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.

Role: QC Analyst

Responsibilities
  1. Perform routine chemical and microbiological testing of raw materials, in-process samples and finished products using approved methods and instruments.
  2. Prepare reagents, maintain laboratory records and complete test documentation according to procedures.
  3. Follow and support data integrity, quality management and good manufacturing practice requirements.
  4. Carry out equipment checks, basic maintenance and participate in calibration and validation activities.
  5. Assist with investigations for out-of-specification results and document findings clearly.
  6. Support training of new analysts and share practical knowledge to help the team deliver accurate results.
Why you?

Basic Qualifications:

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

Preferred Qualification

  1. Experience with stability testing, method transfer or validation activities.
  2. Familiarity with a quality management system and risk-based laboratory practices.
  3. Experience with laboratory instrument troubleshooting and maintenance.
  4. Prior exposure to microbiological testing alongside chemical analysis.
  5. Training or experience in data integrity practices and record keeping.
  6. 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.

إليك الترجمة العربية للإعلان الوظيفي بالكامل:

… (Arabic content retained as provided) …

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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GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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