Commercial Quality Manager

**Site Name**: Jeddah Headquarters Business Park
**Posted Date**: Dec 21 2025
**GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.**

**Role purpose**

Join GSK to lead local and commercial quality activities in Saudi Arabia, ensuring safe and compliant supply to patients. You will partner with commercial, regulatory, medical, supply chain and global quality teams to maintain quality standards, drive investigations and CAPA, and support inspection readiness. This role offers visible impact, career growth, and the chance to help GSK unite science, technology and talent to get ahead of disease together.

**Key responsibilities**

- Provide local commercial quality oversight for products and supply activities in Saudi Arabia.
- Lead and manage quality investigations, root cause analysis, and corrective and preventive actions (CAPA).
- Maintain and improve local Quality Management System documentation, procedures and work instructions.
- Support inspection readiness and act as the local quality contact for audits and regulatory interactions.
- Provide quality input into commercial processes such as product launches, promotional materials reviews, and complaint handling.
- Monitor and report on quality performance metrics and trend analysis to local and global stakeholders.
- Coach and train commercial and cross-functional teams on quality expectations and good practices.
- Participate in or lead internal audits; respond to audit/inspection findings and implement remediation.
- Collaborate with global quality, regulatory and supply partners to implement quality standards and continuous improvements.

**Why you?**

**Basic qualifications**

- Saudi National.
- Bachelor’s degree in life sciences, pharmacy, engineering, or a related field.
- Minimum 5 years’ experience in quality within a regulated healthcare, pharmaceutical, or medical products environment.
- Practical knowledge of Good Manufacturing Practice (GMP) and relevant local regulatory requirements.
- Proven experience leading investigations, root cause analysis and CAPA.
- Strong written and spoken English; Arabic language skills advantageous.
- Ability to work on-site in Saudi Arabia; primarily on-site with occasional hybrid flexibility based on business needs.

**Preferred qualifications**

- Experience with commercial quality, promotional compliance, or supply chain quality activities.
- Familiarity with global quality systems and working within a matrix organization.
- Experience supporting regulatory inspections or audits.
- Training or certification in quality management, auditing, or investigation techniques.
- Strong stakeholder management, coaching skills and experience implementing process improvements or digital quality tools.

**Work Environment**
This is an on-site role based in Saudi Arabia. Travel across the assigned territory may be required.

**How to Apply**

**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**:
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