Commercial Quality Manager
Listed on 2025-12-24
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Quality Assurance - QA/QC
Quality Engineering, QA Specialist / Manager, Regulatory Compliance Specialist
Location:
Jeddah Headquarters Business Park, Saudi Arabia.
Posted:
Dec .
Site Name:
Jeddah Headquarters Business Park.
GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization, in line with hiring, 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. 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.
- 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.
- 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.
- 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.
This is an on site role based in Saudi Arabia. Travel across the assigned territory may be required.
How To ApplyIf you're ready to join us in this impactful role, apply today! Together, we'll get ahead of disease and shape the future of healthcare. You may apply for this position online by selecting the Apply Now button.
Equal Employment OpportunityGSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Seniority Level: Not Applicable
Employment Type:
Full time
Job Function:
Quality Assurance
Industries:
Pharmaceutical Manufacturing
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