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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.
LOC Quality Executive
You will support local quality activities to keep our Quality Management System strong and compliant. You will work closely with operations, supply partners, and the LOC Quality Manager. We value people who are practical, collaborative, and curious. This role offers real growth, the chance to improve processes, and the opportunity to help GSK’s mission of uniting science, technology and talent to get ahead of disease together.
Responsibilities:
This role is based in Algeria-Boumerdes/Boudouaou and will be on-site with flexibility for regional travel to Warehouse at Ain Defla (Khemis Meliana) 2-3 times a week.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Deliver and monitor Local Operating Country (LOC) quality objectives and the LOC quality improvement plan.
- Track and trend quality KPIs to identify improvement opportunities and report progress.
- Maintain and improve the local Quality Management System to meet GSK standards, Good Manufacturing Practices and local regulations.
- In market batch transfers and its related activities
- Support investigations, root cause analysis and corrective actions for deviations, complaints and audit findings.
- Conduct self-inspections and vendor assessments for third-party contractors and service providers.
- Assess quality impact of planned changes and manage change control activities.
Why you?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals
- Degree or diploma in pharmacy, life sciences, or a related technical discipline.
- Minimum 3 years’ experience in quality assurance, quality control, or regulated operations in the life sciences or pharmaceutical sector.
- Practical knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
- Experience with investigations, CAPA process and root cause analysis.- Experience working with third-party contractors, suppliers, or distribution operations.
- Role is on-site in Algeria; full-time on-site commitment is required.
Preferred Qualification:
If you have the following characteristics, it would be a plus:
- Bachelor’s Degree in a scientific field (Biology, Chemistry, Pharmaceutical Sciences or a related area)
- Experience with electronic quality management systems or document control tools.
- Familiarity with auditing, inspection readiness and handling regulatory interactions.
- Experience in warehousing, distribution or secondary repacking operations.
- Strong data analysis skills and experience using KPIs to drive improvement.
- Ability to work effectively across functions and coach operational teams.
Working arrangement
This role is based in Algeria-Boumerdes/Boudouaou and will be on-site with flexibility for regional travel to Warehouse at Ain Defla (Khemis Meliana) 2-3 times a week.
What we value
We look for people who act with integrity and put patient safety first. You communicate clearly and build trust with your colleagues. You make practical, timely decisions and coach others to improve. You are open to learning and welcome collaboration.
Apply now
If this role excites you, we would love to hear from you. Please submit your CV and a short note about why you are interested. We review applications as they arrive and aim to respond quickly.
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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