GSK

life sciences or pharmaceutical sector

LOCQualityExecutive

Boumerdesoudouaou, Algeria; Khemis Meliana, Ain Defla, Algeria FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“LOC Quality Executive at GSK. Skills: Quality Management System, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), investigations, root cause analysis, corrective actions, vendor assessments, change control activities. Support local quality activities to keep our Quality Management System and compliant.. Work closely with operations, supply partners, and the LOC Quality Manager.”

What You'll Achieve.

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.

Industry & Context.

life sciences or pharmaceutical sector
Problems you'll solve

root cause analysis; investigations; deviations; complaints; audit findings

Eligibility Requirements

flexibility for regional travel to Warehouse at Ain Defla (Khemis Meliana) 2-3 times a week.

What They're Looking For.

Must Have

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 full-time on-site commitment is required.

Nice to Have

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., data analysis skills and experience using KPIs to drive improvement., Ability to work effectively across functions and coach operational teams.

What You'll Do.

Support local quality activities to keep our Quality Management System and compliant.

Work closely with operations

and the LOC Quality Manager.

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.

How You'll Work.

Team & Collaboration

Work closely with operations, supply partners, and the LOC Quality Manager.; Ability to work effectively across functions and coach operational teams.

Communication Scope

communicate clearly

Process & Methodology

change control activities

Full 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. **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 regulatio

Free ATS check

Applying for this LOC Quality Executive role?

Most applicants get filtered before a human reads their resume. See if yours makes the cut.

How to Apply on Workday

  • Workday has a multi-step form — save your progress after every section.
  • "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
  • Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
  • Job requisition numbers are useful when following up with HR by email.

ANONYMOUS · UNFILTERED

What do employees actually say about GSK?

Real rants from real employees. Read before you apply.

Read Company Rants →