Scope

You will support and enhance our quality management system and data integrity at the site in Algeria. You will work closely with the quality, manufacturing, engineering, and IT teams to ensure process compliance with regulations and internal standards. We value pragmatic, curious, and collaborative individuals who are eager to learn and grow. This position offers clear career development opportunities, a tangible impact on patient safety, and the chance to contribute to uniting science, technology, and talent to get ahead of disease together.

Key Responsibilities
In this role, you will be responsible for the following:

• Reviewing and maintaining quality system records, including investigations, corrective and preventive actions (CAPA), deviations, and change control.

  
  
  

• Maintaining controlled documents, managing archives, and supporting user administration for quality and document systems:

  
  
  

  • Document lifecycle management: creation, distribution, review, modification, withdrawal of old versions, and proper filing of procedures according to document type via VQD.

    
    
    

  • Keeping the document list up to date.

    
    
    

  • Maintaining binders and files of distributed documents, if applicable.

    
    
    

  • Communicating document links for updates to ensure real-time periodic reviews.

    
    
    

  • Conducting Level 1 periodic reviews of the documentation system: document management, logbooks, reconciliation, batch records.

    
    
    

  • Managing and updating data on VQD.

    
    
    

  • Monitoring the dashboard of key performance indicators (KPIs) related to documentation on VQD.

    
    
    

  • Ensuring the use of VQD for every GxP document, using the backup system unless VQD is unavailable.

    
    
    

  • Relevant documents: LSOP, GUI, reports, protocols, DDL, MC, DC, annexes, logbooks, job descriptions.

    
    
    

• Managing training logistics and organizing the scheduling of local training sessions:

  
  
  

  • Assigning training.

    
    
    

  • Planning training sessions.

    
    
    

  • Recording training.

    
    
    

  • Reporting on training.

    
    
    

  • Administering training-related documentation, such as preparing participant lists, managing post-event documentation, and recording.

    
    
    

  • Ensuring efficient recording of all training in line with agreed processes and standards for business units/functions/sites, such as Good Manufacturing Practices (GQMPs) and Standard Operating Procedures (SOPs).

    
    
    

  • Generating local compliance reports based on agreed metrics.

    
    
    

  • Preparing any necessary documentation regarding training processes and record management for business units/functions/sites to meet audit requirements.

    
    
    

  • Providing basic daily support to learners.

    
    
    

  • Supporting local learning management practices/systems, such as SharePoint sites, local tracking tools, etc.

    
    
    

  • Providing support to the training advisor and training manager for general administrative tasks.

    
    
    

• Supporting data integrity activities and electronic system reviews to ensure records are accurate, complete, and accessible.

  
  
  

• Preparing tracking tables, KPI reports, and status updates for governance meetings and continuous improvement activities.

  
  
  

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• Degree in pharmaceutical sciences, chemistry, life sciences, engineering, or a related field.

  
  
  

• Experience in quality assurance, quality systems, or operations regulated by GMP.

  
  
  

• Practical knowledge of Good Manufacturing Practices (GMP) and quality management systems.

  
  
  

• Experience in investigations, CAPA, deviation management, or change control.

  
  
  

• Strong English and French communication skills, both written and spoken.

  
  
  

• Proficiency in office IT tools and experience with document or quality management systems.

  
  
  

Preferred Qualifications:

• Experience supporting data integrity programs or working with electronic laboratory/quality systems.

  
  
  

• Familiarity with validation concepts or computerized system validation.

  
  
  

• Strong organizational skills and experience managing multiple stakeholders.

  
  
  

• Experience preparing management dashboards and presentations.

  
  
  

This role is based on-site in Algeria. Hybrid or remote work is not offered due to the practical and cross-functional nature of the role.

Application Closure Date: 10th February 2026

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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