Apprentice - Pharmaceutical Quality Manager

Référence du poste : DAC-APPR-EP-2026-02

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Vous avez envie de faire carrière au sein d'un organisme public qui a pour mission de protéger efficacement la santé des populations ? Rejoignez-nous.
 

Santé publique France is France’s national public health agency. A public institution under the authority of the Minister of Health, formed through the merger of several public institutions and established by Ordinance 2016-246 of April 15, 2016, the agency works to promote public health. As a scientific, expert, and public health safety agency, its missions include:

  1. Epidemiological observation and surveillance of the population’s health status; 
  2. Monitoring health risks threatening the population; 
  3. Promoting health and reducing health risks; 
  4. Developing prevention and health education; 
  5. Preparation for and response to health threats, alerts, and crises; 
  6. Issuing public health alerts.

The agency is organized into 12 departments—some scientific, some cross-functional, and some providing operational support. 

The agency’s strategic priorities and work program, established by its Board of Directors, are organized into three areas: Strengthening the capacity for anticipation and rapid response to health threats; Measuring and assessing the extent of diseases and risk factors to guide their prevention and control; Strengthening the health impact of all public policies and the prevention and promotion of health.

Emergency and Crisis Management Directorate (DAC)

Responsibilities

  • Participate in the pharmaceutical company’s quality assurance activities.

Responsibilities

The apprentice will be responsible for supporting the Quality Department’s activities:

  • Participating in the management of deviation handling and corrective and preventive actions (CAPA),
  • Participating in quality monitoring of the Pharmaceutical Facility’s service providers (storage platforms, carriers) by tracking audit discrepancies and evaluating responses to complaints,
  • Participating in the monitoring and improvement of the change control process, particularly in relation to the Pharmaceutical Facility’s relocation project,
  • Participation in drafting procedures, standard operating procedures, logistics quality sheets, and other quality documents,
  • Participation in the project to implement an ERP and EDM system through the execution of qualification tests,

Project—Amendment to the authorization to open a pharmaceutical facility: preparation and implementation

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