Pharma Quality Technician: QMS & Continuous Improvement

Ipsen PharmSciences SAS

Dreux

Sur place

EUR 32 000 - 42 000

Plein temps

Il y a 5 jours
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Résumé du poste

Ipsen PharmSciences SAS is seeking a Quality Technician to support the Quality Management System across Pharmaceutical Development, strengthening compliance and driving continuous improvement. This role requires a scientific background and pharma experience in a highly regulated environment.

You will manage quality records, help with reporting and QMS activities, coordinate training, participate in inspections, and contribute to projects that elevate quality culture globally.

Qualifications

  • Bachelor's degree in a scientific or health-related field or equivalent experience.
  • 2-5 years of experience within a Quality function in the pharmaceutical industry.
  • Knowledge of Quality Management Systems and regulated environments.
  • Strong organisational, analytical, and communication skills.

Responsabilités

  • Support the deployment and continuous improvement of the Quality Management System across Pharmaceutical Development activities.
  • Manage quality records and documentation within electronic quality and document management systems.
  • Support quality reporting, performance monitoring, and Quality Management Reviews.
  • Coordinate training activities and maintain Learning Management System records.
  • Participate in self-inspections and quality compliance activities.
  • Contribute to continuous improvement projects and help promote a strong quality culture across the organisation.

Connaissances

Quality management systems
Analytical skills
Communication skills
Digital systems
French
English

Formation

Bachelor's degree in a scientific field

Description du poste

Ipsen PharmSciences SAS is seeking a Quality Technician to support the Quality Management System across Pharmaceutical Development, strengthening compliance and driving continuous improvement. This role requires a scientific background and pharma experience in a highly regulated environment.

You will manage quality records, help with reporting and QMS activities, coordinate training, participate in inspections, and contribute to projects that elevate quality culture globally.

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