Chargé(e) Assurance Qualité R&d – Alternance – H/f

Pierre Fabre

Toulouse, Haute Garonne, France
Life cycle management of medical devices
Quality management system
Regulatory requirements analysis
You will be integrated into the Quality and Compliance, R&D and Medical team, reporting to the Project Quality Manager

Job Summary

  • You will be integrated into the Quality and Compliance, R&D and Medical team, reporting to the Project Quality Manager.
  • Your main mission will be to structure the QMS for the Life Cycle Management of Medical Devices.
  • Benefits include product allocations, attractive conventional salary, profit sharing, 13th month, and employee savings plan.

Matching Summary

You will be integrated into the Quality and Compliance, R&D and Medical team, reporting to the Project Quality Manager.

Skills & Requirements

Must-have

  • Life Cycle Management of Medical Devices
  • Quality Management System
  • Regulatory requirements analysis
  • Deviations and audits management
  • Document management

Nice-to-have

  • Curiosity and rigor
  • Synthesis skills
  • Interpersonal skills
  • Team collaboration

Key Requirements

  • BAC+5 or higher education
  • Pharmacist, Master 2 Quality, or Engineer
  • Good knowledge of quality and pharmaceutical environment
  • Proficiency in IT tools
  • Fluent French and English

Work Rights

Not specified

Tailored Resume

Cover Letter