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Director of Regulatory Affairs France

il y a 1 mois


Lyon, Auvergne-Rhône-Alpes, France EMD Temps plein
Job Summary

We are seeking a highly skilled Regulatory Affairs Specialist to join our team in France. As a key member of our Regulatory Affairs team, you will be responsible for leading the local submission management process, defining the Health Authority engagement strategy, and serving as the point of contact for local Health Authorities.

Key Responsibilities
  • Develop country product plans based on global/regional strategy and business plans
  • Provide relevant support for clinical trials as applicable and required
  • Enable the development of team members, support their personal growth, and reach their full potential
Requirements
  • PhD in pharmacy required
  • Excellent and up-to-date knowledge and understanding of applicable EU and French regulations
  • High proficiency in French and English
  • Advanced skills in all standard MS office & business applications
About EMD

At EMD, we are committed to creating access and opportunities for all to develop and grow at their own pace. We are a global company with a passion for innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics.