Alternance 12 Mois – Affaires Règlementaires Globales

Sanofi

Gentilly, , France
Preparation and compilation of cmc dossiers
Coordination of regulatory submissions
Regulatory database management
As an intern within the Global Regulatory Affairs CMC team, you will actively participate in the development, registration, and regulatory maintenance of innovative biological medicines

Job Summary

  • As an intern within the Global Regulatory Affairs CMC team, you will actively participate in the development, registration, and regulatory maintenance of innovative biological medicines.
  • Sanofi offers a supportive environment with inspiring mentors, collaborative teams, and opportunities to learn and innovate using the latest digital tools and AI.
  • The position includes attractive remuneration, social benefits, paid exam preparation days, and a commitment to diversity, inclusion, and employee well-being.

Matching Summary

As an intern within the Global Regulatory Affairs CMC team, you will actively participate in the development, registration, and regulatory maintenance of innovative biological medicines.

Skills & Requirements

Must-have

  • Preparation and compilation of CMC dossiers
  • Coordination of regulatory submissions
  • Regulatory database management
  • Support for clinical trial regulatory processes
  • Regulatory impact assessment
  • Cross-functional collaboration

Nice-to-have

  • Analytical and synthesis skills
  • Organizational skills
  • Good interpersonal skills
  • Interest in artificial intelligence
  • Project management knowledge

Key Requirements

  • Bac+5 in pharmacy or regulatory affairs
  • Fluent English

Work Rights

Not specified

Tailored Resume

Cover Letter