Regulatory Site Officer

Sanofi

Riells, Spain
Regulatory site compliance assessment
Draft and review regulatory variation filings
Module 3 dossier preparation
Evaluate the regulatory compliance status of the site

Job Summary

  • Evaluate the regulatory compliance status of the site.
  • Draft and manage product renewals and site registrations.
  • You will learn from the best, work on projects that matter, and see the real impact of your work on millions of patients.

Matching Summary

Evaluate the regulatory compliance status of the site.

Skills & Requirements

Must-have

  • Regulatory site compliance assessment
  • Draft and review regulatory variation filings
  • Module 3 dossier preparation
  • CMC documentation experience
  • High-level English proficiency

Nice-to-have

  • Teamwork and global vision
  • Analytical and synthesis skills
  • French language proficiency
  • Methodical and practical profile

Key Requirements

  • Experience in regulatory dossier Module 3
  • Experience in pharmaceutical product transfers
  • Knowledge of pharmaceutical regulations and guidelines
  • Practical experience with computer tools

Work Rights

Not specified

Tailored Resume

Cover Letter