Junior Regulatory Site Officer

Sanofi UK

Riells I Viabrea, Spain
Regulatory variation dossiers
Module 3 documentation
Cmc documentation
Evaluate the regulatory compliance status of the site

Job Summary

  • Evaluate the regulatory compliance status of the site.
  • Draft and/or review regulatory variation sheets, variation dossiers, complete Module 3 parts or other additional documentation related to products manufactured at the Riells site.
  • Here you will not only have a job; you will have a school of regulatory excellence.

Matching Summary

Evaluate the regulatory compliance status of the site.

Skills & Requirements

Must-have

  • Regulatory variation dossiers
  • Module 3 documentation
  • CMC documentation
  • High-level English proficiency
  • Pharmaceutical regulatory guidelines

Nice-to-have

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

Key Requirements

  • Experience in Module 3 of regulatory dossier
  • Experience in regulatory variations
  • Experience in pharmaceutical transfers
  • Practical experience with IT tools
  • Degree in Pharmacy or Chemistry (valued)

Work Rights

Not specified

Tailored Resume

Cover Letter