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 parts of Module 3 or other additional documentation related to products manufactured at the Riells site.
This is a school of regulatory excellence where you will learn from the best, work on important projects, see the real impact of your work on millions of patients, and build a solid career from day one.
Matching Summary
Evaluate the regulatory compliance status of the site.
Skills & Requirements
Must-have
Regulatory compliance assessment
Regulatory variation dossier drafting
Module 3 documentation
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 Module 3 of the regulatory dossier
Experience in drafting regulatory variations
Experience in pharmaceutical product transfers
Knowledge of pharmaceutical regulations and guidelines