This role serves as the primary authority on Quality Documentation lifecycle management within Sanofi's QualiPSO Content Management System
Job Summary
This role serves as the primary authority on Quality Documentation lifecycle management within Sanofi's QualiPSO Content Management System.
The position requires leading a robust training strategy to ensure GRA personnel are qualified and current on all applicable quality documents.
Sanofi offers a competitive salary range of $113,250.00 to $163,583.33 along with comprehensive benefits including at least 14 weeks' gender-neutral parental leave.
Matching Summary
This role serves as the primary authority on Quality Documentation lifecycle management within Sanofi's QualiPSO Content Management System.
Salary
Base: $113,250.00 - $163,583.33; Bonus/Equity: Not specified; Benefits: Comprehensive health, wellness, and 14 weeks parental leave
Skills & Requirements
Must-have
5+ years relevant experience
2+ years Regulatory Affairs experience
2+ years GxP Quality system management
Advanced proficiency in Veeva CMS
Knowledge of 21 CFR Part 211 and GxP regulations
Document lifecycle management expertise
Nice-to-have
Agile mindset and digital tool adoption
Cross-functional collaboration skills
Data-driven continuous improvement approach
Change agent capabilities
Multicultural environment sensitivity
Key Requirements
BS/BA degree in a relevant scientific discipline
Minimum 5 years of relevant experience
At least 2 years in Regulatory Affairs
Hands-on experience with electronic document management systems