Location
Clayton
Job Type
Full-time
Posted
July 15, 2026
Job Description
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
**Summary**
Maintains regulatory documentation and filing systems in support of the Biopharma North America regulatory team. Maintains accurate files of health authority correspondence in paper and electronic formats as needed and word processing submission documents as needed. This position will support the product managers to meet business objectives for the overall regulatory team.
**Primary Responsibilities**
+ Perform updates, facilitate SME reviews, and ensure proper hard copy and el...
**Summary**
Maintains regulatory documentation and filing systems in support of the Biopharma North America regulatory team. Maintains accurate files of health authority correspondence in paper and electronic formats as needed and word processing submission documents as needed. This position will support the product managers to meet business objectives for the overall regulatory team.
**Primary Responsibilities**
+ Perform updates, facilitate SME reviews, and ensure proper hard copy and el...
Ready to Apply?
Submit your application for Regulatory Documentation Specialist I at Grifols Shared Services North America, Inc
Apply Now