Would you like to join an international team working to improve the future of healthcare?

Grifols is a general healthcare company that since **** 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.

¿We believe that diversity adds value to our business, our teams, and our culture.

MissionPrepare, review and manage complex submissions and follow up of chemistry/manufacturing and controls regulatory activities, ensuring timeliness, accuracy, comprehensiveness, and compliance with regulatory standards.What your responsibilities will bePrepare, review and manage complex submissions and follow up of chemistry/manufacturing and controls (CMC) regulatory activities, ensuring timeliness, accuracy,



comprehensiveness, and compliance with regulatory standards.Keep track of change requests in the appropriate database.Represent the regulatory function in cross-functional project teams as related to worldwide product registrations.Keep track of CMC regulatory activities in the appropriate databases.You have a Bachelor's Degree in Health Sciences.Flexible and adaptable to changing situations/projects within the company/industry.Computer skills (such as MS Office, databases, Document Management System).

You have Advanced level of Spanish and English (C1).

Hybrid ModelFlexible schedule: Monday-Thursday 7-10 to *****h and Friday 8-15h.

(Temporary position#J-*****-Ljbffr

📌 Regulatory Affairs Specialist - Temporal (Barcelona)
🏢 Grifols
📍 Barcelona