About the company
We believe that diversity adds value to our business, our teams, and our culture. Prepare, compile, and maintain registration dossiers and other regulatory documentation for medicinal products and medical devices within the assigned portfolio.
Review and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance.
Maintain up-to-date knowledge of current regulations and regulatory requirements applicable to medicinal products and medical devices, ensuring ongoing compliance.
Coordinate the translation of regulatory documentation, ensuring accuracy, consistency, and compliance with local market requirements.
Collaborate with cross-functional teams and external partners to ensure timely and high-quality regulatory submissions.
You have a Bachelor's Degree in Health Sciences or engineering.
You have Advanced level of Spanish and English (C1) and of MS Office (Excel).
Hybrid Model
Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same adaptable start time).
Contract of Employment: Permanent position.

📌 Regulatory Specialist and Senior Specialist (España)
🏢 Grifols
📍 España