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Regulatory Affairs Specialist

Grifols, S.A

sant cugat del vallès, cataluña, Spain Full-time July 09, 2026

Found Description

About the company

We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.

Mission

The RRAA Specialist will be responsible of the preparation of technical documentation, submission and following up of product registration and/or renewal, variations dossiers, as well as other regulatory documentation.

What your responsibilities will be

  • Prepare, compile, and maintain registration dossiers and other regulatory documentation for medicinal products and medical devices within the assigned portfolio.
  • Prepare, review, and submit regulatory documentation for new registrations, renewals, variations, and other regulatory procedures.
  • Review and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance.
  • Monitor the prog...

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