Full-time

Regulatory Affairs Officer

Posted by Teva Pharmaceuticals • Porto Salvo, Lisbon, Portugal

📍 Porto Salvo, Lisbon 🕒 February 28, 2026

About the Role

The opportunity

We are looking for a Regulatory Affairs Associate/Officer to join us in Teva Porto-Salvo office. We have a hybrid approach to home-working!

You mission will be to coordinate and prepare applications for registration, variations, revalidations and pricing to obtain approvals from the Portuguese and European regulatory authorities, ensuring that the appropriate processes for the registration, launch and maintenance of our products are complied with in a timely manner and that safety and quality control standards are met.

How you’ll spend your day

  • New Registration Applications (National/MRP/DCP/CP) Preparation of registration file and requirements within the established deadlines
    Follow-up of registration, deficiency letters, allegations and responses to authorities, agree final texts with INFARMED to obtain marketing authorization.
    Artworks: elaboration, review and approval of artworks for new r...
  • Ready to Apply?

    Submit your application today and take the next step in your career journey with Teva Pharmaceuticals.

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