An excellent opportunity to join an international pharmaceutical company seeking a Regulatory Affairs Manager to support its global regulatory operations, in the Pre-MA team.

This professional will manage registration procedures and prepare dossiers for Marketing Authorization Applications, ensuring compliance with international guidelines. The role includes coordinating deficiency letters, supporting product launches, communicating with customers and global health authorities, and contributing to regulatory strategies for new submissions and lifecycle management projects. Additionally, this person will maintain up‑to‑date regulatory information, review documentation from CMOs, manage the online audit room, and coordinate cross‑functional product activities.

We are looking for a professional with a degree in a Life Science field and three to five years of experience in Regulatory Affairs within European, national, or other highly regulated markets (US, Canadá). Experience in Pre-MA and Modules 1 and 3 are required. Excellent English and Portuguese communication skills are mandatory.

A chance to join a global pharmaceutical company with international exposure, strategic responsibilities, and opportunities to deepen your regulatory expertise.

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.