Opportunity Description

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are looking for a Regulatory Affairs Specialist to join our team and support regulatory activities across EMEA and LATAM. This position is ideal for a professional with around 3 years of experience in Regulatory Affairs, particularly with strong exposure to CMC documentation and lifecycle management in multinational environments. The role is a full‑time position based in Madrid, starting with a one‑year fully remote assignment on an international project, with occasional travel to the client’s site in Alcobendas during the first year. Responsibilities Support regulatory submissions and activities across EMEA and LATAM markets. Prepare and maintain regulatory dossiers, including Module1 and Module3 documentation...
Full-time Other-General

Interested in this opportunity? Apply now through Expertini.

Apply for this Position