Regulatory Affairs Specialist

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.

❗ ❗ We offer a full-time employment contract based in Madrid , starting with a one-year fully remote assignment on an international project, including occasional travel to the client’s site in Alcobendas during the first year.

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