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

Ready to Apply?

Submit your application today and join our talented team at PQE Group.

Submit Application