Regulatory Affairs Lead - MedTech (CE/MDR)

BD in Limerick, Ireland is hiring a Regulatory Affairs Specialist to support new product development and CE marking from concept to commercialization, collaborating with R&D, Quality and Engineering. The RA role involves applying knowledge of MDR/MDD, preparing regulatory documents, and maintaining compliance across systems.

This position requires a university degree and offers an opportunity to work with cross-functional teams in a dynamic, global environment at the Limerick site.