Global Regulatory Affairs Device Lead, (Brussels, Belgium)

Make your mark for patients

Are you ready to shape the future of cutting‑edge medical technologies? As the Global Regulatory Affairs Devices Lead (GRA‑DL), you’ll play a pivotal role in bringing innovative medical devices and combination products to patients worldwide—spanning Neurology, Immunology, and breakthrough New Medicines, including cell and gene therapies. From advanced Drug Delivery Systems to IVDs and Biomarkers, you’ll influence a diverse portfolio of life‑changing technologies while driving global regulatory strategy in a highly visible, high‑impact role.

This position can be located in Atlanta, GA, or Raleigh, NC.

About the Role

In this role, the Global Regulatory Affairs Devices Lead (GRA‑DL) partners closely with the GRA Device Team Lead to guide regulatory strategy, documentation planning, and submission preparation for medical device programs. You will collaborate with Global Clinical Development (GCD), Globa...