About this role
Embrace the opportunity to become a Device Documentation Lead and play a pivotal role in ensuring robust, compliant documentation for drug–device combination products. Collaborate with cross-functional teams, drive regulatory submissions, and support patient impact across the product lifecycle. Shape the future of medical device documentation with a global leader in biopharmaceuticals.
About UCB
Global biopharma company focused on neurology and immunology therapies for severe diseases. Headquartered in Brussels, Belgium.