Device Documentation Lead – Regulatory & QA

UCB is seeking a Device Documentation Lead to ensure high-quality documentation supporting drug–device combination products. This role, based in Bulle, Switzerland, requires an individual with a Master’s degree and strong knowledge of medical device regulatory frameworks. You will manage documentation activities across development programs and collaborate with cross-functional teams to ensure compliance and readiness for regulatory submissions.

Your solid project management and communication skills are essential for success in this global role. Join us to contribute to patient-focused innovations.