We are looking for a Device Documentation Lead who is methodical, detail‑focused, and quality‑driven to join our Devices, Artwork & Packaging (DAP) team , supporting the development and lifecycle of drug–device combination products. This role can be based in Braine‑l’Alleud, Belgium or Bulle, Switzerland .
As Device Documentation Lead, you will play a key role in ensuring that robust, compliant documentation supports the development and regulatory submission of drug–device combination products. You will define and implement documentation strategies across multiple programs, ensuring consistency, accuracy, and readiness for design reviews and regulatory dossiers.
Working within cross‑functional technical project teams, you will contribute across the full product lifecycle—from development and usability studies to submission, launch, and lifecycle management—ensuring high‑quality documentation that ultim...