- Eysins, Vaud, Switzerland
- Director
- 5+ years
Lead and manage medical device development programs, ensuring regulatory compliance and cross‑functional collaboration.
Responsibilities
- Lead cross‑functional exercises to define targeted device profiles
- Develop device development project plans and budgets with internal and external teams
- Deliver quality products and processes with appropriate validation and regulatory documentation
- Write submission dossiers for FDA and EMA/NbO
- Report and control device development timelines, budgets and risks
Requirements
- Bachelor’s degree in Product Design, Mechanical, Process, Materials Science or Electronic Engineering