Global Device Regulatory Lead — Strategy & Submissions

A global medical technology company in King of Prussia is seeking a Lead in Global Regulatory Affairs Device. The individual will drive regulatory strategies, ensuring compliance for the device portfolio. Responsibilities include liaising with the FDA, managing submissions, and collaborating with various stakeholders. The ideal candidate should possess over 5 years of regulatory experience, strong communication skills, and a relevant degree. This role offers significant opportunities to influence product development and compliance across international markets. #J-18808-Ljbffr