Head of Medical Devices Regulatory Affairs

The Head of Medical Devices Regulatory Affairs at Meta is responsible for leading the regulatory strategy and product approvals for innovative hardware and software as medical device products. This role requires a subject matter expert who can navigate the complexities of regulatory requirements across various global markets, ensuring timely market access and compliance for Meta's growing medical device portfolio. The position involves collaboration with cross-functional teams and external stakeholders to drive regulatory goals and improve the quality system within the organization.