Regulatory Affairs Specialist

Cochlear is seeking a Regulatory Affairs Specialist to join its Global Regulatory Affairs team in Kuala Lumpur, partnering with Product Development and R&D to shape the regulatory strategy for medical devices and software solutions. The role involves providing regulatory expertise throughout the product lifecycle, from pre-market development to post-market sustaining activities, ensuring compliance with global requirements. This position supports a global product portfolio with a primary focus on the United States and European regulatory environments while collaborating with regional teams worldwide.