Regulatory Affairs Specialist

Change people’s lives and love what you do! Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market‑leader in implantable hearing devices, more people choose a Cochlear‑branded cochlear implant system than any other. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives.

Overview & Purpose

The Regulatory Affairs Specialist provides regulatory support across the lifecycle of Cochlear products, focusing on submissions and approvals in APAC, LATAM and EMEA markets. The role contributes regional requirements to global planning, provides regulatory guidance, and manages region‑specific documentation for submissions, tenders and legalization. The specialist oversees regulatory information management to maintain accurate product and certification records. Additionally, the specialist supports engineering and manufacturing te...