ABOUT MED-EL

MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,800 employees around the world.

Our Regulatory Affairs department ensures that products comply with applicable regulations and standards. This includes providing strategic input to product developments, obtaining and maintaining product registrations and approvals, communicating with authorities, and monitoring regulatory changes to ensure continued compliance.

• Lead, organise and support key regulatory projects / tasks and regulatory compliance initiatives
• Organise and support preparation of regulatory submissions, licence renewals, registrations and change notifications to international authorities
• Organise and maintain regulatory documentation to meet regulatory requirements
• Provide regulatory intel to product development projects