**About the Role** We are seeking a Regulatory Affairs Associateto join our team to support the implementation of regulatory strategies, prepare regulatory submissions, and ensure compliance to labelling requirements for Cochlear’s products.In this role, you will support the preparation and maintenance of regulatory submissions, product registrations, and renewals in alignment with company and authority requirements. You will contribute to the development of labelling requirements for instructions for use, packaging labels, and product information and coordinate labelling verification to ensure compliance with international standards and country-specific regulations.**Key Responsibilities:****1. Labelling Compliance and Documentation*** Assist interpretation and application of global and regional medical device labelling standards and regulations.* Support the development and maintenance of a central repository of labelling requirements.* Prepare and deliver labelling requirements spec...