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The Senior Quality Specialist at Cochlear is responsible for managing the Quality Management System, conducting internal audits, and ensuring compliance with medical device regulations. Key responsibilities include facilitating root cause analysis, leading improvement projects, and delivering quality training programs. The role requires 3+ years of quality experience in a regulated industry with knowledge of ISO 13485 and continuous improvement methodologies.

As a Software Product Owner at Cochlear, you will shape the product vision and roadmap, prioritize backlog items, define requirements for the development team, and lead collaborations across different teams to ensure product success and alignment with organizational goals. You will also be a subject matter expert, guiding interactions with various functions and teams.

Responsible for obtaining Customs Rulings, introducing Licenced Manufacturing Warehouse, supporting logistics operations, implementing lean practices, collaborating with departments, ensuring compliance, and optimizing transportation processes. Support project teams and continuous improvement efforts in logistics.