At ResMed, we are committed to transforming our Medical Device labelling capabilities to ensure compliance with the evolving regulatory regulations worldwide. This transformation is crucial for maintaining the highest standards in our industry.

About the Role

We are seeking a Labelling Systems Specialist to support the development and evolution of labelling content within a regulated medical device environment.

This role sits at the intersection of systems, regulatory, and product development, contributing to both the optimisation of existing labelling processes and the transition to our Enterprise Labelling System (ELS).

You will bring a systems-thinking mindset, strong communication skills, and a continuous improvement approach to how content is created, structured, and managed — including exploring the use of AI and emerging technologies to enhance efficiency, scalability, and quality.

Key Responsibilities