Technical Writer

Join the Labelling team and play a pivotal role in the Medical Device Regulations project. If you’re an experienced Technical Writer who thrives on complex documentation, process improvement, and guiding others, this is your opportunity to make a meaningful impact. Responsibilities: Own the end-to-end development, publishing, and release of high-quality, compliant technical product documentation. Ensure all content aligns with ResMed’s standards, processes, and regulatory requirements. Collaborate cross-functionally to gather and validate technical information. Contribute to content governance, style guide improvements, and tooling best practices. Identify opportunities to streamline documentation workflows through AI or automation tools.