Technical Writer - Medical Device Labelling (12 months contract) page is loaded Technical Writer - Medical Device Labelling (12 months contract) Apply locations Sydney, NSW, Australia time type Full time posted on Posted 5 Days Ago time left to apply End Date: June 30, 2025 (17 days left to apply) job requisition id JR_042019L ocation: Bella Vista, Sydney HybridWe're looking for a technically minded, self-driven leader to join our Labelling team and play a pivotal role in our 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 !Let's Talk About the Role :Own the end-to-end development, publishing, and release of high-quality, compliant technical product documentationEnsure all content aligns with ResMed's standards, processes, and regulatory requirementsCollaborate cross-functionally to gather and validate technical informationContribute to content governance, style guide improvements, and tooling best practicesIdentify opportunities to streamline documentation workflows through AI or automation toolsMentor junior team members and contribute to team knowledge growthLet's Talk About You:5+ years of hands-on technical writing experience, preferably in regulated industries (medical device, electronics, pharma )Proven leadership experience - you've led documentation projects or mentored others in a team setting .Strong technical acumen and a process-oriented mindsetProficiency in XML-based CMS platforms, with demonstrated experience using tools like Adobe AEM, Adobe Workfront, InDesign, Acrobat, and JIRA/ConfluenceUnderstanding of how to leverage AI and modern tools to improve documentation efficiency and qualitySelf-motivated and adaptable, with excellent communication skills and a continuous improvement mindsetExcellent communication skills and the ability to translate complex technical input into user-focused content.Preferred:Experience with translation/localisation workflowsBackground in high-volume manufacturing or medical device labellingFamiliarity with agile methodologies and cross-functional collaborationJoining us is more than saying "yes" to making the world a healthier place. It's discovering a career that's challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant. Similar Jobs (1) Engineer,Verification & Validation Eng (12-months contract) locations 2 Locations time type Full time posted on Posted 14 Days AgoResmed (NYSE:RMD, ASX: RMD) creates life-changing health technologies that people love. We're relentlessly committed to pioneering innovative technology to empower millions of people in more than 140 countries to live happier, healthier lives. Our AI-powered digital health solutions, cloud-connected devices and intelligent software make home healthcare more personalized, accessible and effective. Ultimately, Resmed envisions a world where every person can achieve their full potential through better sleep and breathing, with care delivered in their own home. Learn more about how we're redefining sleep health at and