This is a Associate Technical Writer - Medical Devices (12-Month Contract) role with ResMed based in Bella Vista, NSW, AU ResMed Role Seniority - junior More about the Associate Technical Writer - Medical Devices (12-Month Contract) role at ResMed 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 an Associate Technical Writer to support the development and maintenance of labelling technical content within a regulated medical device environment. This role will operate across both existing (legacy) labelling processes and a new enterprise labelling system (ELS) as the business transitions to future ways of working. The role is ideal for someone early in their career who is detail-oriented, eager to learn, and comfortable working in structured, compliance-driven environments. Key Responsibilities Support creation and maintenance of labelling technical documentation Execute labelling updates using established legacy processes and tools Create and update content within the Enterprise Labelling System (ELS) under guidance Perform proofing and quality checks to ensure accuracy, completeness, and compliance to our processes, style guides and brand. Support reviews, approvals, and change management activities Skills & Experience Essential: 2–3 years of experience in a similar role is ideal. Degree in engineering, science, quality, regulatory, or related discipline (or equivalent experience) Strong attention to detail and organisational skills Clear written and verbal communication Ability to follow defined processes and work under guidance Willingness to learn in a regulated environment Desirable: Exposure to regulated documentation (medical devices, pharma, or similar) Familiarity with document or content management systems Basic understanding of regulatory or quality principles Joining 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. Before we jump into the responsibilities of the role. No matter what you come in knowing, you’ll be learning new things all the time and the ResMed team will be there to support your growth. Please consider applying even if you don't meet 100% of what’s outlined Key Responsibilities Supporting documentation Executing updates ✅ Quality checks Key Strengths Attention to detail ️ Communication skills Process adherence Regulated documentation exposure Content management systems familiarity ⚖️ Regulatory principles understanding A Final Note: This is a role with ResMed not with Hatch.