Associate Technical Writer - Medical Devices (12-Month Contract) job opportunity at Resmed.

Home Jobs In Australia Tag: Job Associate Technical Writer - Medical Devices (12-Month Contract) position at Resmed


DateMore Than 30 Days Ago bot
Resmed Associate Technical Writer - Medical Devices (12-Month Contract)
Experience: 3-years
Pattern: full-time
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degreeAssociate
loacation AU Sydney Bella Vista, Australia
loacation AU Sydney Bell..........Australia

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.  

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