other
Posted Apr 20Labelling Systems Specialist (12-Month Contract)
at ResMed
On-site
Requirements
- 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
- Experience in technical writing, regulatory, quality, or engineering roles within a regulated environment Excellent written and verbal communication skills, with the ability to translate complex information into clear, user-friendly content Proven ability to collaborate effectively across multiple stakeholders and functions Strong attention to detail with a solid understanding of compliance-driven environments Desirable
- Experience within the medical device industry or similar highly regulated sectors Exposure to design controls, product development processes, or structured technical documentation Familiarity with document management systems or structured content/authoring platforms Interest or exposure to AI, automation, or digital content solutions Who You Are A proactive and self-motivated learner who takes initiative Curious, with a continuous improvement mindset toward systems and processes Comfortable working in
Additional details
- 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).
- Responsibilities Develop, maintain, and manage labelling content across legacy platforms and enterprise systems Translate regulatory, engineering, and product
- requirements into clear, accurate, and compliant documentation Contribute to content creation, structuring, and governance within the Enterprise Labelling System (ELS), supporting adoption of new ways of working Ensure accuracy, consistency, and traceability of labelling artefacts in alignment with regulatory and quality standards Collaborate cross-functionally with Regulatory Affairs, Quality, Systems Engineering, and Product teams Support continuous improvement initiatives, including process optimisation