Technical Writer - Medical Devices (12-month Contract)
ResMed
Sydney, AU
On-site
Develop and maintain labelling content
Translate regulatory requirements
Collaborate cross-functionally
Transforming Medical Device labelling capabilities to ensure compliance with evolving regulatory regulations worldwide
Job Summary
Transforming Medical Device labelling capabilities to ensure compliance with evolving regulatory regulations worldwide.
Support the development and evolution of labelling content within a regulated medical device environment, transitioning to an Enterprise Labelling System (ELS).
Collaborate cross-functionally with Regulatory Affairs, Quality, Systems Engineering, and Product teams to ensure accuracy, consistency, and traceability of labelling artefacts.
Matching Summary
Transforming Medical Device labelling capabilities to ensure compliance with evolving regulatory regulations worldwide.
Skills & Requirements
Must-have
develop and maintain labelling content
translate regulatory requirements
collaborate cross-functionally
continuous improvement initiatives
structured technical documentation
Nice-to-have
systems thinking mindset
AI and emerging technologies
structured content authoring platforms
design controls
product development processes
Key Requirements
Experience in technical writing, regulatory, quality, or engineering roles within a regulated environment
Excellent written and verbal communication skills
Proven ability to collaborate effectively across multiple stakeholders