Technical Writer
1 week ago
**L**ocation**:Bella Vista,**Sydney | Hybrid**
We’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 documentation
- Ensure all content aligns with ResMed’s standards, processes, and regulatory requirements
- Collaborate cross-functionally to gather and validate technical information
- Contribute to content governance, style guide improvements, and tooling best practices
- Identify opportunities to streamline documentation workflows through AI or automation tools
- Mentor junior team members and contribute to team knowledge growth
**Let’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 mindset**
- Proficiency in **XML-based CMS platforms**, with demonstrated experience using tools like **Adobe AEM**, **Adobe Workfront**, **InDesign**, **Acrobat**, and **JIRA/Confluence**
- Understanding of how to **leverage**AI**and modern tools to improve documentation efficiency and quality
- Self-motivated and adaptable, with excellent communication skills and a continuous improvement mindset
- Excellent communication skills and the ability to translate complex technical input into user-focused content.
**Preferred**:
- Experience with **translation/localisation workflows**
- Background in **high-volume manufacturing**or **medical device labelling**
- Familiarity with **agile methodologies**and cross-functional collaboration
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