Associate Technical Writer role at ResMed. Support labelling content development & maintenance in a regulated med device environment. 2-3 yrs exp, detail-oriented, degree in engineering/science req. #TechnicalWriter #MedicalDevice #Labelling #Regulatory #EntryLevel #ResMedCareers
Launch Your Career in Medical Device Labelling Transformation
At ResMed, we are committed to transforming our Medical Device labelling capabilities to ensure compliance with evolving global regulations. This transformation is crucial for maintaining the highest industry standards and delivering safe, effective products to patients worldwide.
About the Role
We are seeking a meticulous and proactive Associate Technical Writer to join our team. This role is central to developing and maintaining the technical content for our product labelling. You will operate across both existing (legacy) processes and a new Enterprise Labelling System (ELS) as we transition to future ways of working. This is an ideal opportunity for someone early in their career who is detail-oriented, eager to learn, and thrives in a structured, compliance-driven environment.
Key Responsibilities: Support Labelling Excellence & Transition
You will be instrumental in ensuring the accuracy and compliance of our critical labelling documents during a pivotal business transformation.
Core Responsibilities:
- Support Creation & Maintenance: Assist in the creation and maintenance of labelling technical documentation (IFUs, labels, packaging).
- Execute Labelling Updates: Perform labelling updates using established legacy processes and tools, ensuring timely and accurate changes.
- Utilize New Systems: Learn to create and update content within the new Enterprise Labelling System (ELS) under the guidance of senior team members.
- Perform Quality Checks: Conduct thorough proofing and quality checks to ensure all content is accurate, complete, and compliant with processes, style guides, and brand standards.
- Support Review Cycles: Facilitate reviews, approvals, and change management activities within the regulated documentation workflow.
Skills & Experience: The Foundation for Success
You are a structured communicator with a foundational understanding of technical documentation in a regulated setting.
Essential:
- 2–3 years of experience in a similar technical writing, documentation, or quality support role is ideal.
- A degree in Engineering, Science, Quality, Regulatory Affairs, or a related discipline (or equivalent practical experience).
- Exceptional attention to detail and strong organizational skills.
- Clear and effective written and verbal communication skills.
- Ability to follow defined processes precisely and work effectively under guidance.
- A willingness to learn and grow within a regulated medical device environment.
Desirable (What Will Make You Stand Out):
- Exposure to regulated documentation (medical devices, pharmaceuticals, aerospace, etc.).
- Familiarity with document or content management systems (e.g., Veeva, SAP, Loftware, Easy Label).
- Basic understanding of regulatory (FDA, MDR) or quality principles (ISO 13485).
Why Build Your Career at ResMed?
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.
1. Impact Through Precision
- Your work ensures the accuracy of information that guides clinicians and patients in the safe use of life-changing medical devices.
- Be part of a critical global transformation project that shapes the future of ResMed’s compliance.
2. Growth & Learning
- Gain hands-on experience with both legacy and next-generation enterprise systems.
- Develop expertise in medical device regulations and technical writing within a supportive team environment.
- Clear pathways for career development in Technical Writing, Labelling, or Regulatory Affairs.
3. Inclusive & Innovative Culture
- Thrive in a culture driven by excellence that helps you meet and create new goals.
- Be part of a diverse and inclusive workplace that encourages individual expression and innovative ideas.
Ready to Start Your Technical Writing Career in MedTech?
If you are a detail-oriented professional eager to contribute to meaningful work in a regulated industry, we want to hear from you.
Apply now for the Associate Technical Writer position. We commit to responding to every applicant.
