Who is Artrya®
We are an Australian medical technology company advancing new standards of care for the detection, diagnosis, and treatment of coronary artery disease. We’ve developed the first new approach in 50 years for diagnosing heart disease, the global #1 cause of death.
Artrya’s ground-breaking AI-driven Salix Coronary Anatomy solution helps clinicians diagnose cardiovascular disease within 10 minutes at the point of care, so that they can provide personalised, life-saving treatment plans for all patients, while the patient is still in the waiting room.
The Role
As an engineering focused Technical Writer, you will take a hands-on lead in developing end-to-end technical documentation and supporting change management and continuous improvements within design control processes for SaMD products, including AI-enabled software, ensuring deliverables are complete, traceable, and compliant with global regulatory and quality standards.
You'll work day-to-day with software engineers, cloud/infrastructure engineers, AI/ML researchers, QA, and product managers - extracting technical knowledge and producing structured, traceable, regulatory compliant documentation. You don't need to write code, but you will need to understand software development concepts and how they relate to the SaMD products.
The ideal candidate is a former software developer or engineer who has transitioned into technical writing for regulated products.
At a high level this role will be responsible for:
- Documentation Ownership & Authoring of Technical Documentation (E.g. Software design and architecture, UI specifications, Software risk assessments)
- Traceability & Lifecycle Integration
- Change Control & AI/Software Updates
- Planning, Tracking & Program Coordination
- Support for Reviews, Submissions & Audit Readiness
- Process, QMS & Continuous Improvement
About you
We want to hear from you if you are ready for the next step in your career where you will be an integral part of the documentation of our products and processes which can help save lives. To do this you will need:
- A Bachelor’s level qualification in systems engineering or related degree,
- 5+ years of technical writing experience, with at least 3 years in a regulated environment
- Solid experience [JB1] in medical devices, SaMD, or regulated software environments and familiarity with ISO 13485, FDA 21 CFR Part 820/QMSR, IEC 62304, and ISO 14971. Demonstrated understanding of software development concepts including software architecture, version control, cloud infrastructure and CI/CD deployments.
- Proven experience authoring technical documentation in a regulated environment, including design documentation, traceability and version control, and technical files.
- Demonstrated ability to translate complex engineering and AI/ML concepts into clear, structured, and compliant documentation.
- Exceptional written communication with ability to produce clear, structured, compliant documentation
- Strong interpersonal skills with the ability to work across regulatory, engineering, quality, and clinical teams under tight timelines
What we offer
If this sounds like you, be part of Artrya’s journey and be rewarded by knowing you will be instrumental in an organisation that is 100% aligned to its purpose of saving lives. We offer a competitive salary, a supportive work environment with focus on flexibility and professional growth.
The Executive Team are incredibly passionate and motivated to succeed. You will thrive by adding to our dynamic culture that will provide considerable chance for continued personal and professional growth.
How to apply
If you are ready to contribute to Artrya’s future, this is your opportunity to get on board. Click "Apply" and send your resume.
For more information or to see the detailed Job Description, please email us at ********@artrya.com
📌 Technical Writer - SaMD (Software Engineering-focused) (Perth)
🏢 Artrya
📍 Perth