Systems Engineer (12-month contract)

ResMed Inc; Sydney; In loco; AUD 95.000 - 130.000; Tempo pieno

Descrizione del lavoro

ResMed in Sydney is seeking a Systems Engineer to join the Devices Systems team to support the global expansion of sleep therapy technology. You will translate user, clinical and regulatory needs into system requirements and work with cross-functional teams to adapt the product for international markets.

The role focuses on requirements development, design changes, verification, risk management and regulatory activities, with emphasis on robust documentation and collaboration across engineering,

Competenze

• Bachelor's degree in engineering or related field.
• 2+ years of relevant engineering experience.
• Solid understanding of engineering principles and systems thinking.
• Experience with requirements, interfaces, design documentation or verification.
• Strong analytical and methodical problem solving abilities.
• Clear written and verbal communication across multidisciplinary teams.
• Ability to work independently while seeking guidance when needed.
• Interest in medical device regulations, quality systems and development processes.

Mansioni

• Translate user, clinical, business and regulatory needs into clear system requirements.
• Develop and manage system requirements with traceability and documentation.
• Collaborate with software, electronics, mechanical, verification, clinical and regulatory teams.
• Assess regional requirements and adapt products for international releases.
• Evaluate system architecture and interfaces for reliability and performance.
• Investigate and resolve system-level technical issues across disciplines.
• Support system verification, test planning and results documentation.
• Participate in system risk management, hazard analyses and design reviews.
• Contribute to regulatory submissions and design evidence for releases.
• Follow Systems Engineering processes and drive continuous improvement.

Conoscenze

Systems thinking

Requirements traceability

Cross-functional collaboration

Analytical problem solving

Formazione

Bachelor of Engineering (Electrical/ Electronics/ Mechanical/ Software/ Mechatronics)

Strumenti

JIRA

Jama

Confluence

Descrizione del lavoro

Help bring innovative sleep therapy technology to patients around the world. At ResMed, we create connected devices and digital health solutions that help millions of people sleep, breathe, and live better lives. We’re looking for a Systems Engineer to join our Devices Systems team based in Sydney and play a key role in supporting the global expansion of our sleep therapy technology. As a member of the team, you’ll focus on the globalisation of a newly released laboratory system for sleep apnoea titration, working with cross‑functional teams to adapt and extend the product for international markets. You'll support the product through requirements development, design changes, verification, risk management and regulatory activities, helping ensure it meets the needs of customers, clinicians and patients across different regions.

What You'll Do

• Translate user, clinical, business and regulatory needs into clear system requirements and technical solutions to support global product deployment.
• Develop, maintain and manage system requirements, including requirements traceability and technical documentation throughout the product lifecycle.
• Collaborate with software, electronics, mechanical, verification, clinical and regulatory teams to support product changes and system integration.
• Assess regional and market‑specific requirements, identifying necessary product adaptations to support international releases.
• Evaluate system architecture, interfaces and technical design options to ensure compatibility, functionality, performance and reliability.
• Investigate and resolve system‑level technical issues, working across engineering disciplines to identify effective solutions.
• Support system verification and validation activities, including test planning, execution, results analysis and documentation.
• Participate in system risk management activities, including risk assessments, hazard analyses and design reviews.
• Contribute to technical documentation and design evidence required for regulatory submissions and international product releases.
• Follow established Systems Engineering processes and contribute to continuous improvement initiatives.

What You Bring

• A Bachelor of Engineering in Electrical, Electronics, Mechanical, Software, Mechatronics or a related field.
• A minimum of 2 years of relevant engineering experience, ideally in systems engineering or product development.
• A sound understanding of engineering principles, systems thinking and structured problem‑solving approaches.
• Experience working with technical requirements, system interfaces, design documentation or verification activities.
• Strong analytical skills and a methodical approach to investigating and resolving technical challenges.
• Clear written and verbal communication skills, with the ability to collaborate effectively across multidisciplinary teams.
• An ability to work independently on assigned engineering activities while seeking guidance when appropriate.
• An interest in developing knowledge of medical device regulations, quality systems and product development processes.

Nice to Have

• Experience in medical device development or another regulated industry.
• Experience with engineering development tools such as JIRA, Jama, Confluence or similar platforms.
• Experience working with integrated hardware and software systems.
• Familiarity with medical device standards such as ISO 13485, ISO 14971 or IEC 60601

What Sets You Apart

• Systems Thinking: Understand how requirements, hardware, software and system interfaces interact to deliver reliable product performance.
• Collaborative Approach: Build productive relationships and contribute effectively to cross‑functional engineering discussions.
• Quality Focus: Demonstrate attention to detail in engineering documentation, verification and risk management activities.
• Continuous Improvement: Proactively identify opportunities to improve engineering processes, product quality and ways of working.

Why Join ResMed

At ResMed, you'll have the opportunity to contribute to the global expansion of innovative sleep therapy technology, helping make advanced clinical solutions available to more healthcare professionals and patients worldwide. You'll gain exposure to the full product lifecycle, work alongside experienced engineers and collaborate across Engineering, Clinical, Regulatory, Quality and Manufacturing teams. This is an opportunity to develop your systems engineering expertise while making a meaningful contribution to products that help people sleep, breathe and live better lives. 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. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates.

Resmed (NYSE:RMD, ASX: RMD) creates life‑changing health technologies that people love. We’re relentlessly committed to pioneering innovative technology to empower millions of people in more than 140 countries to live happier, healthier lives. Our AI‑powered digital health solutions, cloud‑connected devices and intelligent software make home healthcare more personalized, accessible and effective. Ultimately, Resmed envisions a world where every person can achieve their full potential through better sleep and breathing, with care delivered in their own home.

Learn more about how we’re redefining sleep health at Resmed.com and follow @Resmed.