Systems Engineer, Medical Devices — Sydney

ResMed Inc; Sydney; Vor Ort; AUD 110.000 - 160.000; Vollzeit

Zusammenfassung

ResMed Inc. is seeking a Systems Engineer for the Sydney, NSW team. You will help shape next-generation sleep therapy devices by translating needs into robust system requirements and delivering validated, high-quality solutions across disciplines.

You will collaborate with software, electronics, mechanical, verification, and clinical teams to drive product success. The role emphasizes traceability, risk assessments, and adherence to medical device regulations and standards, with a focus on

Qualifikationen

• Bachelor of Engineering in Electrical, Mechanical, Software, Mechatronics or related field.
• Strong systems thinking and methodical problem solving.
• Clear communication for cross-functional teams.

Aufgaben

• Translate user, clinical, business, and regulatory needs into system requirements, risk assessments, and technical solutions.
• Create, maintain, and support traceability of requirements in a requirements management tool.
• Collaborate with software, algorithm, electronics, mechanical, verification, and clinical teams to develop integrated system solutions.
• Evaluate design options and trade-offs and escalate when needed to senior engineers.
• Support system risk management, including analyses and reviews.
• Follow established Systems Engineering processes and contribute to continuous improvement.

Kenntnisse

System requirements

Traceability

Cross-functional collaboration

Risk assessment

Problem solving

Ausbildung

Bachelor of Engineering

Tools

JIRA

Jama

Confluence

Jobbeschreibung

ResMed Inc. is seeking a Systems Engineer for the Sydney, NSW team. You will help shape next-generation sleep therapy devices by translating needs into robust system requirements and delivering validated, high-quality solutions across disciplines.

You will collaborate with software, electronics, mechanical, verification, and clinical teams to drive product success. The role emphasizes traceability, risk assessments, and adherence to medical device regulations and standards, with a focus on