Mechanical Engineer, Pressure Systems — Medical Devices

ResMed Inc.; Sydney; On-site; AUD 90,000 - 130,000; Full time

Job summary

ResMed in Sydney is seeking a Mechanical Engineer to join the Pressure Systems sub-team. You will design components for high-volume production and evaluate manufacturability and patient-focused performance for sleep apnoea devices.

You will collaborate with multidisciplinary teams, build and test prototypes, and perform verification activities while contributing to DFMEA and quality processes under regulatory requirements. Strong communication and analytical skills are essential.

Qualifications

• Bachelor's degree in Mechanical, Mechatronics, Biomedical Engineering or equivalent.
• Strong communication and teamwork skills.
• Experience with CAD and simulation tools.

Responsibilities

• Develop components, considering design impact on performance, manufacturability and end-user experience.
• Apply design requirements related to patients, usability, therapy performance, environment, cost, quality and assembly.
• Collaborate with multidisciplinary teams across mechanical, electronics, systems, software and manufacturing.
• Build and evaluate prototypes using additive manufacturing and hands-on fabrication methods.
• Design and conduct verification and validation testing to meet requirements.
• Solve design problems using first principles, simulations and empirical methods.
• Create and maintain documentation of designs and testing.
• Communicate progress, risks and challenges with the team.
• Participate in DFMEA and risk management activities.
• Adhere to ResMed's Quality Management System and regulatory requirements.
• Develop technical skills and share learning to improve team capability.

Skills

Communication

Teamwork

Analytical thinking

Education

Bachelor's degree in Mechanical, Mechatronics, Biomedical Engineering or equivalent

Tools

Creo CAD

ANSYS CFD

Job description

ResMed in Sydney is seeking a Mechanical Engineer to join the Pressure Systems sub-team. You will design components for high-volume production and evaluate manufacturability and patient-focused performance for sleep apnoea devices.

You will collaborate with multidisciplinary teams, build and test prototypes, and perform verification activities while contributing to DFMEA and quality processes under regulatory requirements. Strong communication and analytical skills are essential.