About the role
AI summarisedThe Senior Mechanical Engineer leads product development from concept to production within ResMed's Diagnostics Product Team, focusing on sleep disorder monitoring and treatment devices. Responsibilities include designing electro-mechanical systems, mentoring junior engineers, ensuring compliance with medical device quality standards, and collaborating across teams and suppliers. The role requires a degree in Mechanical, Biomedical, or Mechatronics Engineering with significant experience in complex electro-mechanical product development, preferably in the medical industry.
MedTechOnsite
Key Responsibilities
- Collaborate across the project team to efficiently define solutions and processes that deliver the greatest value for ResMed and meet user needs
- Be aware of the interactions between systems in solving engineering problems in connected product solutions
- Work collaboratively with external suppliers and across teams and disciplines to achieve project objectives
- Provide guidance to the mechanical team to help them solve technical issues within a project
- Mentor the engineering team in building technical capability, leadership, ownership and accountability
- Communicate effectively and proactively with peers and business stakeholders to report on project progress and remove project roadblocks
- Work within the regulated medical device environment and advocate for best engineering and quality practice
- Ensure that ResMed engineering best practices and processes are adhered to in the delivery of your work and any projects or sub-systems you are responsible for
- Embody ResMed’s Core Competencies and exemplify ResMed’s values
- Own and execute discipline design activities in a team at both component and sub-system level, and actively contribute to design architecture and innovative thinking
Requirements
- Degree in Mechanical Engineering, Biomedical Engineering, Mechatronics, or equivalent
- Significant experience in a product development role designing complex electro-mechanical systems
- Significant knowledge of product development process, including preparing documentation for the design history file
- Significant knowledge of materials and manufacturing processes
- Proficiency in 3D CAD (PTC – Creo products preferred)
- Significant experience & application of simulation & analysis tools (e.g., Ansys, MoldFlow, Minitab)
- Significant experience in test, verification and validation traced to requirements
- Experience in developing test/process measurement capabilities
- Significant engineering experience within the medical industry (preferred)