Job Description

Join the ResMed Sleep and Respiratory Care Team today!
ResMed is a global leader in connected devices and digital health. We help millions of people sleep, breathe and live better lives. Are you ready to help fuel our growth? As ResMed continues to evolve with the future of healthcare, our customer-centric organization focuses on cloud-connected devices and digital health technologies that are designed to help treat and manage sleep apnea, COPD, and other chronic respiratory diseases that, together, affect over one billion people worldwide.
If you share a passion for transforming care, keeping people healthy and out of the hospital, and lowering healthcare costs, ResMed invites you to apply to an applicable role (e.g. marketing, sales or product development) within the diverse and talented Sleep and Respiratory Care team.


Let’s talk about Responsibilities

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  Conceptualize and develop the design with due consideration to requirements such as human factors engineering, usability, environmental factors, balance patients’ needs, therapy performance requirements, design for manufacturing and assembly.
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  Conduct relevant studies that drive design directions.
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  Pre/post testing, verification and validation of designed products to ensure they meet the necessary requirements and specifications under anticipated usage scenarios and operating conditions.
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  Understanding and applying human factors criteria to product designs, gathering research/customer data and introducing best practices with new product requirements.
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  Be responsible for providing design recommendations that support project deliverables.
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  Cross-functional team leadership interaction with suppliers and internal stakeholders
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  Demonstrate cross-functional team leadership. Assess and communicate effectively with internal customers and suppliers in relation to design issues.
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  Operate with a high level of autonomy whilst interacting effectively with, and seeking input from team members and other areas of the business including marketing, manufacturing, clinical and regulatory affairs to ensure the products being developed are appropriate and satisfy all necessary requirements
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  Assist in the preparation and review of system documentation including System Specifications, Risk Analyses, Regulatory Submissions, etc.
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  Work within the ResMed Quality system, standards, regulatory requirements such as the FDA and maintain training requirements.
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  Self-management of tasks by the individual and directed by the Project Manager and/or Design Managers.

Let’s talk about Qualifications and Experience

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  Degree in Mechanical or Biomedical Engineering.
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  Minimum 5 years of engineering experience in a product research and development environment
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  Knowledge or experience in medical devices or similar regulated industry product development processes will be beneficial.
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  Experience integrating mechanical components/systems into overall product design.
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  Knowledge of manufacturing processes (mainly Injection Moulding) will be beneficial.
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  Strong proficiency with 3D CAD tools.

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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. If this sounds like the workplace for you, apply now!