Job Description

Join Us as a Senior Systems Engineer at ResMed!


Are you ready to make a meaningful impact on the lives of millions? We're seeking a Senior Systems Engineer to join our Masks Systems Engineering team from a base of Sydney or Singapore. This is your opportunity to lead with technical expertise, drive innovation, and collaborate across disciplines to deliver exceptional patient outcomes.


ResMed practices a flexible working environment and achieves its success through diverse collaborative teams. You will have opportunities to develop a network of like-minded people and develop further in your engineering journey. We ask you to be your authentic self, to always speak your mind and to bring your best.


We are in search of a passionate

Senior

Systems Engineer

to join our Product Development team at ResMed, where you will play a pivotal role in defining requirements and delivering innovative, patient-centered solutions. Together, we prioritize patient safety through meticulous and robust testing, while also championing the long-term sustainability of our products across their lifecycle.

Let's talk about the Team

Our team supports the entire lifecycle of ResMed's mask products--from concept development (PD) through to Product Lifecycle Engineering (PLE). We thrive on innovation, collaboration, and technical excellence to deliver world-class therapy solutions. You'll work within a high performing group that values shared ideas, embraces challenges, and prioritizes the patients' experience.

Let's talk about the Role

As a Senior Systems Engineer, you will:

Lead cross-functional and multi-site systems engineering efforts

across new product development programs, aligning teams in Singapore, Sydney, and global partners to deliver cohesive system solutions.

Develop, manage, and maintain high-quality system requirements and specifications

for Resmed's products--integrating user needs, regulatory expectations, and business objectives.

Collaborate across disciplines

including Mechanical Design, Materials, Human Factors, Quality, Regulatory, Clinical, Manufacturing, and Product Management to design safe, effective, and user-centric mask systems.

Drive innovation and system-level architecture

, ensuring that mask performance, comfort, durability, manufacturability, and usability are considered holistically within the broader ResMed device ecosystem.

Work closely with V&V teams

to ensure system requirements are fully tested, verified, and validated in alignment with regulatory and quality expectations. ensuring compliance with Regulations and Standards

Lead system risk assessments

, define mitigation strategies, and ensure robust traceability from design input to post-market surveillance.

Support FDA submissions

, contributing system documentation, verification packages, risk files, and technical justifications for 510(k) pathways.

Act as a hands-on systems engineer

--engaging directly in prototype evaluation, experimental testing, data analysis, bench investigations, and design troubleshooting alongside the team.

Shape system-level decisions through technical leadership and stakeholder management

, facilitating design reviews, handling trade-offs, and ensuring clarity of decisions across global teams.

Provide ongoing support for released products

, focusing on performance improvements, quality investigations, regulatory updates, and lifecycle enhancements.

Mentor and guide team members

, fostering systems-thinking capability, rigor, and effective collaboration across engineering disciplines and geographical locations.

Champion continuous improvement

, embedding lessons learned into future development cycles, tools, and engineering best practices. Your leadership and technical expertise will directly influence the next generation of Resmed's products--delivering superior patient comfort, safety, and therapy effectiveness.

Let's talk about Qualifications:

Education:

Bachelor's or Master's degree in Systems Engineering, Mechanical Engineering, Biomedical Engineering, or related discipline. Minimum

8 years of experience

in systems engineering or product development, ideally within medical devices or other regulated environments. Demonstrated experience working with

multi-site, multi-disciplinary engineering teams

. Experience contributing to

FDA submissions

, especially

510(k)

pathways, including system requirements, verification evidence, and risk management documentation.

Skills & Knowledge:

Deep understanding of

systems engineering principles

: requirements development, architecture definition, design integration, and verification/validation planning. Strong working knowledge of

ISO 13485, ISO 14971

, biocompatibility standards (

ISO 10993

series), and

cleaning/reprocessing standards

(e.g.,

ISO 17664

). Experience generating

technical documentation

, system models, risk files, and verification protocols/reports. Hands-on experience with

prototype evaluation, bench testing, and iterative problem-solving

. Ability to translate user and business needs into system requirements and balanced design decisions.

Attributes:

Strong problem-solving mindset and exceptional communication skills. Proven leadership capability, including mentoring and cross-functional influence. High attention to detail with a passion for product quality, patient safety, and human-centric design. Pragmatic, hands-on engineer who is comfortable in the lab, on the bench, and in design reviews. Collaborative, adaptive, and energized by working in a fast-paced global R&D environment.
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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! We commit to respond to every applicant.