At ResMed, we’re passionate about driving innovation that improves lives. We’re seeking a Project Manager to join our Global Product Quality team on a 12-month maternity leave cover. This is an exciting opportunity to be part of a highly impactful team, contributing to projects that shape patient outcomes worldwide. The role is ideal for a highly motivated senior engineer looking to grow into project management, or for experienced project managers who thrive on navigating complexity, building cross-functional alignment, and driving continuous improvement in a global medical device environment.Job SummaryAs Project Manager – Global Product Quality, you will lead high-impact projects that ensure the safety, performance, and quality of ResMed products worldwide. Acting as a key integrator between Quality, Regulatory, Product Development, Medical Affairs, Supply Chain, and Commercial teams, you will coordinate responses to complex product quality matters and champion improvements to the systems and processes that support our global business.Let’s talk about responsibilitiesManage complex, competing needs between internal groups across Quality, Regulatory Affairs, Product, Engineering, Clinical and Supply Chain and facilitate to achieve optimal solutions for the businessLead and coordinate cross-functional teams to resolve complex product quality challenges and achieve optimal outcomes for the business.Coordinate and develop formal responses to post-market requests received from Regulatory Authorities.Act as a trusted advisor and facilitator across global teams, balancing patient safety, commercial and regulatory priorities.Drive continuous improvement of Quality and Operational systems, embedding best practices that enhance risk management, efficiency, and product lifecycle excellence.Mentor and coach others, fostering a collaborative and positive team environment.Perform other ad hoc duties as required.What You’ll BringInitiative and flexibility in managing rapidly evolving quality problems where data and outcomes are often unclear.Ability to influence and negotiate conflicting points of view across commercial, quality, regulatory, and product development perspectives.Strong problem-solving, analytical, and conceptual thinking skills.A results-driven mindset with the ability to balance competing priorities and manage risks.Proven project management skills, including planning, organization, delegation, and risk management.Excellent communication and stakeholder management skills across multiple time zones, locations, and levels.A passion for improving processes and systems and making a difference to patients and customers.Let’s talk about qualifications and experienceDegree in Engineering, Science, or a related discipline (or equivalent experience).Strong background in regulated industries, ideally healthcare or medical devices.Demonstrated experience leading or contributing to complex, cross-functional projects — either as a project manager or as an engineer driving project outcomes.Proven ability to coordinate across multiple stakeholders and functions on challenging, multi-factorial topics.Working knowledge of medical device regulations (e.g., FDA, ISO 13485, MDR) or the ability to rapidly learn and apply them.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!
