At ResMed, we’re shaping the future of healthcare through breakthrough technology—and quality is at the heart of everything we do. We’re looking for a Graduate Quality Assurance Engineer to join our Global Quality Management Systems (QMS) team and help ensure our products and processes meet the highest standards in global markets.
This is a great opportunity to work cross-functionally, learn from experienced quality professionals, and contribute to meaningful projects that make a difference in people’s lives.
The primary role of Quality Assurance function is to ensure that management systems are established to enable business compliance with multiple regulatory frameworks and to support the entire lifecycle of Resmed products to meet our customer’s requirements.
The Quality Assurance - Quality Systems function supports• The management, maintenance, and optimization of the structure and integrity of the Quality Management Systems (QMS) to ensure ResMed’s products and processes comply with the regulatory requirements applicable to medical devices for the markets in which they are distributed.
• All aspects of the audit program to ensure regulatory compliance, quality best practice, process improvements, and development of supplier quality systems.
• Broad business technical support around QA systems and processes.
Supports and implements significant quality projects across the business and creates and improves quality and business processes.
As a graduate engineer in the Global QMS team, you will work across the business to help implement, maintain, and improve the Global Quality Management System (QMS). The responsibilities and activities for this role vary and present an opportunity to collaborate broadly across the business.
Support the management, maintenance, and optimization of the structure and integrity of the Global Quality Management Systems (QMS) to ensure compliance and alignment with applicable regulatory standards and business requirements.
Support in the development and maintenance of Resmed’s QMS Training program.
Apply critical thinking skills to help resolve issues, identify opportunities for improvement, and work with stakeholders to achieve desired outcomes.
Collaborate with internal customers in relation to quality and business improvements.
Support in the consultation and collaboration with Global Business Process owners to interpret, construct and apply
robust processes into the Global QMS.
Review, analyse and implement opportunities for continual improvement of the Global QMS to meet business needs.
As needed, support internal and external QMS audits through a variety of preparation and support activities.
Undertake other Quality Assurance Systems support and other ad hoc activities as required, including Audits and QMS support.
Let’s talk about Qualifications and Experiences
Strong collaboration, listening, interpretation, and communication skills.
Ability to identify linkages and dependencies between processes.
Ability to think clearly and critically, assess information and evidence to make informed, timely decisions.
Ability to successfully influence others to achieve outcomes.
Agility to adapt and respond quickly while being resilient to overcome obstacles.
You are a team player with a can-do attitude and you’re willing to try, fail and learn from your mistakes.
This role is also open to candidates with 1-2 years of relevant work experience
Preferred:
Bachelor’s degree in science or engineering.
Interest in medical devices, regulatory compliance, or quality systems is a plus
#LI-APAC
#auearlycareers
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!
