The primary role of Manufacturing Quality function is to design, implement and monitoring quality control programs. Key deliverables include, but not limited to, recommending changes to methods, procedures and standards to improve quality of output based on analysis of data and systems. Ensures products are built correctly to specification, quality standards and appropriate regulatory compliance. Reports defects and tracks until resolution.Let’s talk about ResponsibilitiesSupport the Factory Focus teams to achieve current KPI of Quality, Delivery and CostLead and support new products introduction process into manufacturing with active involvement in appropriate XFT deliverables and phase transitions in collaboration with QA counterpart in XFT and QA/RA teamPro-actively improve quality systems to support manufacturing including reviews across all areas of manufacturing and QA production support team to ensure a level of consistency and standardization in ResMed QMS across various manufacturing business units and sitesEnsure risk of non-compliance and related business risks are mitigatedProvide quality / technical leadership through mentoring/coachingEnsure compliance to ResMed QMS; strong knowledge, application of and compliance to FDA Quality System Regulations, GMP, and applicable ISO / regulatory standardsAbility to work collaborative across various QA functions in ResMed (Quality systems & Audit, design, supplier, manufacturing, and customer quality)May perform Quality representative role for Operations projects and business activities that require broad quality expertise and support, eg: site moves / expansions, new process / business ventures, support / integration of acquired companies.Develop Quality Agreements, Quality Plans, Project Based Risk AssessmentPerform or support internal / external / supplier auditsPartner with stakeholders and other functions to understand business & quality requirements and apply appropriate risk-based decision making to achieve successful business and customer outcomesSupport/remote support technical leadership in Quality Engineering across global team.Utilize advanced data analytics, machine learning insights, and statistical methodologies to support root cause investigations, CAPA effectiveness reviews, and risk-based decision making.Ensure AI-enabled quality systems and automated decision-support tools comply with applicable regulatory requirements, quality standards, data governance policies, and validation expectations.Drive continuous improvement initiatives by identifying opportunities for automation, predictive quality monitoring, and intelligent process optimization within the Quality Management System (QMS).​Let’s talk about Qualifications and Experience Required Bachelor’s degree in Engineering or Science with 5 years’ experience in a regulated volume manufacturing industry.Experience in Quality Systems / Manufacturing quality, risk management, requirements management and process validationSelf-starter, with the ability to work with minimal supervision and with a sense of urgency.Good planning and organisational skills; ability to take own initiative and ownership.Strong inter-personal, communication, and negotiation skills with the ability to interact positively with senior management and manage stakeholders.Ability to work effectively with global teams, maintaining good relationships while influencing change.PreferredExperience in Quality and/or Regulatory positions in medical device industry.Experience in Quality System, Manufacturing Quality, process validation and risk manage.#LI-APACJoining 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.