QA Engineer (Manufacturing)

As a QA Engineer (Manufacturing) based in Tuas, you will play a key role in ensuring manufacturing quality, compliance, and operational excellence across regulated production environments. Working closely with Manufacturing Engineering, Operations, and cross-functional teams, you will help deliver reliable, high-quality products by applying proven quality engineering practices, supporting validation and risk management activities, and driving continuous improvement. This is an opportunity to contribute to new product introductions, digital quality initiatives, and advanced manufacturing capabilities while helping build a culture of quality across Resmed.

Responsibilities:

• Support manufacturing operations in achieving quality, availability, and value objectives through the application of established Quality Engineering methods.
• Participate in new product, process, technology, and manufacturing capability introductions, ensuring quality requirements are embedded from the start.
• Contribute to manufacturing readiness activities including quality planning, risk assessments, validation, control strategy execution, and launch support.
• Apply Manufacturing QA standards, tools, and best practices to drive consistency and adoption across manufacturing teams.
• Analyze quality and manufacturing data, identify trends, support investigations, and recommend preventive actions to improve future outcomes.
• Help strengthen quality systems, processes, and engineering practices to improve Right First Time performance and reduce recurring quality issues.
• Provide quality and technical guidance through training, consultation, and coaching on topics such as problem-solving, risk management, validation, and data-driven decision-making.
• Partner with Manufacturing Engineering, Operations, and other stakeholders to ensure quality considerations are integrated into process, equipment, automation, MES, and digital manufacturing changes.
• Support digital quality, automation, advanced manufacturing, and transformation initiatives through testing, implementation, and operational adoption activities.
• Assist with compliance activities including audits, risk mitigation, and adherence to the Resmed Quality Management System and applicable regulatory requirements.

Qualifications:

• Bachelor's degree in Engineering or Science.
• At least 3 years of experience within a regulated, high-volume manufacturing environment.
• Knowledge of Quality Systems, Manufacturing Quality, risk management, process validation, and structured problem-solving methodologies.
• Ability to support investigations, validation activities, quality planning, digital assurance deliverables, and continuous improvement initiatives.
• Data-driven approach with the ability to identify trends, support decision-making, and recommend practical improvements.
• Strong planning, organization, and ownership of assigned work.
• Effective communication and collaboration skills with cross-functional teams.
• Proactive learning mindset with interest in developing expertise across digital quality, automation, advanced manufacturing, and Quality by Design.

Preferred Experience:

• Background in Quality and/or Regulatory roles within the medical device industry.
• Exposure to MES, digital quality systems, CSV/CSA, automation, advanced analytics, or advanced quality planning methodologies.
• Demonstrated use of AI or data-driven technologies to improve efficiency, quality insights, or decision-making.

What Sets You Apart

• Curiosity: Continuously seeks opportunities to learn, improve, and expand technical capability.
• Ownership: Takes initiative and follows through on commitments with accountability and care.
• Collaboration: Builds trusted partnerships across functions to achieve shared outcomes.
• Problem-Solving: Approaches challenges with structure, objectivity, and a focus on root causes.
• Adaptability: Embraces change and contributes positively in evolving manufacturing environments.
• Quality Mindset: Champions high standards and promotes a culture of compliance and continuous improvement.

Why Join Resmed

At Resmed, your work helps improve the lives of people around the world through innovative healthcare and manufacturing excellence. You'll have the opportunity to contribute to products that make a meaningful difference while working alongside talented teams committed to quality, innovation, and continuous improvement. This role offers exposure to advanced manufacturing, digital quality initiatives, automation, and future-focused quality engineering practices, creating strong opportunities for professional growth and long-term career development.

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!