QA Engineer (Manufacturing)

About the role

Resmed is looking for a QA Engineer (Manufacturing) based in Tuas, Singapore, to ensure quality, compliance and operational excellence across regulated production environments. Working with Manufacturing Engineering, Operations and cross-functional teams, the role supports validation and risk management, drives continuous improvement and contributes to new product introductions and digital quality initiatives.

Key responsibilities

• Support manufacturing operations in achieving quality, availability and value objectives using established Quality Engineering methods.
• Take part in new product, process, technology and manufacturing capability introductions, embedding quality requirements from the start.
• Contribute to manufacturing readiness: quality planning, risk assessments, validation, control strategy execution and launch support.
• Apply Manufacturing QA standards, tools and best practices to drive consistency across manufacturing teams.
• Analyse quality and manufacturing data, identify trends, support investigations and recommend preventive actions.
• Strengthen quality systems and processes to improve Right First Time performance and reduce recurring issues.
• Provide quality and technical guidance through training, consultation and coaching on problem-solving, risk management, validation and data-driven decision-making.
• Partner with Manufacturing Engineering and Operations so quality is integrated into process, equipment, automation, MES and digital manufacturing changes.
• Support digital quality, automation and transformation initiatives through testing, implementation and adoption.
• Assist with compliance activities, including audits, risk mitigation and adherence to the Resmed Quality Management System and regulatory requirements.

Required profile

• Bachelor's degree in Engineering or Science.
• At least 3 years of experience in a regulated, high-volume manufacturing environment.
• Preferred: background in Quality and/or Regulatory roles within the medical device industry.
• Preferred: exposure to MES, digital quality systems, CSV/CSA, automation, advanced analytics or advanced quality planning.

Required skills

• Knowledge of quality systems, manufacturing quality, risk management, process validation and structured problem-solving.
• Ability to support investigations, validation, quality planning and continuous improvement.
• Data-driven approach, strong planning and organisation, effective communication with cross-functional teams.