Quality Engineer I - Medical Devices, ISO 13485

Quasar Medical; Singapore; Hybrid; SGD 70,000 - 110,000; Full time

Job summary

Quasar Medical in Singapore is seeking a Sr. Engineer I, Quality Engineering to ensure quality and regulatory compliance across manufacturing of medical devices. You will develop QA plans, oversee production, and support new product transfers.

You will lead quality initiatives, participate in audits, investigate deviations, and drive continuous improvement with cross-functional teams. The role requires a degree in engineering or science and 2–5 years in quality, fluent English, and strong

Qualifications

• Degree in Engineering or Science with 2–5 years in quality roles.
• Diploma in Engineering or Science with >5 years in QA may be considered.

Responsibilities

• Develop and maintain QA plans, procedures, and control measures.
• Monitor production processes to detect quality issues.
• Support audits and regulatory inspections (FDA, ISO 13485).
• Lead investigations into deviations and implement CAPA.
• Ensure traceability and documentation throughout manufacturing.

Job description

Quasar Medical in Singapore is seeking a Sr. Engineer I, Quality Engineering to ensure quality and regulatory compliance across manufacturing of medical devices. You will develop QA plans, oversee production, and support new product transfers.

You will lead quality initiatives, participate in audits, investigate deviations, and drive continuous improvement with cross-functional teams. The role requires a degree in engineering or science and 2–5 years in quality, fluent English, and strong