Quality Engineer

Cyrus Technology; Singapore; On-site; SGD 45,000 - 68,000; Full time

Job summary

Cyrus Technology in Singapore is seeking a Quality Engineer to support the QMS and perform IQC, IPQC and Final QC activities on the production floor. You will review drawings, interpret specifications, and use standard inspection tools to ensure products meet quality standards.

The role requires 2–4 years in Quality, strong problem-solving, and proficiency with MS Office. Collaboration with Engineering, Production and Procurement teams is essential to drive improvements and ensure compliance

Qualifications

• Diploma or Degree in Engineering, Quality, Manufacturing, Biomedical Engineering, or related discipline.
• 2 to 4 years of experience in Quality Engineering, Quality Assurance, or Manufacturing Quality.

Responsibilities

• Support and maintain the QMS in accordance with ISO 13485 requirements.
• Perform IQC, IPQC, and FQC activities.
• Review engineering drawings and specs.
• Conduct inspections and measurements using common inspection equipment.
• Investigate quality issues and support corrective actions.
• Handle non-conforming materials and products.
• Support CAPA, NCR, customer and supplier quality issues.
• Participate in supplier audits and internal audits.
• Prepare and maintain quality records and reports.
• Work with Engineering, Production, Procurement, and Warehouse to resolve issues.
• Support continuous quality improvement projects.

Skills

Engineering drawings

Quality Assurance

Problem solving

Communication skills

Microsoft Office

IQC/IPQC/PQC

Production floor work

Education

Engineering/Quality degree

Tools

Inspection tools

Job description

The Quality Department plays a very important role in maintaining the quality management system and driving quality improvements to deliver high quality products for our customers.

Responsibilities

• Support and maintain the Quality Management System (QMS) in accordance with ISO 13485 requirements.


• Perform Incoming Quality Control (IQC), In-Process Quality Control (IPQC), and Final Quality Control (FQC) activities.


• Review and interpret engineering drawings, specifications and inspection requirements.


• Conduct inspections and measurements using common inspection equipment.


• Investigate material, process and product quality issues and support corrective actions.


• Handle non-conforming materials and products.


• Support CAPA, NCR, customer complaints and supplier quality issues.


• Participate in supplier audits and supplier quality improvement activities.


• Support internal and external audits.


• Prepare and maintain quality records, inspection reports, and related documentation.


• Work closely with Engineering, Production, Procurement, and Warehouse teams to resolve quality issues.


• Support continuous improvement projects and quality initiatives.


• Perform other quality-related duties as assigned.

Minimum Qualifications

• Diploma or Degree in Engineering, Quality, Manufacturing, Biomedical Engineering, or related discipline.


• 2 to 4 years of experience in Quality Engineering, Quality Assurance, or Manufacturing Quality.


• Ability to read and interpret engineering drawings and specifications.


• Familiarity with basic inspection and measurement equipment.


• Good problem-solving and analytical skills.


• Good communication and interpersonal skills.


• Proficient in Microsoft Office applications.


• Hands-on and willing to work on the production floor when required.

Preferred Qualifications

• Experience in Medical Device, Precision Engineering, Electronics, or regulated manufacturing industries.


• Knowledge of ISO 9001, 13485, 14001 Quality Management Systems added advantage.


• Experience in IQC, IPQC, and PQC activities.


• Experience in handling CAPA, NCR, customer complaints, or supplier quality issues.


• Familiarity with quality tools such as 5 Why, Fishbone Diagram and 8D.


• Exposure to supplier audits or internal audits.

What We Are Looking For

• Hands-on and willing to support day-to-day quality operations.


• Able to work independently and take ownership of quality issues.


• Positive attitude and willingness to learn.