Precision QA Engineer — Plastics/Medical Devices

Recruit Now Singapore Pte Ltd; Singapore; On-site; SGD 46,000 - 55,000; Full time

Job summary

Recruit Now Singapore Pte Ltd is seeking a QA Engineer (Plastics/Medical) to join our client’s Loyang site. Responsibilities include supplier management, audits, and qualification activities to assure quality of materials and processes in a high-tech manufacturing environment.

The ideal candidate holds a Diploma in quality management or engineering, with 3–5 years' ISO documentation and audit experience. You will drive CAPAs, MRB meetings, and maintain ISO 9001/14001/13485 systems in

Qualifications

• Diploma in quality management / Engineering / Manufacturing required.
• 3–5 years of relevant experience in handling audits and ISO documentation in manufacturing.
• Knowledge in Supplier Management and Quality Management Standards (ISO 9001/14001/13485).
• Experience with PFMEA, Control Plans and GR&R, 8D and 5W problem solving.

Responsibilities

• Participate in supplier management on-boarding, selection and audit processes.
• Evaluate supplier performance and drive improvement opportunities.
• Support supplier/material qualification ensuring documentation and quality of purchased material.
• Collaborate with Procurement, Warehouse and Manufacturing on qualification projects and CAPA actions.
• Lead MRB meetings to address quality issues and implement corrective actions.
• Maintain ISO 9001/14001/13485 documents and readiness for audits.
• Plan and conduct internal and external audits for third-party certification and management reviews.
• Review audit findings and develop action plans for continuous improvement.

Skills

Supplier Management

PFMEA

GR&R

Control Plans

8D Problem Solving

Audits

Quality Standards

Education

Diploma in quality management / Engineering / Manufacturing

Job description

Recruit Now Singapore Pte Ltd is seeking a QA Engineer (Plastics/Medical) to join our client’s Loyang site. Responsibilities include supplier management, audits, and qualification activities to assure quality of materials and processes in a high-tech manufacturing environment.

The ideal candidate holds a Diploma in quality management or engineering, with 3–5 years' ISO documentation and audit experience. You will drive CAPAs, MRB meetings, and maintain ISO 9001/14001/13485 systems in