Senior Supplier Quality (Medical Device, MNC)

REVUP CONSULTING PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading multinational medical technology firm in Singapore is seeking a Supplier Quality Engineer to safeguard the quality of components sourced from various suppliers. You'll assess, qualify, and monitor suppliers while ensuring compliance with ISO 13485 and FDA regulations. The ideal candidate has a degree in Engineering or Science and 2 to 5 years of experience in Supplier Quality within the medical device or pharmaceutical fields. This role involves interaction with engineering and procurement teams and contributes to enhancing product reliability.

Qualifications

• 2 to 5 years in Supplier Quality within medical device or pharmaceutical fields.
• Experience with ISO 13485 and FDA regulations.

Responsibilities

• Assess, qualify, and monitor suppliers; maintain approved supplier lists.
• Lead supplier audits and corrective action plans.
• Resolve material quality issues quickly.
• Ensure compliance with ISO 13485 and FDA requirements.
• Support new product introductions.
• Track supplier performance metrics.
• Manage supplier changes.
• Partner with engineering and procurement.
• Approve or reject supplier plans.
• Lead and develop a team member.

Skills

Problem solving

Communication

Education

Degree in Engineering or Science

Job description

Supplier Quality Engineer

Join a global multinational leader known for advancing high precision medical technologies; this organisation specialises in developing and manufacturing innovative devices used worldwide to improve patient outcomes. You will play a key role in safeguarding the quality of components sourced from a wide network of suppliers to ensure products reach the market with absolute reliability.

Location: Admiralty
Work arrangements: Onsite

Key Responsibilities

• Assess, qualify, and monitor suppliers; maintain approved supplier lists
• Lead supplier audits, root cause investigations, and corrective action plans through the SCAR process
• Resolve material quality issues quickly and prevent recurrence; support containment and risk mitigation
• Ensure compliance with ISO 13485, FDA requirements, and internal quality systems
• Support new product introductions to embed quality in early stages
• Track supplier performance metrics; report trends and drive improvement initiatives
• Manage supplier changes to prevent production impact
• Partner with engineering, procurement, and production to ensure smooth integration of supplier components
• Approve or reject supplier plans; lead audits; recommend supplier selection and development; act as primary contact in supplier quality matters
• Lead and develop a member under this headcount

Requirements

• Degree in Engineering or Science with 2 to 5 years in Supplier Quality within medical device or pharmaceutical fields; strong problem solving and communication skills; experience with ISO 13485 and FDA regulations

Work Environment

• Office and controlled cleanroom settings; moderate travel to supplier sites