Senior Supplier Quality Engineer

Illumina; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

Illumina in Singapore is looking for a Supplier Quality Engineer who interfaces with development and suppliers to ensure quality in manufacturing processes. The role requires strong problem-solving skills and the ability to manage supplier relationships effectively.

The ideal candidate will possess a bachelor's or master's degree in relevant fields with at least 3 years of experience in quality engineering, focusing on supplier management and risk assessments. This position offers a dynamic work environment with opportunities for both professional growth and travel.

Qualifications

• Minimum of 3 years of experience as a Supplier Quality Engineer or in a related function.
• Ability to conduct vendor audits and supplier risk assessments.

Responsibilities

• Provide solutions using core knowledge in the area of specialization.
• Work with diverse assignments requiring creative problem-solving.
• Manage relationships with internal and external partners.
• Adapt communication style to varying audiences.

Skills

FDA 21 CFR Part 820

ISO 13485

Supplier Management Processes

Problem Solving (CAPA/SCAR)

Risk Management (FMEA)

Negotiation Skills

Communication Skills

Education

Bachelor’s or Master’s degree in Engineering, Life Sciences, or related field

Job description

Position Overview

Interfaces with development and supplier engineering to provide materials and components for company product manufacturing. Communicates product specifications to suppliers and assesses suppliers’ ability to meet engineering and quality requirements. Evaluates suppliers’ internal functions to assess their overall performance and provides feedback in assessment of their operation. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier‑related problems as they occur. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met.

Responsibilities

• Apply core knowledge and understanding of area of specialization to provide solutions in creative and effective ways.
• Assess unusual circumstances and use sophisticated analytical and problem‑solving techniques to identify causes and suggest variations in approach.
• Work on assignments of diverse scope where information is limited and problem solving requires adaptation of existing techniques.
• Enhance internal and external working relationships and networks with senior partners within area of expertise.
• Adapt style to differing audiences and often advise others on difficult matters that require persuasion.
• Work independently and have work reviewed at critical points.
• Use evaluation, judgment, and interpretation to select the best course of action.

Requirements

• Familiarity with FDA 21 CFR Part 820, ISO 13485, and supplier management processes (component qualification, risk assessments, and audits) is an advantage.
• Practical application of Problem Solving (CAPA/SCAR), Risk Management (FMEA), Non‑conformance Handling, and continuous improvement tools.
• Strong cross‑functional collaboration, negotiation, and communication skills to manage relationships internally and externally.
• Willingness to travel domestically and internationally as required (typically around 25%).

Preferred Experience, Education, and Skills

• Bachelor’s or master’s degree in Engineering, Life Sciences, or a related field.
• Minimum 3 years specifically working as a Supplier Quality Engineer or in a closely related Supplier Relationship function.
• Demonstrated track record in component qualification, vendor audits, and supplier risk assessments.
• Deep understanding of failure investigation (CAPA/SCAR), Risk Management (FMEA), First Article Inspection (FAI), and Mistake Proofing.

Equal Opportunity Statement

We are proud to confirm a zero‑net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility.

Illumina is an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.

Background Check and AI Policy

Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact [e-mail].

For more information, see https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf.