425 Supplier Quality jobs in Singapore

PRINCIPAL ACCOUNTABILITIES

SQP oversees critical and non critical supplier mainly mechanical parts in. SQP is responsible in leading before and after FAS (First Article Submission) qualify and monitor quality performance of new / existing suppliers and ensure uninterrupted supplies of materials and services. He/ She should be able to foster close relationships with suppliers and partners and be able to communicate their value to the company.

JOB RESPONSIBILITIES

1. Lead and Drive First Article Submission for new and existing supplier

Supplier Quality Professional develop Quality plan such as Process Flow Diagram (PFD), Manufacturing Process Plan (MPP) & Inspection Test Plan (ITP) to new supplier. Perform supplier audits such as QMS, Process and HSE. This will involve visit/audit and assessing their capability and FAI. SQP shall work with Sourcing and Engineering, to engage and educate suppliers/sub-contractors.

1. Lead quality performance review

Worked closely with suppliers, to monitor conduct audit for vendor performance. Conduct in process audit and drive for closure of audit findings and continuous improvement and reduction of COPQ (Cost of Poor Quality). Lead the discussion with the suppliers and ensure timely response is executed to deliver result to our internal customers. Guide Procurement and team for supplier performance review process.

1. Supplier Development.

SQP shall drive for vendor development, identify and develop new special process to meet turnkey objective and reduce leadtime of supplier.

1. Analyse supply market.

SQP shall propose and execute creative ways to improve supplier process which creates financial value to the organization.

1. Maintain good relationship with stake holders and customer/s

SQP maintain good relationship with stakeholders such as Manufacturing, Procurement, Engineering and Quality. Work with cross functional teams in resolution of process and quality issues related to design, application and manufacturing process. Develop quality consciousness and impart application of quality tools such as FMEA, 8D.

1. Develop Product Quality Control Plan

SQP shall also be in charge in developing Quality Control Plan according to the requirements of the customer. He/She shall ensure that required processes and documentations and surveillance points are identified in the QCP. He/She shall liase closely with the customer during development of the new QCP and revision of the existing QCP and its approval (internal and Customer).

1. Customer /Third Party Inspection coordinator

SQP shall manage Customer and Third Party inspection of products/parts. He/She shall ensure that each Quality Control Plan activity which requires surveillance points are monitored and conducted accordingly. He/She will liase and communicate closely with the internal and external customers to ensure that TPI inspections are executed according to the plan schedule.

1. Perform any ad-hoc duties as and when assigned by the superior.

2. All employee of Completion Products Pte Ltd shall observe the highest standards of ethics and integrity in undertaking purchasing activity and act in a honest and professional manner that supports the standing of Completion Products Pte Lts core value.

3. Ensures 5S is implemented in the work area.

4. Adheres company's guidelines with regards to Safety and Quality.

5. Complies to Company Code of Business Conduct.

6. Support and participate in company-wide or departmental programs such as:

7. Total Quality Management, Lean Manufacturing

8. Social Activities

REQUIRED COMPETENCIES

1. Must complete minimum training required specified in Employee Qualification and OJT Form No. S 1-026F.

2. Ensures Accountability – holding self and others accountable to meet commitments

3. Decision Quality – making good and timely decisions that keep the organization moving forward. Good decisions that are a mixture of analysis, wisdom, experience and judgement.

4. Customer focus – Building strong customer relationships and delivering customer-centric solutions.

5. Drives Result – consistently achieving results, even under tough circumstances. Results might be quantifiable – measured in terms in P&L, sales growth, customer satisfaction ratings, new product launched. Qualitative result - an enhanced reputation among customers, a more vibrant brand that attracts customer and employee talent.

QUALIFICATION GUIDE

1. Education : Minimum Degree in Technical/Engineering course preferably Mechanical

Engineering

1. Communication : Fluent both in oral and wriiten English communication

2. Experience : Minimum 5 years of working on the same field . Experience in Oil and Gas

manufacturing is an advantage.

1. Experienced as Internal Auditor or Supplier Auditor is an advantage

2. With API or ISO Certification is preferred

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Mechanical / Precision Engineering or relevant
• Min 5 years of experience in Oil & Gas industry with experience in Supplier Quality
• Oversea travelling is required

To submit your application, please apply online to - or call for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd

EA License No: 17C8900

Our client is one of the leading players in the Semiconductor sector. Due to business needs, they are now recruiting a Supplier Quality Engineer to be part of their Quality team for ongoing transformation projects. They are located in the East – easily accessible.

Responsibilities of Supplier Quality Engineer :

• Audit, qualify, and manage suppliers to ensure compliance with ISO and industry standards
• Drive supplier onboarding, performance reviews, and continuous improvement initiatives
• Monitor supplier KPIs (PPM, on-time delivery, SCARs) and lead CAPA/root cause investigations
• Review supplier processes, documentation, and quality systems for alignment with requirements
• Partner with cross-functional teams during NPI and supplier transitions to embed quality planning early
• Support incoming inspections and evaluate critical processes (e.g. welding qualifications) where required

Requirements:

• Min Degree in engineering field
• Min 3 years of supplier quality experience in equipment manufacturing industry
• Familiar with quality tools such as FMEA, SPC, MSA, and 8D problem-solving
• Willing to travel to supplier sites when required

We regret that only shortlisted candidate will be notified.

Email:

RecruitPedia Pte Ltd

EA License No: 19C9682

EA Personnel No: R Oh Puey Xin)

The Supplier Quality Engineer (SQE) ensures that all materials, components, and services provided by suppliers meet Cragar Industries' stringent quality standards and regulatory requirements. This role is critical in maintaining product integrity, supporting ISO13485 compliance, and driving continuous improvement across the supply chain.

• Supplier Evaluation & Qualification Assess and approve suppliers based on capability, compliance, and performance metrics.

Conduct supplier audits and process reviews to ensure adherence to ISO13485 and Cragar's quality standards.
- Quality Assurance & Compliance Develop and implement supplier quality plans, inspection protocols, and control systems.

Monitor supplier performance using KPIs such as On-Time Deliver.
- Issue Resolution & Continuous Improvement Investigate non-conformances, perform root cause analysis, and implement corrective actions.

Collaborate with suppliers to drive process improvements and reduce defect rates.
- Cross-Functional Collaboration Work closely with Procurement, Engineering, and Production teams to align supplier quality objectives with business needs.

Support New Product Development (NPI) projects by qualifying new suppliers and materials.
- Documentation & Reporting Maintain accurate records of audits, certifications, and supplier performance evaluations.

Prepare reports for management on supplier quality trends and improvement initiatives.

• Education: Diploma or Bachelor's degree in Engineering, Quality Assurance, or related field.

• Experience: Minimum 3–5 years in supplier quality or manufacturing quality roles, preferably in the biomedical or precision engineering industry.

• Technical Skills: Knowledge of ISO13485, PPAP, APQP, FMEA, SPC, and root cause analysis tools.

Proficiency in statistical analysis and quality management systems.
- Soft Skills: Strong communication, problem-solving, and supplier relationship management abilities.

• Be part of a leading player in the biomedical manufacturing sector.
• Opportunity to influence supplier quality strategy and contribute to global supply chain excellence.

Job Title: Supplier Quality Engineer

Location: Singapore

Industry: Medical Devices Technology

Reporting to: Quality, Senior Manager

Job Overview

Join our team and play a vital role in our Supplier Quality Management Program You will contribute to all aspects of supplier quality, including onboarding, performance monitoring, change management, and corrective actions. Your efforts will make sure that the products our customers receive are of the highest quality. This position requires excellent communication and creative problem-solving skills to collaborate effectively with both internal and external stakeholders.

Key Responsibilities

• Participate in supplier management processes, including onboarding, selection, and approval. This involves assessing supplier profiles, conducting site visits and audits, reviewing supplier quality agreements, and building strong partnerships.
• Develop and manage the Approved Supplier List (ASL) across entities, ensuring a tailored measurement and monitoring framework for each supplier category.
• Evaluate and monitor supplier performance and business risk related to Quality, Delivery, and Service. Collaborate with suppliers to identify opportunities for enhancements and improvements.
• Participate in supplier-related changes through the Supplier Change Management process, evaluating the impact with internal stakeholders using change notices and FMEA risk management.
• Support new product development launches and new supplier/material qualifications by ensuring complete supplier onboarding documentation and that purchased materials meet required standards.
• Communicate and collaborate closely with external suppliers and internal stakeholders (Supply Chain, Incoming Material Engineering, Manufacturing, R&D, and Regulatory Affairs) on supplier/material qualification projects, as well as material quality issues.
• Address purchased material failures/defects and derive preventive and corrective action plans through the SCAR system.
• Gather information from all parties to support the flow of information and identify/support process enhancements.
• Conduct internal audits of internal quality procedures.

Profile of Ideal Candidate:

• Diploma or Bachelor of Engineering or Bachelor of Science in Bioengineering, Materials, or general Engineering relevant to medical fields.
• 1-2 years of relevant experience in Quality Assurance, Supplier Management, or a medical device/manufacturing environment is preferred.
• Expertise in applicable standards (ISO 13485, Regulation (EU) 2017/745, ISO 9001, 21 CFR 210/211/820, etc.) or certification in QMS/Lead/Internal Auditing, preferably in ISO 13485/9001 or equivalent, is preferred.
• Working knowledge of FMEA.
• Highly organised with strong documentation management skills.
• Excellent interpersonal and communication skills to build cross-functional teamwork and support.
• Good capabilities in dealing with suppliers.
• Positive working attitude and comfortable managing administrative processes and ad-hoc assignments.

If you are keen to have a preliminary chat, please send your CV directly to

The data collected is strictly used for recruitment purposes only and will be treated with the utmost confidence. Your profile will also be sent out only after you have given your consent.

Adaba Pte Ltd

EA Licence: 25C2727

Job Title: Supplier Quality Engineer

Location: Singapore
Industry: Medical Devices Technology
Reporting to: Quality, Senior Manager

Job Overview

Join our team and play a vital role in our Supplier Quality Management Program! You will contribute to all aspects of supplier quality, including onboarding, performance monitoring, change management, and corrective actions. Your efforts will make sure that the products our customers receive are of the highest quality. This position requires excellent communication and creative problem-solving skills to collaborate effectively with both internal and external stakeholders.

Key Responsibilities

• Participate in supplier management processes, including onboarding, selection, and approval. This involves assessing supplier profiles, conducting site visits and audits, reviewing supplier quality agreements, and building strong partnerships.
• Develop and manage the Approved Supplier List (ASL) across entities, ensuring a tailored measurement and monitoring framework for each supplier category.
• Evaluate and monitor supplier performance and business risk related to Quality, Delivery, and Service. Collaborate with suppliers to identify opportunities for enhancements and improvements.
• Participate in supplier-related changes through the Supplier Change Management process, evaluating the impact with internal stakeholders using change notices and FMEA risk management.
• Support new product development launches and new supplier/material qualifications by ensuring complete supplier onboarding documentation and that purchased materials meet required standards.
• Communicate and collaborate closely with external suppliers and internal stakeholders (Supply Chain, Incoming Material Engineering, Manufacturing, R&D, and Regulatory Affairs) on supplier/material qualification projects, as well as material quality issues.
• Address purchased material failures/defects and derive preventive and corrective action plans through the SCAR system.
• Gather information from all parties to support the flow of information and identify/support process enhancements.
• Conduct internal audits of internal quality procedures.

Profile of Ideal Candidate:

• Diploma or Bachelor of Engineering or Bachelor of Science in Bioengineering, Materials, or general Engineering relevant to medical fields.
• 1-2 years of relevant experience in Quality Assurance, Supplier Management, or a medical device/manufacturing environment is preferred.
• Expertise in applicable standards (ISO 13485, Regulation (EU) 2017/745, ISO 9001, 21 CFR 210/211/820, etc.) or certification in QMS/Lead/Internal Auditing, preferably in ISO 13485/9001 or equivalent, is preferred.
• Working knowledge of FMEA.
• Highly organised with strong documentation management skills.
• Excellent interpersonal and communication skills to build cross-functional teamwork and support.
• Good capabilities in dealing with suppliers.
• Positive working attitude and comfortable managing administrative processes and ad-hoc assignments.

If you are keen to have a preliminary chat, please send your CV directly to

The data collected is strictly used for recruitment purposes only and will be treated with the utmost confidence. Your profile will also be sent out only after you have given your consent.

Adaba Pte Ltd
EA Licence: 25C2727

The Principal Engineer, Supplier Quality entails the following :

Responsibilities

• Adhere to Good Manufacturing Principles (GMPs) based Quality Management Systems requirements (ISO13485, MDR, etc) for medical devices and medicinal products
• Identify and lead implementation of preventive and corrective actions via CAPAs, audits, NCMRs, and complaint handling systems
• Lead implementation of Supplier Change Requests and utilize Production Part Approval Process (PPAP)
• Key contributor on NPD (New Product Development) projects, ensuring rigorous performance and APQP deliverables (CTQ, PFMEA, control plan, GRR, FAI, IQ/OQ/PQ, PPA, etc.), in collaboration with Procurement, Manufacturing and R&D
• Ensure supplier quality systems adhere to all applicable regulations and standards
• Ability to lead and influence cross-functional teams to drive reduction in patient safety risk and greater levels of regulatory compliance
• Apply experience and knowledge of FDA, MDD (Medical Device Directive), EU-MDR (Medical Device Regulations), ISO Quality Management Systems),cGMP, and Risk Management (ISO to instill a culture dedicated to ensuring patient safety and sustained regulatory compliance
• Drive new process, system implementation within supplier quality lifecycle team
• Identify and lead continuous process/products improvement/excellence initiatives/projects

Qualifications

• Bachelor degree in Science or Engineering, advance Degree preferred.
• 8 + years experience as minimum, of which preferably >5 years in manufacturing quality/Engineering quality/supplier quality in medical device industry, active medical device preferred.
• Solid experience / knowledge of quality process management and tools e.g. APQP, PPAP, SPC, process validation and verification, Statistics Tools and Analysis in development and revision of Quality Sampling Plans based on product and patient risk.
• Apply experience and knowledge of ISO Quality Management Systems), FDA medical device regulations, cGMP, and Risk Management (ISO to instil a culture dedicated to ensuring patient safety and sustained regulatory compliance
• Proficiency in multi-tasking and working in a high-paced, matrixed environment with an awareness of continued impact on compliance and operational performance
• Ability to lead and influence cross-functional teams, including Procurement, Regulatory Affairs, Technical Services and Research & Development to drive reduction in patient safety risk and greater levels of regulatory compliance
• Organized and resourceful with excellent attention to detail and ability to execute on assigned project plans
• Commitment to work within the ethos of the company mission, code of conduct and applicable legal standards/regulations
• Proficient English, working language for reading, writing and oral communication.

• 20% travel expected

  
  

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

Semiconductor Supplier Quality Manager (m/f/d)

We offer an interesting position as Manager Semiconductor Supplier Quality as a member of the global BMW Semiconductor Management Team. Since Semiconductors play an ever more important role in the manufacturing of our cars, the quality of our cars hinges on the quality of semiconductors.

You will work with semiconductor suppliers in all Asia to make sure that BMW can utilize robust semiconductor solutions. The adherence of the entire semiconductor supply chain (Wafer Manufacturing, Assembly and Test) to respective standards (ISO, IATF-16949, VDA, BMW Group Standards) plays a central role in this context. Assessment of suppliers with respect to those requirements as well as the closing of potential gaps will define your daily work. Furthermore, you will be responsible for problem solving activities in case of shortcomings of semiconductor solutions. You will support the global BMW Semiconductor Management organization with local presence and a strong relationship to semiconductor suppliers in China and the Asia Pacific region.

Responsibilities

• Responsible for the supply assurance of active and passive components during allocations
• Responsible for the internal communication and the support regarding SC suppliersrelevant topics
• Responsible for ensuring the supply chain transparency and necessary technical exchange with SC suppliers

Supply Risk Management

• CoC of SC suppliers & main contact person for internal & external partners
• Manages top & executive management meetings
• Manages COS/SRM meetings with top SC suppliers with support from SC Strategy & Data Management teams
• Control gate for consistent data/presentations integrity for A-B program before handing it out to the SC suppliers
• Assesses & evaluates the SC supplier & product portfolios, as well as special approvals
• Evaluates SC roadmaps & request price indication for all OCs from SC suppliers
• Ensures the availability of SC NDAs
• Defines and reviews requirements and supply chain Group Standards
• Negotiates framework contracts with SC suppliers.

Supply Crisis Management

• Actively manages effective measures along the entire supply chain to avoid line-down caused by SC
• Assesses & confirms if spot market scanning and procurement is required
• Tracks, communicates & reports the SC supply crisis issues to PLT/TF and PMO
  Manages the escalation towards SC suppliers

Requirements

• Engineering Degree (Electrical.Engineering, Physics, Chemical and any relevant studies)
• Profound work experience in quality management and/or semiconductor manufacturing
• Project management and leadership experience
• Profound knowledge in the areas of semiconductor technology, electronics processes and manufacturing processes
• Experience regarding the use of quality management systems
• Proficient in both English and Chinese language
• Proactive, ability to think analytically and able to work independently
• Willing to travel for work