1,417 Supplier Quality jobs in Singapore

Overview & Responsibilities

Position Summary:

The Supplier Quality Specialist executes the Ebara Elliott Energy supplier quality control program. The position works closely with procurement and quality departments to ensure that all suppliers have adequate business management systems for the purpose of providing products that meet Ebara Elliott Energy requirements. This is accomplished through the qualification and re-qualification of suppliers based on the results of system audits and the evaluation of their performance as it relates to the on-time delivery, number of defects, and cost. The position also focuses on the prevention of supplier defects through the conveyance of contractual requirements. This is done through the management of pre-manufacturing and in-process meetings conducted at the supplier along with the development of supporting documentation, drawings, quality inspection & test plans, etc. In addition, this position will support source inspection needs.

Key Responsibilities:

• Using Ebara Elliott Energy supplier qualification procedures, identify and qualify new suppliers to improve cost, quality, and lead time.
• Monitor and uphold quality standards of existing approved supplier base. Identify and mitigate quality issues as identified by inspection, NCR, and warranty data inputs.
• Collaborate with Quality and Engineering teams to develop the quality and capability of approved suppliers.
• Resolve supplier questions as they relate to Ebara Elliott Energy drawings and/or processes.
• Lead root cause analysis and corrective action efforts for supplier non-conformances.
• Monitor and audit supplier quality performance; drive corrective actions and continuous improvement.
• Assemble and utilize inspection, NCR, and warranty data inputs to drive supplier quality priorities and corrective action plans.
• Conduct investigations of major supplier problems including customer complaints.
• Prepare technical reports regarding supplier quality procedures, processes, and problems.
• Develop a regional supplier scorecard system to track quality, on-time delivery, responsiveness, and issue resolution.
• Maintain records in the Ebara Elliott Energy approved supplier database.
• Aide in the development and release of component inspection plans.
• Set and maintain receiving inspection requirements / routing in the ERP system for all products received into the warehouse.
• Support on site source inspection needs as required.
• Conduct regular supplier review meetings.
• Support new product launches with supplier readiness assessments.

Qualifications:

• Two year associates degree in Supply Chain, Engineering, related field technical field.
• 5+ years of technical work experience in supplier quality / qualification roles within manufacturing or fabrication industries.
• Ability to read and interpret detailed technical drawings, prints, and bills of material.
• Strong analytical, computer/software, and communication skills.
• Demonstrated manufacturing process knowledge.
• Strong knowledge of procurement and supplier quality systems.
• Experience working with Quality Management Systems, such as ISO 9001or industry-specific quality standards.
• Proficiency with ERP systems (e.g., SAP, Oracle) and supply chain analytics tools.
• A background in lean and/or six sigma principles is preferred.

Key Competencies:

• Ability to conduct supplier audits, process reviews, and compliance checks.
• Understanding of various inspection & testing methods.
• Ability to exercise nonconformance management including corrective / preventative actions, root cause analysis, 5 Why's, etc.
• Skilled in preparing and reviewing quality documentation and reports.
• Familiarity with machining, casting, assembly, and other relevant manufacturing processes.
• Problem solving skills.
• Risk assessment; Ability to evaluate supplier risks in cost, quality, and delivery.
• Attention to Detail. Ensure compliance with specifications, drawings, and standards.

Travel Requirements:

• Up to 50% regional and supplier site travel required.

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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

Responsibilities & Requirements:

• Work with a cross functional team consisting of Business Unit Leaders, OE sites/QRCs Quality Managers, OE sites/QRCs QA Engineers, client approved third parties to ensure smooth execution of our client's Audit Program.
• Responsible for providing regular updates of our client's Audit Program.
• Evaluate and implement appropriate new processes to increase efficiency, execution, and improve collaboration for our client's Audit Program.

Experience / Skills:

• Demonstrate an excellent attention to detail along with the ability to discover errors or inaccuracies related to our client's Audit Program data.
• Demonstrate experience for the ability to plan, organize, and accomplish goals
• Excellent PC knowledge, including MS TEAMS, Microsoft Excel, Microsoft Word and Power Point
• Ability to collaborate across teams to ensure appropriate activities are performed
• Excellent communication skills to convey key information and communicate across multiple layers within the organization
• Good self-motivated, willingness to learn, assertive, positive attitude and work ethics

Rajasekar Shirley Monisha License No.: 02C3423 Personnel Registration No.: R

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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

Summary

• Participates in Supplier Quality Management Program, which includes the Approved Supplier List (ASL) Management, Supplier On-boarding Process, Supplier Change Management, Supplier Quality Agreement Review, Supplier Corrective Action System, and Supplier Performance and Audit Evaluation.
• Achieving of such will require communicating and effecting creative solutions on internal and external stakeholders. This is to ensure that all products that customers received are at their best quality.

Roles and Responsibilities

• To participate in procedures for Supplier Management process such as supplier on-boarding, selection and approval process by assessing and evaluating supplier profile; visiting and auditing of supplier facility and process, initiating supplier quality agreement review, and establishing good partnership with suppliers.
• To develop and manage the ASL across entities and ensure proper measurement and monitoring framework tailored for each supplier category.
• To evaluate and monitor supplier performance and business risk evaluation on the Quality, Delivery and Service aspects, and collaboration with suppliers to identify opportunities for enhancements and improvements.
• To participate in supplier related changes through the Supplier Change Management process, and evaluate the change with internal stakeholders via the initial change notice form and impact assessment/FMEA risk management.
• To support new product development launches and/or new supplier/material qualification by ensuring that all supplier on-boarding related documentations and action are complete, and that quality of purchased material meets the required standards and expectations.
• To communicate and work closely with external suppliers and internal stakeholders (Supply Chain, Incoming Material Engineering, Manufacturing, R&D, and Regulatory Affairs) on supplier/material qualification related projects, material quality related issues. To address on purchased material failures/defects and derive proper preventive and corrective action plans through SCAR system. Additionally, to gather information from both parties to support the flow of information and identify/support process enhancements and improvements.
• Internal audits of internal quality procedures

Requirement

• Diploma or Bachelor of Engineering or Bachelor of Science in Bioengineering, Materials, or general Engineering relevant to medical fields
• Preferred to have 1-2 years of relevant experience in Quality Assurance, Supplier Management, or medical device/manufacturing environment.
• Preferred to have expertise and knowledgeable in applicable standards (such as ISO 13485, Regulation (EU) 2017/745, ISO 9001, 21 CFR 210/211/820, etc) or expertise/certified in QMS/Lead/Internal Auditor preferably in ISO 13485/9001 or equivalent
• Working knowledge in FMEA
• Very organized and in good documentation management
• Excellent Interpersonal and communication skill to build cross-functional teamwork and support, Good capabilities with dealing of suppliers
• Possess positive working attributes and comfortable to manage admin processes and ad-hoc assignments

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.

Summary

• Participates in Supplier Quality Management Program, which includes the Approved Supplier List (ASL) Management, Supplier On-boarding Process, Supplier Change Management, Supplier Quality Agreement Review, Supplier Corrective Action System, and Supplier Performance and Audit Evaluation.
• Achieving of such will require communicating and effecting creative solutions on internal and external stakeholders. This is to ensure that all products that customers received are at their best quality.

Roles and Responsibilities

• To participate in procedures for Supplier Management process such as supplier on-boarding, selection and approval process by assessing and evaluating supplier profile; visiting and auditing of supplier facility and process, initiating supplier quality agreement review, and establishing good partnership with suppliers.
• To develop and manage the ASL across entities and ensure proper measurement and monitoring framework tailored for each supplier category.
• To evaluate and monitor supplier performance and business risk evaluation on the Quality, Delivery and Service aspects, and collaboration with suppliers to identify opportunities for enhancements and improvements.
• To participate in supplier related changes through the Supplier Change Management process, and evaluate the change with internal stakeholders via the initial change notice form and impact assessment/FMEA risk management.
• To support new product development launches and/or new supplier/material qualification by ensuring that all supplier on-boarding related documentations and action are complete, and that quality of purchased material meets the required standards and expectations.
• To communicate and work closely with external suppliers and internal stakeholders (Supply Chain, Incoming Material Engineering, Manufacturing, R&D, and Regulatory Affairs) on supplier/material qualification related projects, material quality related issues. To address on purchased material failures/defects and derive proper preventive and corrective action plans through SCAR system. Additionally, to gather information from both parties to support the flow of information and identify/support process enhancements and improvements.
• Internal audits of internal quality procedures

Requirement

• Diploma or Bachelor of Engineering or Bachelor of Science in Bioengineering, Materials, or general Engineering relevant to medical fields
• Preferred to have 1-2 years of relevant experience in Quality Assurance, Supplier Management, or medical device/manufacturing environment.
• Preferred to have expertise and knowledgeable in applicable standards (such as ISO 13485, Regulation (EU) 2017/745, ISO 9001, 21 CFR 210/211/820, etc) or expertise/certified in QMS/Lead/Internal Auditor preferably in ISO 13485/9001 or equivalent
• Working knowledge in FMEA
• Very organized and in good documentation management
• Excellent Interpersonal and communication skill to build cross-functional teamwork and support, Good capabilities with dealing of suppliers
• Possess positive working attributes and comfortable to manage admin processes and ad-hoc assignments

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.

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Adaba Pte Ltd

EA Licence: 25C2727

Job Responsibilities

• Collaborate with purchasing and engineering teams to evaluate potential suppliers based on quality, reliability, and performance
• Conduct supplier assessments, audits, and qualifications to ensure compliance with quality standards
• Develop and implement supplier quality assurance processes, procedures, and metrics to improve supplier performance
• Establish quality agreements and specifications to ensure supplier consistency and alignment with requirements
• Address supplier issues, non-conformities, and corrective actions in a timely and effective manner
• Provide training, guidance, and support to suppliers to improve their quality management systems
• Maintain strong communication with internal stakeholders and suppliers to ensure alignment on quality expectations

Job Requirements:

• Bachelor's Degree in Engineering, Quality Management, or a related field
• Additional certification (e.g., CQE, Six Sigma) is an advantage
• Minimum 3 years of experience in a manufacturing or supplier quality role
• Strong knowledge of quality management systems, standards, and methodologies
• Experience in supplier auditing, documentation review, and corrective action follow-up
• Proficient in data analysis tools and software (e.g., Excel, Minitab, or similar)
• Good communication and interpersonal skills to collaborate with cross-functional teams and external suppliers
• Experience in manufacturing, automotive, semiconductor is preferred