1,766 Supplier Quality Engineer jobs in Singapore

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

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.

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

• Salary up to $4500
• Location: Kallang Sector
• Monday - Friday, 830am - 6pm
• AWS + 2 months of Variable Bonus

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

Job Requirements:

• Bachelor's Degree in Engineering, Quality Management, or a related field
• Additional certification (e.g., CQE, Six Sigma) is an advantage
• Experience in supplier auditing, documentation review, and corrective action follow-up
• Proficient in data analysis tools and software (e.g., Excel, Minitab, or similar)

We regret to inform that only shortlisted candidates will be notified.

Chong Wei Lian (William) | Registration Number: R

AlwaysHired Pte Ltd | EA Licence No: 24C2293

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

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 Precision Engineering or relevant
• Min 5 years of experience in Metal Machining industry with experience in QC/ Audit
• Oversea travelling is required

To submit your application, please apply online 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

To be a technical focal point for the work cell to work on supplier quality issues directly with the Supplier Quality Engineering group and communicate status on non-conforming parts/suppliers across the work cell product at the site level.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

• Ensure that all non-conforming materials held in Receiving Inspection are released to stock or production floor in a timely manner. Provide feedback of issues encountered to SQE II.
• Provide guidance to Receiving Inspectors.
• To provide documentation to perform Inspection of components per Inspection Plans in SAP.
• To be the focal person for work cell related quality and functional product issues that stem from components being purchased for manufacturing.
• Evaluate component failure rates from production line, collect samples and initiate Failure analysis to drive continuous improvement activity to component manufacturer.
• Assure that non-conforming materials to be returned to vendor due to poor quality have the appropriate documentation that describes the reasons for return (5W, 2H).
• Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor.
• Comply and follow all procedures within the company security policy.

JOB QUALIFICATIONS AND KNOWLEDGE REQUIREMENTS

· Degree or Diploma in Mechanical Engineering or a similar discipline and preferably at least 2 years in Medical Device Manufacturing.

· Well verse in ISO13485:2016, MDSAP and will be advantage with knowledge of the FDA inspection and requirements.

· Technical knowledge in quality control and assurance to effectively assess and manage supplier quality and performance.

· Strong analytical skills to evaluate suppliers' methods, materials, and products, and to resolve any issues that arise.

· Exceptional communication skills to interface with suppliers and cross-functional teams, reporting on supplier performance, and discussing quality improvement strategies.

· Attention to detail and organizational skills to monitor and keep track of multiple suppliers and their performance metrics simultaneously.

· Problem-solving skills to identify and address quality issues, devise improvement strategies, and implement corrective actions with suppliers.

· Understanding of industry-specific regulations and standards, such as ISO 9001, ISO13485 to ensure supplier compliance.

· Project management abilities to coordinate and lead supplier quality-related projects, ensuring they are completed on time and within budget.

· Proficiency in using quality inspection tools and software for data analysis and reporting.

· Mandarin fluency required to liaise with Mandarin-speaking stakeholders