364 Quality Engineer jobs in Singapore

• Well Established Company
• Basic $3,000 - $ 4,000 + Variable Bonus
• Working location: Tampines North
• Working days: Monday - Friday
• Working hours: 9.00am - 6.00pm

Key Responsibilities:

• Develop, implement, and maintain quality assurance protocols and procedures.
• Establish quality management system and programs, conduct regular inspections and audits of assembly processes to ensure compliance with industry standards and company specifications.
• Collaborate with cross-functional teams, including R&D, engineering, production, and supply chain, to identify and resolve quality issues.
• Lead root cause analysis and corrective action initiatives to address defects and non-conformities.
• Monitor and analyse quality performance metrics and report findings to senior management.
• Ensure all quality assurance activities are in compliance with ISO 9001 standards.
• Provide training and guidance to junior quality engineers and other team members on quality best practices, quality programs and quality standards.
• Stay up to date with industry trends and advancements in quality assurance methodologies and technologies.
• Respond to customer inquiries, feedback and complaints regarding product performance and quality, ensure timely and effective resolution of any issues, improve customer satisfaction through quality improvements.
• Oversee all quality-related audits, both internal and external.
• Lead and participate in cross-functional teams to drive quality improvement projects.
• Perform any other duties as assigned by superior.

Qualifications & Experience:

• Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related field.
• Minimum of 1 years of experience in quality assurance within the manufacturing industry.

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

NG JYA YEE (R23119014)
EA Recruitment Pte Ltd
EA License No: 21C0492

This position will be the lead HMCS Quality presence at the site.

They will be responsible for ensuring the desired customer experience by supporting the process development of manufactured products and ensuring conformance to customer specifications and requirements. This includes developing robust statistically based inspection methods, investigating, evaluating, and dispositioning nonconforming products.

The role involves ensuring the effective utilization of Quality systems (ISO 13485) and enforcing compliance with relevant regulations. This position reports to the Site Quality Manager/Leader.

Responsibilities

1. Work with internal/external customers providing inspection, testing, process capability support, qualifications/validations, GRR, Minitab analysis, FAI analysis, and inspection plans promptly.
2. Review and update work instructions related to inspection techniques and equipment, collaborating with Engineering to meet metrology needs.
3. Lead processes for nonconforming material and product, including disposition, investigation, CAPA/corrections, and customer communication.
4. Serve as Key User and lead in ERP (Quality) and EQMS systems.
5. Maintain and coordinate internal and external audits (ISO 13485).
6. Support quality methodologies for process changes and communicate these with the customer.
7. Provide training based on expertise or demonstrated work experience, utilizing training tracking systems and ensuring training requirements are current.
8. Prepare quality documentation and reports by analyzing and summarizing information and trends such as failed processes, stability studies, customer returns, corrective actions, and re-validations.
9. Enhance department and organization reputation by taking ownership of new and different requests and exploring opportunities to add value.
10. Perform other duties or projects as assigned by management and the Global Quality Team.

Education

• Senior Engineer - BA/BS in Engineering with 5-7 years of experience, or in a scientific discipline with 7-10 years in an engineering or technical role.
• Engineer - BA/BS in Engineering with 2-3 years of experience, or in a scientific discipline with 2-4 years in an engineering or technical role.

Experience

• Preferably experience in an ISO 13485:2003 and/or 9001:2000 work environment.
• Medical device experience is a plus.
• ASQ Certified Quality Engineer preferred.
• Ability to utilize MRP or ERP software and Statistical Analysis Software.
• Training in root cause analysis, project management, statistical analysis, SPC, Six Sigma tools, and Geometric Dimensioning and Tolerancing.

This position will be the lead HMCS Quality presence at the site.

They will be responsible for ensuring the desired customer experience by supporting the process development of manufactured products and ensuring conformance to customer specifications and requirements. This includes developing robust statistically based inspection methods, investigating, evaluating, and dispositioning nonconforming products.

The role involves ensuring the effective utilization of Quality systems (ISO 13485) and enforcing compliance with relevant regulations. This position reports to the Site Quality Manager/Leader.

Responsibilities

1. Work with internal/external customers providing inspection, testing, process capability support, qualifications/validations, GRR, Minitab analysis, FAI analysis, and inspection plans promptly.
2. Review and update work instructions related to inspection techniques and equipment, collaborating with Engineering to meet metrology needs.
3. Lead processes for nonconforming material and product, including disposition, investigation, CAPA/corrections, and customer communication.
4. Serve as Key User and lead in ERP (Quality) and EQMS systems.
5. Maintain and coordinate internal and external audits (ISO 13485).
6. Support quality methodologies for process changes and communicate these with the customer.
7. Provide training based on expertise or demonstrated work experience, utilizing training tracking systems and ensuring training requirements are current.
8. Prepare quality documentation and reports by analyzing and summarizing information and trends such as failed processes, stability studies, customer returns, corrective actions, and re-validations.
9. Enhance department and organization reputation by taking ownership of new and different requests and exploring opportunities to add value.
10. Perform other duties or projects as assigned by management and the Global Quality Team.

Education

• Senior Engineer - BA/BS in Engineering with 5-7 years of experience, or in a scientific discipline with 7-10 years in an engineering or technical role.
• Engineer - BA/BS in Engineering with 2-3 years of experience, or in a scientific discipline with 2-4 years in an engineering or technical role.

Experience

• Preferably experience in an ISO 13485:2003 and/or 9001:2000 work environment.
• Medical device experience is a plus.
• ASQ Certified Quality Engineer preferred.
• Ability to utilize MRP or ERP software and Statistical Analysis Software.
• Training in root cause analysis, project management, statistical analysis, SPC, Six Sigma tools, and Geometric Dimensioning and Tolerancing.

Summary

This position will be the lead HMCS Quality presence at the site.

They will be responsible for ensuring the desired customer experience through supporting the process development of product that is manufactured and ensuring conformance to customer specifications and requirements, developing robust statistically based inspection methods, primary support for investigating, evaluating, and disposition of nonconforming product.

They will ensure the Quality systems (ISO 13485) are effectively utilized and compliance to the proper regulations is enforced. This position reports to the Site Quality Manager/Leader.

Resposibilities

The incumbent will:

1. Work with internal/external customers providing inspection, testing, process capability support, Qualifications/Validations, GRR, Minitab analysis, FAI analysis, and inspection plans in a timely manner.
2. Review and update work instructions associated with inspection techniques and inspection equipment. Work with Engineering to meet metrology needs.
3. Leads the nonconforming material and product processes which includes but is not limited to Disposition, Investigation, CAPA/Corrections and customer communication.
4. Key User and lead in ERP (Quality) and EQMS system.
5. Maintain and coordinate internal and external audits (ISO 13485)
6. Support the quality methodologies for process changes. Support communication and process changes with the customer.
7. Provides training to others based on expertise, resume or demonstrated work experience. Uses training tracking system and ensures training requirements are up to date on a regular basis.
8. Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, customer returns, corrective actions, and re-validations.
9. Enhances department and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
10. Any other duties/projects assigned by management & Global Quality Team.

Education:

• Snr Engineer - BA/BS in an Engineering discipline with 5-7 years of Experience, or BA/BS in a scientific discipline with 7-10 yrs in a engineering or technical role.
• Engineer - BA/BS in an Engineering discipline with 2-3 years of Experience, or BA/BS in a scientific discipline with 2-4 yrs in a engineering or technical role.

Experience:

• Experience preferably in an ISO 13485:2003 and/or 9001:2000 work environment.
• Medical device experience a plus.
• ASQ certified Quality engineer preferred.
• Ability to utilize MRP or ERP software and Statistical Analysis Software.
• Root cause analysis training, Project Management, Statistical analysis, SPC, Six Sigma Tools and Geometric Dimensioning and Tolerancing experience.

• Well Established Company
• Basic $6,000 - $ 8,000 + Variable Bonus
• Working location: Tampines North
• Working days: Monday - Friday
• Working hours: 9.00am - 6.00pm

Key Responsibilities:

• Develop, implement, and maintain quality assurance protocols and procedures.
• Establish quality management system and programs, conduct regular inspections and audits of assembly processes to ensure compliance with industry standards and company specifications.
• Collaborate with cross-functional teams, including R&D, engineering, production, and supply chain, to identify and resolve quality issues.
• Lead root cause analysis and corrective action initiatives to address defects and non-conformities.
• Monitor and analyse quality performance metrics and report findings to senior management.
• Ensure all quality assurance activities are in compliance with ISO 9001 standards.
• Provide training and guidance to junior quality engineers and other team members on quality best practices, quality programs and quality standards.
• Stay up to date with industry trends and advancements in quality assurance methodologies and technologies.
• Respond to customer inquiries, feedback and complaints regarding product performance and quality, ensure timely and effective resolution of any issues, improve customer satisfaction through quality improvements.
• Oversee all quality-related audits, both internal and external.
• Lead and participate in cross-functional teams to drive quality improvement projects.
• Perform any other duties as assigned by superior.

Qualifications & Experience:

• Master in Mechanical Engineering, Electrical Engineering, or a related field.
• Minimum of 5 years of experience in quality assurance within the manufacturing industry.
• Certification in quality engineering (CQE) or a related certification is a plus.

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

NG JYA YEE (R23119014)
EA Recruitment Pte Ltd
EA License No: 21C0492

Date Posted:

Country:

Location:

Position Role Type:

Responsibilities:

• Support cells in inspection and gaging issues including inspection plan, equipment and techniques.
• Perform Relentless Root Cause Analysis (RRCA) on product and process non-conformance.
• Maintain, implement and improve quality control procedures and inspection processes.
• Perform Preliminary Material Review, conduct trends analysis and publish reports on non-conformance hardware.
• Participate in internal quality audits to maintain a robust and effective Quality Management System.
• Drive effective improvement projects.
• Participate in performance improvement processes through CORE.
• Lead, educate and instruct shop personnel on Quality procedures and standards compliance.

Requirements:

• Degree in Mechanical / Manufacturing Engineering
• Good working on Quality Management System meeting AS9100 requirements.
• Competent in Microsoft Office applications.
• Knowledge of Co-Ordinate Measuring Machine (CMM), and Non Destructive Testing (NDT) will be added advantages.
• Effective communication and interpersonal skills.
• Generate quality related reports

RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law.

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At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

SUMMARY
To assist the Quality Assurance function as technical support in issues affecting manufacturing. To support and drive corrective action efforts.

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

1. Ensure capability studies are performed on critical processes.
2. Perform first article inspection and review visual aids.
3. Perform defect analysis reporting.
4. Perform MRB on sustained products.
5. Participate in CAC meetings – support continuous improvement.
6. Perform line and product audits.
7. Assist Quality Engineering in APQP.
8. Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor.
9. Comply and follow all procedures within the company security policy.

MINIMUM REQUIREMENTS
Bachelor's degree preferred; or equivalent combination of education and experience.

Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.

• Manage end to end effort for the development and deployment of new production processes and equipment for quality responsibilities.
• Develop the inspection planning, CMM and other inspection gaging requirements.
• Validation of CMM/auto-inspection programs for optimization.
• Identify and design inspection methods for production processes with the goal of process capability and operator feedback
• Maintain and control process documentation of production processes.
• Work with Manufacturing Engineers to develop gauging and systems to support product conformance.
• Troubleshooting and continuous improvement of inspection processes.
• Assist production in the prove-out and debugging of new processes.
• Follow prescribed work rules and safety standards.
• Take ownership of project goals and objectives to ensure project success
  
  

• Manage end to end effort for the development and deployment of new production processes and equipment for quality responsibilities.
• Develop the inspection planning, CMM and other inspection gaging requirements.
• Validation of CMM/auto-inspection programs for optimization.
• Identify and design inspection methods for production processes with the goal of process capability and operator feedback
• Maintain and control process documentation of production processes.
• Work with Manufacturing Engineers to develop gauging and systems to support product conformance.
• Troubleshooting and continuous improvement of inspection processes.
• Develop paperless shopfloor documentation systems.
• Assist production in the prove-out and debugging of new processes.
• Follow prescribed work rules and safety standards.
• Take ownership of project goals and objectives to ensure project success
  
  

• Degree in an Engineering discipline (Mechanical, Manufacturing, Material)
• At least 5 years’ of relevant working experience.
• Knowledge of CMM, auto-inspection method, inspection tooling and metrology technology and ANSI Y14.5 blueprint reading
• Ability to be flexible and adapt to changing priorities
• Develop and manage a project from concept to implementation
• Analyze information and solve problems quickly
• Experience with metrology standards and equipment
• Demonstrate high level of attention to details
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Aviation and Aerospace Component Manufacturing

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Valina Services is a Quality Assurance (QA) and Commissioning, Qualification, and Validation (CQV) solutions provider for the Life Science industry. We offer personalised and focused solutions for customers across the healthcare, pharmaceutical, and manufacturing domain.

As a Quality Engineer, you will be working for our clients, in the respect of the applicable regulations and quality procedures. The main responsibilities of the Engineer will be:

•To maintain an effective Quality Management System (QMS)

•To Conduct and support our clients in their Audits and Inspections

•The Manage the follow up of the Corrective Actions/Preventive Actions (CAPA)

•To understand and address clients findings and quality requirements

•To work with various departments to ensure the respect of the QMS

•To manage the quality complaints from the customers and to improve the quality standards

• Degree (or similar) in IT, Engineering, or Science

•2+ years experience working in GxP environment would be a plus, beginners are accepted and trained

•2+ years experience working in Software Quality Assurance environment would be a plus, beginners are accepted and trained

•Excellent written/verbal English language skills are required. Other languages (French/German/Spanish) would be a plus

•Strong organizational and project management skills

•Familiar with GxP compliance requirements (FDA, EMA, GAMP 5, 21 CFR Part 11, PICs, etc.)

• Competitive basic salary and commission package

•Collaborative and team-oriented culture that embraces diversity

•Comprehensive medical and dental benefits