1,256 Quality Management jobs in Singapore

Maintain and implement quality management systems in accordance with industry standards, ensuring compliance with regulations and procedures. Oversee the quality and safety of assigned workshop operations and manage vendor qualifications.

• Manage Quality Management Systems (QMS) according to AS9100/9110/9120 and ISO14001/ISO45001 standards.
• Conduct audits and investigations for incidents, accidents, and warranty-related issues.

• Min Diploma or Degree in Aerospace Engineering or related fields.
• Experience in Quality Assurance and Safety, preferably in an AMO or MRO environment.
• Certified auditor with knowledge of relevant standards.

In this role, you will be responsible for ensuring the quality management system is compliant with customer requirements.

• Review and revise quality procedures and instructions to maintain high standards.
• Liaise with stakeholders on non-conformance activities, perform root cause analysis, and implement corrective actions to reduce cost of poor quality.
• Perform internal audits to evaluate quality systems, products, and processes.

Requirements:

• Degree in Mechanical or Aeronautical Engineering or relevant discipline.
• Minimum 5 years of experience in Quality Management System and NADCAP.

Key Skills:

• Quality Assurance
• Quality Control
• Root Cause Analysis
• Reliability
• Compliance

Location: Jamiyah Nursing Home, West Coast, Singapore

Job Hours: Monday to Friday

Be a Vital Part of Our Support Team at Jamiyah Singapore.

Join Our Mission to serve the community, grounded in Islamic values and compassion.

Why Join Jamiyah Singapore?

• Purpose with Impact: Be part of a team that directly supports the community.
• Inclusive and Supportive Culture: Work in a multicultural environment where respect, teamwork, and support are core values.

Duties & Responsibilities

• Support the Head of Home in all aspects of operational/compliance audits/reviews of the nursing home.
• Design, implement, and maintain comprehensive quality control processes and establish standard operating procedures (SOPs) for the nursing home.
• Conduct regular reviews of existing procedures to identify areas for enhancement and optimization.
• Plan and conduct risk assessments and quality control reviews to ensure compliance with all statutory, regulatory requirements, and internal compliance requirements.
• Carry out root cause analysis and monitor the effectiveness of action plans to address quality and risk areas of weaknesses.
• Train, coach, develop, and cultivate technical competencies to ensure the capability of designated employees to maintain and comply with quality standards.
• Implement corrective and preventive actions to prevent recurring quality issues.

Requirements

• Degree / Diploma in a relevant discipline
• 5 - 10 years working experience in Quality Assurance/Audit function.
• Strong knowledge and understanding of quality systems and experience in facing quality.
• Good interpersonal and leadership skills.
• Detail-oriented, strong analytical and organizational skill.
• Be prepared to perform other duties as assigned.

Benefits

• Comprehensive Medical & Leave Benefit.
• Supportive and conducive work environment.
• Training & Development opportunities.
• Unlimited opportunities to develop and harness your skills across multi-verticals.
• Being part of a noble organization with a strong heritage in community care.

Location: Jamiyah Nursing Home, West Coast, Singapore

Job Hours: Monday to Friday

Be a Vital Part of Our Support Team at Jamiyah Singapore.

Join Our Mission to serve the community, grounded in Islamic values and compassion.

Why Join Jamiyah Singapore?

• Purpose with Impact: Be part of a team that directly supports the community.
• Inclusive and Supportive Culture: Work in a multicultural environment where respect, teamwork, and support are core values.

Duties & Responsibilities

• Support the Head of Home in all aspects of operational/compliance audits/reviews of the nursing home.
• Design, implement, and maintain comprehensive quality control processes and establish standard operating procedures (SOPs) for the nursing home.
• Conduct regular reviews of existing procedures to identify areas for enhancement and optimization.
• Plan and conduct risk assessments and quality control reviews to ensure compliance with all statutory, regulatory requirements, and internal compliance requirements.
• Carry out root cause analysis and monitor the effectiveness of action plans to address quality and risk areas of weaknesses.
• Train, coach, develop, and cultivate technical competencies to ensure the capability of designated employees to maintain and comply with quality standards.
• Implement corrective and preventive actions to prevent recurring quality issues.

Requirements

• Degree / Diploma in a relevant discipline
• 5 - 10 years working experience in Quality Assurance/Audit function.
• Strong knowledge and understanding of quality systems and experience in facing quality.
• Good interpersonal and leadership skills.
• Detail-oriented, strong analytical and organizational skill.
• Be prepared to perform other duties as assigned.

Benefits

• Comprehensive Medical & Leave Benefit.
• Supportive and conducive work environment.
• Training & Development opportunities.
• Unlimited opportunities to develop and harness your skills across multi-verticals.
• Being part of a noble organization with a strong heritage in community care.

Job Title: Senior Quality Management Specialist

We are seeking a highly skilled Senior Quality Management Specialist to join our dynamic team. The successful candidate will be responsible for developing and maintaining quality control/assurance systems for manufactured products.

The ideal candidate will possess relevant certifications in Quality Management and have a minimum of 3 years' experience in quality management, preferably in the manufacturing industry. Prior experience in leading a team is also essential.

Key Responsibilities:

• Develop and maintain quality control/assurance systems for manufactured products.

• Manage inspection teams and oversee compliance with industry standards (e.g., ISO 9001).

• Address customer feedback and resolve quality-related concerns.

• Implement testing methods to ensure product quality and specifications.

• Drive continuous improvement in production and quality processes.

• Maintain quality records, generate reports, and train staff on best practices.

• Manage budgets, assess risks, and collaborate cross-functionally.

• Conduct audits to evaluate quality management systems.

Required Skills and Qualifications:

• Diploma in Engineering or a related discipline.

• Possess relevant certifications in Quality Management.

• Minimum of 3 years' experience in quality management, preferably in the manufacturing industry.

• Prior experience in leading a team.

• Knowledge of quality standards (e.g., ISO 9001) and testing methodologies required.

• Computer literate.

Benefits:

• Competitive salary package.

• Bonus structure.

If you are a motivated and experienced professional looking for a new challenge, please submit your application by email to

Quality Assurance Manager

• Job Description:

As a Quality Assurance Manager, you will be responsible for designing, implementing and maintaining comprehensive quality control processes and establishing standard operating procedures (SOPs) for the nursing home.

You will conduct regular reviews of existing procedures to identify areas for enhancement and optimization, plan and conduct risk assessments and quality control reviews to ensure compliance with all statutory, regulatory requirements, and internal compliance requirements.

Additionally, you will carry out root cause analysis and monitor the effectiveness of action plans to address quality and risk areas of weaknesses, train, coach, develop and cultivate technical competencies to ensure the capability of designated employees to maintain and comply with quality standards.

Implement corrective and preventive actions to prevent recurring quality issues.

You must have a degree / diploma in a relevant discipline and 5-10 years working experience in Quality Assurance/Audit function. You should possess strong knowledge and understanding of quality systems and experience in facing quality. Good interpersonal and leadership skills are required, as well as detail-oriented, strong analytical and organizational skill.

The company offers comprehensive medical & leave benefits, supportive and conducive work environment, training & development opportunities and unlimited opportunities to develop and harness your skills across multi-verticals.

This is an exciting opportunity to join our team and contribute to the success of our organization. If you are a motivated and dedicated individual who is passionate about quality assurance, we encourage you to apply for this role.

We are seeking an experienced Quality Assurance Expert to join our team. As a key member of the organization, you will be responsible for ensuring the highest quality standards in all aspects of our operations.

• Provide day-to-day operation support in Quality Management (QM) and its corresponding authorization to ensure smooth daily operation.
• Identify gaps, issues and workaround solutions. Creating functional requirements as an input to application design, assist with build, test, and deploy activities for QM module.

You will work closely with business process owners and local users to ensure compliance to global business processes.

• Bachelor's Degree in Computer Science, Engineering, Information Technology, Information System, Info-communications, Science or its equivalent.
• At least 4-5 years of relevant SAP QM, authorization experience in manufacturing environment (Chemical industry preferred) and SAP ECC 6.0 and/or S/4 HANA.
• SAP PP experience will be an added advantage.
• Have strong integration working experience and knowledge of the key integration points between the other SAP modules.

You must have at least one full life-cycle SAP R/3 ECC 6.0 and / or SAP S/4 HANA implementation experience (Project Preparation till Go-Live).

• Strong understanding of QM (primary) and PP (secondary) functionalities and able to apply them to business issues.
• Ability to analyse problems and provide clear recommendations.

You should be able to work independently as well as a team player and can manage own workload with little to no supervision.

• Able to communicate in Mandarin will have advantage.
• Must be familiar with process and project documentation.

• Serves as the management representative to monitor and report on the adequacy, effectiveness, and continuing suitability of our quality management system in accordance with ISO 13485:2016 established policies/procedures, and applicable regulatory requirements.

• Promote awareness of applicable, new, and/or updated in-vitro diagnostic medical device regulations and standards.

• Manage document control, engineering change control, and records control process including external origin documents.

• Evaluate, monitor, and re-evaluate suppliers. Maintain the approved supplier list (ASL).
• Manage the internal audit program to ensure timely execution in accordance with published schedule.

• Manage the calibration program to ensure all monitoring and measuring equipment are inducted, calibrated, reviewed, and monitored in a timely manner.

• Participate in design control, risk management, and software development activities throughout the lifecycle(s) of medical devices. Participate in risk assessment (FMEAs and SHA) and risk control activities of device design, use, and manufacturing.

• Participate in the validation of analytical test methods, process validations, and computer software used in the quality management system, production, and monitoring/testing.

• Participate in the handling of non-conforming products including but not limited to investigation, corrective/preventive actions, and disposition of affected products.

• Participate in the preparation of premarket regulatory submissions for commercial distribution.

Requirements:

• Bachelor of Science degree in a scientific (chemistry, biochemistry, microbiology) or engineering (biomedical) discipline.

• Minimum of 3 years of quality management system (ISO experience in the medical device industry. IVD experience is highly preferred.

• Detailed knowledge and experience in design and development, and risk management of medical device products are strongly preferred.

• Strong verbal and written communication skills. Conversational Mandarin is preferred.
• Strong analytical, time management, and organizational skills.
• Proficient in MS Office applications.
• A positive, proactive, can-do attitude, willing to learn.

• Develop and maintain accurate documentation on our quality management systems.
• Plan and conduct internal and external audits to ensure readiness for certification and customer audits.
• Review audit findings and develop action plans to drive continuous improvements.
• Generate and review quality reports on suppliers' performance and work with suppliers to address non-conforming materials.
• Support the qualification of new suppliers and maintain a healthy pipeline of qualified suppliers.

• Degree in quality management or related field.
• Minimum 3-5 years of relevant working experience in handling audits and ISO documentation in manufacturing industries.
• Knowledge in Supplier Management and quality Management Standards such as ISO 9001, 14001, 13485.
• Familiar with 8D and 5W problem solving methodology and good communication skills.