102 Quality Management jobs in Singapore

Siemens Mobility is an outstanding place to have a career in an innovative environment. Siemens Mobility Rail Infrastructure business supplies the global markets of rail and road-bound transport with innovative products and solutions for Rail Automation, Rail Electrification and in the area of intermodal mobility, apps and backend systems.

Be a part of it, design the future of Mobility and join us for your internship with Siemens Mobility Singapore.

What are my job responsibilities?

The internship in Quality Management department will introduce the Siemens Processes, instructions. The main aim will be to support the Head of QM to prepare materials related to Newcomer Training, Key Performance Indicator collection, liaise with Project teams to provide support related QM activities.

Main tasks and responsibilities

• Support the department Quality managers and Head of Quality in the process updates.
• Support in Annual/Quarterly Key Performance Indicators collection
• Work with the team in Integrated Management System roll out training material preparation
• Support project management in planning and securing milestone results.
• Monitor quality related KPIs or key figures related to projects assigned.
• Defined target values or characteristics as per project target agreement (PM agreement) to be achieved.
• Identify qualification requirements and initiate training for project employees with regards to knowledge of quality methods to be applied, process awareness and expert knowledge.
• Plan and support project audits, assessments, reviews and participate in status meetings.

What do I need to qualify for this role?

• Undergraduate who is undertaking Degree in Engineering or relevant courses
• Willingness to learn the new technology and work in creating template, documents to increase efficiency of the department.
• Good IT Skills, MS Suite
• Cheerful and Can Do attitude

To be eligible for this position, applicants must possess a Valid Student Pass in Singapore or satisfy the Ministry of Manpower's Work Holiday Pass (WHP) requirements.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Job Description: The Technical Support Specialist plays a vital role in the Technical team, responsible for managing day-to-day administrative tasks, performing system data entry, and ensuring the effective organization and maintenance of all quality and technical documentation.

This role requires close collaboration with the front-line team and active involvement to support the development, implementation, and continuous improvement of technical processes and documentation. The successful candidate shall be detail-oriented, dependable, and a strong team player with a commitment to supporting quality excellence.
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• Provide administrative and operational support to the Technical team across all QA/QC functions.
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• Maintain control of technical documentation, ensuring completeness, accuracy, and timely updates-this includes technical drawings, datasheets, checklists, inspection reports, and test reports.
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• Organize and manage both electronic and physical files related to quality and technical documentation.
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• Assist in the preparation of documentation required for product certification, project tender submissions, and internal/external audits.
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• Perform ad hoc administrative tasks to support seamless operations within the Technical team.
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• Support the development, maintenance, and organization of technical content used for training materials and marketing collateral.
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• Liaise with suppliers to ensure compliance with documentation standards and requirements.
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• Coordinate and communicate with external testing and calibration service providers.
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Requirements:

The ideal candidate should possess the following qualifications:

• A minimum of 1 year's experience in steel engineering, preferably.
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• A Certificate/Diploma in relevant engineering faculty.
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• Be committed, hardworking, and able to work independently.
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• Be self-motivated, proactive, and highly independent.
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• Have strong written and oral communication skills.
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• Excellent collaboration and interpersonal skills to work with stakeholders.
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Working Details:

The selected candidate will have the opportunity to work Monday to Friday (9am - 6pm) in Woodlands Close, Singapore, near Admiralty MRT.

Working Hours: Mon to Fri: 815am - 550pm

Company Transport @ Tai Seng and Tuas Cresent

Responsibilities / Duties / Job Description / Job Scope

• Management of certification ISO 9000, 45000, 14000 and customer audits.

• Facilitation of internal and supplier audit program.

• Development and implementation of a training program for internal auditors.

• Maintain internal / supplier audit schedule.

• Assigning internal / supplier audit teams.

• Review of internal / supplier audit reports.

• Conducting follow-up to verify closure of Quality Corrective Action Requests for internal,supplier & customer audits.

• Management of the Quality Corrective Action Request (QCAR) system.

• Ensures the quality controls & quality assurance programs and policies are maintained and modified regularly.

• Management of the control of QMS documentation.

Education / Experience / Skills / Knowledge / Personality

• Bachelor's degree in Quality, Mechanical or Industrial Engineering or equivalent combination of experience and education.

• Quality systems knowledge, including auditing.

• Strong leadership skills with experience in working within a technical team.

Interested candidates who wish to apply for the advertised position, please click APPLY NOW.

Alternatively, you may send your application and resume in MS Words format to or Whatsapp to

We regret that only shortlisted candidate will be notified.

K N Tan

Registration Number: R

EA Licence No: 17C8778 (JIH SUN EMPLOYMENT AGENCY)

R: N12OPS36

The primary goal of this position is to maintain accurate and organized records, as well as ensure that all documentation is properly checked and processed. This role involves maintaining equipment calibration records, creating shipment documents, and performing administrative duties.

• Maintain proper internal and external documentations, adhering to established standards and procedures.
• Verify the accuracy and completeness of incoming and outgoing documentations.
• Keep track of equipment calibration records and follow up on any necessary calibrations.
• Prepare and manage shipment documentations, in addition to performing general administrative tasks.
• Upload Statistical Process Capability reports and oversee In-Process Quality Control reports.
• Establish inspection criteria for products and conduct analysis on internal defects.
• Support quality assurance and control activities, providing additional assistance when required.

• Diploma/Degree in any field, with a preference for quality management/engineering/manufacturing fields.
• At least 1-2 years of relevant experience in quality management within manufacturing industries.
• No prior experience is necessary, but proficiency in MS Office (Excel, PowerPoint, etc) is required.

Job Title: Quality Systems Specialist

This role is responsible for supporting supplier management programs, including performing quality activities such as supplier qualification, periodic performance monitoring, supplier change notification, and decommissioning.

• Perform supplier qualification activities, ensuring that supplier questionnaires are completed with relevant documents, and liaise with stakeholders to assess the suitability of suppliers.
• Liaise with affiliate sites personnel to gather qualified supplier information and assess the leverage of supplier qualification documents.
• Lead or support on-site audits at supplier sites, preparing audit agendas, reports, and coordinating with suppliers to close audit observations.
• Draft quality agreements with new suppliers or review existing agreements for existing suppliers engaged by affiliate sites.
• Perform quality assessments based on company procedures to determine if suppliers can be qualified for GMP use.
• Update qualified supplier lists and perform periodic performance monitoring, supplier change notification, and decommissioning of suppliers.
• Perform other tasks assigned by leadership.

About You:

• Bachelor's degree or higher in a relevant field, such as Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or related fields.
• At least 8 years of working experience in production and/or quality management, with a minimum of 5 years in supplier qualification QA.
• Familiarity with FDA, EMEA, HSA, and PIC/S GMP requirements.
• Experience in leading audits is preferred.
• Proficient in English listening, speaking, reading, and writing.
• Skilled in Microsoft Office applications, SAP, and other relevant tools.
• Strong learning ability and effective communication skills.

Quality Assurance and Control Specialist

Responsibilities:

• Develop, implement, and maintain comprehensive quality management systems.

We are seeking a skilled professional to conduct quality management system (QMS) inspections and ensure compliance with organisational standards.

• Key Responsibilities:
• Conduct thorough inspections to verify processes and documentation meet ISO standards.
• Prepare detailed compliance reports, track non-conformance issues, and recommend follow-up actions.
• Support quality audits by maintaining accurate audit records and monitoring trends.
• Provide administrative support, including documentation, filing, and coordination.

• Essential Requirements:
• Diploma in any discipline; background in quality assurance, compliance, or safety is an advantage.
• Knowledge of ISO 9001 / QMS standards preferred.
• WSQ Graduate Certificate in Workplace Safety and Health or ISO Auditor Certification is an added advantage.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Strong organisational, documentation, and problem-solving skills.

The ideal candidate will be offered a competitive salary package and opportunities for career growth and development.

Our company values diversity and inclusion. We welcome applications from candidates with diverse backgrounds and experiences.

Main Responsibilities:

• Champion a strong quality mindset and actively drive the Zero Defect strategy across internal teams and external suppliers.
• Lead or support qualification of new components and requalification activities (e.g., Product Change Notifications) in line with Continental's Product Life Cycle and APQP (Advanced Product Quality Planning) processes.
• Plan, initiate, and oversee advanced quality measures during the design and development phases to ensure supplier components meet all technical and quality requirements.
• Work closely with global and cross-functional teams including Purchasing, Engineering, Project Management, Local SQM, Customer Quality, and Logistic.
• Participate in the review of corrective actions from VDA 6.3 audits, with a strong focus on early involvement and preventive measures.
• Contribute to lessons learned and best practice sharing across the category, organization, and supplier base.

Requirements:

• Bachelor's Degree in Electrical & Electronic and/or Mechanical Engineering.
• Minimum 3 years working experience in Automotive Industry.
• Good understanding of Component Introduction in design and development phase and APQP management
• Ability to understand, discuss and align technical requirements with high focus on requirements engineering based on drawings and specifications
• Good knowledge in process for plastic overmolding/molding and its secondary process with cosmetic requirement, stamping, press-fit stamping, sub-component assembly, automated inline testing, wire cutting/terminating for cable assemblies
• Strong Knowledge in quality related methodologies and standards (eg. FMEA, 8D review, 5why, Problem Solving, etc)
• Able to work independently and also in team-based environment

EA Licence No.:18S9405 / EA Reg. No.:R

Percept Solutions is expanding and actively seeking talented individuals. We encourage applicants to follow Percept Solutions on LinkedIn at to stay informed about new opportunities and events.

• Great Career Exposure
• Convenient working location
• Competitive Remuneration Package

As a Manager (Clinical Quality Management), you will be responsible for the following duties:

• The Manager, Clinical Quality Management, supports the Director in the strategic and operational oversight of clinical quality, patient safety, infection control, and regulatory compliance within the institution.
• The role entails supervising staff, managing projects, and coordinating with both internal departments and external agencies to uphold and enhance clinical care standards.
• Support and supervise Senior Executives/Executives in the following:
• Ensure accurate, timely collection and analysis of clinical data to support quality initiatives.
• Oversee processes related to audits, licensing (e.g., MOH), and safety inspections.
• Develop and implement education programs on patient safety and clinical quality.
• Monitor and improve IPC practices in line with national and international standards.
• Facilitate cross-functional quality improvement projects across departments.
• Support the establishment and review of clinical practice standards.
• Assist in driving institutional clinical excellence.
• Strategic and Operational Support:
• Assist in setting departmental goals, priorities, and strategies.
• Serve as a key point of contact for Internal stakeholders (management and departmental heads) and external agencies.
• Prepare, review, and present reports and dashboards for management.
• Participate in workforce planning, recruitment, and professional development initiatives.
• Assist in formulating and managing department budgets and resource allocation.
• Support and lead various clinical quality and safety projects as delegated by the Director/HOD.
• Guide and support junior staff in their professional growth and daily functions.

Requirements:

• Degree in Nursing, Healthcare Management, Life Sciences, or a related field.

• At least 5 years' experience in a related job scope in healthcare is preferred.

• Ability to conduct lectures, workshops and teaching sessions.

To apply, simply click on the ''apply'' button in the job advertisement or alternatively, you can send in your resume via email

Email Address:.COM.SG

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

ALLIED SEARCH PTE. LTD.

EA LICENSE : 19C9777