122 Continuous Improvement Methodologies jobs in Singapore
Quality Management Partner
Posted today
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Job Description
The Quality Management Director / Partner will lead firm-wide quality initiatives, manage internal reviews, support regulatory inspection readiness, and provide guidance on complex technical matters. The ideal candidate will be a former ACRA or ISCA Practice Monitoring Programme (PMP) reviewer or someone with equivalent regulatory inspection experience. In addition to overseeing quality management, the candidate will maintain a small portfolio of audit clients and perform in-house monitoring and file inspections.
Key Responsibilities:
Lead the implementation and ongoing enhancement of the Firm’s System of Quality Management (SOQM) in accordance with SSQM 1.
- Oversee internal quality monitoring activities, including engagement inspections, hot and cold file reviews, and root cause analyses.
- Manage firm readiness for external regulatory reviews, including ACRA PMP and ISCA QAR, and lead responses and remediation efforts.
- Maintain a small portfolio of audit clients, ensuring quality and compliance with applicable standards.
- Serve as Engagement Quality Reviewer (EQR) for listed or high-risk engagements where required.
- Provide technical advice on auditing, ethics (EP 100), and quality standards to partners and staff.
- Support the development and tracking of Audit Quality Indicators (AQIs).
- Conduct internal training and coaching to promote a quality-focused culture.
- Collaborate with the PKF International network to align with global methodology and quality policies.
Requirements:
- Bachelor’s degree in Accounting or equivalent.
- Chartered Accountant (Singapore).
- At least 10 years of audit and/or quality management experience, with prior experience at ACRA or ISCA in the PMP or QA function being highly preferred.
- Strong technical knowledge of SSQM 1, Singapore Standards on Auditing (SSA), and EP 100.
- Proven experience in audit quality reviews, internal inspections, and file monitoring.
- Capable of managing audit engagements while maintaining independence in quality oversight roles.
- Excellent communication, analytical, and leadership skills.
- Passionate about audit quality and able to influence at all levels of the firm.
Registration No.
T07LL0568F
Company Size
51 - 200 Employees
Benefits & Others
Miscellaneous allowance, Medical, Birthday Leave
Executive, Quality Management
Posted 17 days ago
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Job Description
You will report to the Deputy Director, Quality Management in ensuring that Quality and Safety related activities and processes are developed, implemented and evaluated,
in support of the department’s key objectives in ensuring the Quality and Safety of patient care in SingHealth Polyclinics (SHP).
Your responsibilities include:
- Implement programmes, projects, and activities relating to Quality and Safety at SHP
- Co-ordinate, support, and participate in Quality Assurance and Improvement initiatives
- Represent the department in committees, workgroups, and meetings, and liaise with internal and external parties on initiatives relating to Quality and Safety
- Provide administrative support for Clinical Governance and other programmes in the SHP Quality Management Framework
- Perform other duties as assigned
Requirements:
Bachelor’s Degree in any discipline
Good verbal and written language skills in English are expected, with fluency in other languages an advantage
Good interpersonal skills and resourceful team player
Strong interest in learning and professional growth
Quality Management Professional
Posted today
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Job Description
Job Title: Quality Assurance Specialist
", "Job Responsibilities:- ", "
- Develop and implement project quality control plans to ensure compliance with industry standards. ", "
- Conduct pre-inspection activities to identify potential issues before client inspection. ", "
- Prepare and submit quality control documentation to clients in a timely manner. ", "
- Liaise with clients to resolve any quality-related concerns or issues. ", "
- Review and analyze inspection reports for accuracy and completeness. ", "
- Oversee daily site activities to ensure they align with project goals and objectives.
- ", "
- Degree in Quality Assurance Engineering or related field. ", "
- Minimum 3 years of experience in QAQC role in construction industry. ", "
- Strong understanding of quality management systems, testing methodologies, and quality standards. ", "
- Proficiency in QA/QC tools and software applications.
Our organization offers a dynamic work environment that fosters growth and development. We provide opportunities for professional advancement and offer competitive compensation packages.
", "Others:This position requires strong analytical and communication skills, as well as the ability to work effectively in a team environment.
"),Quality Management Role
Posted today
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Job Description
Job Title: Quality Management Professional
">Job Description:
">The Quality Management Professional will be responsible for the maintenance and improvement of existing ISO quality systems. This includes investigating and documenting quality non-conformances, leading root cause analysis and corrective actions.
">Key Responsibilities:
">- Conduct periodic audits to ensure compliance with ISO standards, regulatory authorities and customers.
- Maintain all HSE & Quality documentation, procedures, forms and risk assessments.
- Handle reports, government and external audits, inspections and licenses.
- Follow up on latest statutory regulations and compliance for all QHSE.
- Conduct site inspections and audits to ensure safe work practices.
- Work with Operations to identify process gaps and develop improvement plans.
- Prepare and review documentation for customer KPIs.
- Handle customer complaints and process non-conformances, including root-cause analysis and corrective action.
Requirements:
">- Minimum Diploma / Degree in Workplace Safety and Health.
- At least 8 years of relevant working experience in HSE & Quality Management, ideally in logistics.
- Good knowledge of MS Office.
- Knowledge in ISO standards, preferably as a qualified lead auditor.
- Strong analytical and problem-solving skills.
- Excellent communication skills (verbal and written).
Quality Management Specialist
Posted today
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Job Description
We are seeking a Quality Management Specialist to join our team. The ideal candidate will have experience in quality management, preferably in the healthcare and health services sector.
Roles & Responsibilities:
- Maintenance of organization's quality system in compliance with regulatory standards;
- Follow up on deviations/non-conformances (CAPA) in protocols for rectification and process improvement;
- Performance of internal audits and record checking to ensure compliance with regulatory and accreditation standards;
- Assist regional office on quality matters;
Required Skills and Qualifications:
Diploma or degree with 2 years of working experience in quality management;
Good communication skills;
Team player with good coordination;
Meticulous and systematic;
Proficiency in document control systems.
Benefits:
Competitive salary package;
Opportunities for professional growth and development;
Collaborative work environment.
Others:
Audits
CAPA
Hospitals
Food Safety
Process Improvement
Quality Assurance
Quality System
Healthcare
ISO
Compliance
Good Communication Skills
Medical Devices
Quality Management (QM) Partner
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Job Description
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Quality Management Partner
The person will lead firm-wide quality initiatives, manage internal reviews, support regulatory inspection readiness, and provide guidance on complex technical matters. The ideal candidate will be a former ACRA or ISCA Practice Monitoring Programme (PMP) reviewer or someone with equivalent regulatory inspection experience. In addition to overseeing quality management, the candidate will maintain a small portfolio of audit clients and perform in-house monitoring and file inspections.
Quality Management Partner
The person will lead firm-wide quality initiatives, manage internal reviews, support regulatory inspection readiness, and provide guidance on complex technical matters. The ideal candidate will be a former ACRA or ISCA Practice Monitoring Programme (PMP) reviewer or someone with equivalent regulatory inspection experience. In addition to overseeing quality management, the candidate will maintain a small portfolio of audit clients and perform in-house monitoring and file inspections.
Key Responsibilities
- Lead the implementation and ongoing enhancement of the Firm’s System of Quality Management (SOQM) in accordance with SSQM 1.
- Oversee internal quality monitoring activities, including engagement inspections, hot and cold file reviews, and root cause analyses.
- Manage firm readiness for external regulatory reviews, including ACRA PMP and ISCA QAR, and lead responses and remediation efforts.
- Maintain a small portfolio of audit clients, ensuring quality and compliance with applicable standards.
- Serve as Engagement Quality Reviewer (EQR) for listed or high-risk engagements where required.
- Provide technical advice on auditing, ethics (EP 100), and quality standards to partners and staff.
- Support the development and tracking of Audit Quality Indicators (AQIs).
- Conduct internal training and coaching to promote a quality-focused culture.
- Collaborate with the PKF International network to align with global methodology and quality policies.
- Bachelor’s degree in Accounting or equivalent.
- Chartered Accountant (Singapore).
- At least 10 years of audit and/or quality management experience, with prior experience at ACRA or ISCA in the PMP or QA function being highly preferred.
- Strong technical knowledge of SSQM 1, Singapore Standards on Auditing (SSA), and EP 100.
- Proven experience in audit quality reviews, internal inspections, and file monitoring.
- Capable of managing audit engagements while maintaining independence in quality oversight roles.
- Excellent communication, analytical, and leadership skills.
- Passionate about audit quality and able to influence at all levels of the firm.
- Seniority level Mid-Senior level
- Employment type Full-time
- Job function Quality Assurance
- Industries Accounting
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#J-18808-LjbffrSenior Quality Management Professional
Posted today
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Job Description
The ideal candidate will possess strong leadership skills and have experience in managing quality management systems, including post-market surveillance and compliance with regulatory requirements.
- Lead the development and implementation of quality strategies to enhance company efficiency and effectiveness.
- Manage post-market activities, including customer care and communication with relevant departments.
- Develop and execute computer system validation activities related to authoring and executing specifications and validation documentation.
Key Responsibilities:
- Maintain the establishment and upkeep of a quality management system (QMS) that aligns with ISO 13485 QMS and FSCA/FCA requirements.
- Implement and execute quality strategies to enhance business efficiency and productivity concerning FCA/FSCA, product recall, and CSV/SDLC.
- Oversee business change control and quality impact regarding FSCA/FCA and CSV-related activities at the organization.
- Support regional affiliates in implementing post-market activities according to site procedures.
Requirements:
- Bachelor's Degree in Engineering or Science.
- 5 years of Quality Management experience in Medical Device industry.
- 3 years of CSV documentation & processes validation.
- Lead auditor certification to ISO 13485:2016, ISO 9001: 2015, ISO 27001: 2022.
This role is responsible for ensuring that all quality management systems are implemented and maintained effectively throughout the organization.
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Quality Management System Specialist
Posted today
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Job Title: Quality Management System Specialist
">About the Role:
The successful candidate will be responsible for implementing and maintaining quality management system standards, ensuring adherence to regulatory requirements, and conducting internal and external audits.
Key Responsibilities:
- Implement and maintain quality management system standards, including ISO 9001.
- Ensure compliance with regulatory requirements, including civil aviation authorities.
- Conduct internal and external audits to ensure quality and safety standards are met.
- Liaise with stakeholders, including customers and vendors, to ensure quality and safety standards are met.
- Investigate incidents and accidents to identify root causes and implement corrective actions.
Requirements:
- Minimum diploma in aerospace engineering or a related field.
- Minimum 3 years of experience in QMS in the aerospace industry.
- Qualified auditor certification is required.
We Offer:
- A competitive salary package.
- A dynamic and challenging work environment.
- Ongoing training and development opportunities.
How to Apply:
Please submit your resume and cover letter to (insert contact information).
Senior Quality Management Specialist
Posted today
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Job Description
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
Associate, Quality Management Systems
Posted today
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Job Description
As a Associate, Quality Management Systems (QMS) , you will oversee is responsible for GxP training for the site to ensure that quality system is compliant to ISO 13485, MDSAP, EU MDR, Alcon Standards and Policies, and all applicable regulatory requirements.
In this role, a typical day will include:
• Identify improvement opportunities, drive and lead project/implementation activities to improve site's GxP training management process.
• Appointed site's admin for Veeva Quality Learning Management System, manage the user access control and responsible for all training related requests such as processing Training Change Request (TCR), Training Requirement Impact Assessment (TRIA), generating training reports etc.
• Report and monitor training compliance rate and maintain site's Training Master List.
• Perform site impact / gap assessment and remediation against new/revised External Standards and Corporate SOP.
• Site representative for the global Training Community Call.
• Support in internal and external audit as the training's SME (Subject Matter Expert).
• Responsible for the archival of training/certification records.
• Manage quality training for New Hire Orientation.
• Trend, analyze and monitor key performance indicators, suggest improvements and escalate to supervisor/management as necessary.
• Meet quality objectives set by management & comply to Alcon, QMS and Safety requirements.
• Adhere to Alcon standards, in particular quality, ethical, health, safety and environment (HSE) and Business Information Management (BIM) standards.
• Performs any other duties as assigned by Supervisor according to business needs.
.
WHAT YOU'LL BRING TO ALCON:
• Bachelor in Science/ Engineering field a
• Min 1-2 years of working experience in a medical device or pharmaceutical industry in a Quality function, preferably in training
-Transport provided from Kranji, Outram Park and Boon Lay MRT
HOW YOU CAN THRIVE AT ALCON:
- Career Growth & Development - Gain access to continuous learning opportunities, leadership training, and career advancement programs to support your professional journey.
- Collaborative Culture - Work alongside passionate and diverse teams in a dynamic and inclusive environment that encourages innovation and teamwork.
- Impactful Work - Be part of a purpose-driven company that is improving lives by advancing eye care solutions worldwide.
See your impact