1,013 Quality Control Departments jobs in Singapore
Executive, Quality Management
Posted 16 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 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).
Manager, Clinical Quality Management
Posted 14 days ago
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Job Description
Engage with Leaders and Regulators
Opportunity to lead impactful projects
Enhance Patient Care Quality
As a Manager, Clinical Quality Management, you will be responsible for the following duties:
Lead and support the team in managing clinical data, quality assurance activities such as MOH licensing, audits, and safety walks.
Oversee training and education initiatives focused on patient safety, clinical quality, and Infection Prevention and Control (IPC).
Implement and monitor IPC programmes and drive clinical quality improvement projects.
Develop, review, and uphold clinical standards to ensure consistent patient care quality.
Assist the Director in liaising with senior management, department heads, and external agencies like MOH and AIC.
Support departmental planning, reporting, and ongoing service development efforts.
Mentor and supervise staff, while managing manpower planning and team growth.
Help plan budgets and manage resources effectively.
Take on additional projects or responsibilities as assigned by the Head of Department.
Requirements
A degree in Medicine, Nursing, Allied Health, or Healthcare Management from a recognised institution.
At least 5 years of relevant experience in healthcare operations or clinical quality management.
Strong leadership and communication skills, with the ability to conduct training and manage teams effectively.
To apply, simply click on the ‘’apply’’ button in the job advertisement or alternatively, you can send in your resume via email
Email Address:
We regret to inform that only shortlisted candidates will be notified.
ALLIED SEARCH PTE. LTD.
EA LICENSE: 19C9777
#J-18808-LjbffrSenior Quality Management Professional
Posted today
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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.
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 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
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Associate, Quality Management Systems
Posted today
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At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
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.
Alcon Careers
See your impact at alcon.com/careers
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Senior Quality Management Specialist
Posted today
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Job Summary:
We are seeking a skilled Quality Engineer with expertise in supplier management to join our team. In this role, you will be responsible for planning, overseeing, and executing projects aligned with management objectives.
- Main Responsibilities
- Maintain and improve quality, environmental, and water efficiency management systems.
- Ensure compliance with ISO 9001, ISO 14001, ISO 13485, IATF 16949, and ISO 46001.
- Conduct internal audits; coordinate with departments for external customer and vendor audits.
- Manage documentation and serve as Document Control Center.
- Enforce information security across the information life cycle.
- Monitor quality failure costs, yield, and pass rates in production.
- Coordinate corrective and preventive actions with departments and suppliers.
- Handle product and material quality issues, including customer feedback and disposition.
- Provide support on quality, environmental, and technical matters to customers.
Requirements:
To be successful in this role, you will need:
- A degree in engineering or a related field.
- 5 years of relevant working experience in engineering or quality assurance.
- Experience in supplier management and product qualification with APQP, PPAP, MSA, FMEA, and SPC.
- Proficient in 8D problem-solving tools (Fishbone, 5 Whys).
About This Opportunity
This is an exciting opportunity for a Quality Engineer to make a real impact in our organization. If you are a motivated and detail-oriented individual with a passion for quality assurance, we encourage you to apply.
Quality Management Systems Specialist
Posted today
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The Quality Management System (QMS) Specialist is responsible for implementing and maintaining quality processes within the organization.
This role requires collaboration with various departments to ensure effective quality management.
Key Responsibilities:- Develop and implement quality policies and procedures in accordance with applicable regulations and standards.
- Collaborate with cross-functional teams to identify and mitigate quality risks.
- Conduct regular audits and assessments to ensure compliance with quality management system requirements.
- Provide training and guidance to employees on quality procedures and documentation.
- Manage and maintain accurate and complete quality records and documentation.
- Investigate and resolve quality issues and nonconformities in a timely manner.
- Identify areas for process improvements and implement changes as necessary.
- Maintain knowledge of industry trends, regulatory requirements, and best practices related to quality management.
Required Skills and Qualifications:
- Bachelor's degree in a related field (e.g., engineering, science, or business).
- Minimum 5 years of experience in quality assurance or a related field.
- Excellent communication and interpersonal skills.
- Ability to work independently and collaboratively in a team environment.
- Strong analytical and problem-solving skills.
- Proficiency in Microsoft Office and other productivity tools.
Benefits:
- Opportunities for professional growth and development.
- A dynamic and supportive work environment.
- A competitive salary and benefits package.
Other Information:
- Travel may be required for training and auditing purposes.
- Must be able to pass a background check and comply with company security protocols.