95 Continuous Improvement Methodologies jobs in Singapore

Working hours: Monday to Friday (8.00 am to 5.15 pm)
Salary: Up to $5K 

Job Scope: 

• Responsible for collaborating with all Business Units' (BUs) to collate and analyze monthly data for performance trend analysis and prioritize quarterly governance action plans
• Working together with BUs' on external audits, Request For Change (RFC), quality risk assessment, to identify continuous improvement areas, with aim to promote food safety culture within the organization 
• Act as leader for GTQM Resource Database
• Maintain and update resource documents for Group TQM and BUs as per Requirements. Handle user access requests and maintain approval matrices.
• GTQM Document Maintenance
• Support to create Group R&D policies, guidelines, and procedures aligned with international standards.
• New / alternative vendor qualification for ingredient (RM), Packaging (PM), 
• Activities include document review, supplier liaison, technical assessment, and audits to meet F&N standards before listing on the Approved Vendor List.
• New lines / change of equipment Process Qualification PQ
• It involves sterility test plan designing and execution; cleaning and sanitation (CIP) and Hygiene verification to meet requirements, before line approval for commercial runs
  • To develop and maintain Quality Plan program for all Business Units, coordinate and engage BUs' key stakeholders for Quality Plans alignment for implementation
  • Any other assignments /projects that assigned by superior, to meet business needs

Job Requirement

• Min. Degree holder in Food Technology, Food Science or related Science / Engineering fields
• Min. 4- 5 years QA/QC working experience preferably in dairy/ beverage 
• Possess knowledge and experience in food packaging qualification, certified lead auditor are added advantages

For interested applicants, please send your updated resume to:

All candidates' information will be treated with the strictest confidence
Melissa Zhang Zhiqi (Mezzo)
R

Recruit Express Pte Ltd
99C4599

We are seeking a highly skilled Quality Management Professional to join our team. This is an exciting opportunity for an experienced individual who is passionate about quality and safety.

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

Job Scope:

• Quality Performance Dashboard: Collaborate with all Business Units to collect and analyze monthly performance data, identify trends, and prioritize quarterly governance action plans.
• Continuous Improvement: Partner with Business Units on audits, RFCs, and quality risk assessments to identify improvement areas and promote a strong food safety culture.
• GTQM Resource Database Leadership: Maintain and update TQM resource documents, manage user access, and oversee approval matrices.
• Document Management: Support creation and maintenance of R&D policies, guidelines, and procedures in line with international standards.
• Vendor Qualification: Evaluate new/alternative vendors for ingredients and packaging through document reviews, supplier liaison, technical assessments, and audits to meet quality standards.
• Process Qualification: Plan and execute sterility tests, cleaning, sanitation, and hygiene verification for new or modified production lines before commercial approval.
• Quality Plan Development: Develop and maintain quality plans for all Business Units, ensuring alignment and implementation across stakeholders.
• Additional Projects: Undertake other assignments/projects as assigned to meet business needs.

Job Requirements:

• Min. Degree in Food Technology, Food Science, or related Science/Engineering fields.
• Min. 5 years of QA/QC experience in the dairy or beverage industry.
• Willingness to travel for business.
• Knowledge in food packaging qualification; certified lead auditor qualification is an advantage.

For interested applicants, please send your updated resume to:

All candidates' information will be treated with the strictest confidence

Melissa Zhang Zhiqi (Mezzo)

R

Recruit Express Pte Ltd

99C4599

Buona Vista

Salary:Up to $6,000 / month

Mon–Fri, 8:30am–5:30pm

Key Responsibilities:

Audits & Compliance – Plan, conduct, and manage internal/external/supplier audits in line with ISO 9001, ISO 19011 & IATF 16949 standards.

Quality Management System (QMS) – Maintain documentation, train teams, track KPIs, and ensure compliance to QMS processes.

Customer Quality Support – Handle scorecards, PPAP documentation, product change notifications, and major claim analyses.

OEM Qualification – Coordinate customer audits, manage quality agreements, and ensure OEM compliance standards.

Continuous Improvement – Translate Voice of Customer (VoC) into actionable quality initiatives and lead problem-solving using 8D methodology.

Requirements:

Min. Bachelor's Degree in Engineering or Quality Management

Minimum 5 years' experience in automotive / electronics quality

Certified / trained in ISO 9001, ISO 19011 & IATF 16949

Strong communicator with excellent stakeholder management skills

Familiar with automotive core tools (APQP, FMEA, PPAP, MSA, SPC)

Six Sigma or statistical analysis skills a plus

Interested candidates, do submit your resume to or telegram @alexgohhl

Alex Goh Hock Leong

(CEI.No: R l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)

Location: Tuas

Working Hours: Monday to Friday, 8:00 AM – 5:15 PM

Salary: Up to SGD 5,000/month + Variable Bonus

1. Group Quality Performance Dashboard

• Collaborate with all Business Units to collect and analyze monthly quality data.
• Conduct performance trend analysis and develop quarterly governance action plans.

2. Continuous Improvement

• Partner with BUs on external audits, Requests for Change (RFC), and quality risk assessments.
• Identify improvement opportunities and foster a strong food safety and quality culture.

3. GTQM Resource Database Management

• Maintain and update Group TQM and BU resource documents.
• Manage user access requests and approval matrices in accordance with the requirements.

4. Document Maintenance

• Support the creation and upkeep of Group R&D policies, guidelines, and procedures.
• Ensure alignment with international standards and corporate requirements.

5. Vendor Qualification

• Assess and qualify new or alternative suppliers for raw and packaging materials.
• Conduct document reviews, supplier liaison, technical evaluations, and audits.

6. Process Qualification (PQ)

• Design and execute sterility test plans, CIP (clean-in-place) and hygiene verification protocols.
• Approve production lines for commercial runs upon successful qualification.

7. Quality Plan Development

• Develop, maintain, and align Quality Plans across all Business Units.
• Ensure consistency and compliance with quality and safety standards.

8. Other Assignments

• Undertake additional projects or assignments as required to support business objectives.

• Min. Degree in Food Technology, Food Science, or a related discipline.
• Min 5 years of QA/QC experience in the dairy or beverage industry.
• Willingness to travel for business when required
• Knowledge and experience in food packaging qualification and Lead Auditor certification will be advantageous.

If interested, please email me at or telegram @kellynlytan

Kellyn Fullviana (Kellyn Chen)

(CEI.No: R l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599

Quality Management System:

· Facilitate the organization to act according to the processes described in the respective parts of the Quality Management System

· Participate in management reviews, report, and analyze key performance indicators

· Organize and conduct trainings for the local organization and sales teams

· Manage process document control and ensure up-to-date documentation

· Develop and implement contingency plans to mitigate risks

· Responsible for Audit Management Software (CAQ)

Customer Requirements:

· Evaluate and manage customer-specific requirements, provide documentation if needed

· Collect and evaluate customer scorecards. Drive and monitor improvement actions if required.

· Support product change notifications (Global PCN and Local PCN) and customer special requirements.

· Attend customer quality training

· Ensure correct PPAP documentation/submission (main responsibility plants)

· Analyze and report on major claim issues

· Maintain IMDS/CAMDS databases and manage shelf-life statements

Requirements

· Minimum Bachelor's degree in a relevant field (e.g., Quality Management, Engineering - preferably in mechanical engineering, process engineering or equivalent)

· 5+ years' experience in automotive / electronics quality field

· Completed auditor training of applicable QM standards (e.g., ISO 9001, ISO 19011 and IATF 16949)

· Advanced knowledge of applicable QM standards (e.g., ISO 9001, ISO 19011 and IATF 16949) and automotive core tools (APQP, FMEA, PPAP, MSA and SPC)

Interested candidates please send in your resume to:

Topaz Liang Huimin (CEI No. R ), email to:

EA License No: 99C4599

3 weeks ago Be among the first 25 applicants
Key Responsibilities
Develop, implement, and maintain the Quality Management System (QMS) in compliance with ISO 13485, GDPMDS, and other applicable regulations.
Ensure compliance with local and international regulatory requirements, including HSA regulations for IVD devices in Singapore.
Manage documentation processes, including SOPs, work instructions, and records, to ensure accuracy and compliance.
Prepare for and participate in internal and external audits, including regulatory inspections and customer audits.
Conduct training sessions for employees on quality policies, regulatory updates, and best practices in quality management.
Assist in risk assessment and mitigation activities related to product quality and regulatory compliance.
Investigate non-conformances, implement corrective and preventive actions (CAPA), and monitor their effectiveness.
Support supplier audits and evaluations to ensure adherence to quality standards.
Identify opportunities for process improvements and work with teams to enhance efficiency and effectiveness.
Requirements
Bachelor's degree in Life Sciences, Biotechnology, Biomedical Engineering, or a related field.
Minimum of 2 years of experience in quality management, regulatory affairs, or related roles within the medical device or IVD industry.
Familiarity with ISO 13485, GDPMDS, EU IVDR, FDA QSR, and Singapore's HSA regulations.
Strong understanding of quality management principles and regulatory requirements.
Excellent organizational and documentation skills.
Strong analytical and problem-solving skills.
Effective communication and teamwork abilities.
Ability to work independently and manage multiple tasks efficiently.
Certifications (Preferred): ISO 13485 Lead Auditor or other relevant quality certifications.
#J-18808-Ljbffr

Job Responsibilities:

1. Develop, implement, and maintain the Quality Management System (QMS) in compliance with ISO 13485, GDPMDS, and other applicable regulations.

2. Ensure compliance with local and international regulatory requirements, including HSA (Health Sciences Authority) regulations for IVD devices in Singapore.

3. Manage documentation processes, including SOPs, work instructions, and records, to ensure accuracy and compliance.

4. Prepare for and participate in internal and external audits, including regulatory inspections and customer audits.

5. Conduct training sessions for employees on quality policies, regulatory updates, and best practices in quality management.

6. Assist in risk assessment and mitigation activities related to product quality and regulatory compliance.

7. Investigate non-conformances, implement corrective and preventive actions (CAPA), and monitor their effectiveness.

8. Support supplier audits and evaluations to ensure adherence to quality standards.

9. Identify opportunities for process improvements and work with teams to enhance efficiency and effectiveness.

Job Requirements

1. Bachelor’s degree in Life Sciences, Biotechnology, Biomedical Engineering, or a related field.

2. Minimum of 2 years of experience in quality management or related roles within the medical device or IVD industry.

3. Familiarity with ISO 13485, GDPMDS, EU IVDR, FDA QSR, and Singapore’s HSA regulations.

4. Skills:

I. Strong understanding of quality management principles and regulatory requirements.

II. Excellent organizational and documentation skills.

III. Strong analytical and problem-solving skills.

IV. Effective communication and teamwork abilities.

VI. Ability to work independently and manage multiple tasks efficiently.

5. Certifications (Preferred): ISO 13485 Lead Auditor or other relevant quality certifications.