31 Six Sigma jobs in Singapore

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.

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

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

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

SingHealth Polyclinics

Job Category: Administration

Posting Date: 22 Aug 2025

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). You will provide functional team leadership and ensure that the objectives of the team's portfolios are met.

Your responsibilities include:

• Develop, analyse and implement programmes, projects, and activities relating to Quality and Safety at SHP
• Develop, plan and co-ordinate innovation and improvement initiatives, and facilitate support to improvement teams
• Represent the department in committees, workgroups, and meetings, and liaise with internal and external parties on initiatives relating to Quality and Safety
• Co-ordinate administrative support for Clinical Governance and other programmes in the SHP Quality Management Framework

Requirements:

• Bachelor's Degree in any discipline
• Relevant experience in healthcare or quality an advantage
• Good verbal and written language skills in English are expected, with fluency in other languages an advantage
• Good interpersonal skills and resourceful team leader
• Strong interest in learning and professional growth

Req ID: 4275

Kinexcs is a multidisciplinary digital health start-up at the forefront of a rapidly booming industry. It is a data-driven digital therapy platform & wearables company to enable and empower people for mobility and a better life. Kinexcs strives to enable personalised health and evidence-based recovery for musculoskeletal patients.

Website: Kinexcs

Job Summary

We are seeking an experienced professional to lead Clinical Affairs, Quality Management, and Regulatory Compliance within our organization. The role will be responsible for managing clinical evaluations, ensuring compliance with global quality standards, and overseeing regulatory submissions across international markets.

Responsibilities

1. Quality Management System (QMS) Leadership

2. Develop, implement, and maintain QMS in compliance with global standards such as ISO 13485, ISO 9001, and other relevant certifications.

3. Conduct internal and external audits, addressing non-conformities with robust corrective and preventive actions (CAPA).

4. Establish quality policies and procedures, ensuring organization-wide adherence.

5. Train employees on quality standards and foster a culture of continuous quality improvement.

6. Regulatory Affairs Compliance

7. Lead all regulatory submissions, registrations, and compliance activities for domestic and international markets.

8. Ensure alignment with regulations such as FDA, CE, MDR, and other global standards.

9. Stay updated on regulatory changes and implement required adjustments promptly.

10. Act as the primary liaison with regulatory bodies, handling inspections, certifications, and reporting.

11. Sales & Customer Success

12. Identify and qualify leads, conduct product demos, and manage the full sales cycle.

13. Maintain CRM records and collaborate with Marketing and Customer Success teams.

14. Onboard new customers, provide training, and ensure product adoption.

15. Build strong client relationships, act as a customer advocate, and address risks.

16. Gather and relay customer feedback to product and engineering teams.

17. Undertake business travel as required.

18. Clinical Affairs Management

19. Plan, coordinate, and manage clinical evaluations, including Clinical Evaluation Reports (CERs) in alignment with requirements.

20. Support the design and execution of clinical studies, including post-market clinical follow-up (PMCF) where required.

21. Collaborate with R&D, regulatory, and medical teams to collect, analyze, and report clinical data to support regulatory submissions.

22. Maintain up-to-date clinical documentation and contribute to risk management and product lifecycle planning.

• 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 (Health Sciences Authority) 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.

• 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.

• Skills:

• 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.

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.

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

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

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.

Interested candidates, do submit your resume to: OR telegram @jocelynchan

Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R