Total 860 quality control manager job vacancies in Quality Assurance / Control category in Hong Kong

We are seeking a Quality Technician to support our expanding manufacturing site in Singapore. This role is responsible for incoming quality and sampling inspections for critical assemblies, ensuring compliance with quality standards and specifications.

Key responsibilities:

• Perform visual, dimensional, and functional inspections on optical components, mechanical fabricated parts, and cables.
• Conduct First Article Inspection (FAI) for optics and related assemblies.
• Follow established sampling plans, inspection procedures and quality standards.
• Maintain accurate and complete inspection records, logs and reports.
• Assist engineers in the investigation of failures and defects in parts and components.
• Identify quality issues and recommend improvements to enhance inspection effectiveness.
• Support First Pass Yield improvement initiatives and assist in identifying root causes for manufacturing low Yield / quality issues.
• Apply continuous improvement concepts and techniques in daily work activities.
• Performs other duties as assigned by supervisor based on business needs.

Requirements:

• Minimum of three (3) years of experience in Quality inspection, Quality tech or related roles.
• ITE / Diploma or higher in engineering or equivalent.
• Able to read and interpret technical drawings, specifications and manufacturing documents.
• Proficiency in using measurement tools (calipers, micrometers, CMM, etc.).
• Familiarity with optics metrology and laser testing will be an advantage.
• Strong attention to detail and good documentation skills.

Responsibilities

• Prepare and maintain Quality Management Systems procedures.
• Compliance with Customers’ specifications and procedures
• Prepare process inspection plan.
• Plan and implement gauges and equipment calibration systems.
• Conduct QMS audit including at supplier sites.
• Conduct training on QMS and GD&T
• Supervise First Article, Incoming, In-Process and Final inspections and documentations.
• Conduct relentless root cause analysis (RRCA) into production problems.
• Lead in quality improvement projects
• Implement Statistical Process Control (SPC) on production processes.
• Participate in cost reduction and environment, health & safety (EHS) initiatives.
• Co-ordinate good housing keeping (5S) activities

Requirements

• Technical education in Production / Mechanical Engineering, preferably Diplomas level.
• Minimum 2 years working experience in precision manufacturing environment.
• Good knowledge in Geometric Dimensioning and Tolerancing (GD&T).
• Good application of the RRCA tools eg 5 why, Cause and Effect diagram, 8D, DOE.
• Well versed in AS9100 QMS systems.
• Experience in conducting QMS audits.
• Knowledge in Statistical Process Control
• Proficiency in MS Office applications (eg Word, Excel, Power point).
• Good interpersonal and communication skills, both oral and written.
• Good initiative, a team player and motivated individual.
• Customer focus and pro-active in working with business partners.

Salary: Up to 4200
Location: Chai Chee (moving to Tai Seng in Q4)

Responsibilities:

• Manage incidents, feedback & complaints, ensure timely resolution
• Drive quality improvement, patient safety & risk management initiatives
• Support certifications (e.g. DPTM, Bizsafe) and regulatory compliance
• Review workflows, policies & procedures for quality standards
• Track quality indicators, prepare reports for management
• Maintain documentation control & liaise with MOH/AIC/MOM

Requirements:

• Min. Diploma
• Min. 3 years in healthcare quality / patient safety
• Experience in QA/QI, risk management or data protection
• Knowledge in RCA / FMEA is a plus
• Proficient in MS Office (Excel, PowerPoint)
• Familiar with healthcare regulations

If interested, please email me at alexgoh@recruitexpress.com.sg or telegram @alexgohhl

➖

Alex Goh Hock Leong

(CEI.No: R1763413 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)

HAID BIOTECHNOLOGY INDUSTRY (SINGAPORE) PTE. LTD. is seeking a meticulous and experienced Quality Control Inspector to join our new startup team in Singapore. The successful candidate will play a vital role in ensuring our products meet established standards of quality, reliability, and performance by monitoring and auditing all phases of the production process.

品管Quality Control Inspector

一、来料检验职责Incoming Material Inspection

按照检验标准对供应商来料进行外观、细度、性能等检查。

Perform inspections on supplier materials according to established standards, including appearance, fineness, and performance.

对不合格物料进行标识、隔离、记录并及时反馈采购与供应商。

Identify, isolate, and record non-conforming materials, providing timely feedback to Procurement and suppliers.

统计来料不良率，参与供应商质量评估与改善。

Calculate and track the incoming defect rate, and participate in supplier quality evaluation and improvement initiatives.

对检验工具（卡尺、振筛等）进行日常保养与校验状态确认。

Conduct daily maintenance and verify the calibration status of inspection tools (e.g., calipers, vibrating sieves).

二、制程检验职责 In-Process Inspection

按检验计划对生产过程进行首件、巡检、抽检。

Execute first-article, patrol, and sampling inspections based on the inspection plan for the production process.

监督生产按作业指导书、工艺流程执行，发现异常及时制止并上报。

Monitor production to ensure adherence to Work Instructions and process workflows; halt and report any irregularities immediately.

跟踪制程问题的改善过程，确认改善措施的有效性。

Follow up on the correction of process issues and verify the effectiveness of improvement measures.

记录并统计制程不良数据，为工艺优化提供依据。

Record and compile data on in-process defects to provide basis for process optimization.

对关键工序的关键参数进行监控，确保过程稳定。

Monitor key parameters in critical processes to ensure operational stability.

三、成品检验职责Final Product Inspection

按出货标准对成品进行外观、性能等检查。

Inspect finished products for appearance and performance against shipping standards.

对不合格品进行判定、隔离及处理（返工/报废）。

Judge, isolate, and disposition non-conforming products (for rework or scrap).

确保所有出货批次具备完整的检验记录。

Ensure complete inspection records are available for all outgoing batches.

与生产、仓库沟通，避免不良品流入客户。

Liaise with Production and Warehouse to prevent defective products from reaching the customer.

四、质量异常处理 Quality Exception Handling

发现质量异常及时报告并推动异常分析。

Report quality anomalies promptly and drive root cause analysis.

跟进纠正预防措施的落实与验证。

Follow up on the implementation and verification of corrective and preventive actions.

协助组织质量会议，推动跨部门改善。

Assist in organizing quality meetings and driving cross-departmental improvements.

五、质量文件与记录维护 Quality Documentation & Record Maintenance

负责检验记录、检验报告的填写、整理与归档。

Complete, organize, and archive all inspection records and reports.

维护检验标准、作业指导书等质量相关文件。

Maintain quality-related documents such as inspection standards and work instructions.

协助编制和更新检验规范与SOP。

Assist in the compilation and updating of inspection specifications and SOPs.

六、设备与环境管理 Equipment & Environment Management

负责使用的检验设备的日常点检与维护。

Perform daily spot checks and maintenance on assigned inspection equipment.

确保检验区域的 6S 管理符合要求。

Ensure the 6S management standards are met in the inspection area.

协助设备校准与外部计量机构联系。

Assist with equipment calibration and liaise with external metrology agencies.

七、培训与沟通Training & Communication

对新员工进行质量意识、检验标准的培训。

Conduct training on quality awareness and inspection standards for new employees.

与生产、购销等部门沟通质量问题与改善计划。

Communicate quality issues and improvement plans with Production, Purchasing, and Sales departments.

参与客户投诉问题的调查与回复资料准备。

Participate in the investigation of customer complaints and assist in preparing response reports.

Requirements:

· Diploma or higher in Food Science, Biotechnology, Chemistry, Pharmaceutical, or a related field.

· At least 3 years of working experience in a similar role with proven experience.

· Good command of both verbal and written English and Mandarin to liaise with Mandarin-speaking business associates.

· Able to start immediately or with a short notice period preferred.

· Only Singaporeans/PRs may apply.

Job Summary
We are seeking a dedicated and certified Pest Control Technician to join our team. The successful candidate will be responsible for implementing vector control measures to prevent and manage vector-borne diseases in various environments.

Key Responsibilities

• Conduct site inspections and carry out vector surveillance.
• Apply appropriate vector control methods including fogging, larviciding, and residual spraying.
• Maintain records of control activities and findings.
• Adhere to safety protocols and standard operating procedures.
• Report any environmental issues or potential vector breeding grounds.
• Coordinate with team members and supervisors to ensure effective execution of control programs.
  
  Requirements
• Candidates with no experience are welcome
• Workplace literacy and numeracy proficiency in reading, listening, and numeracy.
• Preferably with driving license.
• Must be able to work in various outdoor environments.
• Minimum N Level education or equivalent.
  
  

Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Review and verify executed component batch records for accuracy and compliance with GMP/GDP requirements.
• Perform timely release of raw materials, buffers, and media in SAP in accordance with approved specifications and procedures.
• Support Electronic Batch Record (EBR) review activities for production operations.
• Participate in Quality on the Floor (QOTF), GEMBA walks, and provide real-time guidance to operations personnel on documentation practices and GMP compliance.
• Assist in identifying and escalating documentation or process deviations during record review or shopfloor interactions.
• Collaborate cross-functionally with Production, QC, and Material Management teams to resolve discrepancies or issues related to material release and batch documentation.
• Support QA team in continuous improvement initiatives and data gathering for metrics and trend analysis.
• Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Requirements:

• Diploma in Biomedical Engineering, Biotechnology, Life Science or equivalent
• 1 - 2 years of Quality Assurance/ Manufacturing within a GMP-regulated biologics or pharmaceutical environment.
• Familiarity with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
• Exposure to SAP and Veeva Vault would be preferred
• Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
• Excellent communication skills, both written and verbal, in English

Job Description:

• In charge of performing quality assurance functions with regard to the product, process and maintain quality management system while ensuring compliance with all customers’ requirements
• Responsible for reviewing and revising quality procedures and quality control instructions
• Liaise with customers / vendors / suppliers on non-conformance activities, perform root cause analysis and determine effective corrective actions to reduce or eliminate the cost of poor quality
• In charge of performing internal audits to evaluate quality system, products, and processes
• In charge of performing vendors’ and on-site audits as required
• Drive down monthly Cost of Poor Quality/ scrap

Requirements:

• Degree in Mechanical / Aeronautical Engineering / other relevant disciplines
• Minimum 5 years of experience in QMS, AS9100, NADCAP

To submit your application, please apply online to apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd

EA License No: 17C8900

Position Summary

This position play a critical role in driving compliance and quality programs for Healthcare Transportation & Facilities and supporting the Healthcare Quality Management System to ensure processes and systems are compliant with regional and local regulations and customer requirements.

Job Scope

1. Quality Policies & Procedures: Determine, implement & promote policies and procedures for company’s Network and facilities (hubs & stations) to ensure compliance to standards such as GDP, GCP and others.

2. Quality Assessment & Standards: Write & review SOPs and Work Instructions for transportation & fulfilment solutions pertaining to the healthcare industry.

3. Compliance & Quality Program Management: Implement compliance and quality programs to support local Quality teams to ensure they are kept up-to-date and prepared.

4. CAPA Process Management: Lead in process creation and review of documentation on the implementation and responses to corrective and preventive actions (CAPAs) and monitor action progress until closure.

5. Healthcare Quality Management System: Develop, implement & support the system and processes, develop corresponding training programs, and acts as Super User for eQMS system.

6. Internal Audit Programs: Design & implement robust internal audit processes to ensure readiness of various functions & processes when meeting regulatory agencies & customer audits.

7. Certification Audits: Lead various certification audits with relevant regulatory agencies and certification providers across the region.

8. Operations & Customer Audit Programs: Lead & prepare for regular audit programs / random checks / regulatory activities to achieve successful audit outcomes and proper post audit follow up actions.

9. Healthcare Customer Liaison: Liaise with customers to understand quality requirements / issues / underlying concerns to advise on the way forward, provide advice based on interpretations as applicable to 3PL and resolve issues via conducting root cause analysis.

10. Healthcare Quality Feedback: Liaise, consolidate feedback from different functions to update and prepare final copy for Quality Questionnaires, Agreements and RFQ Proposals for customers.

11. Validation Programs: Lead the validation of transportation lanes and critical equipment like cold chain facilities, and packaging systems.

12. Depot Support: Provide secondary / backup support to healthcare specialists for market depots.

Requirements :

1. Hold local pharmacist license

2. Have at least 5 -7 years of relevant experience in warehouse, quality + QMS for pharmaceutical / healthcare industry in quality related role

3. Experience working in warehouse is desire

4. Have competencies in quality assurance / regulatory affairs, customer relationship management and root cause analysis

5. Have working experience ensuring compliance in accordance to Goods Manufacturing Practise cGMP,)/, Good Clinical Practises cGCP, Goods Distribution Practice (GDP) & ISO13485 for Medical Devices,

6. Experience in local certifications in a warehouse and transportation business.

7. IATA CEIV certification knowledge would be at advantage but not necessary.

8. Experience in conducting external and internal audits for regions

9. Must hold at least Bachelor’s degree in Pharmacy from a reputable local institute in Singapore.

10. Occasionally travel is required to sites and region warehouses.

Competency

1. Accuracy & attention to detail which is crucial to proper compliance to regulatory and standards

2. Problem-solving skills to support customer issue resolution

3. Planning & organization skills to ensure proper audit programs are managed effectively

4. Communication skills to facilitate engagements with customer and regulatory agencies

5. Project management capabilities and familiarity with Process Mapping, Six Sigma, Lean Methodology, Agile or Design Thinking

6. Apply data-driven decision making with the use of data analytics and visualization tools like Power BI and competency in Microsoft Office applications like Excel, Word, and PowerPoint

Working hours:

Mon to Fri 9am-6pm

Job Summary

Responsible for management of Asia Quality System, Policies, Programs and Initiatives. Part of the Global Quality Team to maintain global quality system and drive global initiative.

Role and Responsibilities

Quality System

1. Develop, implement and maintain QMS documentation to maintain compliance with applicable standards such as ISO 9001, ISO 13485 or GMP

2. Monitor regulatory changes and update the QMS accordingly

3. Conduct internal audits and support external audits (external auditing bodies, suppliers and customers)

4. Analyze quality data and metrics to identify trends and areas for improvement

5. Collaborate with cross functional teams to ensure that the quality standards are integrated into processes

Management Representative

1. Reports on QMS performance to top management and recommend improvement

2. Point of contact for certification bodies

3. Lead Management Review and follow up action items

Product Quality Management

1. Analyze and capture recurring product complaints, collaborate with Operation and Technology teams to address compound specified failures

2. Operational Quality Support. To facilitate continuous improvement initiatives, by providing on the floor support through use of quality tools and coaching teams to build ownership and proactive engagement with quality processes.

Customer Complaints Management

1. CCAR Manager. Manage the customer complaints handling process to ensure that all complaints are logged with right information for investigation till auditing process

2. Collaborate with cross functional team during the investigation, resolution and communication of customer complaints

3. Review interim CCAR reports to ensure that root cause is data driven and corrective action(s) address the root cause

Supplier Complaints Management

1. SCAR Manager. Approve SCAR – Supplier related complaints and defects, review and monitor the effectiveness of corrective actions

2. Collaborate with Procurement, Supplier and internal stakeholders to investigate issues and resolution

3. Collaborate with Procurement, Operation and Technology to assess risk and quality impact of raw material on finished goods

Global Quality Team Collaboration

1. Support the implementation of global quality initiatives, systems and tools

2. Ensure that local QMS aligns with global practices and corporate policies

3. Share best practices and lessons learned across global sites

Support Quality Contracts/Documentation

1. Review customer documents and quality related agreements for compliances to ensure clauses are relevant, assess the risks.

2. Response to customer request for certifications, compliance/quality related/audit documents

System

1. Conduct training for staff in Quality Procedure, Standards and Tools.

2. Lead processes identified by the Global Quality Team such as PPAP, QIR, CCAR, SCAR and Mastercontrol for the Asia Region

Requirements:

· Degree or equivalent experience in a field of study such as chemistry, business, accounting, engineering, etc.

· Certificate in Quality Engineering is preferred.

· 4-6 years of quality management experience. Junior with 1-2 experience in related field can also apply

· Demonstrates introductory understanding and ability and with guidance, applies competency in typical situations.

· Able to design quality systems to meet customer expectations and internal needs. New approaches and continuous improvement must be ongoing.

· Good experience into customer & supplier audit and able to conduct training

· Good interpersonal skills to be able to communicate and collaborate with all stakeholders and deal with situation proactively

· Occasionally overseas travel and weekly conference call is required for the role

· This position required to communicate closely with vendors in China.

Working hours:

Mon to Fri 8.30am - 5.30pm ( 1 day hybrid )

Position Overview

The IPQC Technician plays a vital role in ensuring product quality during the manufacturing process. By conducting in-process checks and monitoring production activities, this role helps prevent defects and supports compliance with company and industry standards.

Key Responsibilities

• Perform in-process inspections at various stages of production.

• Monitor and record key process parameters to ensure compliance with specifications.

• Identify and report non-conformities promptly to supervisors.

• Assist in root cause analysis and corrective actions for process deviations.

• Ensure proper documentation of inspection results in line with ISO/GMP requirements.

• Collaborate with production and engineering teams to maintain continuous quality improvement.

• Maintain and calibrate inspection tools and equipment.
  

Qualifications

• Diploma/Certificate in Engineering, Manufacturing, or Quality Assurance.

• Fresh graduates or candidates with up to 2 years of experience in quality control are welcome.

• Basic knowledge of manufacturing processes and quality standards (ISO 9001, GMP, etc.).

• Strong attention to detail and ability to follow procedures.

• Good communication and teamwork skills.

Job Description:

• In charge of performing quality assurance functions with regard to the product, process and maintain quality management system while ensuring compliance with all customers’ requirements
• Responsible for reviewing and revising quality procedures and quality control instructions
• Liaise with customers / vendors / suppliers on non-conformance activities, perform root cause analysis and determine effective corrective actions to reduce or eliminate the cost of poor quality
• In charge of performing internal audits to evaluate quality system, products, and processes
• In charge of performing vendors’ and on-site audits as required
• Drive down monthly Cost of Poor Quality/ scrap

Requirements:

• Degree in Mechanical / Aeronautical Engineering / other relevant disciplines
• Minimum 2 years of experience in Quality Management System and NADCAP

To submit your application, please apply online apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd.
EA License No: 17C8900

Job Description:

• In charge of performing quality assurance functions with regard to the product, process and maintain quality management system while ensuring compliance with all customers’ requirements
• Responsible for reviewing and revising quality procedures and quality control instructions
• Liaise with customers / vendors / suppliers on non-conformance activities, perform root cause analysis and determine effective corrective actions to reduce or eliminate the cost of poor quality
• In charge of performing internal audits to evaluate quality system, products, and processes
• In charge of performing vendors’ and on-site audits as required
• Drive down monthly Cost of Poor Quality/ scrap

Requirements:

• Degree in Mechanical / Aeronautical Engineering / other relevant disciplines
• Minimum 2 years of experience in Quality Management System and NADCAP

To submit your application, please apply online to apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd
EA License No: 17C8900