Total 1,035 quality control manager job vacancies in Quality Assurance / Control category in The Philippines

Job Responsibilities:

• Handle customer quality claims and drive effective Corrective & Preventive Actions, including verifying action effectiveness and supporting cross‑site closure.

• Lead or participate in MRB to ensure only conforming products are shipped.

• Maintain SAP/QM systems, including Quality Notifications.

• Conduct quality‑related trainings (e.g., QMS, FMEA, SPC) and support implementation of quality tools such as FMEA, QFD, SPC and Edit Notes.

• Prepare and report quality data, including process/product capability and Cpk monitoring to meet internal and customer requirements.

• Work with relevant departments to ensure accuracy of CofC and compliance with customer requirements.

• Perform internal audits, support customer audits, and monitor quality performance against goals.

• Contribute to continuous improvement initiatives and support documentation such as procedures, training materials, and SPC manuals.

• Perform other ad‑hoc assignments as assigned from time to time.

Job Requirements:

Degree in Engineering, B. Sc (Physics or Chemistry)

2 – 5 years in QA, experience in implementation of SPC and QA control measures in semiconductor environment.

Strong in statistical techniques and use of statistical tools.

Critical thinking skills

Knowledge in use of quality tools – FMEA, SPC, DOE, PPAP, APQP, MSA

Basic knowledge of quality management systems (ISO 9001, IATF 16949), with audit experience advantage

High level of PC skills – excel, word & powerpoint

Experience in handling non-conformance(claim, MRB), root cause analysis and SPC is a MUST

Fresh graduate are welcome to apply

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

Job:

• Check and approve repackaging requirements of products and materials according to Client and regulatory requirement. Full review of batch records to ensure compliance per the repackaging instruction and GMP standards.
• Verify correct execution of repackaging activity against approved / updated repackaging instructions.
• Perform required quality checks and create quality inspection lots in SAP.
• Record Inspection Results and perform Usage Decision and stock posting. Issue necessary documents to facilitate release.
• Authorize to stop any repackaging activities when deviation is observed, when necessary.
• Perform other QA release (e.g. inbound QA release, cold chain temperature release, outbound release) if required.
• Perform back-up and other duties as assigned.
• Perform QA sampling, inspection and release of incoming packaging materials.
• Filing and maintenance of packaging material specifications.
• Updating of logs and trackers as required.
• Ensure general cleanliness and hygienic conditions of each workstation.
• Ensure compliance to ISO procedures, GxP and all regulatory requirements.
• Work closely with inter-departments personnel to ensure quality is maintained throughout the organization.
• Conduct internal audits, training and general communication to achieve and sustain a high level of quality performance throughout the organization so as to properly support the business and regulatory (ISO, GMP, GSDP) requirements in the most efficient manner.
• Support QA administrative functions when necessary.
• Participate in any ad hoc projects as assigned by management from time to time.

Requirements:

• Diploma in any related discipline or good knowledge in Quality / Compliance areas in manufacturing can be considered.
• Preferably relevant experience in Quality Control / Quality Assurance works in manufacturing / production / assembly / Operation environment.
• Knowledge in ISO, GMP and GSDP preferred.
• Quality-oriented.
• Demonstrate integrity and strong work ethic.
• Good team player with good verbal and written communication skills in English.
• Meticulous with good attention to details.
• Must be able to work in a fast-paced environment.
• Willing to work in cold room environment to perform cold chain QA release.
• Willing to work flexible and extended hours on weekday, weekend and public holidays to support operations and depending on the exigencies of service.
• Able to start immediately.

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 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

Responsibilities:

• Maintain accurate and up-to-date ISO 9001, ISO 14001, and ISO 13485 documentation, including Quality Manuals, procedures, work instructions, and records, to ensure system compliance and management review readiness.
• Plan, coordinate, and conduct internal and external audits to ensure organizational readiness for third-party certification, management reviews, and customer audits.
• Collaborate with internal stakeholders to support and participate in customer and supplier audits to ensure compliance requirements are met.
• Review audit findings, develop corrective action plans, and drive continuous improvement initiatives.
• Generate and review supplier quality performance reports, work closely with suppliers to resolve non-conformances, and promote continuous improvement.
• Issue, monitor, and follow up on Supplier Corrective Action Requests (SCAR), ensuring effectiveness and timely closure.
• Support qualification and onboarding of new suppliers to maintain a robust pipeline aligned with production requirements.
• Manage calibration schedules and preventive maintenance programs for equipment to ensure operational reliability and compliance.
• Address quality issues arising from production and customer feedback by working closely with production teams to implement corrective actions and resolve customer complaints with proper documentation.
• Ensure timely closure of Corrective and Preventive Actions (CAPA), non-conformance reports, and customer complaints, and publish quality performance reports.
• Lead Material Review Board (MRB) meetings with cross-functional teams to perform root cause analysis, implement corrective actions, and verify effectiveness.
• Supervise and lead QC inspectors to ensure parts inspection compliance with engineering drawings and quality standards.

Qualifications:

• Diploma in Quality Management, Engineering, Manufacturing, or a related field.
• Min 3 years of relevant experience in quality or manufacturing environments, with exposure to audits and documentation.
• Basic understanding of supplier management and quality coordination.
• Familiarity with commonly used quality management standards (e.g. ISO systems).
• Working knowledge of quality tools and process control methods.

We regret only shortlisted candidates will be contacted. All applications will be handled confidentially. By submitting your application, you agree to the collection, use, retention, and disclosure of your personal information to prospective employers.

Wecruit Pte Ltd

EA License No: 20C0270

EA Personnel: Nyon Hock Sen (Aden)

EA Personnel Reg No: R24124070

• Drive quality excellence in a growing medical technology environment
• Lead process improvements and influence cross‑functional decisions

About Our Client

Our client is a global medical technology manufacturer known for delivering high‑precision products used in healthcare settings worldwide. They are expanding their quality function and seeking experienced professionals who can elevate operational standards and support long‑term growth.

Job Description

• Oversee quality management systems and ensure strong regulatory compliance across manufacturing operations
• Develop, implement, and maintain quality assurance procedures aligned with FDA, ISO 13485, and other relevant standards
• Support both internal and external audits, ensuring all documentation and processes meet compliance requirements
• Monitor production processes to identify quality gaps and resolve issues proactively
• Conduct product investigations, lead root‑cause analysis, and implement effective corrective and preventive actions (CAPA)
• Support new product transfers by ensuring quality requirements are built into early development and production phases
• Lead validation activities including IQ, OQ, PQ, process validation, and test method validation
• Drive continuous improvement initiatives to enhance product quality and operational efficiency
• Manage customer feedback and complaints, ensuring timely resolution of quality‑related concerns
• Communicate any necessary process changes or updates to customers and internal teams
• Provide technical guidance and quality‑related support to internal and external stakeholders
• Maintain accurate quality documentation, inspection records, and monthly/annual quality reports
• Train manufacturing personnel on quality procedures, standards, and best practices
• Promote a strong culture of compliance, quality ownership, and continuous improvement

The Successful Applicant

• A degree in Engineering or Science, Diploma holders with extensive experience
• Quality experience, preferably in medical devices
• Strong knowledge of FDA regulations and ISO 13485
• Strong analytical and problem‑solving skills with a structured approach to troubleshooting
• Ability to collaborate effectively with cross‑functional teams and communicate clearly
• Experience working in cleanroom or controlled environments is an advantage

What's on Offer

• Opportunity to drive quality excellence in a regulated and fast‑growing sector
• Exposure to new product transfer projects and key validation activities
• Collaborative work culture and cross‑functional project involvement
• Career growth in an established, innovation‑driven medical technology organisation

Contact

Vanessa Chan (Lic No: R2197577/ EA no: 18S9099)

Quote job ref

JN-032026-6959737

Phone number

+65 6643 9742

Michael Page International Pte Ltd | Registration No. 199804751N   

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Mechanical / Precision Engineering or relevant
• Min 5 years of experience in Oil & Gas industry with experience in Supplier Quality
• Oversea travelling is required

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

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Precision Engineering or relevant
• Min 5 years of experience in Metal Machining industry with experience in QC/ Audit
• Oversea travelling is required

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

Quality Assurance Controller (Precision Engineering)

Employment Requirements / Eligibility

• Open to Singapore Citizens, Permanent Residents, and foreign applicants (Work Permit Holders)

• 3-5 years of relevant QA/QC experience in precision engineering or manufacturing environment

• Familiar with inspection tools (e.g. vernier calipers, micrometers, height gauges; CMM is an advantage)

• Able to read and interpret engineering drawings and specifications

• Basic knowledge of ISO 9001 quality management systems and documentation

• Meticulous, hands-on, and able to work independently

• Basic computer skills (e.g. MS Excel for reporting and documentation in English)

• Good communication skills to coordinate with production team

Preferred Attributes

• Experience in handling customer audits and quality issues

• Knowledge of root cause analysis and corrective/preventive actions (CAPA)

• Able to start work within short notice is an advantage

Working Hours

• 5.5-day work week

• Monday to Friday: 8:30 AM – 5:30 PM

• Saturday: 09:00 AM – 13:00 PM

质量保证管控员（精密工程）

聘用要求 / 资格条件

• 欢迎新加坡公民、永久居民及外籍 (普通工作准证）申请者申请

• 具备2–4年精密工程或制造业相关质量保证/质量控制（QA/QC）经验

• 熟悉检测工具（如游标卡尺、千分尺、高度规；具备三坐标测量机 CMM 经验者优先）

• 能够阅读和理解工程图纸及技术规格

• 具备 ISO 9001 质量管理体系及相关文件的基本知识

• 工作细心、动手能力强，能够在小型团队环境中独立工作

• 具备基本电脑操作能力（如使用英文版 MS Excel 进行报告及记录）

• 具备良好的沟通能力，能够与生产团队协调

优先考虑条件

• 具备处理客户审核及质量问题的经验

• 熟悉根本原因分析及纠正/预防措施（CAPA）

• 能够在短时间内到岗者优先

工作时间

• 每周工作 5.5 天，

周一至周五：上午 8:30 至下午 5:30，周六：上午 9:00 至下午 1:00

Responsibilities:

• Work with the R&D team on quality planning from the early stage of product development.
• Manage overall quality activities across the Business Unit, including product development, customer requirements, sales support, inventory, and product transition.
• Set quality goals for the BU and support departments in achieving them.
• Build and improve quality systems, project development processes, and IPD processes.
• Identify project risks, monitor product quality performance, and drive corrective and preventive actions.
• Handle customer complaints, major quality issues, and product quality problems, ensuring proper follow-up and closure.
• Monitor project process compliance and lead technical review assessments.
• Use data analysis to identify problems and improve processes continuously.
• Organize stage review meetings during the R&D phase.
• Conduct process training and strengthen team quality capabilities.
• Promote quality awareness and a strong quality culture across the BU.

Requirements:

• Bachelor's degree or above, with at least 5 years of experience in quality-related roles, including at least 3 years in a managerial position. Experience in R&D quality is preferred.
• At least 5 years of experience in quality-related work, preferably in R&D quality.
• Familiar with ISO9001 and quality tools such as 8D, QC tools, APQP, FMEA, Six Sigma, and QCC.
• Good communication, interpersonal, and problem-solving skills.
• Able to work well under pressure.
• Familiar with hardware, software, FPGA, and mechanical development processes.
• Knowledge of IPD processes; experience in setting up or implementing IPD is an advantage.

We regret that only shortlisted candidates will be notified.

GMPTechnologies (S) Pte Ltd | EA Licence 11C3793 | EA Personnel: Novita Widjaja |Registration No: R22105960

Job Summary:​​

We are seeking a motivated and detail-oriented female individual to join our team as a Quality Document Controller. This is an excellent opportunity for a candidate with document control experiences and a commitment to maintaining high standards of quality documentation system. The primary responsibility of this role is to provide administrative support in the tracking, controlling, distribution, and archiving of quality management system documents and applications. The ideal candidate should be able to work effectively under scheduled timelines in a dynamic environment.

​Key Responsibilities:​​

· Responsible for handling quality document control cycle, including collecting, numbering, logging, tracking, distributing, archiving of quality documents (e.g., procedures, RFIs, ITPs, quality reports) in both electronic and hard copy formats, from subcontractors, client, third party and company internal sections.

· Maintain master summary lists of controlled quality documents to ensure accuracy and up-to-date status.

· Work with Novade APP (On-line RFI management software; training will be provided), PTS (On-line document transmittal App), and iSEPCO3 (APP as a Cloud Drive).

· Provide clerical support to the Quality team, including data entry, Collecting, photocopying, and scanning.

· Preparation of quality meeting minutes as required.

· Learn and adhere to company quality policies and Document Control procedures.

· Collaborate with team members to ensure the efficiency and integrity of the document management system.

​Qualifications and Requirements:​​

· Diploma or higher qualification in engineering. A background in ​Civil Engineering, mechanical engineering, Information Technology, or other construction related field is considered a strong advantage.​​

· Proficient in the use of Microsoft Office applications (Word, Excel, PowerPoint, Outlook) and PDF Apps.

· Meticulous attention to detail and a high level of accuracy in work.

· Good organizational and time management skills.

· Ability to work effectively both independently and as part of a team.

· Must be able to adapt and perform under a certain degree of work pressure.

​Working Conditions:​​

· ​Site office-based.

· Standard Working Hours:​​ 5-day work per week, 9 hours per day (including break), 44 hours per week.

​

• Coordinate and monitor construction activities to ensure work progresses according to the project schedule.
• Plan and track site works in line with the master programme and detailed work schedules.
• Liaise with the Professional Engineer on matters relating to temporary works and technical requirements.
• Work closely with consultants and subcontractors to resolve technical issues and ensure smooth site operations.
• Conduct site inspections, maintain construction quality standards, and address engineering issues promptly.

Requirements:

• Diploma in Civil Engineering or equivalent
• At least 5 years of relevant experience in construction projects with LTA infrastructure works.
• Experience with diaphragm wall (D-wall), bored piling, or tunnelling works.
• Able to coordinate site teams, subcontractors, and consultants effectively.
• Strong problem-solving skills and ability to manage site operations in a structured manner.

If you are keen to apply for the position, kindly email your detailed resume in MS Word to hr@recruit-expert.com

Please note that only shortlisted candidates will be notified.

For more job opportunities, please visit our website at www.recruit-expert.com

EA Licence: 19C9701

Registration: R21100996

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Precision Engineering or relevant
• Min 5 years of experience in Metal Machining industry with experience in QC/ Audit
• Extensive travelling is required

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

Jobscope:

• Set and monitor R&D quality targets.
• Support teams to achieve quality goals and improve performance.
• Manage quality activities across product development and lifecycle.
• Investigate quality issues, handle customer complaints, and implement corrective actions (8D).
• Support quality planning and control during new product development (IPD process).
• Conduct quality reviews and track improvement actions.
• Improve quality systems, processes, and standards.
• Analyze data to identify issues and drive continuous improvement.
• Promote quality culture, training, and improvement activities.

Requirements:

• Bachelor’s degree or above, with at least 5 years of experience in quality-related roles.
• Experience in R&D quality is preferred.
• Familiar with ISO9001and quality tools (8D, FMEA, APQP, Six Sigma, QC tools).
• Strong communication and problem-solving skills.
• Able to work under pressure.
• Knowledge of hardware, software, or engineering development processes.
• Familiar with IPD process (preferred).

To apply, please visit www.gmprecruit.com

To learn more about this opportunity, please contact Fiona Koh | fiona.koh@gmprecruit.com

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh| Registration No: R11092398

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By submitting your application for this position, you consent to the collection, use, and disclosure of your personal data by GMP Recruitment Services (S) Pte Ltd and its recruitment partners, including Employment and Employability Institute Pte Ltd, for the purpose of i) employment facilitation and ii) data and statistical analysis. You may find out more information on the PDPA policies at GMP Recruitment Services (S) Pte Ltd’s website and [https://www.e2i.com.sg/pdpa/]