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

Responsibilities

·               Developand drive a strategic roadmap for yield improvement and defect reduction acrosscritical process modules.

·               Leadthe design and maintenance of advanced, real-time Statistical Process Control(SPC), Fault Detection and Classification (FDC), and Advanced Process Control(APC) systems to stabilize and optimize all fabrication steps.

·               Cross-contaminationmanagement to achieve balance between research and development flexibilities inintegration runsheet flow path vs process tools health and processrepeatability.

·               Smallvolume prototype protocol and product and process control plan alignment andset-up with requestor, process margin runs till demonstration of product SPCrepeatability and line defect and electrical yield.

·               Serveas the technical expert and primary quality interface for key customers,leading customer audits, addressing quality-related concerns, and drivingcustomer-specific quality improvement plans.

·               Directand oversee high-level, cross-functional root-cause analysis (RCA) andcorrective and preventive action (CAPA) teams for major process excursions,non-conformances, and field returns, utilizing methodologies like 8D or SixSigma

·               Overseethe selection, qualification, and maintenance of all in-line and off-linemetrology and defect inspection tools, ensuring measurement system accuracy(Gage R&R) and high data quality.

·               Collaboratewith Process Integration and R&D teams to define, qualify, and stabilizerobust manufacturing process windows for all new product introductions (NPI),ensuring Design for Manufacturability (DFM) principles are met.

·               Leveragelarge-scale manufacturing data (Big Data) to identify subtle process drifts,predict failures, and proactively implement controls.

·               Lead,mentor, and manage a team of Quality Engineers, Process Control Engineers, andTechnicians, setting performance goals, developing career paths, and fosteringa culture of ownership and data-driven decision-making.

·               Collaborateclosely with all stakeholders to balance the trade-off between qualitystability, process efficiency, and tool uptime.

Requirements

·               Degreein Engineering, Materials Science, Chemical Engineering, or a related technicalfield.

·               Preferable10+ years of experience in the semiconductor industry, with a minimum of 5years in a leadership/management role focusing on Process Control, QualityAssurance, or Yield Engineering within a Fab environment.

·               Technicalknowledge of semiconductor fabrication processes in different modules.

·               Expert-levelknowledge of Statistical Process Control (SPC), Design of Experiments (DOE),Failure Mode and Effects Analysis (FMEA), and Lean/Six Sigma methodologies(Black Belt certification highly preferred).

To find out more about thisopportunity, please contact Lionel Liew atlionel.liew@gmprecruit.com.

We regret that only shortlisted candidates willbe notified.

GMP Technologies (S) Pte Ltd  |   EA Licence: 11C3793|   EA Personnel: Lionel Liew   |  Registration No: R1330693

This is in partnership with the Employment andEmployability Institute Pte Ltd (“e2i”).

e2i is the empowering network for workers andemployers seeking employment and employability solutions. e2i serves as abridge between workers and employers, connecting with workers to offer jobsecurity through job-matching, career guidance and skills upgrading services,and partnering employers to address their manpower needs through recruitment,training, and job redesign solutions. e2i is a tripartite initiative of theNational Trades Union Congress set up to support nation-wide manpower andskills upgrading initiatives.

By applying for this role, you consent to GMPTechnologies (S) Pte Ltd’s PDPA and e2i’s PDPA.

• Semiconductor Industry

• Monday - Friday (8.30am - 5.30pm)

• Basic salary up $7000 + AWS + VB + Allowance

• North Area

Job Responsibilities:

• Be responsible for on-site quality control of the company's silicon photonics chip production process (wafer testing, wafer dicing, chip visual inspection, etc.).

• Monitor production process quality data, analyze process fluctuations using quality tools such as SPC and FMEA, identify potential quality risks, propose process improvement measures and promote their implementation.

• Lead the investigation, analysis and solution of quality abnormalities in the production process (such as dicing chipping, visual inspection defects, test parameter abnormalities, etc.), formulate corrective and preventive actions, track and verify the effect, and reduce the process defect rate.

• Be responsible for the formulation and update of quality inspection standards for the production process, train front-line operators and inspectors to ensure that they master quality requirements and operating specifications.

• Regularly conduct process quality reviews, summarize quality data of each station, form process quality reports, and promote continuous quality improvement in the production link.

• Cooperate with PDQE, FA and other positions to participate in new product introduction, failure analysis and other work, and provide process quality related support.

Job Requirements

• Microelectronics, Semiconductor or related majors, with more than 3 years of PQE work experience in the semiconductor or silicon photonics chip industry; familiarity with wafer dicing, chip testing, visual inspection and other processes is preferred.

• Master process quality control methods and tools (SPC, FMEA, 8D, 5Why, etc.), and be able to independently carry out process quality analysis and improvement work.

• Familiar with the silicon photonics chip production process; those with a process background are preferred; understand the working principle and quality control points of equipment at each station (dicing equipment, test equipment, visual inspection equipment).

• Strong ability in problem analysis, communication and coordination, and execution, able to quickly respond to quality problems in the production process.

• Familiar with the ISO9001 quality system, with basic English/Mandarin reading and writing skills, able to read English/Mandarin technical documents."

Job Title: Quality Document Controller

Department: Quality Assurance / Quality Control (QA/QC)
Location: Jurong Island, Singapore
Work Type: Full-Time
Working Hours: 5-day work week, 44 hours per week
Work Environment: Site Office-Based

Job Summary

We are seeking a motivated and detail-oriented individual to join our QA/QC team as a Quality Document Controller. This role is responsible for managing the full document control lifecycle, ensuring all quality-related documents are properly tracked, maintained, distributed, and archived in accordance with project and company standards.

The ideal candidate should be highly organized, able to work under deadlines, and comfortable working in a dynamic project environment.

Key Responsibilities

• Manage the full document control cycle, including collection, numbering, logging, tracking, distribution, and archiving of quality documents (e.g., procedures, RFIs, ITPs, quality reports) in both electronic and hard copy formats.
• Coordinate with subcontractors, clients, third parties, and internal teams to ensure timely submission and proper handling of documents.
• Maintain and update master lists of controlled documents to ensure accuracy and traceability.
• Use document control systems and platforms such as Novade, PTS, and iSEPCO3 (training will be provided).
• Provide administrative support to the QA/QC team, including data entry, scanning, photocopying, and filing.
• Prepare meeting minutes for quality-related meetings as required.
• Ensure compliance with company quality policies and document control procedures.
• Collaborate with team members to maintain an efficient and well-organized document management system.

Qualifications & Requirements

• Diploma or higher qualification, preferably in Engineering or related fields such as Civil Engineering, Mechanical Engineering, Information Technology
• Prior experience in document control or administrative support in a construction or engineering environment is an advantage.
• Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook) and PDF tools.
• Strong attention to detail with high accuracy in documentation.
• Excellent organizational and time management skills.
• Ability to work independently and as part of a team.
• Able to perform under pressure and meet deadlines.

Working Conditions

• Based in a site office environment on Jurong Island.
• Standard working hours: 5 days per week, 9 hours per day (including break), 44 hours per week.
• Overtime is not frequent and will be compensated in accordance with Singapore labour regulations.

SCOPE OF RESPONSIBILITIES

1. Communication

1.1. Serves as the communication point to project teams with regard to quality assurance (QA) study audits

1.2. Follows up with project teams with regard to resolution of PSI QA study audits

1.3. Liaises with PSI divisions/operational offices with regard to internal systems, process, and location audits

1.4. Liaises with vendors with regard to vendor qualification audits

1.5. Serves as the communication point for PSI Operations staff with regard to issues related to quality assurance

1.6. Serves as the communication point for PSI clients with regard to QA audits contracted to PSI

2. Planning and scheduling

2.1. Prepares, conducts, and reports QA study audits

2.2. Assembles QA study audits documentation

2.3. Takes part in the preparation, conduct, and reporting of internal systems audits

2.4. Takes part in the preparation, conduct, and reporting of internal locations audits

2.5. Takes part in the preparation, conduct, and reporting of vendor qualification audits

2.6. Takes part in the preparation, conduct, and reporting of internal process audits

3. Training

3.1. Trains PSI Operations staff in quality management topics

Sang Chow Wong Pte. Ltd. is a trusted Singapore-based manufacturer and distributor of food seasonings and condiments. With over 36 years of experience, we have been serving restaurants, hawkers, food manufacturers, and wholesalers with a diverse range of Halal-certified sauces made for excellence.

Responsibilities:

• Ensure all food products are produced in compliance with food safety standards, regulatory requirements, and company policies
• Oversee the entire quality assurance processes
• Conduct regular internal audits for the organization, manage external inspections and liaise with regulatory agencies for annual audits
• Ad-hoc duties with production and operations on a daily basis, e.g. maintenance and pest control
• Collaborate with cross-functional teams and assist with new R&D product projects

Requirements:

• Candidate must possess at least a Diploma / Bachelor's degree in Food Science, Food Technology or equivalent
• At least 1 Year of working experience in the Food Manufacturing is required for this position
• Proficient with Microsoft Office and able to communicate in English. Mandarin is also preferred in order to liaise with & Mandarin speaking associates from Export Markets
• Prior experience with FSSC Certification process will be preferred

Key Job Purpose:

The Quality Management (QM) Specialist is to support the QMR in ensuring the organization and its affiliates adhere to all applicable local, regulatory and quality standards associated with Enterprise Risk Management. As Subject Matter Expert (SME) for Enterprise Risks per ISO31000 and other ISO Standards for QMS, such as ISO13485, ISO14971, ISO27001, ISO14001 and WSH regulations.

The role serves to maintain a high standard of compliance, effectiveness, and continuous improvement throughout the organization's identified risks. The role will coordinate with Process Owners and appointed Risk Management PICs in Affiliates, monitor identified risks are managed in an effectiveness and timely manner. Report the progress of Enterprise Risks to Risk Management Committee in a biyearly manner.

Job Description

Risk Management

• Coordinate and work with Process Owners to address and manage the identified risks, including the execution of their effective controls.
• Ensure effectiveness of risk control measures are executed by Process Owners where documented evidence indicated in the Risk Register are available and uploaded.
• Follow-up with QMR and relevant HODs on new processes or products or business model which may an impact to operational and governance processes.
• Analyse and do trending of enterprise risks within SAP and across the region which requires escalation or proposed sources of improvement to QMR. .
• Support QMR in coordinating the Risk Management Committee meeting at SAP in biyearly manner. Assist to prepare updates and follow up actions from the Risk Management Committee meeting.
• Extend consistent practices of Enterprise Risk Management to Affiliates.
• SME for Risk Management and provide training on Risk Managements to SAP and affiliates.

Audit Support (Internal and external)

• Assist in the planning, execution, and follow-up of internal audits, ensuring compliance with regulatory standards and company policies.
• Support external audits by coordinating audit activities, preparing documentation, and ensuring audit readiness associated with Enterprise Risks
• Ensure that audit findings associated with Enterprise Risks are addressed through effective corrective actions and continuous improvement.
• Perform analysis trending on Corporate Audit findings for all affiliates in SAP and share result to QMR for reporting to Top Management.

 Environmental & WSH Support

• Support in coordinating with relevant stakeholders and assessing the impact of environmental / WSH information to the organization.
• Identify environmental issues that impact the organization, associated risks are included in Legal Risk Register and control measures are effectively put in place.

Job Requirements

• Diploma or Degree in a relevant field
• Minimum 2 years of experience in a Quality Assurance role within the Medical Devices industry
• Certified Internal Auditor for ISO 13485, ISO 9001, ISO 31000 and/or ISO 14001
• Strong knowledge of ISO standards (ISO 13485, ISO 9001, ISO 27001, ISO 14001, ISO 31000)
• Understanding of Environmental Management Systems (EMS)
• Knowledge of Workplace Safety and Health practices
• Proficient in Microsoft Office applications
• Experience in risk management activities, data trending, and analysis

Company Overview   

Amperesand is reinventing how the world powers its most critical systems.

We are facing a once-in-a-generation opportunity for infrastructure disruption. Electricity demand is skyrocketing, driven by AI factories, electric vehicles, and modern industrial growth. Energy supply is shifting to incorporate a more diverse mix of resources – including solar, gas, and batteries – at a massive scale.

And yet the power infrastructure behind our latest mega-projects hasn’t meaningfully changed in nearly 100 years. Supply chains for today’s infrastructure equipment can’t match the pace and sophistication of critical energy projects. Ampersand is building hardware and software that rewrites this broken power infrastructure playbook to support a new era of energy abundance.

We’ve built a new class of intelligent, software-defined power infrastructure products leveraging a decade of advanced medium voltage Solid State Transformer research that’s now ready for commercial deployment.

Our products and solutions go far beyond the capabilities of traditional electrical equipment. We make power systems that are faster to deploy, dramatically smaller and more efficient, and capable of supporting modern, dynamic energy needs for tomorrow’s most demanding energy consumers.

Scalable in-house advanced manufacturing capability is our foundation for meeting timeline and quality expectation to serve infrastructure customers around the world.

Amperesand is led by breakthrough energy hardware development veterans and funded by top tier investors who share our vision of building a category-defining energy technology company.

With hubs in San Francisco, Reno, and Singapore, our global team is laser focused on building foundational technology to solve the most pressing problems in power infrastructure at scale.

Join us in building the power foundation of the future!

Role Summary

As our Senior Power Electronics Control Engineer you will focus on control and system behavior of advanced power converters, including AC-DC and DC-DC topologies, used across low-voltage and medium-voltage power conversion systems. The role emphasizes multilevel power converter architectures and resonant power conversions used in solid-state transformers (SST). You will work hands-on across control design, modeling, analysis, laboratory debugging, and validation, and collaborate closely with hardware, firmware, and system engineers to bring robust power electronics solutions from concept through validation.

Responsibilities:

• Design and implement digital control algorithms for advanced AC-DC and DC-DC power converters across low- and medium-voltage applications.

• Develop small-signal and large-signal models to support stability analysis, loop compensation, and transient optimization.

• Support development of control strategies for advanced power conversion stages, including multilevel or resonant topologies and AC-DC / DC-DC stage interactions.

• Implement real-time control algorithms on DSP/MCU/SoC platforms.

• Lead hands-on debugging and root-cause analysis across simulation, firmware integration, hardware bring-up, and lab testing.

• Collaborate with hardware and firmware teams to optimize sensing, protection, and control-loop performance.

• Support validation activities including loop stability measurement, transient response testing, and fault handling verification.

• Own complex control subsystems and contribute to system-level design under technical leadership.

Qualifications:

• Technical degree or equivalent industry experience in Electrical Engineering or a closely related field, with a strong focus on power electronics and control systems.

• 3+ years of experience designing and deploying digital control for power converters, with demonstrated ability to own and execute complex technical tasks.

• Strong understanding of resonant power conversion principles and their control implications across isolated and non-isolated power converter architectures.

• Solid foundation in control theory, including loop compensation, stability margins, frequency-domain and time-domain analysis, and nonlinear system behavior.

• Proven experience implementing real-time control algorithms on embedded platforms.

• Hands-on laboratory experience debugging power converters.

• Ability to translate theoretical control concepts into practical, robust implementations.

• Strong problem-solving and analytical skills, with the ability to work through technically ambiguous challenges.

• Familiarity with modeling and simulation tools such as MATLAB/Simulink and PLECS.

• Proficiency in embedded C for real-time control implementation and debugging.

Bonus Qualifications:

• Exposure to medium-voltage power electronics systems.

• Exposure to bidirectional power conversion and power flow control.

• Experience supporting products from R&D through validation and deployment.

Please note: This role requires working on-site 5 days a week. We do not offer hybrid or remote options.

How to apply: Please submit your application through our careers page: https://job-boards.greenhouse.io/amperesand/jobs/4164340009

Summary

The Manager/Senior Manager, Quality Assurance & Regulatory Affairs (QA/RA) will be responsible for establishing, implementing, and maintaining a compliant and robust Quality Management System (QMS) in accordance with ISO 13485, EU MDR2017/745, and FDA 21 CFR Part 820 (QMSR).

This role will lead Quality Assurance (QA), Quality Engineering (QE), and Regulatory Affairs (RA) functions to support the development and manufacturing of Class III implantable medical devices, including pericardial patches and biological heart valves.

The position will play a critical role in ensuring regulatory compliance, product quality, and successful market access (CE mark and FDA approval).

Responsibilities

·       Lead and support the development and execution of regulatory strategies for CE marking and FDA submissions.

·       Lead and facilitate regulatory inspections, including Notified Body audits and FDA Pre-Approval Inspections (PAI).

·       Drive quality engineering initiatives, including process validation, risk management, processo ptimization, and continuous improvement.

·       Oversee key quality systems, including CAPA, internal audits, complaint handling, and supplier quality management.

·       Collaborate cross-functionally with Engineering, Manufacturing, and R&D, and act as the management representative for quality and regulatory compliance.

·       Establish and maintain the Quality Management System documentation, including the Quality Manual, SOPs, document control, and records management.

Requirements

·       Bachelor’s degree or higher in Biomedical Engineering, Life Sciences, Chemical Engineering, or a related discipline.

·       Minimum 10 years of relevant experience in the medical device or pharmaceutical industry, including at least 5 years in a leadership capacity.

·       In-depth knowledge of FDA 21 CFR Part 820, EU MDR2017/745, ISO 13485, and ISO 14971.

·       Familiarity with industry standards such as ISO 14644 (cleanroom manufacturing), ISO 10993, and ISO 5840 would be advantageous.

·       Proven experience in regulatory submissions (CE Mark and FDA) for Class III implantable medical devices is highly preferred.

·       Demonstrated strong leadership and team-building capabilities, with the ability to operate effectively in a start-up or greenfield environment.

·       Excellent communication and stakeholder management skills, with the ability to engage senior management, regulatory authorities, and external partners.

·       Strategic mindset with hands-on execution capability, coupled with a high level of accountability and attention to detail.

Responsibilities: 

• Develop and maintain an operational risk management framework that aligns with the organization's objectives, ensuring it meets all necessary requirements. 

• Implement and embed the operational risk management policy across multiple local entities. 

• Collaborate with first-line management to support and maintain the internal control framework and testing methodologies. 

• Deliver internal control testing campaigns, documenting results in the risk management tool and reporting outcomes through appropriate channels. 

• Oversee the Quarterly Control Evaluation (QCE) process across local entities, including the reporting of management results and remediation plans. 

• Contribute to the implementation of the Operational to Secure Subsidiaries (OSS) framework. 

• Engage in community calls to communicate key updates between the risk management and internal control functions. 

• Build and maintain strong relationships with stakeholders in Risk, Compliance, and Internal Audit to ensure effective oversight of the control framework. 

• Maintain a risk and control tracker to ensure management teams are aware of their commitments to audits and regulators. 

• Participate in risk management forums and governance meetings to provide oversight and support for operational risk management initiatives. 

Requirements: 

• Degree-level qualification or equivalent is essential. 

• A minimum of several years of experience in Audit, Finance, or Risk Management within a regulated environment. 

• Familiarity with the insurance sector, particularly international health, is preferred but not mandatory. 

• Knowledge of technology, security, and data risks and their control frameworks is advantageous. 

• Strong understanding of material risk exposures in financial services and internal control frameworks. 

• Expertise in Technology Risk Frameworks (e.g., COBIT, ISF, ISO27001 series) is a plus. 

• Excellent skills in report writing, organization, and analysis, with the ability to influence stakeholders at all management levels. 

• Competence in navigating a matrix organization effectively. 

• Understanding of the Solvency 2 risk environment is preferred but not required. 

Interested candidates who wish to apply for the advertised position, please click on “Apply”. We regret that only shortlisted candidates will be notified. 

EA License No.: 01C4394 (Persol Singapore PTE LTD) 

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Responsibilities

• Establish and maintain PV quality management system, ensuring the full compliance with GVP, relevant regulatory requirements, as well as all applicable health authority requirements mainly in EU and China.
• Manage PV controlled procedures, including policy, SOP, etc.
• Conduct PV quality activities, including audits, change control, deviation and CAPA management, KPIs  (Key Performance Indicators) monitoring, training management, etc.
• Qualifies PV CSO (Contract Service Organization).
• Manage PSMF (Pharmacovigilance System Master File).
• Manage the drafting and updating of Safety Agreements, and ensure the periodic reconciliations with partners.
• Manage any PV Inspection from Health Authorities or PV Audit form Partners
• Handle the other ad hoc tasks as required by Superiors.

Requirement

• At least bachelor degree in clinical medicine, pharmacy, life science, etc.
• 7-9 years or above experiences of PV operation or quality management, and at least 3-5 years experiences of PV quality management.
• Familiar with GVP and applicable regulatory requirements for China, EU, etc.
• Experience in pharmaceutical, biotech, CRO, or related regulated environments is preferred.
• Extensive knowledge of PV quality assurance principles, practices and standards.
• Good understanding, communication and learning skills.
• Fluent in English and Chinese for effective communication with Chinese-speaking stakeholders and review of regulatory documents

Company Overview

Turntech Precision is a Microturning Jobshop in Singapore specializing in Swiss-Type CNC machining for small precision turned parts. We serve contract manufacturers and OEMs in electronics, semiconductor, and medical device industries across Southeast Asia.

Job Summary

Support QC/QA engineers by inspecting in-process parts, reporting quality issues, and assisting in quality control tasks to ensure production meets standards and continuous improvement goals.

Responsibilities

• Assist QC/QA Engineer with daily quality control tasks and ad-hoc assignments to support production quality
• Inspect in-process parts periodically using micrometers, microscopes, profile projectors, vernier calipers, and gauges to verify dimensional accuracy
• Report out-of-specification dimensions promptly to Quality Engineer and Production Engineer/Operator for corrective action
• Generate quality reports for QC/QA Engineer and help enforce corrective actions on the production floor
• Troubleshoot engineering and quality issues arising during daily production to minimize defects
• Implement and maintain 5S standards in quality control and production areas to ensure workplace organization and safety
• Lead workplace improvement initiatives that enhance company competitiveness and product quality
• Continuously develop individual skills and knowledge to improve quality control effectiveness

• Position: Quality Control Specialist/Assistant
• Location: Sunview - Jurong Working hours: 5 days, Monday to Friday (8.30am to 6.00pm)
• Salary (commensurate on experience): Up to $2600 + AWS + OT + Medical/Dental
• Duration: Permanent
• Industry: Logistics - MNC

Main Responsibilities

• Inspect, test and sample materials or assembled parts or products for defects and
• deviations from specifications
• Observe and monitor production operations and equipment to ensure conformance to specifications and make or order necessary process or assembly adjustments
• Discuss inspection results with those responsible for products and recommend necessary corrective actions
• Discard or reject products, materials and equipment not meeting specifications
• Maintain records of testing, information and various metrics such as number of defective products per day etc.
• Inspect procedures of the entire production cycle to ensure they are efficient and comply with safety standards
• Documents inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database
• NCR data collections and photos taking

Requirement

• Minimum 1-year relevant experience in quality control
• Minimum ITE above Proficient in MS Word, Excel, Outlook etc.
• Basic computer skills is preferred

Email me at joie@searchpersonnel.com.sg

 ***We do not charge our candidates nor bind them with any contract.***

 Joie Chang

 Deputy Consulting Director

Reg no.: R2090601 | EA No: 13C6684

Thank you for your interest in this position. Our shortlisting period is 3 working days. Only shortlisted candidates will be contacted for further consideration.

If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend that you continue your job search to maximize your opportunities. We wish you all the best and should we have any suitable roles that match your experiences/ qualifications/ preferences, we will reach out to you.

What you'll be doing

• Design, develop, and implement robust machine control software for complex manufacturing equipment

• Collaborate with cross-functional teams to integrate software solutions with hardware components

• Troubleshoot and resolve software-related issues in production environments

• Continuously optimize and enhance existing software systems to improve performance and reliability

• Document code, processes, and procedures to ensure maintainability and traceability

• Stay up-to-date with industry trends and best practices in machine control software engineering

What we're looking for

• Bachelor's degree in Computer Science or a related field

• Minimum 3 years of experience in machine control software development, preferably in the semiconductor or manufacturing sectors

• Proficiency in programming languages such as C++, C#, Python, and PLC programming

• Strong understanding of real-time embedded systems, control theory, and industrial automation protocols

• Excellent problem-solving and analytical skills to identify and resolve complex software issues

• Ability to work collaboratively in a team environment and communicate effectively with cross-functional stakeholders

• Familiarity with software development best practices, including version control, testing, and documentation

HOW TO APPLY:

Interested applicants, please click on “Apply Now” or submit your resume to ref68@trustrecruit.com.sg

We regret only shortlisted candidates will be notified.

Important Note: Trust Recruit Pte Ltd is committed to safeguarding your personal data in accordance with the Personal Data Protection Act (PDPA).

Please read our privacy statement on our corporate website www.trustrecruit.com.sg 

Trust Recruit Pte Ltd

EA License No: 19C9950

EA Personnel: John Angeline

EA Personnel Reg No: R1544851

• 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

What you'll be doing

• Developing and implementing effective quality control processes and procedures

• Conducting thorough inspections and testing of raw materials, work-in-progress, and finished products

• Analyzing data and generating reports to identify and address quality issues

• Collaborating with production and engineering teams to improve manufacturing processes

• Ensuring compliance with industry standards, regulations, and the company's quality management system

• Training and mentoring junior quality assurance personnel

• Continuously seeking ways to enhance quality and efficiency

What we're looking for

• Diploma / Degree in Mechanical Engineering or a related field

• Min 2 years of experience as a QA Engineer in the precision engineering or machining industry

• Experience in NADCAP processes is an advantage

• Excellent knowledge of quality control principles, methodologies, and best practices

• Strong technical aptitude and hands-on experience with a variety of testing and measurement equipment

• Proficiency in data analysis and report generation using relevant software tools

• Problem-solving and critical thinking skills to identify and resolve quality issues

• Excellent communication and interpersonal skills to collaborate effectively with cross-functional teams

Interested applicants, please click on “Apply Now” or submit your resume to ref68@trustrecruit.com.sg

We regret only shortlisted candidates will be notified.

Important Note: Trust Recruit Pte Ltd is committed to safeguarding your personal data in accordance with the Personal Data Protection Act (PDPA).

Please read our privacy statement on our corporate website www.trustrecruit.com.sg 

Trust Recruit Pte Ltd

EA License No: 19C9950

EA Personnel: John Angeline

EA Personnel Reg No: R1544851