Total 698 Quality Assurance / Control job vacancies

Are you our next creator of change?

Are you looking for a career in an inspiring, global environment where your expertise makes a difference? At Neste, you will be working for the world’s leading producer of renewable diesel and sustainable aviation fuel. Together we can help our customers to reduce their greenhouse gas emissions.

We are looking for you,

Process Control Engineer
to join our Technical Department, Process Control Engineering Team in Neste Tuas Singapore.

As the owner of the refinery process control systems, you will focus on ensuring operational availability, productivity, flexibility & safety through continuous process control improvement initiatives, process control optimization & troubleshooting where required.

In this job, you will also work closely with Operations, Maintenance, Safety and Other Engineering functions to strive for Operational Excellence through process improvement initiatives & projects. 

Together with you as the process control subject matter expert (SME) in the Singapore renewable diesel & sustainable aviation fuel (SAF) production refinery, we can make an impact today through meaningful work that drives Neste forward.

Reasons to join
We operate in an inspiring and evolving business environment as a global leader in renewable fuels. We contribute to Neste’s success by living our values every day: we care, we have courage, we cooperate.

We always prioritize safety and in every location. We strive to create a positive and impactful work environment.

Transformation brings new possibilities and fosters our courage and curiosity. As a global company, we support personal development with versatile learning and career opportunities. Collaboration is key, and we believe in flexible, smart ways of working.

More about the job

Your role in our team

• As the owner of the process control systems in the Pre-Treatment Units, Heat Treatment Unit & Tank farm, you will develop & improve refinery processes by following up, developing & executing modifications / improvements to the Distributed Control System (DCS), Safety Instrumented System (SIS) & other automation system applications
• Troubleshoot process deviations and lead major non-conformance investigations to resolve problems related to process control applications or safety interlock systems.
• Develop and drive alarm management workflow related to your area of responsibility.
• Develop and drive management of change (MOC) as change manager for PCS & SIS modifications
• Lead or support capital investment projects involving changes to the DCS, SIS or other automation system applications.
• Ensure process safety through functional safety / periodic proof tests, standards and specifications development and risk evaluation processes (Process Hazard Analysis, HAZOP, LOPA, SIL etc…)
• Process control systems related competence development at Singapore refinery in your area of responsibility.
• Develop and maintain documentation and specifications related to process/plant control and automation logics.
• Utilizes process monitoring & optimization management tools to optimize plant performance
• Sharing and implementation of best practices and common initiatives from Rotterdam and Porvoo refineries.
• Participate as proof test leads to execute SIS proof testing during unit turnarounds

Keys to success in this role / The best combination to succeed in this role

• B Sc. or higher degree in chemical engineering or relevant field and understanding of Renewable products chemical processing unit operations and engineering.

• At least 6 years of work experience in process control engineering and operations in the oil and gas, refining or petrochemical industry
• Strong knowledge in Instrumentation and control design engineering management, engineering drawing interpretation ability
• Process Control engineering application / operating skillsets on Emerson DCS and SIS is considered an advantage
• Process Control experience on refining pre-treatment units, heat treatment units and/or tank farm operations is considered an advantage
• Good understanding on functional safety lifecycle management (design, operations & maintenance) is considered an advantage

• Responsible attitude and safety-oriented mindset
• Strong problem solving, communication and computational thinking skills
• Strong Interpersonal and planning skills
• Good ability to influence in both local and global matrix organization with cultural awareness, performance driven and active networking attitude

Let’s get you started

We look forward to receiving your CV and application (with a salary request).

Due to security and confidentiality, please submit your application through our recruitment system. Applications sent via email will not be considered.

We will do our best to contact you within 2 weeks after the application time has ended. The recruitment process will include interviews and a possible aptitude assessment. (The person selected for the position must pass a health examination including a drug test. A security clearance is obtained with your consent.)

Neste in brief
Neste (NESTE, Nasdaq Helsinki) creates solutions for mitigating climate change and accelerating a shift to a circular economy. The company is the world’s leading producer of sustainable aviation fuel (SAF) and renewable diesel, enabling its customers to reduce their greenhouse gas emissions. Neste refines waste, residues and other renewable raw materials to high-quality renewable fuels at its refineries located on three continents. The company’s annual renewable fuels production capacity will be increased to 6.8 million tons in 2027.

Neste has high standards for sustainability and the company has consistently been recognized by several leading sustainability indices. In 2024, Neste's revenue stood at EUR 20.6 billion. Read more: neste.com

At Micron, we offer an outstanding opportunity for a dedicated and ambitious Contamination Control Technician to join our diverse team at FAB 10. As a key player in the environment quality control sector, you will collaborate with Facilities, Equipment, Fab support, Production Teams and area engineering teams. Your role will involve environmental samplings, quality control checks, contamination troubleshooting, state-of-the art sensors maintenance to prevent environment/chemical contamination (such as particle, airborne molecular contamination, liquid particle contamination) to the manufacturing process. You will consistently adhere to world-class standards and successfully implement coordinated reaction mechanism to prevent fab excursion.

Responsibilities:

• Responding to ERT and Security alerts and ensuring that gowning room logistics are adequate when evacuation occurs.

• Responding to contamination alarms and reporting abnormal conditions to engineering and other stake holders.

• Sampling various areas of the Fab for contamination (swab, bacteria, airborne and liquid particles and airborne molecular contamination) and working with the chemical lab to have the samples analyzed and obtaining the data in a timely manner.

• Ensuring that real time monitoring systems are Operating and recording properly.

• Carrying out primary investigation on contamination Issues and providing contamination data to engineering for analysis.

• Carrying out primary investigation on contamination control analyzers.

• Completing special projects as well as supporting contamination control engineering projects.

• Ensuring team members are practicing approved cleanroom protocol.

• Acting as contamination control resources to the Fab, Probe, Facilities and other supporting groups.

• Be a contributing member in your areas of responsibilities.

Requirements:

• Chemical Engineering/Chemistry/Material Diploma is preferred or related field of study

• Candidiates without experience are welcome to apply

• Must be able to work in cleanroom environment

• Good interpersonal skills with the ability to collaborate effectively with a diverse variety of people.

• Basic proficiency in PC skills, including MS Office Word, Excel, and PowerPoint.

• Strong analytical and problem-solving abilities.

• Basic knowledge of analytical technique, such as Ion chromatography, gas chromatography and particle analyzers, etc. is a plus

• Must be able to work a 12-hourly shift and open to night shift

Quality Control Manager (Maternity Coverage)

4-6 Months Contract

Location : Gul Circle

Salary Up to $8,000 depending on experience

Industry: Pharmaceutical

Our client delivers vital healthcare solutions worldwide, powered by the precision and dedication of its Manufacturing & Supply teams. With your talent, they can expand their impact—protecting more people and offering hope to patients and their families.

Job Summary    

• Responsible for assisting the Head of Site Quality to implement quality control processes to ensure product meets the standards and regulatory requirements.
• Manage quality control systems and drive continuous improvement initiatives to enhance quality control operational efficiency and effectiveness.

Responsibilities:

• Developing and implementing the annual quality control objectives in alignment with the organizational strategy, vision, and objectives
• Implementing quality control processes supporting the right operation of the quality control activities, in accordance with the Sanofi global procedures
• Ensuring compliance of the quality control processes with internal and external quality requirements, regulations, and certifications
• Ensuring that any investigation related to quality control activities is performed in a timely manner to support final decision
• Maintaining a system to ensure compliance and that quality risks are properly identified, tracked, and mitigated for the quality control activities
• Ensuring a quality control schedule is in place to support the timely release of products and the adherence of the test’s execution to the committed standard times
• Ensuring the testing and release of all incoming materials
• Concluding on the conformance of analytical test results with regards to specifications to support the release of product batches
• Ensuring the use of validated analytical methods in compliance with the regulatory dossiers and the maintenance, qualification, and calibration of equipment to ensure accuracy and reliability of the QC activities
• Establishing metrics and monitoring data for the quality control activities, to identify trends and issues and to implement action plan
• Establishing and monitoring key performance indicators (KPIs) and metrics for the quality control activities, to report on the performance and effectiveness
• Promoting a culture of quality throughout the quality control organization
• Identifying and driving continuous improvement initiatives and projects to enhance the quality control efficiency and effectiveness fostering a culture of continuous improvement
• Evaluating and recommending new technologies, tools, and methods to enhance quality control processes and outcomes
• Leading and managing the quality control team, including hiring, training, coaching, and performance evaluation
• Ensuring management of budget allocation to QC department, and ensuring optimized expenses for the QC activities
• Preparing and participating in regulatory inspections and audits, providing expertise on quality control

Requirements

• Degree or background in Chemistry is ideal
• Microbiology background or experience managing a Microbiology lab team

Lim Pey Chyi - Apple.lim@manpower.com.sg

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Job Responsibilities

• Conduct detailed inspections of residential and commercial properties to identify pest infestations
• Carry out pest control treatments using approved methods, including chemicals, baits, and traps
• Handle and apply pesticides safely in accordance with company procedures and regulatory guidelines
• Educate clients on pest prevention methods and proper sanitation practices
• Maintain accurate service records and documentation for all jobs completed
• Respond to client inquiries and service requests in a timely and professional manner
• Stay updated on industry trends, pest control techniques, and new products
• Comply with company policies, safety standards, and industry regulations

Working Hours

• 5.5 working days per week
• Monday to Friday: 8 hours per day
• Saturday: 4 hours

Requirements

• Valid NEA Vector Control Technician/Worker License
• Class 3 driving license is an advantage
• Willing to work outdoors and in various environmental conditions
• Good teamwork and positive attitude
• Strong communication and customer service skills
• Mature candidates are welcome to apply

• Salary up to $6,000
• 5 days work week
• Jurong East MRT

Our client is an emerging MNC with a global presence — headquartered in Singapore, with R&D and technical operations across Asia and customers in worldwide data-centre and high-speed optical markets.

SOX 404 Compliance & Implementation

• Lead the design, documentation, and implementation of SOX 404-compliant internal controls over financial reporting (ICFR)

• Develop comprehensive process documentation, including risk control matrices (RCMs), flowcharts, and control descriptions

• Execute management's assessment of internal control effectiveness in accordance with SEC and PCAOB requirements

• Coordinate external auditor SOX 404 testing and manage remediation of identified deficiencies

IPO Readiness Support

• Support the Company's U.S. listing preparation by ensuring timely establishment of IPO-ready internal control environment

• Align internal control framework with U.S. GAAP, SEC regulations, and PCAOB auditing standards

• Collaborate with legal, finance, and business teams to address control gaps identified during IPO readiness assessments

• Prepare SOX-related disclosures for registration statements and periodic SEC filings

Risk Assessment & Control Optimization

• Conduct annual fraud risk assessments and entity-level control evaluations

• Identify key financial reporting risks and design preventive and detective controls

• Monitor control operating effectiveness through ongoing testing and continuous auditing techniques

• Drive automation of controls and implementation of data analytics for control monitoring

Cross-functional Collaboration

• Partner with process owners across business units to embed control consciousness into daily operations

• Provide SOX 404 training and guidance to finance and operational teams

• Serve as primary contact for external auditors on ICFR matters

Requirements

• Bachelor's degree or above in Accounting, Finance, or a related field, with CPA, CIA, or CISA certification preferred.

• Minimum 4 years of experience in internal control, internal audit, or external audit, preferably with a Big 4 background.

• Hands-on experience with SOX 404 compliance is essential, including involvement in first-year implementation or remediation projects. Prior direct experience in U.S. IPO or SEC reporting readiness is highly desirable.

• Strong technical proficiency in U.S. GAAP, PCAOB standards, and the COSO 2013 Framework, as well as practical experience with ERP systems such as SAP, Oracle, or NetSuite and data analytics tools.

• Industry-specific experience in semiconductor is preferred.
  
  R22107887 | Gladys Chang Si Min

Job Responsibilities:

• Plan and implement the Abnormal Handling (ABS/PAR/IEAR/BPD) system, assisting the FAB reviewing process abnormalities establishing an early warning notification system, with the aim of reducing quality loss and cost for the company and customers, and supervising the effectiveness of system execution.

• Plan and implement the MRB (Material Review Board), assisting the FAB reviewing waived products resulting from process abnormalities, in order to reduce quality loss and cost for the company and customers, and supervising the effectiveness of the system.

• Plan and implement internal audits, assisting the FAB in identifying processes and systems with quality risks, and supervising the effectiveness of improvements to risk processes.

• Plan and implement the MSA (Measurement System Analysis) system, assisting the FAB in performing calibration and capability assessment of measuring instruments to ensure the reliability of measurement values and thus ensure product quality.

• Implement the automotive service package, assisting the FAB in planning executable methods and systems, and auditing and supervising the execution process for automotive products.

Job Requirements:

• Minimum Bachelor degree in engineering (ex. Electronics, Material science, Chemistry, Physics, Statistics, Data Science, Math)

• Candidates with more than 3 years of semiconductor process/quality/integration experience will be considered for a senior role

• Knowledge of problem solving (8D methodology), statistical techniques, Measurement System Analysis(MSA) and planning/project management is an advantage

• Knowledge of ISO9001/ISO/TS16949 or VDA6.3 standards, Lead Auditor qualification and audit handling/experience is preferred

• Collaborate with cross-functional teams to resolve quality issues and customer requirements to drive product quality improvements

• Good communication and negotiation skills, with the ability to collaborate with FAB module, PEI and Customers

Whether you’re looking for your first role or your next career move, UMC is where your future can take shape.

Step into your future with us. Apply Now.

About United Microelectronics Corporation

United Microelectronics Corporation (UMC) is a leading global semiconductor foundry with over 40 years of innovation powering technologies across AI, automotive, consumer electronics, connectivity, and IoT. As one of the industry’s most established players, we enable breakthrough technologies through precision-engineered semiconductor manufacturing for customers across every major sector of the electronics world.

Headquartered in Taiwan, UMC has been present in Singapore since 2004 and continues to invest in local talent, technology, and advanced manufacturing. Our recent Fab expansion reflects our long-term commitment to building Singapore as a key hub for semiconductor innovation, and to creating stable, meaningful careers through innovation, teamwork, and progress.

Join a team that invests in your future from day one. With best-in-class training, hands-on experience and access to cutting-edge tools, UMC equips you to lead tomorrow’s tech landscape, right down to the nanometre.

The Quality Technician Auditor is responsible for performing in-process quality control audits and inspections throughout the manufacturing process. This role ensures that products meet internal and customer quality standards by identifying process deviations, supporting corrective actions, and driving continuous improvement in production quality.

Key Responsibilities

• Provide guidance and training to operators on quality requirements and best practices.

• Conduct regular in-process audits and inspections at various stages of manufacturing to verify compliance with quality standards and procedures.

• Utilize measurement tools and equipment (e.g., calipers, micrometers, gauges) to assess product and process conformity.

• Document audit findings, non-conformances, and corrective actions in detailed reports for traceability.

• Collaborate with production, engineering, and quality teams to address process deviations and implement corrective/preventive actions.

• Monitor and verify the effectiveness of corrective actions and process improvements.

• Support root cause analysis for quality issues and participate in cross-functional problem-solving teams.

• Ensure strict adherence to quality and safety protocols.

• Maintain 6S standards in the production and audit areas.

• Present audit results and improvement recommendations to supervisors and cross-functional teams.

Qualifications

Minimum:

• Nitec/Higher Nitec/Diploma in Engineering, Science, or related technical field.

• Ability to work on 12 hours shift and work in the production line.

• Good communication and documentation skills.

• Strong attention to detail and analytical skills.

• Proficient in Microsoft Office applications, with the ability to apply them effectively in daily work.

Preferred:

• Experience in in-process quality control or manufacturing audits preferred.

• Familiarity with manufacturing processes, quality standards, and inspection techniques is preferred.

• Fundamental knowledge of AI tools is an advantage.

• Good project management skills and continuous improvement knowledge is preferred.
  

  Assists engineers in testing and inspecting products at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products. Implements methods and procedures for inspecting, testing, and evaluating products, processes and/or production equipment. Report such data to management and production engineering so problematic areas may be addressed.

JOB DESCRIPTION

Department: Quality Assurance

Report to: Head of Supplier Quality Engineering Section

Functional Relationships with: Quality Assurance & Control Division

POSITION PROFILE:

Based in: Singapore

Job site: Tuas

The successful candidate will:

• Manage, monitor & assure good incoming part quality.

• Manage part quality issues, deploy effective corrective & preventive measures.

• Audit, qualify to introduce parts & vendors.

• Monitor & work with vendors to improve part quality.

KEY DUTIES & RESPONSIBILITIES:

• Ensure all parts are correctly verified & fit for use promptly. Drive, resolve supplier-related quality issues promptly and effectively to ensure continuous supply of good quality parts.

• Monitor & analyse part data & supplier’s performance to identify risks; develop plans to improve parts, suppliers to meet quality expectations.

• Train & enable technicians to function as effective detection and prevention gates of incoming materials to ensure good part quality.

• Audit, qualify, manage suppliers & parts. Map suppliers’ development plan with existing and potential suppliers.

• Audit, verify suppliers’ quality systems, controls and processes to ensure their conformance to the requirements and standard.

• Review, improve / refine the SQE workflows, jobs, process efficiency & productivity of SQE operations.

• Manage, enable safe and efficient inspection process & operating environment.

• Manage the SQE equipment to ensure their validity, fitness & correct functions.

• Manage a small team of technicians to conduct effective operations.

• Review, update & maintain SQE-related ISO documents periodically.

• Generate reports as necessary.

ABILITY/COMPETENCY REQUIRED:

• Degree in Engineering disciplines (mechanical, materials, chemical, quality or manufacturing).

• At least 3-5 years of relevant working experiences.

• Must be able to use Microsoft Office applications effectively.

• Experience in plastic injection and/or metal stamping will be excellent.

• Knowledge of using SolidWorks, JMP, Minitab will be good.

• Good communication and negotiation skills.

• Good analytical, logical and troubleshooting skills.

JobDescriptions:

• Maintain and continuously improve the QualityManagement System (QMS).
• Serve as the document controller for theQuality Manual, Standard Operating Procedures, Specifications, WorkInstructions, Forms, Charts, Records and Quality Reports.
• Ensure compliance with GMP, PIC/s, ICH, ASEANGuidelines, FDA, and other regulatory requirements.
• Prepare the annual Product Quality ReviewReport and Management Review Reports.
• Manage and follow up on change controls.
• Conduct process deviation investigations andfollow up on CAPA implementation for closure.
• Handle quality issues in manufacturingoperations.
• Manage customer complaints, product recalls,returns, and counterfeits cases.
• Review and control artwork anddrawings for packaging materials.
• Ensure machine testing, trial runs, qualifications, and validationmeet compliance requirements.
• Monitor accelerated and real-timestability programs.
• Ensure that Good Documentation Practices and traceability are in place.
• Undertake any additional tasks asassigned from time to time.

Job Requirements:

• Degree inPharmaceutical Science, Engineering, or a related field.
• At least 2 - 5 years of experience in quality assurancewithin the pharmaceuticals, manufacturing, or medical devices industries
• Strong knowledge of QMS (e.g. ISO 9001, cGMP) withhands-on experience in documentation control and implementation.
• Proven expertise in QA processes, includinginvestigations, change control, CAPA management, audits, and processvalidation.
• Excellent follow-up, communication, and interpersonal skills
• Meticulous and well-organised, and detail-oriented.
• Proficient in Microsoft Officeapplications.

We regretto inform you that only shortlisted candidates will be notified.

Responsibilities:

• Assist in the implementation and management of food safety (HACCP & ISO 22000) and quality assurance programmes across the Central Kitchen and outlets (local and overseas).
• Conduct training for staff on Standard Operating Procedures (SOPs), food hygiene, and proper food handling practices.
• Support QA testing programmes and new product development initiatives.
• Perform regular inspections and audits to ensure compliance with food safety and quality standards.
• Investigate feedback from customers, outlets, and Central Kitchen, and recommend corrective actions.
• Ensure strict adherence to SOPs across all operational sites.
• Liaise with vendors and contractors on maintenance and compliance matters related to food safety and QA.
• Support continuous improvement initiatives to enhance food safety and quality standards.

Requirements:

• Diploma in Food Science & Technology or a related field.
• Minimum 3 years of relevant QA experience in the F&B industry (e.g., central kitchen, manufacturing, or inspection environments).
• Basic knowledge of food safety standards such as HACCP and ISO 22000.
• Good communication skills in English and Mandarin to liaise with Mandarin-speaking stakeholders.
• Detail-oriented, proactive, and self-motivated with a strong sense of initiative.

EA License No: 18C9123

EA Personnel: R25126753 (Samuel Tan Zihui)

Job Description:

• Develop and execute automated test scripts using Playwright.
• Design and maintain scalable automation frameworks and ensure high test coverage.
• Perform SIT and UAT automation aligned with business requirements.
• Collaborate with developers, product owners, and stakeholders to understand user stories.
• Participate in Agile ceremonies and contribute to test strategy.
• Ensure stability, reliability, and continuous improvement of automation suites.

Requirements:

• 3+ years in software testing with strong automation experience.
• Hands-on expertise in Playwright (TypeScript).
• Experience with Salesforce testing (preferred).
• Good understanding of Agile/Scrum.
• Strong skills in requirement analysis and stakeholder communication.
• Experience with CI/CD integration is a plus.

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