669 Qa Specialists jobs in Singapore

QA Engineer (Process Quality Control) is responsible for developing and deploying inspection procedures to ensure the conformance of materials to be released. Candidates with experience in a semiconductor manufacturing environment are encouraged to apply for this position.

Responsibilities

1. Responsible for backend semiconductor packaging processes such as ball drop, bumping, singulation, backgrind, and mounting.
2. Provide engineering support to meet production output, product quality, efficiency, productivity, yield, cycle time, and safety requirements.
3. Analyze process data to identify improvement actions and work on implementing improvements.
4. Drive permanent solutions to resolve chronic process and quality issues.
5. Evaluate new products, materials, and processes during pilot runs to ensure process readiness.
6. Maintain the relevance of Work Instructions, Control Plans, FMEA, and Process Control documents.
7. Prepare the line for internal and external audits and follow-up on corrective actions.
8. Perform any other ad-hoc duties as assigned.

Requirements

1. Bachelor’s Degree in Engineering (Mechanical, Electrical, Materials, Chemical, or related field).
2. Experience in semiconductor packaging processes (ball drop, bumping, singulation, backgrind, mounting) is advantageous.
3. Experience in process engineering, yield improvement, and quality control.
4. Proficiency in data analysis and statistical process control (SPC).
5. Familiarity with FMEA, Control Plan, and Process Control documentation.
6. Hands-on experience with new product/material/process evaluations.
7. Ability to work in a fast-paced manufacturing environment.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Engineering and Quality Assurance

Industries

• Semiconductors and Manufacturing

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Position Summary

QA Engineer (Process Quality Control) is responsible to develop & deploy inspection procedures to ensure conformance of material to be released. Candidates with experience in semiconductor manufacturing environment are encouraged to apply for this position.

Responsibilities

• Responsible for backend semiconductor packaging processes which ball drop, bumping, singulation, backgrind and mounting.
• Effectively providing engineering support in order to meet production output, product quality, efficiency, productivity, yield, cycle time and safety requirements.
• Responsible to analyse the process data and identify improvement actions and work on the improvement.
• Drive permanent solutions to resolve chronic process and quality issues.
• Responsible to evaluate new product/material/process during the pilot run and ensure process readiness.
• Responsible for the relevance of the Work Instructions, Control Plan, FMEA & Process Control documents.
• Responsible to prepare the line for internal & external audits and the follow-up actions.
• Any other ad-hoc duties as assigned.

Requirements

• Bachelor’s Degree in Engineering (Mechanical, Electrical, Materials, Chemical, or related field).
• Prior experience in semiconductor packaging processes (ball drop, bumping, singulation, backgrind, mounting) would be advantageous.
• Experience in process engineering, yield improvement, and quality control.
• Proficiency in data analysis and statistical process control (SPC).
• Familiarity with Failure Mode and Effects Analysis (FMEA), Control Plan, and Process Control documentation.
• Hands-on experience with new product/material/process evaluations.
• Ability to work in a fast-paced manufacturing environment.

• Well Established Company
• Basic $2500 - $3200 + OT + Allowance + AWS + Variable Bonus
• Excellent Welfare and Benefits + Career progression
• Working Location : East
• Working hours : 5 working days (8am to 5pm)

Job Responsibilities:

• Conduct detailed inspections of finished products to identify defects, non-conformities, and deviations from quality standards
• Support quality in handling defective found during the production
• Collaborate with the quality control team to resolve material quality issues and determine disposition (accept, reject, or rework)
• Collaborate with the production, quality teams to identify root causes of defects and non-conformities
• Perform First Article (FA) report and propose process improvements
• Collect parts for 2 hourly to visual inspection
• Key in data
• Other ad-hoc duties as assigned

Job Requirements:

• Minimum GCE ‘O’ Level / Nitec / Diploma in Quality Assurance or equivalent with 1-2 years of related work experience
• Able to use Smart Scope, Keyence, Micrometer & others measuring equipment
• Able to interpret 2D drawings

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

LIONG ZHAO GUAN (R22107632)

EA Recruitment Pte Ltd

EA License No: 21C0492

Candidates with experience in Manufacturing and mechanical area are encouraged to apply for this position.

- Prepare & submit FAI / Inspection report to customer.

- Maintain the documentation control for FAI / Inspection report / NCR and calibration system.

- Prepare inspection reports and analysis on Non-Conformance report.

- Support to provide 8D report for handling customer complaint.

- Assisting in failure analysis of internal and external defects.

- Provide support and training for the QC inspector.

- Assist in preparation of work instruction, procedure and inspection requirement.

- Support the supplier management by providing feedback on material quality to supplier.

- Prepare Certificate of Conformity, declaration of ROHs, REACH and other related report.

- Ensure the achievement of Quality Goal/objective in Key Performance Index Target.

- Perform dimensional inspection using CMM

- Conduct internal process audit

- Prepare & Conduct ISO 2001:2015 audit

- Maintain FA tools and working environment to meet the 5S and safety requirement.

- Able to plan and execute tasks within datelines and anticipate any problems before hand.

- Work well under pressure and able to finish by datelines.

- Motivated and can multitask.

- Able to work and interact with people from different backgrounds.

- Able to handle and work under stress conditions.

- Able to work independently with minimal supervision.

- Other ad-hoc activities assigned by the reporting manager

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Primary Function

Responsible for maintaining the laboratory quality system in-line with ISO/IEC 17025. Responsible for internal audits, quality & safety policy directives. Responsible for document control of all quality system documentation, standards, clients supplied procedures and specifications.

• Responsible for of all quality control practices in the laboratory. Plan and implement appropriate QC tools such for quality assurance purposes and as requested or stipulated by clients.
• To represent lab in discussion with HSEQ on execution of HSEQ matters, such as internal lab inspection & QM revision.
• Oversee proficiency sample receipt, results generation and reporting, evaluation of round robin reports and initiating corrective action requests for outliers.
• Overall control of the calibration and maintenance program for all laboratory equipment.
• Ensure that the laboratory facilities and environment are adequate to facilitate the correct performance of the required tests as specified either by the standards or SAC-SINGLAS.
• In-charge of change management process related to quality implemented in the laboratory.
• Assist the Laboratory Manager in establishing the HSE system for laboratory. This shall include provision of correct PPE for technicians, training on specific safety activities, analyzing and assessing risks for changes in processes and periodic walk-through assessments to insure that the safety program is functioning, practical and effective.
• Ensure that all computer-generated data is properly and periodically validated and implement suitable security measures (password protection etc.) to prevent unauthorized tampering of routines.
• Perform any other tasks as assigned by management, including testing and analysis during periods of heavy workload. To be on call 24 hours a day 7days a week for queries from lab staff.
• Initiate “error and safety study” on test procedures.
• Initiate and organize investigation on quality problem.
• To feedback to management on quality of audits, SQC and round robin testing.
• Ensure availability of lab reference materials (ASTM Test Methods, CRM etc.) and maintenance and standardization of laboratory reagents.
  
  

Primary Function

Responsible for maintaining the laboratory quality system in-line with ISO/IEC 17025. Responsible for internal audits, quality & safety policy directives. Responsible for document control of all quality system documentation, standards, clients supplied procedures and specifications.

Principal Duties/Responsibilities

• Responsible for of all quality control practices in the laboratory. Plan and implement appropriate QC tools such for quality assurance purposes and as requested or stipulated by clients.
• To represent lab in discussion with HSEQ on execution of HSEQ matters, such as internal lab inspection & QM revision.
• Oversee proficiency sample receipt, results generation and reporting, evaluation of round robin reports and initiating corrective action requests for outliers.
• Overall control of the calibration and maintenance program for all laboratory equipment.
• Ensure that the laboratory facilities and environment are adequate to facilitate the correct performance of the required tests as specified either by the standards or SAC-SINGLAS.
• In-charge of change management process related to quality implemented in the laboratory.
• Assist the Laboratory Manager in establishing the HSE system for laboratory. This shall include provision of correct PPE for technicians, training on specific safety activities, analyzing and assessing risks for changes in processes and periodic walk-through assessments to insure that the safety program is functioning, practical and effective.
• Ensure that all computer-generated data is properly and periodically validated and implement suitable security measures (password protection etc.) to prevent unauthorized tampering of routines.
• Perform any other tasks as assigned by management, including testing and analysis during periods of heavy workload. To be on call 24 hours a day 7days a week for queries from lab staff.
• Initiate “error and safety study” on test procedures.
• Initiate and organize investigation on quality problem.
• To feedback to management on quality of audits, SQC and round robin testing.
• Ensure availability of lab reference materials (ASTM Test Methods, CRM etc.) and maintenance and standardization of laboratory reagents.
  
  

Competency Requirements

• Possess Bachelor’s Degree or Diploma in Chemistry/Chemical Engineering.
• Minimum five years of working experience in petroleum or petrochemical laboratory industry.
• Good knowledge on ISO/IEC17025 requirements, SAC SINGLAS Requirements and client requirements
• ISO/IEC 17025 Internal Auditor Trained.
• Able to work independently and possess good analytical skills, problem solving skills.
• Able to communicate effectively in both verbal and written English.

Seniority level

• Seniority level Mid-Senior level

Employment type

• Employment type Full-time

Job function

• Job function Research, Analyst, and Information Technology

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**It's more than a job**
When you work in Freight Logistics and Operations at Kuehne+Nagel, you play a key role in optimising processes and ensuring that inventory and shipments move efficiently. But that is not all. Your work also helps ensure that vital medicines reach patients on time and supports other essential deliveries, from wind turbines to semiconductors. At Kuehne+Nagel, our contribution counts in more ways than we imagine.
**?**
**How you create impact**
You will be part of the Quality & Compliance Unit within QuickSTAT, adding your expertise to drive quality assurance, regulatory compliance, and operational excellence in pharmaceutical and healthcare logistics. Based in Singapore, you will lead the implementation, development, and maintenance of our Quality Management System (QMS), ensuring full compliance with GDP and ISO standards while serving as the Quality Lead for our Singapore office.
**What we would like you to bring**
You will do this by managing regional compliance, supporting global initiatives, and engaging internal and external stakeholders, while focusing on the following key objectives:
+ To lead the continual development and maintenance of the QuickSTAT Quality Management System in alignment with GDP and ISO 9001 standards.
+ To manage day-to-day Quality & Compliance activities in Singapore, while supporting regional and global QuickSTAT offices.
+ To oversee the implementation of policies and practices that ensure compliance with company quality initiatives and external regulatory requirements.
+ To drive the local audit program, manage internal CAPAs, and ensure Management Reviews are conducted with documented actions for continuous improvement.
+ To oversee training programs, ensuring compliance with SOPs and timely completion of required learning for staff.
+ To manage the qualification and ongoing assessment of regional suppliers, including supplier audits, corrective actions (SCARs), and maintenance of the Approved Supplier List.
+ To provide quality oversight on facility validation, calibration, and qualification protocols and reports.
+ To support mapping and supplier qualification projects within the Singapore Control Tower and ensure alignment with GDP requirements.
+ To deliver quality and compliance training and support operational teams with guidance aligned to the duties of the Responsible Person under EU GDP.
+ To manage internal audits, self-inspections, and quality walkthroughs, ensuring findings are actioned and documented.
+ To collaborate with commercial and operational teams in promoting and embedding a culture of compliance.
+ To support QuickSTAT's vendor compliance program, from selection and onboarding to audits and performance monitoring.
+ To ensure compliance with Health, Safety, and Environmental (HSE) regulations and company-wide policies.
+ To lead or contribute to special projects as required by regional or global Quality & Compliance leadership.
**What's in it for you**
As an employer, Kuehne+Nagel stands for equal opportunity and we are committed to diversity in our teams with regards to people with disabilities. We believe that you can make a valuable contribution to Kuehne+Nagel and look forward to receiving your application.
**Who we are**
Logistics shapes everyday life - from the goods we consume to the healthcare we rely on. At Kuehne+Nagel, your work goes beyond logistics; it enables both ordinary and special moments in the lives of people around the world.
As a global leader with a strong heritage and a vision to move the world forward, we offer a safe, stable environment where your career can make a real difference. Whether we help deliver life-saving medicines, develop sustainable transportation solutions or support our local communities, your career will contribute to more than you can imagine.
We kindly advise that placement agencies refrain from submitting unsolicited profiles. Any submissions of candidates without prior signed agreement will be considered our property and no fees will be paid.
Kuehne + Nagel is an equal employment/affirmative action employer. If you require an accommodation for any part of the online application process due to a disability, please contact the Employee Services HR Help Desk at 1- during the hours of 8:00am - 5:00pm EST; Monday through Friday or via e-mail at: with the nature of your request. We will answer your inquiry within 24 hours.

Description

Responsible for overseeing manufacturing, testing and validation activities, ensuring compliance with internal procedures and regulatory requirements.

Responsibilities:

• Oversee routine quality control for on-site GMP production and testing, ensuring all GMP activities are executed in strict adherence to company procedures.
• Contribute to the establishment of an effective quality system and ensure its efficient operation across all GMP functions and processes in daily operations.
• Provide quality oversight for validation and re-qualification activities, ensuring validation status is consistently maintained
• Accountable for QA Review of all Qualification and Validation protocols and reports, including computer system validation.
• Ensures that the data integrity of all documentation and electronic data complies to all application regulations and SOP requirements
• Participate in site operational readiness programs, including self-inspection and data integrity surveillance for GMP and client audits.
• Manage quality events, including deviations, change controls, CAPA, and lab investigations etc.
• Carry out additional tasks as assigned by leadership.

About You:

• Bachelor’s degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields.
• At least 3-5 years of relevant QA experience in Biopharma or Pharmaceuticals
• Familiar with FDA, EMEA, and PICS GMP requirements.
• Knowledgeable in biological product manufacturing and related quality control requirements.
• Experience in biopharma commercial supply is preferred.
• Experience with a new site start-up is preferred.
• Proficient in English listening, speaking, reading, and writing.
• Skilled in Microsoft Word, Excel, PowerPoint, etc.
• Strong learning ability.
• Excellent cross-functional communication and collaboration skills.
• Strong logical thinking and conflict management abilities.
• Demonstrates strong ownership.

Based in Tuas, company transport provided.

6- 12 months contract.

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Industry

Other

Category

Management & Operations

Sub Category

Management & Leadership

Description

Core Responsibilities:

• Inspection and Testing: Conducting thorough inspections and testing of materials, components, and finished products throughout the production process. This includes visual inspections, dimensional checks, and potentially using non-destructive testing (NDT) methods like ultrasonic testing or magnetic particle testing.
• Quality Control Plans and Procedures: Developing and implementing quality control plans, inspection test plans, and standard operating procedures (SOPs) for manufacturing processes.
• Data Analysis and Reporting: Analyzing data from quality control activities to identify trends, root causes of defects, and areas for improvement. Generating reports on quality metrics and findings.
• Non-Conformance Management: Addressing quality issues and non-conformances by investigating the root cause, implementing corrective actions, and ensuring preventative measures are in place.
• Collaboration: Working closely with production teams, engineering, and other relevant departments to resolve quality issues and improve overall product quality.
• Audits and Compliance: Participating in internal and external audits to ensure compliance with quality standards, such as ISO 9001, and relevant industry regulations.
• Documentation and Record Keeping: Maintaining accurate records of all quality control activities, including inspection results, test data, and non-conformance reports.
• Training and Development: Providing training to production staff on quality control procedures and best practices.

Specific Skills and Knowledge:

• Blueprint Reading: Understanding technical drawings and specifications is crucial.
• Welding Processes: Familiarity with welding procedures, welder qualifications, and related standards (AWS D1.1, BS EN, ISO) is often required.
• Non-Destructive Testing (NDT): Knowledge of NDT methods for detecting flaws in metal components.
• Quality Management Systems: Understanding and experience with quality management systems like ISO 9001.
• Problem-Solving Tools: Familiarity with tools like 8D, Fishbone diagrams, and Pareto analysis for root cause analysis.
• Computer Proficiency: Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and other relevant software.
• Liaising with clients: Communicating with clients on quality-related matters and addressing their concerns.
• Attending to customers' quality queries: Responding to and resolving customer inquiries regarding product quality.
• Supervising quality assurance specialists and inspectors: Providing guidance and support to other quality control personnel.
• Maintaining quality programmes: Ensuring compliance with relevant quality programs such as ISO 9001.
• Working in a multicultural environment: Singapore is a diverse country, so cultural sensitivity and communication skills are important.

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Industry

Other

Category

Engineering

Sub Category

Quality Engineering

Description

Key Responsibilities:

• Developing and Implementing Quality Systems: Designing, implementing, and maintaining quality control and assurance systems for the company's metal products.
• Overseeing Quality Control: Managing and supervising teams of inspectors and quality control personnel.
• Ensuring Compliance: Ensuring the company's quality management system (QMS) meets requirements of relevant standards like ISO 9001 and other industry-specific standards.
• Customer Interaction: Working with project management and customer service teams to address customer requirements, complaints, and feedback related to product quality.
• Product Testing and Evaluation: Overseeing the implementation of testing and evaluation methods to ensure products meet quality standards and specifications.
• Continuous Improvement: Identifying areas for improvement in the production process and quality control procedures to enhance product quality and efficiency.
• Documentation and Reporting: Maintaining accurate quality records, generating reports on quality performance, and communicating findings to relevant stakeholders.
• Training and Development: Providing guidance and training to quality control personnel on quality standards, testing procedures, and best practices.
• Budget Management: Managing the department's budget and ensuring sufficient resources are available for quality assurance activities.
• Risk Assessment: Identifying potential quality risks and developing strategies to mitigate them.
• Collaboration: Working with other departments (e.g., production, engineering, sales) to ensure quality is integrated throughout the product lifecycle.
• Auditing: Conducting or overseeing internal and external audits to assess the effectiveness of the QMS.

Required Skills and Experience:

• Technical Expertise: Strong understanding of quality control principles, testing methodologies, and relevant industry standards (e.g., ISO 9001, API Q1).
• Leadership and Management: Proven ability to lead and manage a team of quality control professionals.
• Communication Skills: Excellent communication and interpersonal skills to effectively interact with various stakeholders.
• Problem-Solving: Strong analytical and problem-solving skills to identify and resolve quality issues.
• Experience: Typically requires a minimum of 3-6 years of experience in quality management, with experience in the metal industry preferred.
• Certifications: Relevant certifications in quality management (e.g., Certified Quality Engineer, Certified Quality Manager) or specific industry certifications (e.g., Certified Welding Inspector).
• Knowledge of Metallurgy: Familiarity with metallurgy properties of metal products can be advantageous.
• Computer Skills: Proficiency in using quality management software and other relevant computer applications.

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Industry

Other

Category

Management & Operations

Sub Category

Quality Management & Operations