116 Quality Control Analysts jobs in Singapore

**THE FUTURE IS WHAT WE MAKE IT.**
**_QA Engineer (NDT Level 3) - Aerospace_**
**_Joo Koon, Singapore_**
Start your career by making an impact and real connections with some of the most meaningful challenges around. When you join Honeywell, you become a member of our performance culture comprised of diverse leaders, thinkers, innovators, dreamers, and doers who are changing the future.
**Make the Best You.**
Working at Honeywell is not just creating incredible things. You will have the opportunity to work with our talented and friendly team of professionals and be part of a global team of future shapers.
**Join Us and Make an Impact.**
We are seeking a dedicated **_QA Engineer (NDT Level 3)_** to join our **_Aerospace_** team in **_Joo Koon, Singapore_** . The ideal candidate will possess a keen eye for detail and a commitment to ensuring products meet the highest quality standards.
**Key Responsibilities:**
+ Ensure process compliance with Site NDT Manual and NADCAP requirements
+ Support Network and 3rd party audits, conduct Site level Self Audit
+ Maintain NADCAP certification of Penetrant Inspection (FPI) & Magnetic Particle Inspection (MPI)
+ Develop and maintain site NDT Manual, NDT related procedures and work instructions.
+ Conduct training and certifications of site NDT personnel.
+ Perform Non-Destructive Testing (FPI and MPI) of production parts as needed
+ Perform Rejection Analysis and Quality Improvement Plan
+ Perform other functions as assigned as Site NDT Level 3 & Source Certifying Agent (SCA)
+ Support production quality engineering tasks as assigned
+ Adherence to Health, Safety and Environmental requirements for NDT personnel
**MUST HAVE:**
+ NAS 410 certified Level 3 in FPI and MPI
+ Familiar with NADCAP certification requirement
+ Good understanding of Quality Management System (eg. AS9100, ISO 9001)
+ Audit experience is a plus
+ Self-driven with strong analytical and problem- solving skills
+ Team player with good interpersonal communication skills
**WE VALUE:**
+ Ability to work independently and prioritize workload to meet project timelines in a fast-paced environment
+ Some knowledge of continuous improvement, quality and lean principles
+ Familiarity with safety, health regulations and the ability to adhere to safety protocols while performing inspections
+ Initiative, analytical and motivated
**About Us**
The world is changing. And it's a familiar story at Honeywell. Our $36 billion business was founded on a legacy of firsts spanning 130 years. We're building a safer, smarter, and more sustainable world through our technology and software across each of our 930 sites globally. Our impact is seen in every shape and size around the world. Our solutions are felt daily in aerospace, buildings and cities, retail, chemicals and materials, safety, industrial and manufacturing, safety, and supply chains.
**Discover More**
We've been innovating for more than 100 years and now we're creating what's next. There's a lot more available for you to discover. Our solutions, our case studies, our #futureshapers, and so much more. Learn more at careers.honeywell.com/us/en/
If you believe what happens tomorrow is determined by what we do today, you'll love working at Honeywell.
The future is what we make it. So, join us and let's do this together.
Honeywell is an equal opportunity employer, and we support a diverse workforce. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, gender, religion, or veteran status. Aboriginal and Torres Strait Islander peoples are encouraged to apply.
**Copyright © 2025 Honeywell International Inc**
Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable.
Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.

**Position: Quality Control Senior Analyst (Raw Material)**
+ Hiring Manager: Manager, QC Raw Material & Lab Service
+ Location: Tuas, Singapore
**About the job:**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi has added two new Evolutive Facilities to our global industrial footprint. These production units (EVF) represent the future of manufacturing. They allow us to increase our capacities while making production more flexible and respectful of the environment.
Fully digitalized, our Evolutive Facilities (EVF) will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our EVFs will help improve people's lives by giving them faster access to more treatments.
In this context, we are looking for one Quality Control Senior Analyst (Raw Material) to support raw material testing and participate in the setting up of the new QC laboratory for our new site based in Singapore.
**Main responsibilities:**
+ Responsible for QC test for raw material samples including compendial tests and identification tests.
+ Participate in method validation/ verification for raw material testing.
+ Perform QC sampling of incoming raw materials.
+ Author/ revise raw material specification and other QC related documents.
+ Support the laboratory start-up activities, participate in equipment qualification activities including generation of user requirement specifications.
+ Support laboratory activities such as housekeeping and equipment maintenance.
+ Train newcomers for QC lab activities and testing
+ Participate and contribute to laboratory continuous improvement.
+ Contribute to laboratory performance (eg, deviation/OOS rate, sample turnaround time)
**Education and Experience**
+ Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 4-5 years of experience in QC lab operations and raw material testing.
+ Experience in method validation/ verification in the pharmaceutical or biotechnology industry preferred.
**Key technical competencies and soft skills:**
+ Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
+ Discipline and assertiveness in decision-making and execution in laboratory start-up activities. Experienced in routine laboratory operations and continuous improvements.
+ Experienced/participated in method transfer, method validation and method verification for raw material testing will be advantageous.
+ Experienced in start-ups will be advantageous.
+ Fluent in English speaking and writing.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

Direct message the job poster from Golden Agri-Resources (GAR)

About the Company - When you join GAR, you join something bigger. Big in scale, big in opportunities to grow, and big in impact. With over 100,000 employees across 14 countries, spanning Asia, Europe, North, and South America, Golden Agri-Resources (GAR) is one of the largest agribusinesses in the world. We manage over half a million hectares of palm oil plantations, including smallholder farms, across Indonesia. Since 1997, we have prioritized sustainability, working closely with farmers, communities, and partners to deliver food, fuel, and a better future.

Our business is rooted in palm oil, expanding into other crops like sugar, soybean, sunflower, and coconut. Our people are our strength. We invest in their growth through global opportunities, cross-border exposure, and continuous learning, because developing our people is key to building a better business. Here, your career contributes to something meaningful — for the planet, for people, and for future generations.

About the Role - Responsible for trade control accounting and preparing daily management reports for the Trading Business Unit (Palm).

Responsibilities -

1. Stay updated on global commodity market developments and inform management of market movements/developments that could affect our Positions/PNL.
2. Update trade details and generate Daily Mark-to-Market reports for realized PNL of closed positions and unrealized PNL of open positions.
3. Liaise with Traders to reconcile trader’s PNL with Trade Control’s Net Position Report daily.
4. Provide analysis on PNL & Position movements for weekly management reviews.
5. Implement and maintain internal controls and ensure operational and financial process efficiencies.
6. Coordinate to ensure smooth month-end book closures.
7. Liaise with Traders to reconcile trader’s PNL with Trade Control reported figures.
8. Analyze driving factors for PNL from a value chain perspective.
9. Prepare charts and commentaries on Business Unit performance for monthly updates to senior management.
10. Assist in preparing ad-hoc reports requested by management and work on annual budgeting exercises.
Seniority level

• Associate

Employment type

• Full-time

Job function

• Finance

Industries

• Wholesale and Food and Beverage Manufacturing

Referrals can double your chances of interviewing at GAR.

Get notified about new Control Analyst jobs in Singapore, Singapore .

#J-18808-Ljbffr

· Quality Control is responsible for the activities at the plant by the inspection, sampling, and disposition of products used in the manufacturing processes throughout the organization.

· As a member of the Quality Control department, a Quality Control Analyst will be expected to successfully execute the responsibilities relating to the sampling, testing, and inspection of all product lots received by the quality control department. These activities include Chemical raw materials, component inspection, and final packaging.

Responsibilities include:

· Demonstrate proficiency in a task by completion of an On the Job Training.

· Maintain proficiency in training per curricula on all governing procedures.

· Perform all aspects of QC responsibilities as it pertains to release activities that will include but is not limited to: sampling, testing, and disposition of raw materials and final packaging/ component lots

· Support additional areas of QC including Rejected, Quality Hold, and Non-conforming materials.

· Perform all activities adhering to strict cGMP guidelines

· Maintain on-time completion of all training requirements

· Perform simple laboratory instrument up keep including the cleaning, calibration, and the preventative maintenance of the instrument as outlined within the departments governing procedures

· Participate in department initiatives to support the continuous improvement of the quality systems of the QC department

· Practice safe work habits and adhere to safety procedures and guidelines

Requirements:

• Min Degree in Science or equivalent with at least 2 years of relevant experience in the pharmaceutical / chemical industry.
• Experience in operating laboratory equipment such as HPLC, GC , KF Titrators.
• Working knowledge of cGMP and regulatory requirements related to Quality is an advantage
• 5 days office hours

If you are interested in the position, do kindly drop your most updated resume to (Attn: QC Analyst)

Thank You.

Leon Leong De Cong
R1551708

Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599

Under direct supervision assists with the monitors, tests and inspects all processes involved in the production of a product and product itself. Ensure the quality standards are met by every component of the product or service provided by a company.
+ Responsible for inspecting products using established inspection tools and techniques.
+ Performs and documents First Article, In-Process, and Final inspections on parts in production to ensure that customer requirements and quality standards are met.
+ Inspects material and product received from outside sources to ensure compliance with quality standards and customer specifications.
+ Timely complete all assigned technical and safety trainings.
+ Work in the field (outside conditions) providing assistance with the movements of materials for Inspection.
+ Clean drilling tools and rig equipment for inspection.
+ Learn and maintain the cleaning machinery which includes mechanical brushing unit, steam cleaner and high-water pressure jetting equipment.
+ Take responsibility for the safety of all cleaning machinery and responsibility for environmental control over the working areas.
+ Report any unsafe conditions or acts to the Supervisor.
+ Ensure that work assignments are performed in accordance with approved plans, schedules and programs.
+ Provide technically correct operation of equipment and other fixed assets under responsibility of the department.
+ Apply Weatherford, and where appropriate Client Company Quality, Health, Safety & Environment Policy and Management Systems.
+ Must understand and comply with all safety rules and company policies of Weatherford.
+ Work assignments carried out to the highest quality level.
+ Perform various other duties and activities as assigned by supervisor within the physical constraints of the job.
+ Min secondary school graduates, or high or ITE/ technical education is a plus.
+ Minimum 3 years of related experience in QC inspection.
+ Above average verbal and written communication skills in English.
+ Prior knowledge of products and/or inspection process.
+ Ability to use measurement devices such as tape measures, micrometres, callipers and scales.
+ Ability to read and understand basic and advanced blueprints and charts.
+ Ability to effectively work with employees and supervisors.
+ The physical ability to immediately respond to emergency situations.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System ( which makes everything possible.
The Quality Control Specialist is responsible for ensuring products and processes meet established quality standards and regulatory requirements. This role involves conducting inspections, testing, and audits, as well as supporting continuous improvement initiatives to maintain high levels of product quality and operational efficiency.
This position reports to the Quality Control Manager and is part of the Quality department located in Singapore, 25 Tuas South Street 1 and will be an on-site role.
What you will do:
+ Leading/providing oversight in OOS investigation, deviation report writing and CAPA planning
+ Provide general oversight on QC routine operations, ensuring that the product and raw material testing schedules are on-track with minimal backlog
+ Approximately 30% of time dedicated to performing Quality Control (QC) testing activities, 70% of time focused on supporting various QC operational activities
+ Driving adherence to quality KPI's and ensure timely reporting of data and trend to relevant stakeholders
+ Ensure that validation of new QC laboratory equipment and method is performed
Who you are:
+ University graduate (Science) with reasonable work experience OR equivalent relevant work experience
+ Possess at least 3 to 5 years of experience working in a QC Laboratory environment
+ Extremely detail and accuracy-oriented with good written and verbal communication skills
+ Experience in writing Laboratory Investigation details, Deviation records with root cause analysis and Change Control records
+ Knowledge and experience of a GxP environment or other regulated industry
It would be a plus if you also possess previous experience in:
+ Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos, graphic, and technical writing skills (create and edit procedures)
+ Reasonable laboratory experience operating laboratory equipment, i.e. UPLC, Endotoxin plate readers, pH meters, microbial testing etc. #LI-SS3 #LI-Onsite
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

LUXOMETAL Pte. Ltd. Is a local trading company on metal accessories for Fashion and Luxury business.

What will you do?

We are running a search for metal hardware professionals specializing in Quality Control and Quality Assurance for the Singapore office!

- Visual control of surface, colours, comparison with validated masters

- Visual check of no scratches, dots, stains

- Sizes measurements with micrometer and digital comparator

- Write the QC (Quality Control) report

- Communicate effectively with asian suppliers to ensure company standards are

- Initiate Meetings with management and asian suppliers to brief / debrief about QA / QC results

The candidate should:

- Langages: Mandarin will be welcomed to communicate with our asian / chineese suppliers.

- Be at ease with measurements tools and 2D/3D CAD drawings

Half or Full Time job, 5 days / week

In this role, you will be responsible for inspecting incoming materials, in-process components, and finished products to ensure they meet established quality standards and customer specifications. Your work plays a critical role in ensuring the long-term success of our customers through consistent product quality.

Responsibilities

• Develop and implement quality control methodologies to ensure compliance with quality assurance standards and guidelines.
• Conduct audits and inspections of products and processes to ensure they meet established quality standards.
• Investigate and troubleshoot product or production issues, developing corrective actions as necessary.
• Monitor the performance of the quality management system, producing data and reports on performance against set standards.
• Communicate quality control information to relevant departments and initiate and collaborate with cross-functional teams to improve product quality and efficiency.
• Interpret technical drawings and understand inspection tolerances and specifications. Develop inspection determination matrix and inspection plan
• Train technicians on inspection methods and equipment maintenance.

Job Requirements:

• A degree in Mechanical Engineering, Quality Assurance, or a related field is required.
• ISO 9001:2015 Internal Auditor and ASME Y14.5/ISO 14405 GD&T certifications preferred
• Minimum 5 years of relevant work experience in a manufacturing environment, preferably high-precision manufacturing.
• Strong knowledge of quality control standards, methodologies, and best practices, as well as experience with quality testing machines and systems.
• Excellent knowledge of data analysis and statistical methods, with the ability to interpret technical specifications and drawings.
• Advanced knowledge of Geometric Dimensioning and Tolerancing (GD&T); proficiency with inspection instruments and metrology software.
• Proficient in using a range of inspection and measuring instruments. Experience with CMM operation is an advantage.
• Familiarity with industry standards: ISO 9001, DNV 2.7‑1/2, API 7, ASME BPVC and ATEX/CSA documentation.
• Strong analytical mindset, excellent problem-solving and cross-functional collaboration skills to identify and resolve quality issues effectively.

Job Title: Quality Control Executive

Location: Tampines industrial, Singapore (only site)

Company: Panorama Antennas PTE Ltd

Reports To: Site Manager

Job Summary:

We are seeking a highly skilled and motivated Quality Control Executive to join our growing team at Panorama Antennas, a leading manufacturer in the telecommunications sector. The Singapore manufacturing site is undergoing rapid expansion to meet the growing global market demand. The successful candidate will be responsible for overseeing quality control of inbound deliveries, & production line processes alongside overseeing the ISO9001 audit. This role requires strong analytical and problem solving skills along with communication skills to interact with the production operators, the Quality Team Manager and head office in London.

Principle Responsibilities:

1. ISO 9001 Quality Management System

· Maintain and improve the ISO 9001 QMS.

· Conduct internal audits and support external audits.

· Ensure documentation and procedures are up to date and compliant.

2. Inbound/Finished Good Inspection

· Oversee inspection of incoming raw materials and components.

· Follow inspection criteria and sampling plans.

· Coordinate with HQ to resolve quality issues.

· Maintain records of inspection results and supplier performance.

· Perform checks on finished products according to our quality control plan to ensure they meet all required standards (100% checks).

3. In-Production Process Control

· Monitor and audit in-process production to ensure compliance with quality standards.

· Follow Statistical Process Control (SPC) and implement other quality tools.

· Work with production team & engineering to identify and resolve quality issues.

· Support root cause analysis and continuous improvement initiatives.

3. Reporting & Documentation

· Prepare quality reports and present findings to management.

· Maintain quality documentation such as inspection plans, SOPs, and work instructions.

4. Cross-functional Collaboration

· Liaise with engineering, production, and procurement teams.

· Train employees on quality standards and procedures.

Qualifications:

- Bachelor’s degree or higher in Engineering, Science or related technical field

- Diploma holders with strong experience may also be considered

Certifications (preferred but not required)

- ISO 9001:2015 Internal Auditor or Lead Auditor certificate

- Certified Quality Engineer (COE) or Certified Quality Auditor (CQA) from ASQ

Professional Experience:

- 3–5 years of relevant experience in quality assurance or quality control in a manufacturing environment.

- Hands-on experience with ISO 9001 implementation and audits.

- Familiarity with supplier quality and in-process inspection.

- Knowledge of how to use a network analyser would be beneficial.

- Experience with soldering and connector fitting is a plus but not essential.

Personal Attributes:

The ideal candidate will be expected to possess the following personal attributes:

- Organised and methodical, so that documentation, audits and inspections can be conducted methodically.

- An informed decision maker who is alive to the importance of their role and the key part information and the sharing of information plays within it.

- Strong written, verbal and presentation skills to communicate their ideas to the wide variety of partners they encounter within the role.

- Able to work independently as well as part of an international team (colleagues based abroad).

Remuneration: SGD42K to SGD54K

Hours of work: 40 hours per week

8:30am to 5:30pm Monday to Friday, with one hour lunch break unpaid

Benefits:

· Company events

· Annual Wage Supplementation

· Health Insurance

· 15 days holiday + 1 extra day per year of service, capped at 20 days.

· Sick pay

· Childcare leave

· Casual dress

· Benefit Hub

Panorama Antennas is an Equal Opportunities Employer