1,550 Qa Engineers jobs in Singapore

Responsibilities

• Implement and maintain all quality and food safety control processes in compliance with company standards, HACCP, ISO, local statutory requirements, and Halal standards.
• Oversee and implement QC & QA procedures across production.
• Conduct inspections on raw materials, in-process, and finished goods.
• Schedule and keep track of product testing activities.
• Maintain and calibrate QC tools and equipment to ensure accuracy.
• Handle audits, documentation, and corrective actions.
• Collaborate with production teams to uphold consistent product quality.
  Perform ad-hoc duties as assigned by management.

Requirements

• Diploma in Food Science, Food Technology, or related field.
• Minimum 2–3 years of working experience in a QA/QC-related field within the food industry.
• Positive work attitude and strong self-initiative.
• Good knowledge of GMP, HACCP, MUIS Halal, ISO 22000, FSSC 22000, and related standards.

Key Responsibilities:

• Perform Incoming Quality Control activities to ensure only qualified materials delivered.
• Support all daily activities assigned by supervisor.

• Support on IT solution development for productivity improvement.

• To auto update the information between 'QVL and Sampling Frequency List Fields, Data Setting Maintenance> system and 'Sampling Grade', 'Sampling time' & 'Conformance Test'.

• To notify the IQC by email when a new RT is created by warehouse personnel.
• To notify SQM should any material inactive for >2 years via email.
• Auto email to supplier for requesting the sample.

Qualifications:

• Candidates pursuing diploma or Degree are welcome
• Strong attention to detail and organizational skills.
• Familiarity with Microsoft office (e.g., Microsoft Word, MS Excel, MS PowerPoint, PDF editors).

Job Description:

The Quality Control (QC) Supervisor for Mechanical will support Site Management Team in monitoring quality and compliance throughout the construction of a Power Plant project located in Jurong Island. Reporting to the QA Manager and working closely with the Mechanical Manager, the QC Supervisor for Mechanical is responsible for overseeing the mechanical execution works performed by the EPC contractors, ensuring strict adherence to contractual quality requirements, engineering specifications, applicable codes, and international best practices.

Key Responsibilities:

• Conduct site inspections, audits, and tests to verify that mechanical installations and repairs adhere to design technical specifications, codes, and quality standards
• Ensure all mechanical work complies with relevant industry codes, project specifications, company policies, and contractual obligations
• Oversee critical mechanical activities including material inspection, installation, welding, Non-Destructive Testing (NDT), pressure testing, and final alignment and pre-commissioning checks
• Maintain detailed, accurate, and auditable records of all inspection activities, equipment history, non-conformance reports, and quality documentation
• Identify, document and track quality documentation
• Identify, document, and track quality defects
• Ensure all quality control activities are performed in full compliance with company Health, Safety, and Environment (HSE) policies and local regulatory requirements
• Support and facilitate quality-related meetings with contractors, engineers, and inspectors to resolve issues and drive continuous improvement
• Review and comment contractor-submitted Inspection & Test Plans (ITPs), method statements, and quality documentation prior to execution
• Ensure all mechanical systems are installed, tested, and documented in accordance with punch list and commissioning readiness requirements

Requirements:

• Minimum 10 years' field experience, with relevant inspector's qualification/certification in mechanical works preferably in Oil & Gas, Shipyard or Power Plant industries
• Strong knowledge of mechanical systems, equipment and construction practices
• Familiarity with international standard, especially ASME code, and inspection methods
• Ability to plan, schedule and allocate work to ensure efficient operations and minimal downtime
• Effective communication in good coordination with other departments
• Proficiency in managing project quality plans, inspection and test plans (ITPs) and reports
• Ability to identify and resolve technical issues effectively

• 5 Days Work
• Annual Leave
• Performance Bonus
• Career development opportunities

Responsibilities:

• Conduct quality audits and inspections on incoming and outgoing products to ensure compliance with company standards.
• Carry out QC processes such as product checks, reworks, repairs, and defect documentation.
• Maintain accurate records of QC data, supplier invoices, and stock handling procedures.
• Support continuous improvement initiatives in production and quality processes.
• Perform other quality-related and ad-hoc duties as assigned.

Requirements:

• Minimum Nitec qualification with at least 1 year of quality control experience (retail jewellery or manufacturing preferred).
• Strong attention to detail with basic knowledge of production processes and MS Office.
• Good communication skills, able to multi-task, and quick to learn.

Please submit your updated resume in MS Word format via the "Apply Now" button.

We regret that only shortlisted candidates will be notified.

StaffKing Pte Ltd (20C0358) | Stanley Chin (R

The Quality Control Team Leader is responsible for leading and executing quality control activities, ensuring that Pall products meet internal specifications, customer expectations, and regulatory standards. This role requires strong leadership, technical expertise in analytical testing, and a commitment to maintaining a safe and compliant laboratory environment.

This position is part of the Quality Control Department reporting to the Senior Quality Manager and will be located in Benoi Sector, Singapore.

In this role, you will have the opportunity to:

• Lead the QC team in performing inspections and analytical testing of raw materials, SFG and FG products.
• Develop and maintain QC protocols, SOPs, and documentation aligned with Pall Filtration standards and applicable regulations. Ensure compliance with ISO, GMP, and other relevant quality and regulatory frameworks.
• Monitor and report on quality metrics, including defect rates, test results, and process capability. Conduct root cause analysis and implement corrective and preventive actions (CAPA) for quality issues.
• Collaborate with cross-functional teams including Manufacturing, Engineering, R&D, and Quality Assurance to resolve quality-related issues.
• Support internal, customer, and regulatory audits, ensuring readiness and compliance. Drive continuous improvement initiatives focused on product quality, process efficiency, and team capability.
• Ensure safety and risk assessment (RA) protocols are implemented and followed in the QC laboratory, including chemical handling, equipment usage, and emergency preparedness.
• Maintain calibration and validation of QC equipment and ensure proper documentation.

The essential requirements of the job include

• Bachelor's degree in chemistry, Chemical Engineering, or a related discipline.
• Minimum 5 years of experience in quality control or assurance, ideally within filter manufacturing or similar sectors.
• Proven ability to lead QC teams and oversee laboratory operations efficiently.
• Deep understanding of filtration technologies, materials science, and chemical manufacturing processes.
• Well-versed in ISO standards, GMP, and other relevant regulatory frameworks.
• Skilled in advanced test methods including ICP-MS, GC-MS, NVR, LPC, and TOC.
• Strong analytical thinking, problem-solving capabilities, and effective communication skills.

It would be a plus if you also possess previous experience in:

• PhD or Master's Degree in Chemistry or a related scientific discipline.
• Experience in chemical or filter manufacturing, membrane technologies, or advanced material testing. Proficiency in ICP-MS, GC-MS, NVR, LPC, and TOC test methods.
• Experience with statistical process control (SPC), risk assessment, and laboratory information management systems (LIMS).

Pall Corporation, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond. 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.

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

JOB DESCRIPTION

• Conduct inspection of incoming, in-process and final inspection on machined parts, weldments and assemblies as per technical drawings, customer's specifications and requirements through the use of various types of inspection equipment set up
• Perform dimension check on parts, components and tools using micrometers, calipers, comparators, indicator, CMM & CREAFOAM
  
  Perform visual, mechanical and functional check on components.
  
  Report non-compliance parts to QA Engineer
• Performs visual and dimensional inspection of incoming and outgoing components/parts
• Understand current specifications involving inspection tolerances, limitations, and procedures.
• Responsible for conducting inspection in accordance with approved technical data.

REQUIREMENT

• GCE 'O' / 'A' Level with minimum 3 year working experience or
  
  Diploma in Mechanical / Manufacturing / Quality Management with minimum 1 year working experience.
• Good interpersonal skill and ability to communicate with all levels.
• Good understanding of technical drawing
• Familiar with all inspection methods and techniques
• Basic understanding of General Dimension & Tolerance control
• Proficient in the use of various types of inspection equipment and visual inspection aids
• Preferred: Able to communicate in simple Mandarin to liaise with Mandarin-speaking colleagues and vendors.

At Xandro Lab, we're building the future of longevity and wellness science — from advanced supplements to high-performance skincare. We're looking for a meticulous and motivated Quality Control (QC) Staff member to join our growing team and ensure every product that leaves our facility meets the highest standards of quality, safety, and compliance.

As part of our production and lab operations team, you'll:

• Oversee quality control across supplements and skincare production.
• Check and verify ingredients, formulas, and manufacturing processes to ensure compliance with GMP, ISO, and other certification requirements.
• Manage batch testing — coordinate with accredited labs for microbiological, stability, and safety tests.
• Identify and evaluate new testing labs where needed, comparing capabilities, costs, and turnaround times.
• Maintain detailed QC documentation and assist in internal audits and CAPA implementation.
• Support the Regulatory Affairs team with technical and QC data for product registration and certification.

• Diploma or Degree in Chemistry, Biotechnology, Pharmaceutical Science, or related fields.
• 2–4 years of experience in QC/QA within supplement, cosmetic, or pharmaceutical manufacturing.
• Strong understanding of GMP and ISO 22716 / ISO 22000 standards.
• Excellent attention to detail, documentation discipline, and problem-solving ability.
• Team player who can work cross-functionally with production, R&D, and regulatory teams.

• Familiarity with Singapore's HSA/SFA regulatory requirements.
• Hands-on experience with analytical testing (e.g., HPLC, microbiological assays).
• Experience in both nutraceutical and cosmetic product categories.

At Xandro, we're on a mission to make science-based longevity and performance nutrition mainstream. You'll be part of a passionate, fast-growing team working at the intersection of science, health, and innovation, ensuring every product meets the highest global standards.

If you're detail-driven, quality-obsessed, and want to shape the next generation of wellness products — we'd love to meet you.

Quality Control Associate

• Up till $2800 basic + Variable Bonus
• Geylang
  Monday to Friday, 8.30am to 5.30pm

Roles & Responsibilities

This position is responsible for conducting audit checks to ensure that products meet the established standards, This role also supports the achievement of Company quality target.

1. Confirm to quality standard and quality processes

2. Inspect in-coming and outgoing products according to policies standard.

3. Perform all product processes within section (eg, QC,SAO), Reworks, Repairs, Defective photo-taking

4. Contribute to continuous improvement

5. Maintain Integrity accuracy and completeness of Supplier invoice data and QC data in system

6. Establish standard operating procedures and conditions for handling storage and checklist of stock.

7. Perform other ad-hoc duties as assigned.