2,077 Quality Engineer jobs in Singapore

• Develop, implement, and oversee project-specific QA/QC plans, inspection protocols, and checklists.
• Ensure construction works meet BCA CONQUAS and Quality Mark standards.
• Lead quality inspections, audits, and evaluations across all trade disciplines.
• Collaborate with consultants, subcontractors, and internal teams to address and resolve quality-related issues.
• Monitor on-site activities to ensure compliance with project specifications and quality requirements.
• Review and approve materials and method statements in line with project standards.
• Maintain accurate records of inspections, non-conformance reports, and corrective actions taken.
• Train and support site teams in adhering to quality standards and implementing best practices.
• Prepare the site for CONQUAS and Quality Mark assessments, including mock-up inspections and scoring strategies.
• Drive continuous improvement initiatives to enhance overall quality performance.
• Oversee material testing, as well as mock-up, PMU, and VMU processes for façade works.

Description

• Plan, execute, and document temperature mapping studies for chambers (cold rooms, freezers, incubators, stability chambers).
• Prepare and review validation protocols, reports, and deliverables in Kneat or equivalent systems.
• Perform data integrity assessments and ensure compliance with GDP and ALCOA+ principles.
• Draft and maintain SOPs for temperature mapping and chamber qualification.
• Support deviation management, change control, and CAPA implementation.
• Provide technical input for requalification planning and continuous improvement.
• Collaborate with QC, QA, and Engineering to support audit and inspection readiness.

Responsibilities

• Good experience in temperature mapping of chambers within pharmaceutical/biotech or regulated industries.
• Knowledge of GDP, ALCOA+ principles, and qualification practices.
• Familiarity with mapping across a variety of chambers is advantageous.
• Experience with validation documentation and use of Kneat preferred.
• Strong technical writing, data review, and teamwork skills.

We are seeking a highly skilled and detail-oriented Quality Control Engineer to join our dynamic team. The successful candidate will play a critical role in ensuring that our products and processes meet the highest standards of quality, safety, and compliance.

• Develop, implement, and maintain quality control systems, standards, and procedures.
• Conduct inspections, testing, and audits to ensure compliance with specifications and regulatory requirements.
• Identify quality issues, analyze root causes, and implement corrective and preventive measures.
• Collaborate with cross-functional teams including production, engineering, and suppliers to resolve quality concerns.
• Prepare and maintain accurate documentation, reports, and quality records.
• Drive continuous improvement initiatives to enhance product reliability and process efficiency.
• Ensure compliance with ISO and other relevant quality management standards.

• Bachelor's degree or Diploma in Engineering (Mechanical, Electrical, Manufacturing, or related field).
• Proven experience in quality control, assurance, or engineering
• Strong knowledge of quality management systems, standards, and methodologies.
• Proficiency in quality tools such as FMEA, Six Sigma, and root cause analysis.
• Excellent problem-solving, analytical, and communication skills.
• Ability to work independently as well as collaboratively in a fast-paced environment.

• Competitive salary between SGD 9,000 – 11,500 .
• Professional growth opportunities and continuous learning.
• A supportive and innovative working environment.
• Exposure to advanced quality systems and processes.

We are hiring Quality Control Engineer - Temperature Mapping with below requirements;

• Plan, execute, and document temperature mapping studies for chambers (cold rooms, freezers, incubators, stability chambers).
• Prepare and review validation protocols, reports, and deliverables in Kneat or equivalent systems.
• Perform data integrity assessments and ensure compliance with GDP and ALCOA+ principles.
• Draft and maintain SOPs for temperature mapping and chamber qualification.
• Support deviation management, change control, and CAPA implementation.
• Provide technical input for requalification planning and continuous improvement.
• Collaborate with QC, QA, and Engineering to support audit and inspection readiness.

Responsibilities

• Good experience in temperature mapping of chambers within pharmaceutical/biotech or regulated industries.
• Knowledge of GDP, ALCOA+ principles, and qualification practices.
• Familiarity with mapping across a variety of chambers is advantageous.
• Experience with validation documentation and use of Kneat preferred.
• Strong technical writing, data review, and teamwork skills.

Position title : Quality Control Engineer

Location: Admiralty

Working Days:  5 Day A Week

Working hours : 9:00am - 6:00pm

Salary : $3000 - $4500 (depends experience)

Key Responsibilities

Job Descriptions:

• To support in ensuring the product quality in satisfying company and customer need and requirements
• To support in ensuring quality control through documentation such as maintaining of QC report, SOP specifications and test methods are available.
• Perform internal and external audit to compliance with QMS requirement.
• Support Production on all quality-related activities, including working closely with supplier and Engineering
• Participate in investigations and ensure CAPA findings, risks, recommendations, Non-Conformances reporting and outcomes are appropriate and are clearly documented and communicated
• Oversee implementation and improvement of IQC, IPQC, OQC process related to customer's products in a timely, efficient, and effective manner.

Requirements

• Experience in Quality control under semi-conductor manufacturing equipment.
• Minimum Diploma qualification

Interested applicants, WA your resume to ‪‪ ‬‬ or email your resume to

TAN YEN ZHEN (CHEN YANZHEN) REG NO: R

THE SUPREMEHR ADVISORY PTE LTD EA NO: 14C7279

Position title : Quality Control Engineer

Location: Sembawang

Working Days:  5 Day A Week

Working hours : 9:00am - 6:00pm

Salary : $3000 - $4500 (depends experience)

Key Responsibilities

Job Descriptions:

• To support in ensuring the product quality in satisfying company and customer need and requirements
• To support in ensuring quality control through documentation such as maintaining of QC report, SOP specifications and test methods are available.
• Perform internal and external audit to compliance with QMS requirement.
• Support Production on all quality-related activities, including working closely with supplier and Engineering
• Participate in investigations and ensure CAPA findings, risks, recommendations, Non-Conformances reporting and outcomes are appropriate and are clearly documented and communicated
• Oversee implementation and improvement of IQC, IPQC, OQC process related to customer's products in a timely, efficient, and effective manner.

Requirements

• Experience in Quality control under semi-conductor manufacturing equipment.
• Minimum Diploma qualification

Samuel Siaw

The Supreme HR Advisory Pte Ltd

EA No: 14C7279

Reg No: R

About Us:

VisionPower Semiconductor Manufacturing Company Pte Ltd ( VSMC ) is a new joint-venture 300mm semiconductor wafer manufacturing facility to be built in Singapore. We are looking for committed, resilient and passionate talents to launch a promising future that power the next generation devices and systems. If you share the same passion to pursue excellence, join us to make an impact and be part of something special

Role Summary:

You will be responsible for ensuring quality control in semiconductor manufacturing processes, managing internal audit activities, managing engineering changes, resolving production issues, and driving continuous improvement.

Key Responsibilities :

• Develop, implement, and maintain quality control measures for semiconductor manufacturing processes.
• Manage internal audit system and perform internal & Supplier audit
• Monitor production data to identify trends and initiate corrective actions to improve yield and reliability.
• Review and validate quality systems and specifications for new equipment and processes.
• Ensure smooth integration of new technologies into the production line with a focus on maintaining quality standards.
• Manage quality control for engineering changes in wafer fabrication, including reviewing change requests, conducting risk assessments, and ensuring compliance with quality standards.
• Oversee the quality of incoming raw material through inspections and audits.
• Collaborate with raw material suppliers to identify quality issues, implement corrective actions, and drive continuous improvement initiatives.
• Lead the response to major abnormal events in the wafer fab, including root cause analysis and corrective actions.
• Manage RMAs and work with customer quality teams to resolve issues and improve customer satisfaction.

Education Qualification & Essential Experiences:

• Bachelor's degree or higher in Electronics, Physics, Materials Science, or other related engineering fields.
• At least 2-3 years of relevant work experience.

Personal Attributes:

• Excellent coordination and communication skills, with the ability to work independently and manage multiple tasks effectively in a fast-paced environment.
• Able to be reliable and accountable in all tasks and responsibilities.
• Have the drive to achieve goals and complete tasks independently.
• Proficient in effectively conveying information through both written and verbal communication.

VSMC promotes diversity and inclusivity in our workforce; and hiring will be conducted in phases.

Job Descriptions :

• To support in ensuring the product quality in satisfying company and customer need and requirements

• To support in ensuring quality control through documentation such as maintaining of QC report, SOP specifications and test methods are available.

• Perform internal and external audit to compliance with QMS requirement.

• Support Production on all quality-related activities, including working closely with supplier and Engineering

• Participate in investigations and ensure CAPA findings, risks, recommendations, Non-Conformances reporting and outcomes are appropriate and are clearly documented and communicated

• Oversee implementation and improvement of IQC, IPQC, OQC process related to customer's products in a timely, efficient, and effective manner.

Requirement : -

• Ability to work under pressure

• Experience in Quality control under semi-conductor manufacturing equipment.

• Able to work independently

• Minimum Diploma qualification

• Able to work late if require.

Role Overview

We are seeking a QC Engineer with strong experience in Computer System Validation (CSV) for analytical laboratory instruments /equipment. The role ensures compliance with 21 CFR Part 11, data integrity, and global validation standards in a regulated GMP environment.

Key Responsibilities

• Lead CSV activities for analytical equipment or instruments and lab computerized systems (e.g., HPLC, GC, UV, LIMS, Empower).
• Develop and execute validation deliverables: URS, risk assessments, IQ/OQ/PQ, RTM, and summary reports.
• Ensure compliance with 21 CFR Part 11, Annex 11, ALCOA+ principles, and data integrity controls.
• Evaluate and validate audit trails, security settings, and user access controls.
• Support integration between instrument, PC, network, and enterprise systems.
• Draft, review, and maintain SOPs, validation documentation, and audit readiness materials.
• Contribute to lifecycle management of systems including periodic reviews, upgrades, and change control.
• Collaborate with QA, QC, and IT to support inspection readiness and continuous improvement.

Requirements

• Bachelor's degree in chemistry, Life Sciences, Engineering, or related discipline.
• 3–10 years' experience in analytical instrument/equipment CSV within pharmaceutical/biotech QC labs.
• Strong knowledge of cGMP, GAMP 5, 21 CFR Part 11, Annex 11 .
• Hands-on experience with microbiology analytical equipment is an advantage.
• Familiarity with electronic validation tools (e.g., Kneat ) is preferred.
• Strong documentation, troubleshooting, and cross-functional collaboration skills.