280 Precision Engineering Firms jobs in Singapore

We are looking for a Quality Control (QC) Technician who will be responsible for performing document management, defect analysis, quality inspections, and reporting to ensure product quality and compliance with standards. The role involves coordination with various departments and external partners to maintain high-quality standards across all stages of production and shipment.

• Perform document review, revision, circulation, training, and retention for both hard copy and soft copy; maintain document storage area housekeeping.
• Conduct failure analysis on field return samples and in-process defect samples.
• Arrange test samples for testing at Batam factory, Japan headquarters, and external test labs.
• Perform incoming material quality inspections and liaise with vendors regarding non-conformity issues.
• Conduct finished goods outgoing quality inspections, packaging, and prepare quality documentation for shipment.
• Carry out quality patrol inspections to monitor ongoing quality standards.
• Lead quality-related meetings and disseminate meeting minutes.
• Evaluate new and changed samples for quality, and present findings using PowerPoint.
• Update daily, weekly, and monthly quality reports.
• Communicate with BT factory on special shipment instructions and follow up until issues are resolved.

• NTC (National Trade Certificate) or equivalent diploma/NITEC in relevant fields such as Electronics, Mechanical, Quality Assurance, or related technical disciplines.

• Understanding and practical application of quality management systems and tools such as ISO 9001, SPC (Statistical Process Control), FMEA (Failure Mode and Effects Analysis), FTA (Fault Tree Analysis), and 8D methodology.
• Ability to interpret technical drawings and specifications.
• Proficiency in operating measurement microscopes and other inspection tools.
• Ability to work in a clean room environment, including wearing appropriate protective gear.
• Fluent in English and Chinese (both spoken and written) for effective communication and documentation with shipping vendors across China region.
• At least 1 year of working experience in a similar electronic or manufacturing environment, particularly in quality inspection, defect analysis, or QC-related tasks.
• Open to fresh graduates without prior experience, provided they demonstrate relevant skills and knowledge.

• Open-mindedness and adaptability to job changes.
• Effective communication and presentation skills.
• Willingness to work overtime if required.

• Great exposure to a large MNC
• Hybrid work arrangement
• Medical, Dental & Leave benefits
• Access to the Company Gym and Karaoke room
• Company-sponsored training for professional development
• Work location within walking distance from Bedok MRT
• Work hours: Mon to Fri (8am - 5pm)

Join Panasonic Industry, a company with over 100 years of expertise in device technologies, committed to transforming society by delivering innovative solutions that exceed customer expectations. Be part of a team that drives meaningful, impactful change through advanced technological solutions.

Job Responsibilities

• Oversee and provide guidance to QC Inspection Team to ensure implementation of all inspection-related activities according to standards, including proper disposition and handling of non-conforming material/product.
  - Pre-inspection of designated goods (at warehouse).
  - Sampling and QC inspection of incoming materials (pre-shipment samples, raw materials, bulk, semi-finished and finished products, packaging materials) and out-going products.
  - In-process inspection to ensure that quality, hygiene, and safety standards are met.
• Identify and investigate OOS (out-of-specification) or NC (non-conformance) cases, analyse the root causes, and monitor closely the resolution and correction status.
• Investigate product feedbacks, analyse quality-related problems, and recommend problem resolution.
• Perform testing on samples of new raw materials, products, packaging etc., or arrange for lab testing (including stability study as required).
• Perform QC inspection and product-related performance data measurement and analysis.
• Work with relevant parties to establish specifications and quality attributes of raw material, packaging and product, confirm appropriate test method for each QC parameter, and document evidence.
• Contribute for establishing and improving relevant QC SOP and inspection/testing-related work instructions (in compliance with GMP and ISO requirements).
• Ensure proper QC documentation including Master Specifications, QC Records (including electronic logs), QC Test Reports, Lab Test Reports, Non-Conformance Reports, COA etc.
• Establish and maintain product stability testing guideline.
• Support and assist Quality Assurance on External Provider Quality Management.
• Ensure cleaning and environmental monitoring programmes for the site are done accordingly.
• Manage retention room for retention, reference and post-inspection samples, and sample retention system.

Requirements

• Degree in Science or Engineering (preferably in Cosmetic Science, Chemistry, Pharmacy, Nutrition or relevant field)
• Preferably 2 years of working experience in the quality control of cosmetics, pharmaceuticals, dietary supplement, food, or skincare/medical device. Fresh Graduates are welcome to apply too.
• Experience in a GMP environment or with knowledge of GMP.
• Knowledge of relevant product standards, quality control and test methods.
• Stringent compliance to procedures, guidelines, standards, and regulations.
• Self-starter, good at working well independently with initiatives.
• Meticulous & detail oriented.
• Analytical & problem-solving skills.
• Time management skills (scheduling, prioritising) to meet deadlines.

Job Responsibilities

• Oversee and provide guidance to QC Inspection Team to ensure implementation of all inspection-related activities according to standards, including proper disposition and handling of non-conforming material/product.
  - Pre-inspection of designated goods (at warehouse).
  - Sampling and QC inspection of incoming materials (pre-shipment samples, raw materials, bulk, semi-finished and finished products, packaging materials) and out-going products.
  - In-process inspection to ensure that quality, hygiene, and safety standards are met.

• Identify and investigate OOS (out-of-specification) or NC (non-conformance) cases, analyse the root causes, and monitor closely the resolution and correction status.

• Investigate product feedbacks, analyse quality-related problems, and recommend problem resolution.

• Perform testing on samples of new raw materials, products, packaging etc., or arrange for lab testing (including stability study as required).

• Perform QC inspection and product-related performance data measurement and analysis.

• Work with relevant parties to establish specifications and quality attributes of raw material, packaging and product, confirm appropriate test method for each QC parameter, and document evidence.

• Contribute for establishing and improving relevant QC SOP and inspection/testing-related work instructions (in compliance with GMP and ISO requirements).

• Ensure proper QC documentation including Master Specifications, QC Records (including electronic logs), QC Test Reports, Lab Test Reports, Non-Conformance Reports, COA etc.

• Establish and maintain product stability testing guideline.

• Support and assist Quality Assurance on External Provider Quality Management.

• Ensure cleaning and environmental monitoring programmes for the site are done accordingly.

• Manage retention room for retention, reference and post-inspection samples, and sample retention system.

Requirements

• Degree in Science or Engineering (preferably in Cosmetic Science, Chemistry, Pharmacy, Nutrition or relevant field)

• Preferably 2 years of working experience in the quality control of cosmetics, pharmaceuticals, dietary supplement, food, or skincare/medical device. Fresh Graduates are welcome to apply too.

• Experience in a GMP environment or with knowledge of GMP.

• Knowledge of relevant product standards, quality control and test methods.

• Stringent compliance to procedures, guidelines, standards, and regulations.

• Self-starter, good at working well independently with initiatives.

• Meticulous & detail oriented.

• Analytical & problem-solving skills.

• Time management skills (scheduling, prioritising) to meet deadlines.

Ventós is a distributor of aroma chemicals and essential oils for flavors and fragrances industries all over the world. Young, dynamic, highly-specialized professionals make up our team of technicians, accountants, sales, purchases, logistics and production.

With more than 3.500 products permanently available in stock we can offer a just-in-time response to our customers needs. We have established commercial agreements with important producers of raw materials, which give Ventós a leading position as agents or distributors of their products.

We are looking to strengthen our team in Singapore by adding a Quality Control Specialist.

Responsibilities:

• Ensure the quality control of raw materials and finished products through routine analytical testing (GC, GC-MS, physical properties, etc.), in compliance with internal specifications and international standards.
• Conduct thorough inspection and testing of incoming materials, in-process production, and finished goods to ensure compliance with established quality standards and specifications.
• Develop and maintain detailed QC documentation, including inspection reports, test records, non-conformance logs, and trend analysis.
• Prepare and maintain technical documentation (CoAs, TDS, SDS, IFRA certificates, allergen declarations, etc.) for internal use and for customer requests.
• Collaborate with production and R&D teams to ensure regulatory compliance of products across different markets (EU, US, Asia, etc.).
• Monitor and implement updates to relevant legislation and international regulatory frameworks (REACH, CLP, IFRA, FDA, etc.).
• Assist with internal and external audits, ensuring all records are up to date and accessible.
• Support the Regulatory Affairs Manager in preparing product dossiers and registration files when required.
• Coordinate with suppliers to collect technical and regulatory documentation of raw materials.
• Participate in continuous improvement projects to optimize quality and compliance processes.
• Maintain accurate and organized records in compliance with ISO and GMP standards.

Profile:

• Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, or a related scientific field. Additional training in Regulatory Affairs or Quality Management is a plus.
• Minimum of 2–3 years of experience in a similar role within the chemical, fragrance, cosmetics, or food industry.
• Solid understanding of international regulatory frameworks (REACH, CLP, IFRA, GHS, etc.).
• Familiarity with analytical techniques such as GC and GC-MS is highly desirable.
• Excellent organizational and multitasking abilities, with strong attention to detail.
• Fluent in English; additional languages (especially Spanish) are an advantage.
• Proficient in Microsoft Office and experience working with ERP systems (Navision highly valued).

Additional Information:

• Working hours: From 8am to 5pm with 1 hour for lunch
• Employment Type: Permanent contract with 3-month probation period

Would you like to join our team? Send us your application!

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Chemical Manufacturing and Wholesale Chemical and Allied Products

Referrals increase your chances of interviewing at Ernesto Ventós by 2x

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Queenstown, Central Singapore Community Development Council, Singapore 5 days ago

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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.

Key Responsibilities

• Manage the storage and inventory of laboratory samples
• Conduct analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samples
• Ensure strict compliance with cGxP standards, including data integrity requirements
• Execute and document stability testing (if not centralized), including storage, testing, and reporting to cGxP standards
• Follow all Health, Safety, and Environment (HSE) guidelines
• Identify and report safety risks or potential incidents, and propose preventive solutions
• Participate in mandatory training and retraining programs
• Support operations during rotating day/night shifts

Role Requirements

Essential Qualifications and Experience

• Prior experience in a laboratory setting within the pharmaceutical industry (QA, production), with exposure to aseptic techniques preferred
• Proficiency in administrative and documentation tasks compliant with GMP and HSE standards
• Demonstrated strengths in:
• Breakthrough analysis and problem-solving
• Resilience and adaptability
• Operational efficiency and continuous learning
• Digital fluency and technical skills

Technical Competencies

• Hands-on knowledge of laboratory instruments and QC testing procedures
• Strong command of GxP, TQM principles, and lab excellence standards
• Ability to maintain QC IPC/DS laboratory equipment and systems in accordance with cGMP compliance
• Competent in executing product testing within timelines and contributing to validation and method transfer protocols
• Skilled in performing routine in-process, release, and stability testing, including documentation review
• Capable of supporting lab investigations and leading root cause analysis
• Detail-oriented in preparing and verifying QC documentation to ensure accuracy, consistency, and regulatory compliance
• Proactively identifies opportunities to optimize testing procedures
• Supports audit readiness and participates in internal audits and inspections by health authorities

Join to apply for the Quality Control Specialist role at Cytiva

Join to apply for the Quality Control Specialist role at Cytiva

Direct message the job poster from Cytiva

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

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
  
  

• 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
  
  

• 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.
  
  

• Seniority level Not Applicable

• Employment type Full-time

• Job function Quality Assurance
• Industries Biotechnology Research, Medical Equipment Manufacturing, and Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Cytiva by 2x

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

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.

Responsibilities:

• Online Quality Checking (Metal Detector, Cooker, Pasteurizer, Steamer)
• Online Finished Product Testing
• Monthly Verification of CCP (Critical Control Point)
• Online Verification Sampling for Microbial Analysis
• Internal Calibration of Weighing Scales
• Verification on goods return
• Handle Customers’ Complaint
• Conduct routine physical, chemical, sensory and other analyses accordingly.
• Take appropriate decisions for rework of material based on historical trend and in consultation with seniors
• Raise non-conformation for quality deviations of Raw Material/Finished Goods and follow up with proper closure of corrective and preventive action
• Initiate actions to investigate customer complaint in consultation with relevant team members
• Collect comprehensive evidence/crucial data, provide sound reasoning and propose possible root cause for customer complaints and internal rejection
• Maintain up-to-date quality control programs, policies, process workflows, procedures and work instructions

REQUIREMENTS:

• Diploma / Degree in Food Science preferred
• At least 2 years of relevant experience will be considered for Senior position
• Experienced and passionate in Continuous Improvement
• Exceptional problem-solving skills
• Good Knowledge of Quality Management Systems (HACCP, BRC, ISO 22000)
• Good Communication, Organizational and Analytical Skills
• Strong ability to work well in a team and independently
• Excellent IT skills, particularly in MS Excel, PowerPoint, Word, Access
• Ability to work with multiple priorities in a fast-paced environment is required.
• 5 Days Work Week + 1 Saturday
• Undertake any other ad-hoc projects/ tasks assigned
• Job Scope, Work Day and Work Hours subject to changes depending on work requirement
• Fresh grads are welcome
• Salary package commensurate with experience