1,485 Quality Control Specialists jobs in Singapore
Quality Control Specialist
Posted 16 days ago
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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- Seniority level Mid-Senior level
- Employment type Full-time
- Job function Quality Assurance
- Industries Chemical Manufacturing and Wholesale Chemical and Allied Products
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#J-18808-LjbffrQuality Control Specialist
Posted 25 days ago
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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 .
Quality Control Specialist
Posted today
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The role of a Quality Control Specialist is pivotal in ensuring the precision and quality of manufactured parts.
To achieve this, performing regular inspections using measurement tools such as calipers, micrometers, height gauges, and CMM machines are essential duties of this position.
Key Responsibilities:
- Conducting dimensional and visual inspections to ensure products meet engineering drawings and customer specifications are performed regularly.
- Inspectors accurately record inspection results on quality forms and maintain proper documentation for traceability and audits.
- Detecting non-conformities or defects and reporting them, with assistance provided for root cause analysis and corrective actions.
- Maintaining adherence to quality procedures, work instructions, and safety standards throughout the production process.
In addition to these responsibilities, carrying out any other assigned tasks by management is expected.
Requirements:
- A minimum of 1 year of experience in a related field is required.
- Candidates with a Mechanical Engineering background are preferred.
Quality Control Specialist
Posted today
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About the Role
We are seeking a skilled Quality Control Specialist to join our team.
Main Responsibilities:
- Perform analytical testing of incoming raw material samples using FTIR, wet chemistry identity testing and other approved compendial methods.
- Manage sample receipt, storage and reagent preparation according to cGxP requirements.
- Conduct raw material method validation/verification and routine release testing.
- Document analytical activities in compliance with GMP, HSE and data integrity standards.
- Support stability testing and associated sample management when applicable.
- Participate in laboratory investigations and support related change controls.
- Maintain the QC Raw Materials laboratory in full cGMP compliance and support audits/inspections.
- Contribute to continuous improvement projects within the QC laboratory.
About You
To be successful in this role you will need:
Required Skills and Qualifications:
- A degree in Chemistry, Biochemistry or Pharmaceutical Sciences, or equivalent scientific field.
- 3-5 years experience in pharmaceutical laboratory environments, preferably in quality control or quality assurance.
- Experience with analytical testing of raw materials, including FTIR and wet chemistry identity tests.
- Knowledge of GMP and cGxP compliance requirements.
- Excellent communication and problem-solving skills.
Quality Control Specialist
Posted today
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Quality Control Specialist - Food Manufacturing
About the JobWe are seeking a Quality Control Specialist to join our team in the food manufacturing industry. As a Quality Control Specialist, you will be responsible for ensuring that all products meet the required standards of quality and safety.
Main Responsibilities:
- In charge of day-to-day inspection of in-process and finished products.
- Ensure hygiene standard of process workers and processing facilities are maintained.
- Responsible for reporting any non-conformance of products/process/hygiene violation in a timely manner.
- Assist in guiding production leaders/operators in implementing corrective actions and continuous improvement in production area.
- Ensure proper records of product and hygiene inspections.
- Implementation / maintenance of SFA, MSC/ASC, Halal, FSSC 22000, HACCP certifications and any other relevant certification.
- To liaise with authorities (eg, SFA) on related Food Safety / License issues when required.
- In charge of health certificate application and laboratory reports arrangement and maintenance of such records.
To be successful as a Quality Control Specialist, you should possess the following qualifications:
- Minimum Diploma in Food Science or Microbiology.
- At least 1 year of experience as QC in the Food Manufacturing industry.
- Understanding FSSC 22000/HACCP/GMP/ Halal requirements is an added advantage.
Benefits
We offer competitive remuneration packages including:
- Meal Provided
- Outpatient Medical & Dental Benefits
How to Apply
If you are interested in this role, please email your resume to us for further consideration.
Quality Control Specialist
Posted today
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Job Description:
">- We are seeking a Quality Control Specialist to join our team. As a Quality Control Specialist, you will be responsible for evaluating and grading green coffee beans for defects, moisture, density, and overall quality. You will also maintain records of supplier samples and quality results for traceability. ">
- You will conduct regular cupping sessions with the QC team to assess flavor, aroma, body, and overall profile of coffee. You will also monitor roasting consistency to ensure adherence to roast profiles and quality standards. ">
- In addition, you will record and analyze quality control data for both green and roasted coffee. You will prepare quality reports and highlight any deviations or concerns to the Head of Coffee. ">
- You will assist in ensuring proper storage conditions for green and roasted coffee to preserve freshness and quality. You will report quality issues, non-conformances, or supplier inconsistencies promptly. ">
- You will collaborate with procurement and production teams on incoming and outgoing product inspections. Additionally, you will provide administrative support and perform other ad hoc duties as assigned by management.
Quality Control Specialist
Posted today
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Job Description
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Your Role:
Quality Control (QC) Specialist is to promote and integrate quality into every aspect of our BioReIiance biologics safety testing business in Singapore. Duties of the role include the support of QC operations (environmental monitoring and release of critical raw materials), data integrity and systems administration to ensure that laboratory testing operations are in full compliance with sound scientific practice, GxP and Standard Operating Procedures (SOPs). As a QC Specialist, you will ensure quarantine materials are received and released for use as per appropriate quality procedures. The ability to develop and maintain effective working relationships with operational, support services and quality assurance personnel will be critical for success in this role.
Who You Are:
- Graduate degree in life sciences or microbiology or higher related degree
- Minimum of 2-3 years of experience
- Demonstrable scientific expertise in microbiology related works
- Previous experience working in a Quality Control materials release environment
- Previous Pharmaceutical experience would be ideal; however, other industry backgrounds would be considered
- You will have previous work experience within a GLP / GMP regulated environment would be highly desirable
- You are strongly focused on quality and safety, with strong planning and organisational skills
- You have good communication and interpersonal skills and are highly self-motivated, with strong initiative and drive
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity
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Quality Control Specialist
Posted today
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Seeking a detail-oriented and organized individual to maintain quality standards by approving incoming materials, in-process production, and finished products. The Quality Assurance Assistant will uphold safety regulations and supervise the production process to ensure all products meet GMP expectations.
Responsibilities:- Perform regular quality assessments on incoming materials from vendors and outgoing products for delivery.
- Manage and qualify products and material quality to meet compliance and industry standards.
- Recommend improvements to the production process to ensure quality control.
- Resolve quality-related issues in a timely manner.
- Keep inventory update of materials, documents, and data to meet GMP standards.
- Maintain QC records.
- Approve all finished products by confirming specifications and conducting required tests.
- Document and update inspection results by completing reports and logs.
- Keep measurement equipment operating by following operating instructions and calling for repairs.
- Maintain a safe work environment by following standards and procedures and complying with legal regulations.
The ideal candidate will possess excellent communication and leadership skills, with a keen attention to detail. They will be able to devise sampling procedures and directions for recording and reporting quality data, plan and conduct testing and inspections, document internal audits, and investigate customer complaints and non-conformance issues.
Quality Control Specialist
Posted today
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Job Description
- Perform routine microbiological testing on raw materials, finished products, water, and environmental samples.
- Conduct microbial limit tests, sterility testing, endotoxin testing, and microbial identification.
- Prepare culture media and maintain laboratory equipment in compliance with quality standards.
- Apply Good Laboratory Practices (GLP) and follow Standard Operating Procedures (SOPs).
- Support the investigation of non-conformities and participate in root cause analysis.
- Document and review test results in laboratory notebooks and LIMS systems.
- Assist with validation and verification of microbiological methods.
- Ensure all activities are aligned with regulatory and client-specific requirements
- Academic background: degree in Microbiology, Life Sciences, or related fields.
- Around 1 year of relevant experience in a QC microbiology role.
- Experience with microbiological techniques in pharmaceutical or biotech environment
- Experience with endotoxin testing, bioburden testing, and microbial identification
- Knowledge of GMP/GLP requirements and aseptic techniques
- Familiarity with environmental monitoring programs and cleanroom classifications
- You have an ability to synthetize and prioritize while maintaining strong attention to detail
- Comfortable with working in shift
Quality Control Specialist
Posted today
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Job Summary:
We are seeking a Quality Control Supervisor to lead our team of inspectors in ensuring that products meet the highest quality standards.
- The ideal candidate will have at least 1-2 years of experience in manufacturing quality control, with a strong understanding of QC tools and equipment.
Responsibilities:
- Implement and maintain Quality Control policies throughout production
- Oversee QC sampling, inspections, and use measuring tools for quality checks
- Guide the team in preparing samples and testing to meet standards
- Work with the production team to quickly resolve quality issues
- Keep detailed records and create reports on QC findings for management
Requirements:
- Strong analytical and problem-solving skills
- Excellent communication and leadership skills
- Ability to work independently and as part of a team
What We Offer:
- A competitive salary package
- Ongoing training and development opportunities
- A dynamic and supportive work environment
Apply Now:
- Submit your application by clicking the link below