998 Control Specialist jobs in Singapore
Quality Control Specialist
Posted 8 days ago
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Get AI-powered advice on this job and more exclusive features.
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
Referrals increase your chances of interviewing at Ernesto Ventós by 2x
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#J-18808-LjbffrQuality Control Specialist

Posted 17 days ago
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Job Description
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
Job Viewed
Job Description
Get AI-powered advice on this job and more exclusive features.
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
Employment type
Full-time
Job function
Job function
Quality AssuranceIndustries
Chemical Manufacturing and Wholesale Chemical and Allied Products
Referrals increase your chances of interviewing at Ernesto Ventós by 2x
Sign in to set job alerts for “Quality Assurance Specialist” roles.
Associate Specialist, Quality Assurance (WDA)
Assistant Vice President, Quality Assurance Specialist
Assistant Vice President, Quality Assurance Specialist
Assistant Vice President, Quality Assurance Specialist
Assistant Vice President, Quality Assurance Specialist
QA Specialist - 15 months training programme
Assistant Manager, Training and Quality Assurance
TikTok LIVE - Content Quality Assurance Specialist (English Speaking)
Manufacturing Quality Assurance (MQA) - Train & Place Program
Quality Assurance & Risk Oversight Specialist
Anti-Money Laundering Operations Quality Assurance - MariBank
Pharmacovigilance (PV) & Quality Assurance (QA) Specialist
Healthcare Quality Assurance Associate Manager
Lifescience Healthcare (LSH) Quality Assurance Manager
Healthcare Quality Assurance Associate Manager
TikTok LIVE - Content Quality Assurance Specialist (Bahasa Indonesia Speaking)
Anti-Money Laundering Operations Quality Assurance - MariBank
Healthcare Quality Assurance Associate Manager
QA Specialist (Compliance) (PCP) 15 months training programme
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-LjbffrQuality Control Specialist
Posted today
Job Viewed
Job Description
Job Title: Quality Assurance Specialist
The ideal candidate will be responsible for overseeing the quality inspection process and ensuring compliance with established standards.
Main Responsibilities:
- Oversight of daily quality inspection processes.
- Timely inspection and verification of finished parts.
- Approval of incoming materials by confirming specifications.
- Creation of quality inspection reports.
- Raising notifications for quality control issues.
Requirements:
- Nitec in any Engineering discipline or equivalent qualification.
- At least 1 year of experience in a Quality related role within Manufacturing environment.
- Ability to work in a cleanroom environment.
This is a permanent position with working hours from Monday to Friday, 8:00am – 5:15pm. Company transport is provided. Medical & dental benefits are also available.
The successful candidate should possess a strong understanding of quality control processes and be able to work independently as part of a team.
Benefits Summary:
- Paid leave and sick days.
- Outpatient medical & dental coverage.
- Company transport assistance.
What We Offer:
- A stable and secure working environment.
Quality Control Specialist
Posted today
Job Viewed
Job Description
We are seeking a highly skilled Quality Control Specialist to join our team. The ideal candidate will have extensive knowledge of quality management principles and be able to implement them effectively.
Key Responsibilities:
- Familiarize yourself with the usage of commonly-used QC testing/measuring instruments.
- Develop and maintain a methodical approach to ensure quality standards are met.
- Perform product inspections, in-process inspections, and final inspections prior to delivery.
- Prepare detailed QC reports and communicate with vendors to resolve any issues that may arise.
Requirements and Qualifications:
- Proven experience in quality control or a related field.
- Excellent communication and interpersonal skills.
- Able to work independently and as part of a team.
- Strong analytical and problem-solving skills.
Benefits:
- Opportunity to work with a dynamic team.
- Professional development opportunities.
- A competitive salary and benefits package.
Why this Job?
This is an excellent opportunity for a motivated individual to join a growing organization and contribute to the success of our quality control team. If you are passionate about delivering high-quality products and services, we encourage you to apply.
Quality Control Specialist
Posted today
Job Viewed
Job Description
Job Opportunity: QC Analyst
Job Description
We are seeking a skilled and detail-oriented QC Analyst to join our team. As a QC Analyst, you will be responsible for ensuring the quality of raw materials, intermediates, and final products in our laboratory.
You will conduct chemical testing, maintain accurate records, and ensure compliance with cGMP and GLP requirements.
This is a 12-hour rotating day/night shift position with a site allowance and shift allowance.
Required Skills and Qualifications
To succeed in this role, you should have:
- Biochemistry knowledge and laboratory experience.
- Laboratory Safety skills and ability to work independently.
- Microbiology and laboratory medicine expertise.
A strong understanding of laboratory procedures and protocols is essential.
Benefits
As a valued member of our team, you will enjoy:
- Competitive compensation package.
- Site allowance of $500.
- Shift allowance of $50.
- Day shift pay of 21.
- Night shift pay of 55.
Others
If you are a motivated and detail-oriented individual with excellent laboratory skills, we encourage you to apply for this exciting opportunity.
Please submit your resume to:
Quality Control Specialist
Posted today
Job Viewed
Job Description
Job Title: Quality Control Specialist
We are seeking a highly skilled Quality Control Specialist to join our team. The successful candidate will be responsible for ensuring that all products meet the highest quality standards and customer requirements.
Responsibilities:
- Inspect raw materials, in-process items, and finished products to ensure they meet quality standards.
- Record and update quality inspection data accurately.
- Identify and report any defective or non-conforming items.
- Work with production team to resolve quality issues.
- Maintain a clean and safe working environment.
- Assist in calibration and maintenance of QC tools and equipment.
- Perform other QC tasks as assigned by supervisor.
Requirements:
- No experience required; training will be provided.
- Able to stand for long hours during shift.
What We Offer:
- A competitive salary package.
- The opportunity to work with a dynamic team.
- Ongoing training and development opportunities.
How to Apply:
Please submit your resume and a cover letter outlining your relevant skills and experience. We look forward to hearing from you!
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Quality Control Specialist
Posted today
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Job Description
Job Title: Quality Control Specialist
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Quality Control Specialist
Posted today
Job Viewed
Job Description
The Quality Control Specialist plays a crucial role in ensuring the quality of our products. The ideal candidate will have excellent inspection skills, be able to identify defects, and possess strong communication skills.
Responsibilities:
- Familiarity with commonly-used QC testing/measuring instruments
- Organized, methodical, meticulous, proactive approach to work
- Visual Inspection of products
- Able to communicate effectively with colleagues and vendors to ensure quality requirements are met
- Perform product inspections, in-process inspections, and final inspections prior to delivery
Tell Employers What Skills You Have
communication, Quality Control , Collaboration, Quality Management , Process Improvement, Quality Assurance , Quality System, proactive, organized, Project Management , quality requirements, Inspection , Manufacturing, on-time, Testing
Quality Control Specialist
Posted today
Job Viewed
Job Description
Basic information:
- Mon - Fri, 8.30am to 5.30pm
- Salary UP $3000 + Bonuses + Salary Increment
- Location: East
Job scope:
- Perform daily quality checks on QC tools and verify accuracy of reports during shift handovers.
- Conduct inspections of incoming materials, in-process items, and outgoing shipments per customer specifications.
- Use digital tools (Kizeo, ERP) for routine and customer-specific inspections.
- Manage non-conformance crates in SAP (Y7/Y8 processes).
- Coordinate with internal teams including OPS, admin, and logistics.
- Carry out ad-hoc tasks as assigned by supervisors or management.
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