857 Quality Control Specialist jobs in Singapore

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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.

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

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Get notified about new Quality Assurance Specialist jobs in Tuas, West Region, Singapore .

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

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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 the fields of 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 your unique viewpoint matters. 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 customers undertake activities ranging from fundamental biological research to developing vaccines, medicines, and cell and gene therapies.

At Cytiva, you will have the opportunity to improve yourself and us—working on meaningful challenges with caring colleagues, customers, and patients. Take your next step toward a 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 quality standards and regulatory requirements. This involves conducting inspections, testing, audits, and supporting continuous improvement initiatives to maintain high product quality and operational efficiency.

This position reports to the Quality Control Manager and is based on-site in Singapore, 25 Tuas South Street 1.

• Leading oversight of OOS investigations, deviation report writing, and CAPA planning.
• Monitoring QC routine operations to ensure testing schedules for products and raw materials are on track with minimal backlog.
• Approximately 30% of time dedicated to performing QC testing activities; 70% supporting QC operational activities.
• Driving adherence to quality KPIs and ensuring timely data reporting and trend analysis.
• Validating new QC laboratory equipment and methods.

• University graduate in Science or equivalent relevant experience.
• 3 to 5 years of experience in a QC Laboratory environment.
• Detail-oriented with strong written and verbal communication skills.
• Experience in laboratory investigations, deviation records, root cause analysis, and change control.
• Knowledge of GxP or similar regulated environments.

• Proficiency with Word, Excel, Oracle, and electronic documentation systems.
• Laboratory experience with equipment such as UPLC, endotoxin readers, pH meters, and microbial testing.

#LI-SS3 #LI-Onsite

Join our team today. Together, we’ll accelerate the impact of science and technology. We partner globally to solve complex challenges and bring science to life.

For more information, visit .

At Danaher, we value diversity and believe in the power of different perspectives, both visible and not, in our workforce and markets.

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This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

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 managing a team of QC associates and ensuring that QC routine operations are carried out as per plan.

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
• 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
• Developing and maintaining specialized technical expertise in order to provide support for existing products and ongoing GxP operations as required
  
  

• 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 Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Medical Device

Referrals increase your chances of interviewing at myGwork - LGBTQ+ Business Community by 2x

Johor Bahru, Johore, Malaysia 10 hours ago

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• Perform visual inspection of product
• Inspect finished goods and verify parts
• Maintain quality records
• Conduct QA inspections and ensure adherence to product quality standards
• Generate inspection and non-conformance reports
• Ensure a secure environment to safeguard confidential information
• Assist in the development of corrective action plans

• A team player with excellent communication skills
• Able to lift and handle heavy objects
• Able to understand and read simple engineering drawings
• Able to lift heavy objects up to 10kg

We are seeking a highly skilled Quality Control Manager to join our team. As a key member of the quality assurance department, you will be responsible for overseeing the operations of our Quality Control Lab and ensuring that all lab analyses are conducted in a timely and accurate manner.

The ideal candidate will have a strong background in chemistry and laboratory experience, with hands-on experience in GC and Analytical Method Validation. They must also possess excellent communication skills and be able to work effectively in a team environment.

Responsibilities:

Job Title: Quality Control Specialist

We are seeking a skilled and detail-oriented Quality Control Specialist to join our team. In this role, you will be responsible for ensuring the quality of our products by monitoring machining activities, reporting any issues, and proposing solutions.

Key Responsibilities:

• Monitor Machining Activities: Ensure that all machining activities meet our quality standards by conducting regular inspections and tests.
• Report Issues: Document any quality issues or defects found during inspections and report them to the relevant teams.
• Propose Solutions: Collaborate with cross-functional teams to develop and implement solutions to address quality issues.
• Implement Process Changes: Work with process owners to identify areas for improvement and implement changes to enhance quality.
• Perform SAP Transactions: Complete SAP transactions after completion of QC operations.

Requirements:

• Experience: A minimum of 3 years of hands-on experience in quality control or a related field.
• Skills: Ability to understand and interpret complex blueprints/technical/engineering drawings, perform inspection using precision measuring equipment, and possess good interpersonal and communication skills.