1,050 Quality Control Specialist jobs in Singapore
Quality Control Specialist
Posted today
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Overview
MiRXES is a Singapore-headquartered molecular diagnostic company with R&D, manufacturing, and clinical lab operations in Singapore, USA, Japan, and China. We specialize in microRNA technologies and the development, manufacturing, and provision of diagnostic test kits and clinical services. Our mission is to enable early disease detection and provide insights for better patient care by harnessing the power of microRNA to augment traditional testing. Our vision is to be the world’s leading developer and provider of accurate, actionable, and affordable microRNA-powered diagnostic tests.
Job Location: 2 Tukang Innovation Grove, JTC MedTech Hub, Singapore
Job SummaryThe QC Specialist will work as part of the Quality team, supporting day-to-day QC operations and maintaining accurate and detailed records of all the assigned tasks. This role involves inspecting products at various stages of the manufacturing process, including incoming raw materials, intermediates, in-process materials and finished goods. This person will also participate in investigations of nonconforming products and assist in implementing corrective actions arising from these inspections.
Roles and Responsibilities- Perform routine QC testing of incoming raw materials, in-process materials and finished goods.
- Plan and schedule daily routine and ad hoc QC runs assigned by line manager.
- Evaluate data and generate reports, highlighting any deviations from standard operating procedures (SOPs).
- Raise nonconformance for failures observed during QC runs.
- Support troubleshooting and investigation of nonconformance to determine root causes.
- Draft and revise QC work instructions as required.
- Support validation and stability studies for lab development and Diagnostic products, when necessary.
- Perform general laboratory support activities, including housekeeping, equipment maintenance, document archival, and inventory tracking of laboratory reagents, etc.
- Contribute to the continuous improvement of laboratory procedures and processes to ensure compliance with GMP requirements.
- Apply Good Documentation Practices (GDP) to all records to ensure traceability, transparency, and audit readiness.
- The tasks and responsibilities listed are essential to the role, however, reasonable accommodations may be made to support additional responsibilities based on evolving business needs.
- Degree/ Diploma in Biomedical Science, Biotechnology, Molecular Biology, Biochemistry, Life Science related courses or equivalent.
- Knowledge and hands-on experience with qPCR, including operation of qPCR machines will be an advantage.
- Proficient in using standard laboratory equipment such as pipettes, centrifuges, etc.
- Familiar with basic laboratory procedures; experience in assay-based workflows and QC testing is an advantage.
- Able to work independently with minimal supervision, as well as collaboratively with cross-functional teams.
- Excellent organizational and time management skills.
- Demonstrate a high degree of initiative and ownership.
- Possess a positive, proactive and willing-to-learn attitude.
- Strong interpersonal and communication skills.
- Basic computer competency, including proficiency in Microsoft Office applications.
- 2-3 years of relevant experience in quality control, preferably within the medical device manufacturing industry.
- Good understanding of Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) is preferred.
This position is based in Singapore.
We appreciate your interest in the above-mentioned position, however, only shortlisted candidates will be contacted.
#J-18808-LjbffrQuality Control Specialist
Posted 11 days ago
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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
We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Job details- Seniority level: Associate
- Employment type: Full-time
- Job function: Quality Assurance and Science
Quality Control Specialist
Posted 27 days ago
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Job Description
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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 today
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Job Description
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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Job Description
We are seeking a detail-oriented and experienced Quality Control Specialist to ensure that products meet required standards before they reach the customer.
The Quality Control Specialist will be responsible for inspecting materials, identifying defects, and ensuring compliance with company and regulatory specifications.
- Key Responsibilities:
- Verify compliance with quality standards, specifications, and procedures
- Conduct measurements using tools such as calipers, and other inspection equipment.
- May require standing
- Working Environment: clean, organized, and fully air-conditioned
- Transport: transport provided from designated pick-up points
- Training: on-the-job training provided
Quality Control Specialist
Posted today
Job Viewed
Job Description
The Role:
We are seeking a detail-oriented and organized Quality Control Specialist to join our team. The ideal candidate will have a strong understanding of quality control principles and be able to work independently in a fast-paced environment.
Responsibilities:
* Conduct daily incoming job inspections and prepare reports
* Perform routine maintenance on equipment and ensure all tools and instruments are calibrated and functional
* Collaborate with production teams to resolve quality-related issues
* Maintain accurate records of inspection results and quality metrics
Requirements:
* 2-5 years of experience in production or manufacturing process planning
* Diploma in Mechanical Engineering or related field
* Proficiency in technical drawing and computer literacy
* Strong communication and problem-solving skills
Quality Control Specialist
Posted today
Job Viewed
Job Description
Job Summary:
As a QC Laboratory Expert, you will play a pivotal role in ensuring the quality of raw materials used in pharmaceutical production. Your primary responsibilities include:
- Developing and executing method validation protocols for raw material testing.
- Supporting laboratory start-up activities, including equipment qualification, generation of user requirement specifications, SOPs, and configuration specifications.
- Performing quality control tests for raw material samples, including compendial tests and identification tests.
- Conducting quality control sampling of incoming raw materials.
- Authoring and revising raw material specifications and other quality-related documents.
- Assisting with laboratory activities such as housekeeping and equipment maintenance.
Requirements:
The ideal candidate will have a Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, or related life sciences or technology, with at least 5-7 years of experience in QC raw material testing. Additionally, they should possess expertise in method validation/verification, good laboratory practices, and data integrity requirements. Experience with routine laboratory operations and participation in method transfer, method validation, and method verification for raw material testing is highly desirable.
What We Offer:
We provide a dynamic and challenging work environment that allows professionals to grow and develop their skills. Our team is passionate about delivering high-quality results and making a meaningful impact in the industry.
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Quality Control Specialist
Posted today
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The role of Quality Assurance Manager is a pivotal position that oversees the entire quality assurance function within an organization.
">- Ensures adherence to product specifications and standards
- Liaises with internal departments to identify and address potential quality issues
- Develops and implements quality control processes to prevent nonconformity
- Coordinates external audits and ensures compliance with regulatory requirements
- Leads a team of quality professionals to achieve quality excellence
Key qualifications include:
">- Diploma in a relevant field or equivalent experience
- At least 10 years of working experience, with at least 5 years in a relevant industry
- Excellent communication, analytical, and problem-solving skills
- Proficiency in Microsoft Office applications and industry-specific software
This is an exciting opportunity for a highly motivated individual who is passionate about quality and customer satisfaction.
Quality Control Specialist
Posted today
Job Viewed
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
Quality Control Specialist
Posted today
Job Viewed
Job Description
Job Overview:
We are seeking an experienced Quality Control Specialist to join our team.
Key Responsibilities:- Quality Assurance: Conduct regular quality checks on incoming products and in-process goods to ensure they meet our high standards.
- Process Improvement: Develop and implement Standard Operating Procedures (SOPs) for analytical methods, ensuring compliance with industry regulations.
- Inventory Management: Oversee the inventory of laboratory consumables, chemicals, and samples, maintaining accurate records and minimizing waste.
- RCA & CAPA: Perform root cause analyses and implement corrective and preventive actions to address product quality issues.
- SQAs: Conduct supplier quality audits to ensure vendors meet our quality requirements.
- Tech Maintenance: Regularly inspect and calibrate test equipment to guarantee accuracy and precision.
- Educational Background: Diploma in Chemical Engineering, Chemistry, Science, or a related field.
- Work Experience: Minimum 1 year of relevant experience in the chemical/petrochemical industry.
- Technical Knowledge: Proficiency in Certificate of Analysis (COA), Internal Quality Control (IQC), and Final Quality Control (FQC).
- Skills: Self-motivated, independent, resourceful, excellent communication and observation skills, and Microsoft Office proficiency.