1,343 Quality Assurance Specialist jobs in Singapore
Quality Assurance Specialist
Posted today
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Job Responsibilities:
- Contribute to Life Science projects for Antaes Asia clients.
- Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
- Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
- Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
- Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
- Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
- Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
- Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
- Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
- Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
- Contribute to the promotion of Antaes services on top of assistance provided to clients.
Job Requirements:
- Bachelor’s degree in Biotechnology, Pharmaceutical or related field.
- 3-5 years of experience in quality assurance within the pharmaceutical or biotechnology industry.
- Experience with product and raw material release processes and related documentation.
- Strong knowledge of GMP (Good Manufacturing Practices) and regulatory compliance.
- Hands-on experience in conducting GEMBA or GMP walk-throughs and identifying quality risks.
- Proficient in reviewing and approving procedures such as SOPs, forms, and batch records.
- Strong attention to detail and ability to work in a fast-paced, regulated environment.
- Excellent communication and collaboration skills to work with cross-functional teams.
- Good communication and problem-solving skills.
Quality Assurance Specialist
Posted 4 days ago
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• We are looking for a Quality assurance specialiststo lead the digital capabilities deliveries from the business side on our Digital Platforms (primarily on Online Banking, Mobile Banking, Pre-Login Website and Online Real-time Onboarding platform).
• Having keen eye for detail and a good understanding of UX and customer journeys is a big plus.
• Project management skills are also desirable as the selected candidate will be managing multiple streams of digital product deliveries.
• The candidate will ensure that our digital experiences across digital touch points work as intended.
• Develop and execute test plans to ensure that all objectives are met.
• Identification of current test script deficiencies and candidates for additional scripted coverage.
• Implement and monitor test scripts to assess functionality, reliability, performance, and quality of the service or product.
• Identify and remedy defects within the production process.
• Recommend, implement, and monitor preventative and corrective actions to ensure that quality assurance standards are achieved.
• Review, analyze digital journeys and support in User Acceptance Testing
• Ensure that user expectations are met during the testing process.
• Collaborate with various POs to review/develop the right product features
• Communicate with internal business and tech stakeholders
• Gain in-depth understanding of business processes to articulate use-cases/user-stories for identified features/ capabilities for the identified platforms.
• Provide support in efforts to increase adoption rates, through user engagement and acquiring feedback
• Good understanding of Agile principles and familiarity in different development & testing methodologies
• Maintain regular connect and engagement with key stakeholders periodically to refine platform
• Document all testing according to required standards.
• Work with cross-functional teams to ensure quality throughout the software development lifecycle.
Regulatory & Business Conduct
• Display exemplary conduct and live by the Group’s Values and Code of Conduct.
• Take personal responsibility for embedding the highest standards of ethics, including regulatory and business conduct, across Standard Chartered
Quality Assurance Specialist
Posted 14 days ago
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Job Description
CDI
Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
- Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
- Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
- Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
- Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
- Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
- Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
- Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
- Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
- Contribute to the promotion of Antaes services on top of assistance provided to clients.
Job Requirements:
- Bachelor’s degree in Biotechnology, Pharmaceutical or related field
- 3-5 years of experience in quality assurance within the pharmaceutical or biotechnology industry
- Experience with product and raw material release processes and related documentation
- Strong knowledge of GMP (Good Manufacturing Practices) and regulatory compliance
- Hands-on experience in conducting GEMBA or GMP walk-throughs and identifying quality risks
- Proficient in reviewing and approving procedures such as SOPs, forms, and batch records
- Strong attention to detail and ability to work in a fast-paced, regulated environment
- Excellent communication and collaboration skills to work with cross-functional teams
- Good communication and problem-solving skills
Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis.
#J-18808-LjbffrQuality Assurance Specialist
Posted today
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Job Description
We are seeking a highly skilled and detail-oriented Quality Assurance Specialist to join our team. In this role, you will be responsible for ensuring the quality of our products by conducting thorough tests and inspections.
Responsibilities:
- Conduct rigorous testing on raw materials and finished products to ensure they meet our quality standards.
- Create and maintain accurate inspection reports and records.
- Evaluate the quality of raw materials and finished products to ensure compliance with specifications.
- Identify and report any quality issues to relevant stakeholders in a timely manner.
- Collaborate with other departments to address quality-related concerns and implement corrective actions.
- Communicate effectively with suppliers regarding quality concerns and negotiate resolutions.
- Support the development and implementation of quality-related initiatives and processes.
Requirements:
- Bachelor's degree in Food Science or a related field.
- A minimum of 6 months' contract commitment.
- Able to start work immediately.
- Work location: Boon Lay.
- Working hours: 8am-5pm.
Quality Assurance Specialist
Posted today
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We are seeking a detail-oriented and experienced Quality Assurance Specialist to lead our ISO 17025 compliance, SAC-SINGLAS accreditation, and Indoor Air Quality (IAQ) testing programs.
This role is critical in ensuring our laboratory meets international standards while delivering accurate and reliable IAQ assessments for clients.
Quality Assurance Specialist
Posted today
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The role of a Quality Assurance Specialist in a laboratory setting involves ensuring the accuracy and reliability of equipment used in testing processes.
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Quality Assurance Specialist
Posted today
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Job Title: Quality Assurance Specialist
About the RoleWe are seeking a highly skilled and detail-oriented Quality Assurance Specialist to join our team. The ideal candidate will have a strong understanding of quality management systems, industry standards, and customer requirements.
Key Responsibilities- Assist in implementing and maintaining quality management systems processes aligned with ISO standards
- Support the development, review, and update of quality documentation, including policies, procedures, and work instructions
- Participate in establishing and ensuring adherence to quality assurance processes to guarantee compliance with industry specifications, standards, and customer requirements
- Implement corrective and preventive actions to address identified quality issues promptly and effectively
- Strong understanding of quality management systems, industry standards, and customer requirements
- Excellent communication and interpersonal skills
- Ability to analyze data and identify trends and deviations
- Proficiency in MS Office and other software applications
We offer a competitive salary, comprehensive benefits package, and opportunities for professional growth and development.
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Quality Assurance Specialist
Posted today
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We are seeking a Quality Assurance Specialist to join our team. The successful candidate will be responsible for developing and maintaining the project quality plan, ensuring compliance with ISO requirements, and supporting the Project Manager on day-to-day QAQC matters.
Key Responsibilities:- Develop and maintain the project quality plan in accordance with ISO standards
- Ensure compliance with ISO requirements through regular audits and reviews
- Support the Project Manager in preparing QAQC reports and managing submission of QAQC documentation
- Maintain accurate records of QAQC activities and ensure all project documentation is kept up-to-date
To be considered for this role, you should have:
- Excellent communication and organizational skills
- Proven experience in quality assurance and control
- Familiarity with ISO standards and procedures
- Ability to work independently and as part of a team
We offer a competitive salary and benefits package, including:
- A comprehensive training program to support your professional development
- Ongoing support and guidance from experienced colleagues
- The opportunity to work on a variety of projects and contribute to system improvement
This is an exciting opportunity to join our team and make a real difference in the quality of our projects. If you are a motivated and detail-oriented individual with a passion for quality assurance, we encourage you to apply.
Quality Assurance Specialist
Posted today
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Job Description
We are seeking an exceptional Quality Assurance Specialist to join our team. As a key member, you will play a pivotal role in ensuring the quality of our products throughout the development process.
- Evaluate product structure and design for safety and functionality requirements.
- Review processes to ensure continuous improvement and drive cross-functional projects for optimization.
- Investigate root causes of incidents and implement countermeasures using problem-solving tools.
- Develop test plans for complex elements to identify risks during production.
- Determine test methods in the development stage and ensure suppliers conduct tests accordingly.
- Pilot production at vendors' plants, evaluate, and qualify manufacturing processes.
- Take ownership of professional growth by continuously improving skills and transforming knowledge into tangible results.
- Support supplier quality management, including audits and customer claim handling.
- Identify visual quality according to LEGO Error definition and VQG guidelines.
- Maintain a safe work environment for all employees.
- Exercise authority to approve/reject testing methodologies, escalate quality risks, and declare equipment performance results.
- Verify and validate development performance against development agreements.
- Contribute risk findings to project teams using quality tools like CTQs, FMEA, SPC, CPK, and PPAP.
- Monitor development weaknesses or challenged points impacting mass production stability.
- Provide quality input for novelty developments at earlier stages.
- Align PS tests with PS and supplier teams.
- Approve test diagrams for physical testing to drive PP approval.
- Improve supplier development quality management and provide quality input to high-complexity projects.
- Check with QID for D-FMEA and add local quality input.
- Review development data to evaluate performance.
- Initiate P-FMEA to minimize development process risks and verify reliability for key measurements and testing.
A successful candidate will have:
- Proven experience in quality development or design engineering in plastic/injection molding industries with relevant education.
- A strong quality mindset to ensure uncompromising quality.
- Expertise in plastic materials, molding, or related processes is preferred, as well as experience in the toy industry and international toy safety standards.
- Knowledge in APQP, PPAP, PFMEA, SPC, and MSA application is required.
- Supplier quality development and management experience in Thailand is preferred.
- Project management skills, good communication skills, and fluency in English (reading, writing, speaking) are required; proficiency in Mandarin is a plus.
The ideal candidate should possess:
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
- Ability to work effectively in a team environment.
- Fluency in English (reading, writing, speaking).
- Proficiency in Mandarin is a plus.
We offer a dynamic and supportive work environment that fosters growth and development. If you are passionate about quality assurance and committed to excellence, we encourage you to apply.
Quality Assurance 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 Assurance Specialist is to promote and integrate quality into every aspect of our BioReliance biologics safety testing business in Singapore. The role is to perform batch record review (i.e. data audits) to support all aspects of quality operations to ensure that laboratory testing operates in full compliance with sound scientific practice, GxP and Standard Operating Procedures (SOPs). The scope of responsibility is to contribute or impact the results of the QA team and is accountable for the quality of own work, solve problems of low complexity independently by identifying and selection solutions and by analyzing information.
The post holder will be able to perform the following functions independently, with minimal guidance.
What You Do
- Batch record review: Review and approval of GxP documents, including Protocols, Technical Specification (TS), Batch Records, Workbooks, SOPs and all other QMS documentation.
- Batch record review: Comply with all applicable policies, procedures and guidelines.
- Batch record review: Conduct in-process or final audits and approval on manufacturing or testing documentation as they comply with the stated regulatory standards and the approved TS, protocol or SOPs.
- Batch record review: Release of the certificate of analysis for GMP testing against the TS and associated documentation.
- Batch record review: Prepare QA statement within each GLP final report specifying inspections date, and dates findings were reported to the Study Director and management.
- Review and approve deviations, anomalous results, OOS, positive results and CAPAs.
- Assist in investigations from events, complaints or data audits.
- Conduct trend analysis for deviations and review / approve applicable CAPA records.
- Assist self-inspections to ensure continuous improvement.
- Perform and support client audits, regulatory inspections.
- Perform and support internal audits.
- Perform and support supplier audits.
- Comply with Health and Safety Executive regulations and undergo relevant training modules when required and actively takes necessary action when encountering unsafe situations.
- Perform their duties according to the principles of Good Laboratory (GLP), Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP).
Who You Are
- Graduate degree in life sciences or higher related degree
- Minimum of 2 - 4 years of experience, within a similar Quality Assurance role i.e. batch record review.
- Shows a desire and motivation to work in Quality and regulated environment.
- Awareness of Biologics regulatory environment and GMP manufacturing topics.
- A proactive approach to all aspects of Quality.
- Fluent in both written and spoken English.
- Good communicator, dealing directly and effectively with operational teams and site QA and lab colleagues routinely.
- Strong analytical and problem solving abilities.
- Organized and logical in defining workload and delivering projects.
- Technical and problem solving skills
- Has the functional and technical knowledge and skills to do the job
- Can learn new skills and knowledge quickly
- Uses logic to solve problems with effective solutions
- Makes good decision
- Energy and Drive
- Self-motivating; is action-oriented and full of energy for the things he / she sees challenging
- Pursues everything with energy, drive and the need to finish, especially in the face of resistance and setbacks
- Can be counted on to achieve goals, constantly and consistently, pushes self and others for results
- Professional and interpersonal skills
- Relates well to all kinds of people in the organization, builds constructive and effective relationships using diplomacy and tact
- Is seen as a team player, cooperative, easily gains support of peers, encourages collaboration
- Global mindset and to be willing to engage in conference calls at out-of-office hours.
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity
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