Total 6 Quality Assurance / Control job vacancies in Central Singapore

The Construction Quality Manager oversees quality assurance and quality control activities throughout the construction phase of a project. The role works closely with the project team to ensure on‑site work meets agreed standards for quality, safety, and performance.

Key Responsibilities

• Oversee and support quality assurance and quality control processes on site.
• Review and monitor contractor quality plans and ensure alignment with project requirements.
• Work with project teams to promote consistent quality practices and standards.
• Identify quality issues and support corrective actions to maintain scope, schedule, and budget.
• Plan and carry out quality audits and inspections.
• Track, analyse, and report quality data, non‑conformance, and improvement actions.
• Support continuous improvement of quality processes and controls.
• Maintain clear documentation of audits, issues, lessons learned, and outcomes.
• Stay informed on relevant construction standards, regulations, and best practices.
• Provide guidance and training to project stakeholders on quality processes and expectations.
• Support the use of systems and tools to improve efficiency, transparency, and traceability in quality management.

• Perform QC inspections on raw materials, in-process, and finished IVD products
• Ensure production activities comply with established quality standards and SOPs
• Manage and monitor warehouse conditions (e.g., storage, temperature control, FIFO/FEFO)
• Oversee inventory accuracy, stock control, and traceability of materials and products
• Handle non-conformance, deviations, and support CAPA implementation
• Maintain QC records and documentation in compliance with QMS (e.g., ISO 13485)
• Support internal/external audits and regulatory inspections
• Collaborate with production, supply chain, and QA teams to drive continuous improvement

• Diploma/Degree in Life Sciences, Biomedical, Chemistry, or related field
• At least 2 years of experience in QC within medical devices / IVD / pharmaceutical industry
• Familiar with ISO 13485, GMP, and regulatory requirements
• Knowledge of QC processes, warehouse management, and inventory control
• Strong attention to detail and documentation skills
• Able to work in a fast-paced, regulated environment

We’re Hiring: QA Engineer (Regtech / Fintech, B2B SaaS)

Location: Singapore/Malaysia (Hybrid)

Employment Type: Full Time (Monday to Friday (40 hrs/week)

Workplace Type: Hybrid

About Us

AsiaVerify is one of Singapore's leading regulatory technology companies, building automated compliance solutions trusted by businesses across Asia and the UK. Our core products span KYB, KYC, AML, and UBO — delivered via API and portal to clients who need fast, reliable, and accurate compliance data.

We're headquartered in Singapore, with teams across Asia and the UK. We move fast, take ownership, and invest in people who are eager to grow.

The Role

We're looking for a mid-level QA Engineer to own quality across our backend services and frontend portal. You'll work across the full testing spectrum — from manual exploratory testing to building automated test suites — with a particular focus on API/integration testing and performance validation.

Our stack is Java/Spring Boot on the backend and Vue 3/Nuxt on the frontend. You'll be embedded in the delivery team, working closely with engineers and PMs to catch issues early and ship with confidence.

Responsibilities

• Design, build, and maintain automated test suites covering API, integration, and end-to-end flows.
• Conduct manual and exploratory testing for new features, regression cycles, and edge cases.
• Write and maintain API test cases across REST endpoints — validating request/response payloads, error codes, and integration behaviour with third-party data providers.
• Design and execute performance and load tests; identify bottlenecks and work with engineering to resolve them.
• Collaborate with PMs to understand requirements and contribute to acceptance criteria and test plans early in the development cycle.
• Identify, document, and track defects clearly; follow through to resolution.
• Maintain and improve test infrastructure, tooling, and documentation over time.
• Contribute to a quality-first culture — advocating for testability in product and system design.

Requirements

• 2–4 years of QA experience in a SaaS, fintech, or technology product environment.
• Hands-on experience with test automation frameworks (e.g. Selenium, Playwright, Cypress, or similar).
• Solid API testing skills — comfortable with tools such as Postman or RestAssured; able to read and validate REST/JSON responses independently.
• Experience with performance/load testing tools (e.g. JMeter, k6, or similar).
• Familiarity with Java or JavaScript/TypeScript sufficient to read and contribute to test code.
• Understanding of CI/CD pipelines and how automated tests integrate into the delivery process.
• Strong analytical mindset — able to identify edge cases, reproduce issues reliably, and communicate findings clearly.
• Experience working in Agile/Scrum environments.

Nice to have:

• Hands-on experience working in Linux environments, with the ability to perform debugging, log analysis, and basic system-level troubleshooting.
• Solid experience with databases such as MySQL, PostgreSQL (including AWS-managed databases), and/or MongoDB, with the ability to write queries for data validation, debugging, and test setup.
• Proficiency in using tools like Jira for defect tracking, test management, and participation in Agile workflows.
• Demonstrated ability to produce clear, well-structured, and maintainable documentation, including test cases, test plans, and technical notes.

We are looking for a Transaction Surveillance & Screening (TSS) Associate who is passionate about taking on a new challenge within the payments, financial services and FX industry.

As a TSS Associate, you will form a critical part of our day‑to‑day Transaction Monitoring controls, with a specific focus on supporting APAC clients, particularly those operating in or connected to China. You will use our systems to ensure that Compliance risks are adequately identified, assessed, monitored, controlled and reported in line with regulatory and internal requirements.

This role is based in Singapore and will operate Monday to Friday, 10:00am – 6:00pm Singapore Time.

The Details:

• Perform day‑to‑day Transaction Monitoring, identifying potentially fraudulent, suspicious or illegal activity.
• Review and analyse transactions relating to APAC clients, with a particular focus on China‑related activity.
• Analyse payment and compliance data from multiple sources to identify trends, patterns and emerging risks.
• Proactively escalate urgent or high‑risk cases to the MLRO/DMLRO for further review.
• Conduct screening on PEPs and sanctioned entities, including investigation of potential matches.
• Use Mandarin language skills to review client information, transactional data and supporting documentation where required.
• Work closely with internal teams and stakeholders to resolve operational compliance queries efficiently.
• Complete Compliance administration tasks, including maintaining accurate and up‑to‑date client records.
• Assist with the review of existing Transaction Monitoring processes and suggest enhancements to controls and systems.
• Stay informed of current and emerging regulatory requirements and financial crime typologies relevant to APAC and China‑focused activity.

This is a hybrid position. Expectation of days in office will be confirmed by your hiring manager.

The Product Control Analyst (PC) role supports all day-to-day running of the trading desk, ensuring a detailed position summary is kept for the traders and for the matrix as a whole (if applicable) and that the traders' exposures are monitored. This may involve the consolidation of data for the trading matrix. 

The PC is also accountable for a broader range of activities on the desk, e.g. risk/ exposure of trades and ensuring exposure is properly documented and calculated in a consistent manner, the monitoring of futures that are near expiry (where applicable), and determining what to hedge (upon checking with traders).

The PC is expected to provide commentary on the daily profitability reports to explain P&L movements - this requires the PA to have a strong understanding of the P&L and other relevant market information related to the matrix. 

The PC provides all management information and decision support to the traders, e.g. creating reports and/or undertaking general trading, market, or other modeling and analysis on behalf of the traders.  In some cases, this may involve other activities such as rolling storage or internal projects such as supporting the setup of a new business and working with the MIS/ IT team.

Clinigen is at the forefront of delivering critical medicines and support to healthcare professionals and patients. As part of our ongoing commitment to excellence, we are seeking a Quality Control / Quality Assurance Associate to join our esteemed team in Singapore. In this pivotal role, you will be instrumental in upholding our quality management standards as we expand our operations in the Southeast Asia region.

Your primary responsibilities will include:

• Overseeing documentation processes for our Quality Management System (QMS)/electronic QMS (eQMS)
• Facilitating product releases to ensure compliance with established quality standards
• Conducting vendor and customer approvals and validations
• Providing support for secondary packaging processes
• Assisting with validation activities to maintain operational efficacy
• Collaborating with warehouse and cleanroom facilities to ensure adherence to quality parameters

The ideal candidate will possess the following qualifications and skills:

• A tertiary qualification in Science, Pharmacy, or a relevant technical discipline, or equivalent professional experience
• Minimum of 2 years of experience in a quality assurance or quality control role; experience within a warehouse and cleanroom environment in the Healthcare, Pharmaceutical, or Food industries is highly desirable
• Familiarity with Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) quality management systems
• Exceptional communication skills, both verbal and written
• The ability to cultivate collaborative relationships with cross-functional team members
• Strong organizational and time management skills, with a focus on detail-oriented execution
• A commitment to excellence in administrative and documentation practices
• A proactive attitude, with a willingness to contribute positively to our mission of enhancing patient care

• In return for your valuable contributions and commitment to our organization, we are pleased to offer you an attractive and comprehensive benefits package that includes:
• A competitive monthly salary that reflects your experience, skills, and the industry standards, ensuring that you are fairly compensated for your hard work and dedication.
• A performance bonus designed to reward exceptional performance and achievements, providing you with additional financial incentives as you excel in your role.
• Ongoing professional development opportunities, including training programs, workshops, and access to resources that will help you enhance your skills and advance your career within our organization.