Top QA Engineer Jobs in the Netherlands

Own the Integrations team’s QA strategy, combining exploratory testing with automated API, contract, and Playwright end-to-end tests. Write Gherkin acceptance specifications, test integrations and API changes, investigate edge cases, manage regression runs in GitHub Actions, resolve flaky tests, conduct security scans, and make release go/no-go decisions. The role also includes migrating legacy tests, coaching developers on quality practices, and coordinating QA initiatives across product teams.

Lead and improve QA across business change initiatives by establishing risk-based testing standards, coaching teams, coordinating functional, integration, API, regression, data migration, and end-to-end testing, managing defects and evidence, and assessing release readiness. The role partners with business, technology, project, compliance, and supplier stakeholders while driving continuous improvement and maintaining alignment with requirements, risks, DORA, and Solvency II.

Provides real-time QA oversight for pharmaceutical manufacturing operations, ensuring GMP compliance across commercial and clinical production. Responsibilities include shop-floor quality guidance, deviation and CAPA management, investigations, risk assessments, change controls, inspection readiness, documentation approval, MES and SAP quality processes, operator coaching, and continuous improvement. The role supports aseptic and biologics manufacturing while maintaining independent quality judgment across extended shift operations.

Owns quality assurance across in-space propulsion products and customer programs, covering quality plans, audits, nonconformances, corrective actions, production controls, traceability, calibration, safety reviews, and continuous improvement. The role partners with engineering, manufacturing, customers, and certification bodies from prototype development through small-series production while applying aerospace standards such as AS9100 and ECSS.

Own end-to-end quality for Xsolla’s Web3 smart wallet on an Ethereum-compatible ZK rollup. Test account abstraction, signing, smart contracts, token standards, transaction lifecycle, counterfactual deployment, indexer synchronization, wallet security, and partner integrations. Build Playwright and TypeScript automation, use chain forking and transaction tracing, validate testnet-to-mainnet releases, configure AI coding tools, and mentor QA engineers.

Performs manual exploratory testing and develops automated UI and API tests to ensure product quality. Designs test cases, investigates defects, analyzes CI/CD test failures, verifies data integrity, and documents testing procedures. Collaborates with developers and stakeholders throughout the development lifecycle, contributes to QA process improvements, and supports reliable product delivery using tools such as Playwright, Git, Docker, and observability platforms.

Leads the QA Shopfloor program for a cell therapy manufacturing facility, overseeing GMP compliance across manufacturing, warehouse, and quality control operations. Manages batch record and logbook review, deviations, CAPAs, change controls, inspection readiness, quality systems, and continuous improvement. Acts as deputy to the Associate Director, provides QA oversight during GMP events, supports team training and development, and collaborates with cross-functional and network stakeholders.

Provides strategic quality assurance leadership for Elekta’s Brachy business line. Develops quality strategy, leads international quality teams, oversees QMS implementation, audits, management reviews, regulatory compliance, risk escalation, and quality approvals. Supports regulatory authority interactions, mergers and acquisitions, organizational change, budgeting, and team development while fulfilling Person Responsible for Regulatory Compliance responsibilities for Nucletron B.V.

Own QA strategy across three product teams, combining exploratory and manual testing with automated end-to-end testing. Write Gherkin specifications, develop and review Playwright tests in TypeScript, monitor CI regression runs, resolve flaky tests, and triage bugs. Run release regression and security scans, determine automation priorities, coordinate cross-team QA days, and coach developers to take ownership of testing.

Performs pharmaceutical quality assurance activities in a GMP- and GLP-regulated environment. Responsibilities include deviation and CAPA review, investigations, root cause analysis, shopfloor QA support, SOP development, audit and inspection support, documentation review, and cross-functional quality projects. The role also mentors junior staff and coordinates complex assignments related to manufactured products and regulatory compliance.

Inspect incoming fashion products against purchase orders, document non-compliance, conduct basic quality tests, and operate measuring equipment. Lead and train junior QA staff, audit inspection work, troubleshoot quality issues, and support warehouse inventory operations while following safety and environmental procedures.

Reviews and approves manufacturing and laboratory investigations, CAPAs, effectiveness checks, risk assessments, and deviation reports under cGMP and regulatory requirements. Assesses root causes, supports inspections, analyzes quality metrics, develops training, leads cross-functional meetings, and drives continuous improvement across manufacturing, laboratory, facility, materials, and computer-system quality events.

Evaluates customer support interactions, leads QA calibration, audits AI-powered quality tools, and translates grading data into actionable coaching. Maintains knowledge-base documentation, training materials, and macros, delivers refresher training, supports onboarding, and handles a limited number of Zendesk tickets during regular and peak periods. Requires strong feedback and communication skills, target orientation, customer support experience, and fluency in Dutch or German plus professional English.

Designs, analyzes, and improves manufacturing processes and production tools for high-precision parts. Assesses drawings for manufacturability, develops and validates processes, documents PFMEAs and test methods, identifies bottlenecks, advises on equipment and tooling investments, and supports prototypes through volume production. The role connects customers, engineering, quality, operators, and the shop floor across semiconductor, analytical, medical, and high-tech manufacturing.

Support GMP compliance in biotechnology manufacturing by reviewing batch records, quality documents, deviations, CAPAs, investigations, and change controls. Provide on-floor quality oversight, support batch disposition and labeling, maintain documentation, contribute to quality metrics, and participate in continuous improvement. Responsibilities and independence vary by experience level.

Validate wireless RF and addressable RS485 communication systems across fire and security products. Execute performance, robustness, protocol, and installation tests; support test automation; prepare compliance evidence for EN 50131; and maintain test plans, reports, and defect documentation. The role collaborates with R&D, product management, and compliance teams while analyzing logs, traces, and serial output.

Validate wired and wireless security sensors and peripheral devices across functional, fault, power, recovery, battery, environmental, and robustness scenarios. Develop test plans, reports, and defect documentation; translate requirements into test scenarios; support EN 50131 compliance evidence; and collaborate with R&D, product management, and compliance teams.

Develop and maintain automated UI and API tests using C#, enhance front-end and back-end testing frameworks, conduct performance and manual testing, monitor QA results, support UAT, estimate QA efforts, and help define automation strategy. The role also includes coaching QA colleagues, collaborating within a Scrum team, and testing cloud-based microservice applications on Microsoft Azure.

Test web applications across frontends and APIs, validate AI-driven and asynchronous outputs, identify and document defects, maintain test documentation, and advocate for quality throughout the development lifecycle. The role involves collaborating with product, development, and customer support teams, using SQL and CLI tools, and contributing to test automation and software architecture discussions.

Manage pharmaceutical distribution quality systems for Ferring’s global trading entity. Responsibilities include GDP compliance, inspection readiness, CAPA oversight, quality audits, supplier and customer qualification, technical agreements, deviation assessments, batch disposition, regulatory surveillance, and acting as Responsible Person Delegate. The role also supports distribution centers, maintains QMS documentation, and drives continuous improvement.

Leads a team of 8–12 QA specialists overseeing GMP quality for commercial manufacturing and supporting digital systems. Partners with Operations, Warehouse, QC, Maintenance, and MSAT; resolves complex compliance issues; improves quality processes; governs ERP, MES, BI, validation, and qualification activities; and supports inspection readiness and regulatory inspections.

Supports quality and regulatory compliance across engineering, manufacturing, order fulfillment, and other functions. Responsibilities include quality metrics analysis, audit planning and execution, corrective and preventive actions, nonconformity resolution, controlled document changes, and regulatory requirement interpretation. The role contributes to continuous improvement, internal and external audits, and effective quality management system processes in a medical device environment.

Design and execute comprehensive test plans for dApps and smart contracts, perform unit/integration/end-to-end testing, run security audits and vulnerability assessments, automate tests within CI/CD pipelines, monitor quality metrics, debug issues, and collaborate with developers and product managers to ensure reliable DeFi/EVM-compatible applications.

Designs and maintains end-to-end automated testing across AWS web applications and Salesforce workflows. Automates cross-platform user journeys, Salesforce Lightning UI tests, REST APIs, integrations, webhooks, secure queues, and database verification. Integrates test suites into Git-based CI/CD pipelines while validating secure synchronization of enterprise DevOps data between cloud microservices and Salesforce metadata.

Provides on-site quality assurance support for GMP shopfloor operations in a 24/7 shift environment. Responsibilities include batch record and material review, batch release support, documentation lifecycle management, deviation and OOS/OOT investigations, CAPA, change controls, audits, and inspection readiness. The role requires strong organizational skills, attention to detail, teamwork, regulatory awareness, and fluency in English. Experience with radiation, PET, or radiopharmaceuticals is desirable.