Top QA Engineer Jobs in the Netherlands

Leads quality assurance and Responsible Person activities for pharmaceutical distribution entities and 3PL partners. Manages a team of three, ensures GDP and regulatory compliance, oversees quality documentation and training, supports recalls and product holds, evaluates distribution processes, and drives continuous improvement to reduce quality risks and costs. Requires Dutch MOH Responsible Person registration, quality systems expertise, strong analytical and communication skills, and fluency in Dutch and English.

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.

Provide QA oversight for equipment, automation, processes, and computerized-system validation in GMP-regulated life sciences environments. Review and approve validation documentation, risk assessments, technical changes, and qualification activities. Support CSV, data integrity, device and combination-product activities, FMEA, change control, and quality risk management while advising engineering, manufacturing, product development, and information systems teams.

Supports pharmaceutical QA and regulatory compliance for clinical and commercial products. Responsibilities include batch release documentation, GMP/GDP record review, quality event tracking, document workflows, supplier qualification records, quality metrics, audit readiness, and inspection preparation. The role collaborates with Qualified Persons, Technical Operations, Supply Chain, Regulatory Affairs, and external partners while identifying documentation gaps and maintaining compliant quality systems.

Own the site's Quality Management System and ensure compliance with internal standards and food safety regulations. Lead process optimization, internal audits, GMP rounds, and external audit preparation. Partner with production and logistics teams to embed quality practices, manage supplier non-conformities and consumer complaints, and drive continuous improvement across fulfillment operations.

Supports quality assurance for pharmaceutical distribution and logistics operations under GDP and GMP requirements. Maintains quality systems and documentation, advises staff on compliant processes, supports training, metrics, audits, change management, investigations, and continuous improvement initiatives. Works with planning and customer service teams to ensure compliant shipment preparation and execution.

Provides strategic leadership for Computer System Validation, automation compliance, data integrity, and lifecycle management of GMP computerized systems supporting pharmaceutical manufacturing. Serves as the site subject matter expert for DCS, SCADA, MES, historians, building management systems, and related automation platforms. Leads validation strategies, inspection readiness, regulatory compliance, cross-functional initiatives, continuous improvement, and mentoring across Automation, Quality, Engineering, QC, and IT teams.

Ensure the quality and reliability of embedded software across microcontroller systems and single-board computers. Responsibilities include analyzing requirements, designing test plans, executing functional, integration, system, and hardware-software integration tests, investigating defects, maintaining traceability, building regression campaigns, supporting ASPICE and MISRA compliance, performing static analysis, and documenting verification evidence. The role collaborates with software and hardware teams on firmware flashing, interfaces, reproducibility, and root-cause analysis.

The QA Manager owns quality strategy across Harver’s platforms, leads and develops QA Engineers, and drives quality-left practices. Responsibilities include defining acceptance criteria and test contracts, overseeing automation architecture, monitoring production health, leading incident response, and implementing AI-assisted quality pipelines. The role requires hands-on expertise with Playwright, Node.js, TypeScript, MongoDB, PostgreSQL, and AI-assisted engineering tools, alongside strong leadership, automation, test architecture, and production-quality judgment.

Senior Mobile QA Engineer responsible for designing and executing Android and iOS test strategies, automating native and hybrid application testing with Espresso and XCUITest, and validating APIs, backend integrations, data flows, security, and secure transactions. The role integrates automated tests into Azure DevOps CI/CD pipelines, uses Postman, WireMock, Proxyman, and Charles Proxy for testing and debugging, and applies shift-left quality engineering, monitoring, alerting, and quality metrics.

Lead Qualified Person activities and GMP/GDP quality assurance for investigational and commercial medicinal products. Responsibilities include batch certification and release, supply-chain oversight, deviation and CAPA management, audits, quality agreements, inspection readiness, regulatory compliance, and cross-functional support across manufacturing, clinical, commercial, and distribution operations.

Provides cGMP and quality guidance for commercial pharmaceutical operations, leads investigations and CAPA implementation, supports FDA and EMA inspections, approves change controls and validation documentation, and drives risk management and continuous improvement. The role requires strong pharmaceutical quality assurance experience, knowledge of regulatory expectations, and fluency in Dutch and English.

QA Engineer responsible for manual, exploratory, risk-based, and automated testing of software. The role includes building and maintaining end-to-end, integration, and regression test suites; integrating quality controls into CI/CD pipelines; documenting and verifying defects; assessing release readiness; and collaborating with developers, architects, product managers, and designers. The engineer will also improve testing frameworks, quality metrics, and processes while exploring AI-assisted testing approaches.

Supports GMP compliance and product quality throughout manufacturing product introduction and lifecycle management. Reviews electronic batch records, raw materials, GMP documentation, and change controls; supports batch disposition, Qualified Person release packages, quality systems, regulatory compliance, and continuous improvement. Collaborates with Operations, Quality Control, Engineering, and Development teams while promoting a strong quality culture.

Lead a QA team and act as Qualified Person for large-molecule commercial products. Oversee GMP compliance, investigations, CAPA implementation, inspection readiness, and cross-functional quality oversight to maintain site quality and regulatory alignment.

Reviews batch records and customer-facing documentation for GMP compliance, certifies finished goods for release, and supports non-conformance, rework, QMS, and routine quality assurance activities. The role is on-site in Medemblik, Netherlands, and requires a scientific background, quality or production experience, attention to detail, communication skills, and a collaborative mindset.

Owns quality assurance, reliability, and regulatory compliance for radar systems. Maintains QMS governance, develops quality plans and SOPs, leads root-cause analysis and corrective actions, oversees testing and calibration, reviews technical documentation, audits suppliers, manages incoming inspections, and tracks defects and process maturity. Collaborates with Operations, Engineering, Procurement, Service, and suppliers to ensure compliant, reliable products before production handover.

Own release quality across web funnels, mobile apps, payment flows, and subscriptions. Build test plans, validate end-to-end journeys, reproduce and document defects, assess severity, and make release readiness decisions. Expand automated UI testing using JavaScript or TypeScript, test APIs and analytics events, verify fixes, and document scalable QA processes. Collaborate with engineering and product teams while using AI tooling to accelerate test generation, debugging, and automation.

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.

Leads GMP-focused audits across pharmaceutical, biotechnology, and CRO operations, including processes, systems, vendors, facilities, and documentation. Supports clinical development quality activities, evaluates regulatory compliance, identifies risks, drives corrective and preventive actions, advises stakeholders on quality systems and audit readiness, and contributes to inspection readiness and continuous improvement. The role requires significant pharmaceutical or CRO quality assurance experience, GMP audit leadership, strong clinical research knowledge, and approximately 35% international travel.

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.

Monitors affiliate and sales managers’ partner communications across Telegram, Skype, and email. Reviews tone, accuracy, compliance, response times, and SLA adherence; identifies risks and escalates critical cases. Provides constructive feedback, maintains communication standards and error records, prepares quality reports, and supports process improvements. The role requires strong written English, objectivity, responsibility, stress resilience, and the ability to understand affiliate and iGaming operations.

Provides on-site, shift-based quality assurance oversight for manufacturing, QC laboratory, warehouse, and packout operations. Reviews records, assesses discrepancies, approves deviations, performs verification, supports inspections, and ensures compliance with cGMP, approved procedures, aseptic techniques, and quality systems. The role also identifies operational issues, supports remediation, authors documents, assists with maintenance oversight, and helps integrate new team members.

Lead and maintain the site Quality Management System (ISO 9001/13485), ensure regulatory compliance, manage QA team, support production floor quality, drive corrective/preventive actions, lead audits and product investigations, and enable new product transfers.

Interns will learn the supply chain execution application and agile software delivery practices. Responsibilities include writing and executing automated tests from manual scripts, reviewing peer tests, collaborating with global development teams, and contributing to high-quality software solutions. Candidates need Java fundamentals, curiosity, and the ability to work from the Rotterdam office. Familiarity with Git, Selenium WebDriver, and Postman is helpful.