Top QA Engineer Jobs in the Netherlands

Supports product assurance and safety activities for ESA spacecraft programs, including requirements baselines, contractor reviews, audits, inspections, testing, acceptance reviews, non-conformance and waiver tracking, safety reviews, dashboards, and launch campaigns. Coordinates multidisciplinary PA&S experts, supports manufacturing, assembly, integration and testing, prepares reports and meeting documentation, and contributes to technology assessments, training, and lessons learned. The role is based at ESTEC in the Netherlands with frequent international travel and possible prolonged missions.

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.

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.

QA Analyst responsible for testing web applications throughout the software testing life cycle. Duties include creating and executing test scenarios, maintaining regression test cases, analyzing results, documenting and tracking defects, and supporting resolution. The role also uses AI tools to generate test scenarios, query testing data, and maintain QA documentation. Candidates should have 0–3 years of software testing experience, familiarity with bug tracking and version control, and an understanding of SDLC processes. Automation, scripting, CI/CD, and ISTQB certification are preferred.

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.

Supports EMEA Quality Assurance digital communication initiatives by optimizing SharePoint user experience, conducting usability assessments, creating visual content, integrating Power BI dashboards, improving digital QMS solutions, and exploring AI-enabled workplace tools. Collaborates with Quality Assurance, IT, Communications, and Operational Excellence stakeholders to improve employee engagement, communication, and visibility of quality initiatives.

Conduct manual testing for Paper.io 2, identify and document defects, create test plans, improve QA processes and tools, monitor technical KPIs, and collaborate with design, development, and central technology teams. The role owns QA activities across development and release stages while providing feedback on game mechanics, quality, and player experience.

Lead a multi-site laboratory Quality Management System across the UK, Ireland, and United States. Harmonize quality procedures, documentation, audits, CAPA, accreditation activities, change management, and continuous improvement. Monitor quality metrics, manage auditor relationships, apply risk-based principles, and coach site Quality Representatives. Requires international collaboration and 15–20% travel.

Provides QA oversight for advanced therapies manufacturing, ensuring GMP compliance, inspection readiness, and product quality. Responsibilities include reviewing investigations, deviations, CAPAs, change controls, validations, technology transfers, risk assessments, and product disposition decisions. The role supports aseptic processing, Annex 1 compliance, facility and equipment projects, regulatory inspections, GMP training, and quality improvement initiatives. It partners cross-functionally with manufacturing, QC, warehouse, MSAT, and other teams, and participates in a rotating 24/7 on-call schedule.

Lead quality assurance and testing across capital markets, derivatives, and securities financing projects. Develop Java/Cucumber/Gherkin test automation, create test plans and cases, coordinate testing phases, manage defects in Jira and Zephyr, and report progress and results. Provide production support as a risk-systems subject matter expert, collaborate with risk teams, perform hands-on testing, investigate root causes, and ensure software quality through release. Linux, SQL, Oracle, Agile, DevOps, and financial clearing experience are important.

Lead the strategic direction, operations, financial performance, and organizational development of the Quality department. Oversee customer audits, regulatory inspections, quality KPIs, processes, and compliance with clinical research regulations and client expectations. Represent Quality in leadership and client meetings, maintain client satisfaction, support business development, and build strong internal and external relationships.

Leads global quality assurance projects across AbbVie’s pharmaceutical distribution and supplier network. Coordinates cross-functional project execution, regulatory impact assessments, quality system improvements, supplier governance, performance metrics, compliance initiatives, and operational process standardization across sites and regions.

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.

Support the site Quality Management System and GMP compliance through quality documentation, training administration, deviations, CAPAs, change controls, risk assessments, supplier qualification, audits, inspections, and continuous improvement. Collaborate with site and global stakeholders to manage supplier activities, maintain inspection readiness, strengthen quality culture, and improve compliance processes in a pharmaceutical manufacturing environment.

Oversee and strengthen the site Quality Management System, lead deviation and quality event reviews, approve CAPAs and change requests, maintain QMS documentation, support audits and regulatory inspections, deliver GMP and compliance training, and drive continuous improvement across quality processes.

Lead and develop a QA team supporting Cell and Gene Therapy manufacturing. Oversee batch record review, deviations, CAPAs, change controls, product disposition, investigations, audits, inspections, and quality metrics while ensuring cGMP and regulatory compliance. Partner with manufacturing, supply chain, regulatory affairs, and other departments to resolve quality issues and drive continuous improvement.

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.

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.

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.

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.