Top QA Engineer Jobs in Italy

The role involves supervising manufacturing processes to ensure safety and quality standards, performing loss analysis, and supporting line operations and team development.

The Site Manager will oversee construction projects, ensure compliance with regulations, manage contractor activities, and maintain safety standards. They will also liaise with clients throughout the project lifecycle.

The Process Quality Engineer oversees product quality in manufacturing, develops operational plans, and drives improvements in processes and procedures.

As a Quality Assurance Intern, you'll participate in testing, validation, and enhancing processes for wearable products, producing certification reports, and assisting the Product team.

The role involves managing quality control activities, ensuring compliance with quality standards, conducting audits, and collaborating with development teams to improve processes within R&D for control systems products.

The Kazakh Localization QA Tester/Proofreader will review localized Kazakh content for accuracy, execute testing on products, identify bugs, and ensure a high-quality user experience through attention to detail and cultural understanding.

As a QA Engineer, you will ensure software reliability by developing test plans, optimizing automated test suites, validating security implementations, and collaborating with developers to maintain high quality and performance standards.

As a Quality Assurance Specialist, ensure compliance with quality oversight in manufacturing radioactive sterile injectables, manage audits, training, and improve quality metrics.

As a Senior QA Engineer, you'll lead E2E testing efforts, develop test automation frameworks, and collaborate with cross-functional teams to ensure software quality.

Lead quality assurance in renewable energy projects, managing quality plans, supplier requirements, inspections, and compliance across the engineering and construction lifecycle.

Oversee GMP compliance and quality oversight for sterile production: review batch records, support batch release, manage GMP documentation, investigate deviations/OOS/complaints, support audits, and contribute to validation, SOPs, and CAPA/change control activities while working shift patterns.

The role supports the operationalization of pilot plant processes through quality system management, compliance assurance, and audit preparations. Responsibilities include documentation, qualification, validation activities, and KPI monitoring.

The TRD QA Specialist supports quality assurance in pharmaceutical manufacturing, overseeing compliance, managing quality systems, conducting audits, and maintaining documentation while ensuring adherence to GMP standards.