• Testowanie istniejących oraz powstających funkcjonalności systemu Base • Efektywne zgłaszanie i weryfikacja błędów w działaniu aplikacji • Tworzenie i utrzymywanie czytelnych i przejrzystych przypadków testowych i planów testów • Przeprowadzanie i dokumentowanie wykonanych testów manualnych • Bliska współpraca z zespołem developerskim, Tech Leaderem i Product Ownerem • Współpraca z projektantami, zespołami wsparcia oraz utrzymania • Udział w tworzeniu i wsparcie w udoskonalaniu procesu testowania

• Test REST APIs using tools like Postman or similar platforms • Report bugs and track issues with the development team • Assist in regression and functional testing • Maintain testing documentation and reports

• Perform functional, regression, integration, and end-to-end testing for Workday applications and integrations. • Create and maintain test plans, test cases, test scripts, and testing documentation. • Validate Workday modules such as HCM, Payroll, Recruiting, Time Tracking, Absence, Compensation, Benefits, and Financials. • Execute manual and automated testing activities based on project requirements. • Analyze business and functional requirements to ensure complete test coverage. • Identify, document, track, and retest defects using defect management tools. • Coordinate with developers, functional consultants, and business users during SIT and UAT phases. • Support Workday implementation, enhancement, and production support projects. • Participate in requirement reviews and provide quality assurance recommendations. • Ensure compliance with testing standards, QA methodologies, and best practices.

• Author, maintain and implement study-specific Clinical Quality Audit Plan(s) for assigned clinical program(s) and trial(s) to ensure the execution of a phase-appropriate, fit-for-purpose Audit Program • Represent Quality at cross-functional clinical program meetings and Clinical Study Team meetings and operational activities to provide appropriate Quality guidance on GCP compliance matters to internal departments. • Identify, mitigate, or escalate clinical quality risks by leveraging GCP knowledge and best practices across all phases of clinical development. • Maintain program oversight and influence proactive quality management through quality related activities with regard to vendor management, study conduct, and study • Author and/or review QMS controlled documents which may include standard operating procedures (SOPs) in accordance with applicable regulatory requirements (e.g., ICH E6, FDA, EMA, MHRA, local regulations) • Oversee the implementation of appropriate and timely Deviation, Investigations and • Participate in risk review meetings and review study Risk Management • Conduct QA reviews of essential documents including as applicable Clinical Protocols, Study Plans/Manuals, Investigator Brochures, Investigator’s Brochure, for ensuring quality, accuracy, and completeness • Collaborate with internal and/or external stakeholders to ensure management of GCP quality issues, CAPAs, and change controls • Identify process improvements to build compliance into the design and conduct of clinical activities • Actively support the development and deployment of Inspection Readiness/Management program to support competent authority inspections for sponsor and clinical sites & vendors