Quality Assurance Engineer

• May 2023 - Present

Junior Software Test Engineer

• Oct 2021 - May 2023

• Preparation and execution of test cases according to the requirements • Identification and maintenance of defects • Execution of regression tests for new releases • Preparation of test summary reports • Maintenance of automated tests (Selenium and APIs functional tests) • Participation and leading of Agile/Scrum ceremonies • Preparation and execution of test cases according to the requirements • Identification and maintenance of defects • Execution of regression tests for new releases • Preparation of test summary reports • Maintenance of automated tests (Selenium and APIs functional tests) • Participation and leading of Agile/Scrum ceremonies

Quality Assurance Specialist

• Nov 2018 - Oct 2021

• Meeting all regulatory compliance requirements of the Quality System • Preparation and update of QS procedures in accordance to ISO 13485 and FDA requirements • Coordination of Corrective Action Preventive Action (CAPA) program • Participation in the external and internal audits • Coordination and implementation of the internal audit program • Meeting all regulatory compliance requirements of the Quality System • Preparation and update of QS procedures in accordance to ISO 13485 and FDA requirements • Coordination of Corrective Action Preventive Action (CAPA) program • Participation in the external and internal audits • Coordination and implementation of the internal audit program

Quality Engineer

• Mar 2017 - Nov 2018

▪ Preparation of documentation for devices registration and certification. ▪ Establishment and updating of company‘s quality procedures, work instructions and testing records. ▪ Supervision of medical device Quality System requirements according ISO 13485 and FDA. ▪ Participation in external and internal audits. ▪ Control of CAPA system. ▪ Preparation of documentation for devices registration and certification. ▪ Establishment and updating of company‘s quality procedures, work instructions and testing records. ▪ Supervision of medical device Quality System requirements according ISO 13485 and FDA. ▪ Participation in external and internal audits. ▪ Control of CAPA system.