Medical Device QA Specialist — ISO 13485 Focus
pEssilorLuxottica is seeking a QA Specialist to join the Quality Regulatory Affairs team in Bologna. You will support maintenance and continuous improvement of the Quality Management System, ensuring compliance with medical device requirements across the product lifecycle. /ppResponsibilities include drafting and reviewing procedures and records, managing changes, supporting audits, handling non-conformities and CAPA activities, and coordinating supplier quality initiatives. /p #J-18808-Ljbffr