pVivaBioCell S.p.A. in Udine, Italy, is seeking a Senior QA / Regulatory Affairs Specialist to ensure GMP and ISO compliance. The role is hybrid, reporting to the Quality Regulatory Department, and requires leading regulatory activities and supporting audits. /ppYou will manage quality documentation, contribute to the ongoing improvement of the quality system, and collaborate with cross-functional teams to maintain compliance with 21 CFR Part 11 where applicable. /p #J-18808-Ljbffr
Mostra le tue capacità professionali all'azienda, compila il form e lascia un tocco personale nella lettera di presentazione, aiuterà il recruiter nella scelta del candidato.