Senior Regulatory Affairs

RequisitiISO/IEC 27001, ISO/IEC 42001.L'innovazione sanitaria deve arrivare ai pazienti, non fermarsi al regolamento.Ardeevo affianca i fabbricanti di dispositivi medici e di dispositivi medico-diagnostici in vitro nel percorso di conformità al Regolamento (UE) 2017/745 (MDR) e al Regolamento (UE) 2017/746 (IVDR), con servizi di Regulatory Affairs e Quality...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biologics and vaccines. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance.The role supports variations, renewals, market expansions, and annual reports,...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biologics and vaccines. The role involves post-approval regulatory activities, worldwide submissions, and close collaboration with manufacturing, QA, QC, and regulatory teams to drive submission strategies and risk mitigation.This position supports variations, renewals, and market...

Ardeevo cerca professionisti per rafforzare il nucleo regolatorio e QA nel contesto MDR/IVDR. Revisionerete output regolatori generati da una piattaforma AI-Native, fornendo verdetti motivati e miglioramenti di processo.La posizione prevede supporto ai clienti, collaborazione con il team prodotto e contatto con Organismo Notificato. Si valuta esperienza su...

Klk Oleo in Lombardy, Milano area seeks a Senior Regulatory Affairs Expert to drive regulatory compliance and product stewardship across Europe.Tutti i candidati sono invitati a leggere attentamente la seguente descrizione del lavoro e le relative informazioni prima di candidarsi.You will support systems, monitor EU regulations, and provide guidance to...

Aufgaben und Verantwortlichkeiten As a Senior Regulatory Affairs Expert, you will play a key role in ensuring regulatory compliance and product stewardship across our European operations. Your main responsibilities include: Supporting the development, implementation, and continuous improvement of Regulatory Affairs and Product Stewardship...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance.Responsibilities include developing post-approval CMC submission...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biological and vaccine products. This role involves post-approval regulatory activities, collaboration across manufacturing, QA, QC, and regulatory teams, and support for variations, renewals, and market expansions. Remote options in Europe are offered.The role emphasizes writing and...

As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. Your work supports variations, renewals, and market expansions, delivering...