Senior International Regulatory Affairs Specialist

Manpower Salerno cerca una risorsa per ruolo di International Regulatory Affairs Senior Specialist presso Palomonte (SA). Responsabilità chiave includono sviluppo ed implementazione di strategie regolatorie, gestione dossier e rapporti con enti regolatori internazionali, con focus su conformità e trasferimenti. Offerta: inserimento diretto, RAL tra 38.000...

INTERNATIONAL REGULATORY AFFAIRS SENIOR SPECIALISTFaccia ora il prossimo passo nella sua carriera: scorra verso il basso per leggere la descrizione completa del ruolo e invii la sua candidatura.Manpower Salerno ricerca, per importante azienda farmaceutica con sede a Palomonte (SA), una risorsa da inserire nel ruolo di:International Regulatory Affairs Senior...

INTERNATIONAL REGULATORY AFFAIRS SENIOR SPECIALIST Manpower Salerno ricerca, per importante azienda farmaceutica con sede a Palomonte (SA) , una risorsa da inserire nel ruolo di: International Regulatory Affairs Senior Specialist La risorsa sarà responsabile dello sviluppo e dell'implementazione delle strategie regolatorie a supporto dell'espansione...

pParexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines, with remote options across Europe. You will collaborate with manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance across variations, renewals, and market expansions. /ppThe role...

Overview 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,...

Overview As an RSU Specialist, you will lead country-specific site activation and regulatory activities within IQVIA's FSP team in Italy. You will act as the primary liaison for investigative sites and project teams, ensuring compliant, timely site activation and regulatory documentation. You will leverage local regulatory expertise to support timelines,...

Overview In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international setting....

Overview In this role, you lead a Europe-wide team of Regional Research Managers to steer the research, innovation, and academic collaboration strategy. You will build and manage high-impact partnerships with academia, healthcare providers, and government bodies to advance scientific innovation and business growth. You will engage executives and key...

Overview As Senior Global Patient Safety Physician at Chiesi, you lead safety science for assigned products, shaping proactive risk management and safety surveillance. You collaborate across Clinical Development, Medical Affairs, Regulatory, Quality and external partners to integrate safety data into development plans and submissions. You drive science-led...