Italy Regulatory Affairs Lead

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

Un'agenzia di recruitment cerca un Responsabile Regulatory Affairs per un'azienda di produzione di prodotti innovativi per la salute degli animali. La figura si occuperà della gestione delle pratiche regolatorie e collaborerà con vari reparti, tra cui Farmacovigilanza. È richiesta una laurea in medicina veterinaria e almeno 1-2 anni di esperienza nel...

Overview In this role you will lead labeling strategy within Global Regulatory Affairs to align CCDS, dCCDS, USPI and EU SmPC across products. You will influence product development plans, ensure compliant labeling and support commercial opportunities. You’ll collaborate with GRA, GCD, GCSP and cross-functional teams to maintain global consistency and...

Johnson & Johnson Innovation in Italy is seeking a Medical Affairs Manager, Neuroscience to shape and execute the medical strategy for our Neuroscience portfolio in Italy, including autoimmune neurological diseases and neurodegenerative disorders.Reporting to the Therapeutic Area Medical Lead, you will build scientific partnerships, advance evidence...

Overview In this Regulatory Affairs Lead role, you shape IVD regulatory strategies, guiding performance evaluation and marketing authorizations. You will act as the regulatory lead for global project teams, coordinating interactions with authorities and ensuring compliant submissions. The role supports lifecycle management and continuous improvement within...

Location: Milan, Italy Contract Type: Permanent contract, Fulltime Department: Regulatory Affairs The Opportunity In this role, you will serve as the primary regulatory representative for Italy, ensuring compliance with local regulations, leading interactions with Health Authorities, and supporting product registrations and lifecycle management activities....

Parexel is seeking a Regulatory Affairs Consultant - CMC vax/bio (home or office based) in Teramo, Abruzzo, Italy. You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products and collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions.You will manage regulatory...

Overview In this role you will provide strategic medical leadership across the Rare Diseases portfolio, guiding medical affairs and evidence generation to support growth. You will partner with clinical development, regulatory, and commercial teams to shape global medical strategies while upholding ethics and patient centricity. As a scientific external...