Senior Regulatory Affairs Lead

Sentinel Diagnostics, leader in the Development and Production of Diagnostic Kits for Clinical Chemistry, Immunology, Molecular Biology, Chromatography and Rapid Tests, in order to expand the RA Team, is looking for a: Senior Regulatory Affairs Specialist FDA & International Registrations Key Responsibilities Define and implement regulatory strategies to...

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...

IQVIA on behalf of Chiesi Farmaceutici seeks a Global Regulatory Affairs Manager to join our international team for a fixed-term maternity cover. Based in Italy, you will partner with GRL and GRT to shape regulatory strategies across EU and global markets.The role requires 3–4 years in international regulatory affairs, with preferred experience in rare...

Select how often (in days) to receive an alert:Di seguito, troverà un'analisi completa di tutti i requisiti per i potenziali candidati e le istruzioni su come candidarsi. In bocca al lupo!Senior Manager, CMC Regulatory Affairs, Global Rare DiseasesDate: 1 Oct 2026Department: GRD Regulatory AffairsBusiness Area: R&D, Pharmacovigilance & Regulatory AffairsJob...

About usChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we...

Chiesi Farmaceutici S.p.A.Scorra verso il basso per una panoramica completa dei requisiti di questo lavoro. È la persona giusta per questa opportunità?seeks an experienced Senior Manager, CMC Regulatory Affairs for its Global Rare Diseases portfolio.The role focuses on post-approval CMC activities, coordinating with global teams and CMOs to ensure...

About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as...

Seeking a Senior Manager for CMC Regulatory Affairs in Global Rare Diseases. Responsible for CMC regulatory documents, submissions, and strategy for commercial

Chiesi Farmaceutici S.p.A. seeks an experienced Senior Manager, CMC Regulatory Affairs for its Global Rare Diseases portfolio. The role focuses on post-approval CMC activities, coordinating with global teams and CMOs to ensure high-quality submissions.You will shape regulatory strategies across development and marketed products, maintain timelines, and drive...