Regulatory Affairs Specialist

Select how often (in days) to receive an alert: Job Title: Regulatory Affairs Specialist Job Requisitions No.: 18302 Job Description: Role Details The role has primary responsibility for supporting all local regulatory affairs workflow including preparation of dossiers and applications for new registration and maintain existing products life-cycle as well as...

Overview In questa posizione, ti occupi di gestire le attività regolatorie per dispositivi medici a livello nazionale ed internazionale, garantendo conformità normativa, sottomissioni e manutenção delle registrazioni. Lavorerai a stretto contatto con sedi estere, distributori e funzioni interne per facilitare l accesso ai mercati e l introduzione di...

Overview Quality Assurance Regulatory Affairs (QARA) Specialist – Dedalus. Remote in Italy. Part of the Global Quality and Assurance Team to drive quality and regulatory excellence in healthcare technology. What you’ll achieve As a QARA Specialist you will ensure compliance with Quality and Regulatory standards across the company, contributing to better...

Select how often (in days) to receive an alert: Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa. Over three years ago, we embarked on a transformative journey...

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...

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,...

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,...

## Regulatory and Start Up Specialist - ItalyApply: Milan, Italy: Full time: Posted Today: R1572752### RSU Specialist**Level:** Senior Associate **Location:** Italy (Home Based) ### About IQVIAIQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights to the life sciences industry. With more...

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...