Remote Ivd/Cdx Regulatory Affairs Expert
1 settimana fa
A global healthcare consulting firm is seeking an experienced Regulatory Affairs professional specializing in in vitro diagnostics (IVD) and Companion Diagnostics (CDx).This role involves developing regulatory strategies, collaborating with cross-functional teams, and managing submissions for regulatory approvals.Candidates must have at least 5 years in Medical Device regulatory affairs, a university degree in a scientific field, and excellent English skills.The position offers flexibility in work location across Europe.#J-*****-Ljbffr
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Remote IVD/CDx Regulatory Affairs Expert
1 settimana fa
Milano, Italia Parexel A tempo pienoA global healthcare consulting firm is seeking an experienced Regulatory Affairs professional specializing in in vitro diagnostics (IVD) and Companion Diagnostics (CDx). This role involves developing regulatory strategies, collaborating with cross-functional teams, and managing submissions for regulatory approvals. Candidates must have at least 5 years in...
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Regulatory Affairs Consultant
1 settimana fa
Milano, Italia Parexel A tempo pienoWhen our values align, there's no limit to what we can achieve. About the Role We are seeking an experienced Regulatory Affairs professional specializing on in vitro diagnostics (IVD) and Companion Diagnostics (CDx) to join our Global Regulatory Affairs team. In this strategic role, you will provide expert guidance on regulatory pathways for IVD and CDx...
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Regulatory Affairs Consultant
3 giorni fa
Via Milano, Italia Parexel A tempo pienoWhen our values align, there's no limit to what we can achieve. About the Role We are seeking an experienced Regulatory Affairs professional specializing on in vitro diagnostics (IVD) and Companion Diagnostics (CDx) to join our Global Regulatory Affairs team. In this strategic role, you will provide expert guidance on regulatory pathways for IVD and CDx...
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Regulatory Affairs Consultant
2 giorni fa
milano, Italia Parexel A tempo pienoWhen our values align, there's no limit to what we can achieve.About the RoleWe are seeking an experienced Regulatory Affairs professional specializing on in vitro diagnostics (IVD) and Companion Diagnostics (CDx) to join our Global Regulatory Affairs team. In this strategic role, you will provide expert guidance on regulatory pathways for IVD and CDx...
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Regulatory Affairs Consultant
5 giorni fa
Milano, Italia HAYS A tempo pienoSocietà di Consulenza - Aziende Farmaceutiche - Affari Regolatori - Regulatory Affairs Consultant - Milano **La tua nuova azienda** Il nostro cliente è una rinomata Società di consulenza che fornisce servizi alle azienda farmaceutiche in merito alle autorizzazioni necessarie per la commercializzazione dei loro prodotti. In un’ottica di ampliamento...
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Regulatory Affairs Specialist
1 settimana fa
Milano, Italia Pharma D&S A tempo pieno**Regulatory Affairs Consultant** Pharma D&S ricerca per la sede di Cassina de' Pecchi (MI) un/una Regulatory Affairs Consultant - Lifecycle Management, con almeno due anni di esperienza nel ruolo. La risorsa selezionata si occuperà di: - Gestione della sottomissione regolatoria e valutazione dei dati tecnici di tutte le procedure regolatorie -...
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Regulatory Affairs Manager
2 giorni fa
milano, Italia Cpl Life Sciences A tempo pienoManaging Consultant - Regulatory Affairs & Quality @ Cpl Life Sciencesob Title: European Regulatory Affairs ManagerLocation: Milan, Italy - HybridRemuneration: Competitive salary and packageRegulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is...
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Regulatory Affairs Associate Director
5 giorni fa
Milano, Italia Alira Health A tempo pieno**REGULATORY AFFAIRS ASSOCIATE DIRECTOR/DIRECTOR (DRUG)** Alira Health is a very dynamic company who aims to provide best in class regulatory services adapted to the needs of our clients. Our regulatory department is growing, and we are looking for a Director in drug regulatory affairs to be a key contributor by providing sound experience in the field of...
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Medical Device
3 giorni fa
Milano, Italia Resourcing Group A tempo pienoMedical Device – Regulatory Affairs DirectorResponsibilitiesLine management of 10 Regulatory Line ManagersEstablish and implement regulatory strategies ensuring new and existing products comply with the latest global requirementsTrain the team on EMEA / FDA requirementsQualificationsMinimum 8 years in regulatory affairs in the medical device...
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Medical Device
2 giorni fa
milano, Italia Altro A tempo pienoMedical Device – Regulatory Affairs DirectorResponsibilitiesLine management of 10 Regulatory Line ManagersEstablish and implement regulatory strategies ensuring new and existing products comply with the latest global requirementsTrain the team on EMEA / FDA requirementsQualificationsMinimum 8 years in regulatory affairs in the medical device...