Senior Regulatory Affairs Specialist

2 settimane fa


Roma, Lazio, Italia Cosmo Intelligent Medical Devices A tempo pieno

Cosmo IMD is a division of the Cosmo Pharmaceutical group focusing on medical devices integrating artificial intelligence. Cosmo IMD has developed in recent years unrivaled expertise in multiple aspects related to the AI MedTech business, such as medical device Hardware and Software design, healthcare Artificial Intelligence development, medical data harvesting, clinical development, scientific production, and regulatory expertise in the US and worldwide. Cosmo IMD team is manufacturing GI Genius,



  • Roma, Lazio, Italia Angelini Pharma A tempo pieno

    Requisition ID: 6227- Location: Roma, IT- Company: ANGELINI PHARMA SPA- Professional area: Medical, R&D- Job Description:- _We have an opportunity for a _**_Regulatory Affairs Specialist._****_Main activities:_**- _ Definition and development of regulatory strategies, supporting the Regulatory Affairs Director and in line with the Company's needs._- _Exploit...


  • Roma, Lazio, Italia Cosmoimd A tempo pieno

    Senior Regulatory Affairs Specialist of Cosmo Intelligent Medical Devices. Work Location: Rome – Italy – Viale Ostiense 131/L Key Responsibilities: Assess medical device safety by providing input/review to the risk management activities throughout the whole product lifecycle, health hazards evaluations, and clinical evaluation reports. Review and...


  • Roma, Lazio, Italia Cosmoimd A tempo pieno

    Senior Regulatory Affairs Specialist of Cosmo Intelligent Medical Devices.Work Location: Rome – Italy – Viale Ostiense 131/LKey Responsibilities:Assess medical device safety by providing input/review to the risk management activities throughout the whole product lifecycle, health hazards evaluations, and clinical evaluation reports. Review and provide...


  • Roma, Lazio, Italia Cosmoimd A tempo pieno

    Senior Regulatory Affairs Specialist of Cosmo Intelligent Medical Devices. Work Location: Rome – Italy – Viale Ostiense 131/L Key Responsibilities: Assess medical device safety by providing input/review to the risk management activities throughout the whole product lifecycle, health hazards evaluations, and clinical evaluation reports. Review and...


  • Roma, Lazio, Italia JR Italy A tempo pieno

    Social network you want to login/join with:Senior Regulatory Affairs Specialist, RomaClient:Location:Job Category:OtherEU work permit required:YesJob Reference:516766534730147430433710Job Views:4Posted:23.03.2025Expiry Date:07.05.2025Job Description:Cosmo IMD is a division of the Cosmo Pharmaceutical group focusing on medical devices integrating artificial...


  • Roma, Lazio, Italia TN Italy Lavoro a distanza Freelance A tempo pieno

    Company OverviewTN Italy is seeking a highly skilled and experienced Regulatory Affairs professional to join our team as Contractor Regulatory Manager.The successful candidate will be responsible for providing regulatory support and expertise to our clients, ensuring compliance with all relevant regulations and guidelines.Key Responsibilities:Initiate,...


  • Roma, Lazio, Italia Jr Italy A tempo pieno

    Social network you want to login/join with:Senior Regulatory Affairs Specialist, RomaClient:Location:Job Category:OtherEU work permit required:YesJob Reference:516766534730147430433710Job Views:4Posted:10.03.2025Expiry Date:24.04.2025Job Description:Cosmo IMD is a division of the Cosmo Pharmaceutical group focusing on medical devices integrating artificial...


  • Roma, Lazio, Italia Cosmoimd A tempo pieno

    Job OverviewAt Cosmo Intelligent Medical Devices, we are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring the compliance of our medical devices with regulatory requirements.About the RoleWe are looking for an experienced professional with...


  • Roma, Lazio, Italia Coswell S.p.A. A tempo pieno

    Sei alla ricerca di una sfida professionale in un contesto dinamico e internazionale? Allora questo è il ruolo che fa per te Stiamo cercando un–Junior Regulatory Affairs Specialist. Principali task: Gestione delle schede di sicurezza (SDS): valutare le schede di sicurezza per i prodotti chimici tramite workflow approvativi; preparare e aggiornare SDS e...


  • Roma, Lazio, Italia Mantell Associates A tempo pieno

    Mantell Associates is partnered with a Cell & Gene Therapy organisation, who is seeking a CMC Regulatory Affairs Manager to join their growing team. CMC Regulatory Affairs Manager - Responsibilities:Help the team implement and manage CMC regulatory strategies for gene therapy projects, ensuring everything aligns with regulatory requirements. Contribute to...


  • Roma, Lazio, Italia Aretè & Cocchi Technology A tempo pieno

    JSB Solutions - azienda leader nei servizi life sciences con focus su consulenza, gestione studi clinici e sviluppo software - ricerca per il potenziamento del proprio organico un Regulatory Affairs Specialist (JSB.PPL.25.008) da inserire all'interno della propria divisione degli Affari Regolatori . Chi siamo: con quattro sedi operative in Italia...


  • Roma, Lazio, Italia Productlife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma.Chi siamoIntexo Società Benefit, una realtà di consulenza del gruppo ProductLife, opera nel settore healthcare con l'obiettivo di garantire un accesso rapido, trasparente e sostenibile alle...


  • Roma, Lazio, Italia Cosmoimd A tempo pieno

    **Job Overview**We are seeking an experienced Regulatory Affairs Specialist to join our team at Cosmo Intelligent Medical Devices.


  • Roma, Lazio, Italia PQE Group A tempo pieno

    Sei pronto per entrare a far parte di una società di consulenza leader mondiale nell#39;industria farmaceutica e dei Medical Device? PQE Group è affermata in questo settore dal 1998, garantendo una presenza internazionale grazie alle 45 filiali e i 2000 dipendenti in Europa, Asia e nelle Americhe. Lavorare in una realtà di consulenza come PQE Group ti...


  • Roma, Lazio, Italia ProductLife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma. Chi siamo Intexo Società Benefit, una realtà di consulenza del gruppo ProductLife, opera nel settore healthcare con l'obiettivo di garantire un accesso rapido, trasparente e sostenibile...


  • Roma, Lazio, Italia Leo Pharma A tempo pieno

    **Company Description**At LEO Pharma, we are at a pivotal point in our transformation journey to advancing medical dermatology by developing new biologics, in a mostly unexplored therapeutic area in the world today.Every day, we seek inspiration from people living with skin diseases.We are passionate about identifying and addressing their greatest health...


  • Roma, Lazio, Italia Leo Pharma A tempo pieno

    Company DescriptionAt LEO Pharma, we are at a pivotal point in our transformation journey to advancing medical dermatology by developing new biologics, in a mostly unexplored therapeutic area in the world today.Every day, we seek inspiration from people living with skin diseases.We are passionate about identifying and addressing their greatest health needs,...


  • Roma, Lazio, Italia ProductLife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma.Chi siamoIntexo Società Benefit, una realtà di consulenza del gruppo Product Life, opera nel settore healthcare con l'obiettivo di garantire un accesso rapido, trasparente e sostenibile alle...


  • Roma, Lazio, Italia TN Italy Lavoro a distanza Freelance A tempo pieno

    **Job Description**TN Italy is seeking a highly skilled Regulatory Affairs Manager to join our team in Rome. As a key member of our regulatory team, you will be responsible for ensuring compliance with relevant regulations and guidelines.**Key Responsibilities**Initiate, review, and approve regulatory changes through Pfizer's enterprise system for changes...


  • Giuliano di Roma, Lazio, Italia Cosmo Intelligent Medical Devices A tempo pieno

    Company OverviewCosmo Intelligent Medical Devices is a division of the Cosmo Pharmaceutical group, specializing in medical devices integrating artificial intelligence.About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist Junior to join our team. As a key member of our Regulatory Affairs department, you will play a crucial role in...