Job Title: AI Translator & Digital Health Lead Introduction to role: Are you ready to turn AI and Digital Health ideas into scaled solutions that deliver measurable value for patients and the business? Do you thrive
Who we are Amplifon is an Italian multinational company and the global leader in hearing care solutions and services. More than 20,000 professionals every day, in a network of 9,500 points of sale across 24 countries,
About Us Sophos is a cybersecurity leader defending 600,000 organizations globally with an AI-driven platform and expert-led services. Sophos meets organizations wherever they are in their security maturity and grows with them to defeat cyberattacks. Its
As a Senior Quality Assurance Specialist, you will play a key role in ensuring compliance with quality and regulatory requirements for both our current and future product portfolio. Initially, your primary focus will be on our
Why Orthofix? Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want
Named Account Manager – Security Operations (SecOps) (Italy) Role Overview Join Fortinet, a cybersecurity pioneer with over two decades of excellence, as we continue to shape the future of cybersecurity and redefine the intersection of networking
At TD SYNNEX, we are a leading global distributor and solutions aggregator for the IT ecosystem, operating in more than 100 countries with over 23,000 employees worldwide. We help our partners accelerate growth through innovative technologies,
Pharma Point Srl è alla ricerca di un/una Regulatory Affairs Specialist – Medical Device da inserire nel team dedicato a dispositivi medici. Sede di lavoro: Liguria. Il ruolo prevede supporto alle attività di preparazione, aggiornamento e
B. Braun Avitum Italy cerca un Regulatory Affairs Junior Manager per la sede di Mirandola (MO) per sostituzione maternità, con esperienza di almeno 3 anni nel settore medicale/farmaceutico. Ruolo incentrato sulla registrazione di dispositivi medici fuori
Una società di consulenza IT sta cercando un Project Manager nellambito Healthcare per gestire progetti di sviluppo e implementazione di sistemi applicativi. Il candidato ideale avrà esperienza comprovata nella gestione di progetti tecnologici complessi e una
B. Braun Melsungen AG, presso la sede di Mirandola, cerca un Regulatory Affairs Junior Manager per una sostituzione maternità nel dipartimento di Regulatory Affairs. Richiesta unesperienza di almeno 3 anni nel settore medicale o farmaceutico con
Stealth Healthcare AI Startup, a Europe-focused medical software startup, seeks a Product Manager with hands-on MDR experience to bridge product, engineering, clinical, and QA/regulatory functions. The role emphasizes regulatory-ready product decisions from day one. You will translate
Sinclair is looking for a Risk Manager in Italy to oversee risk management for medical devices and aesthetic products, ensuring compliance with ISO standards. The role involves leading risk management activities, coordinating with cross-functional teams, and
Integrity360 is seeking a Product Owner for their MDR Platforms in Rome. In this role, you will drive the development of the Online Portal, enhancing cybersecurity services and customer engagement. Ideal candidates should have 5+ years of
About Us Integrity360 is a leading independent cybersecurity and PCI specialist operating across Europe, Africa, the Caribbean, and North America. The company has office locations in Ireland, the UK, Bulgaria, Italy, Sweden, Spain, Lithuania, Ukraine, Africa,
Unagenzia per il lavoro cerca un Regulatory Affairs Specialist per unazienda nel settore metalmeccanico a Villafranca di Verona. La risorsa si occuperà di sviluppare e gestire i fascicoli tecnici per dispositivi medici secondo la normativa MDR, gestire
MAW cerca per unazienda nel settore Medical Device uno Specialista Qualità ISO 13485 e MDR con almeno 2 anni di esperienza in Quality Assurance e Regulatory Affairs. Gestirà la documentazione tecnica dei dispositivi medici e supporterà il
Teoresi MedTech cerca un Regulatory Affairs Specialist per supportare la verifica e laggiornamento della documentazione tecnica di dispositivi medici presso la sede di Bologna. È richiesta laurea in Ingegneria Biomedica e minimo 2 anni di esperienza
Per conto di un\azienda operante nel settore Medical Device , si ricerca un* Specialista Qualità ISO 13485 e MDR con almeno 2 anni di esperienza in ambito Quality Assurance e Regulatory Affairs. Attività principali: Gestione e aggiornamento
At Cedic we offer solutions for living. Our diverse product portfolio, specialising in fluid delivery, is designed with the main objective of improving the patient’s quality of life. That is why we continually invest in our