Lavori attuali relativi a Quality Assurance Lead — Medical Devices, MDR - roma - Kiranet


  • Roma, Italia Kiranet A tempo pieno

    Overview Un\'azienda innovativa nel settore sanitario cerca un QUALITY ASSURANCE SPECIALIST per gestire e migliorare il Sistema di Gestione Qualità, assicurando il mantenimento delle certificazioni ISO 9001 e ISO 13485. Richiesta laurea in ingegneria, esperienza di almeno 3 anni nella gestione qualità, e conoscenza delle normative (MDR, GDPR). Offriamo...


  • roma, Italia Nordberg Medical A tempo pieno

    Regulatory Affairs Specialist -Medical DevicesJoin to apply for the Regulatory Affairs Specialist -Medical Devices role at Nordberg MedicalRegulatory Affairs Specialist -Medical DevicesJoin to apply for the Regulatory Affairs Specialist -Medical Devices role at Nordberg MedicalGet AI-powered advice on this job and more exclusive features.The Regulatory...

  • Senior Quality

    7 giorni fa


    roma, Italia Hantech Medical A tempo pieno

    A medical device company in Italy is seeking a Quality Manager to lead Quality Operations and Regulatory Affairs. The ideal candidate will have at least five years of experience managing quality management systems, including a minimum of three years specifically in medical devices. Responsibilities include overseeing compliance with European regulations,...


  • giuliano di roma, Italia Hantech Medical A tempo pieno

    A medical devices company is seeking a Quality Operations Engineer in Villamarzana, Italy, to ensure ISO 13485 compliance and maintain product integrity. The role requires monitoring in-process quality, managing calibration of equipment, and driving continuous improvement initiatives. Ideal candidates should have a bachelor's degree in a scientific or...


  • giuliano di roma, Italia Hantech Medical A tempo pieno

    A medical devices company is seeking a Quality Operations Engineer in Villamarzana, Italy, to ensure ISO 13485 compliance and maintain product integrity. The role requires monitoring in-process quality, managing calibration of equipment, and driving continuous improvement initiatives. Ideal candidates should have a bachelor's degree in a scientific or...


  • Roma, Italia Page Personnel Italia SPA A tempo pieno

    Una multinazionale nel settore Healthcare cerca un Sr. Quality Assurance Specialist per gestire audit interni, garantire la compliance normativa e monitorare i fornitori. Il candidato ideale ha una laurea in discipline scientifiche e circa 5 anni di esperienza in Quality Assurance nel settore medicale. È richiesto l'inglese fluente e capacità di lavorare...


  • Roma, Italia Page Personnel Italia SPA A tempo pieno

    Sr. Quality Assurance Specialist Importante multinazionale specializzata nella produzione di dispositivi medici. Azienda L'azienda è una realtà multinazionale affermata nel settore Healthcare, tra le principali aziende europee produttrici di apparecchiature per la chirurgia di riferimento. Offerta Responsabilità principali Audit & Compliance Pianificare,...

  • Technical Reviewer

    2 giorni fa


    roma, Italia BSI A tempo pieno

    Great that you're thinking about a career with BSI!Job title: Technical Specialist & Scheme Manager - Active DevicesLocation: Home-based position located in the UK or Europe with up to 20% travel for training.BSI is seeking experienced R&D Engineers to join our Active Medical Devices team as a home-based Technical Specialist & Scheme Manager (Technical...


  • roma, Italia Alchimia Srl A tempo pieno

    A leading medical devices company in Italy seeks a Temporary Project Manager specializing in regulatory compliance for EU medical devices. This role involves planning, executing, and monitoring compliance efforts within a high-pressure environment. Candidates should have project management training, experience with medical device regulations, and fluency in...


  • roma, Italia Alchimia Srl A tempo pieno

    A leading medical devices company in Italy seeks a Temporary Project Manager specializing in regulatory compliance for EU medical devices. This role involves planning, executing, and monitoring compliance efforts within a high-pressure environment. Candidates should have project management training, experience with medical device regulations, and fluency in...

Quality Assurance Lead — Medical Devices, MDR

4 giorni fa


roma, Italia Kiranet A tempo pieno

Un'azienda innovativa nel settore sanitario è alla ricerca di un QUALITY ASSURANCE SPECIALIST per gestire e migliorare il Sistema di Gestione Qualità, garantendo il mantenimento delle certificazioni ISO 9001 e ISO 13485. È richiesta una laurea in ingegneria, esperienza di almeno 3 anni nella gestione qualità e conoscenza delle normative MDR e GDPR. Questa posizione offre un'opportunità di crescita professionale in un contesto dinamico e in espansione.#J-18808-Ljbffr