Regulatory Affairs Lead – Medical Devices

1 settimana fa


WorkFromHome, Italia W&H Sterilization s.r.l. A tempo pieno

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  • Medical Affairs Lead

    1 giorno fa


    WorkFromHome, Italia Clinigen A tempo pieno

    Role Description In this role, you will be responsible for establishing and maintaining strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the medical community. You will play a pivotal role in supporting the company's medical strategy and ensuring the accurate and ethical dissemination of medical...


  • WorkFromHome, Italia ResMed Inc A tempo pieno

    A global healthcare technology firm in Italy is looking for an Advanced Regulatory Affairs Specialist to join their team. You will participate in all regulatory activities related to the import and distribution of medical devices within the EMEA region, ensuring compliance with regulations. The role requires a Bachelor's degree and experience in the medical...


  • WorkFromHome, Italia ResMed Inc A tempo pieno

    Advanced Regulatory Affairs Specialist page is loaded## Advanced Regulatory Affairs Specialistlocations: Vimercate, Italy: Didcot, United Kingdom: Kista, Swedentime type: Full timeposted on: Posted Todayjob requisition id: JR\_ **We are looking for our future Advanced Regulatory Affairs Specialist to join our Regulatory team in Italy, GB or Sweden.****Let's...


  • WorkFromHome, Italia ResMed Inc A tempo pieno

    A leading global healthcare company is seeking an Advanced Regulatory Affairs Specialist in Vimercate, Italy. In this role, you will participate in regulatory activities tied to the import and distribution of medical devices across the EMEA region. The ideal candidate has a Bachelor's Degree in Science or Engineering and at least 5 years of relevant...

  • Remote QA

    4 settimane fa


    WorkFromHome, Italia SGS Australia A tempo pieno

    A leading company in testing and certification is seeking a Quality Assurance professional for a remote role focused on maintaining the medical device quality management system. The ideal candidate should have a degree in Biomedical Sciences, strong knowledge in QA systems, and experience in medical devices. This position involves managing complaints,...


  • WorkFromHome, Italia Weekday AI A tempo pieno

    This role is for one of the Weekday's clients Min Experience: 8 years Location: Europe JobType : full-time We are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory operations and system implementations. The ideal candidate will play a critical role in...


  • WorkFromHome, Italia Weekday AI (YC W21) A tempo pieno

    Lead - Regulatory Information Management 1 day ago Be among the first 25 applicants This role is for one of the Weekday's clients. Minimum experience: 8 years. Location: Europe. Job type: full-time. We are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory...


  • WorkFromHome, Italia Clinigen A tempo pieno

    A medical affairs organization in Italy is seeking a professional to establish and maintain relationships with key opinion leaders and support medical strategies related to haematology and oncology. This role involves conducting educational programs for healthcare professionals, supporting clinical trials, and ensuring ethical dissemination of medical...


  • WorkFromHome, Italia Analog Devices, Inc. A tempo pieno

    Director, Field Medical Affairs (Rare Diseases) EUR 100.000 - 130.000 Director, Field Medical Affairs (Rare Diseases) Join to apply for the Director, Field Medical Affairs (Rare Diseases) role at Regeneron We’re hiring a Medical Director, Field Medical Affairs (Rare Diseases) to help advance care in cardiovascular, muscle, and bone conditions. This hybrid...


  • WorkFromHome, Italia Perrigo Company plc A tempo pieno

    A global healthcare provider in Italy is seeking a Regulatory Affairs Manager to lead regulatory strategy for biocidal products. The successful candidate will manage a high-performing team and ensure compliance with evolving regulatory standards. Ideal candidates have 5+ years of experience in regulatory affairs, strong project management skills, and a...