Aktuelle Jobs im Zusammenhang mit Regulatory Compliance Expert - Innsbruck, Tirol - MED-EL Medical Electronics


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    Software Project ManagerAt MED-EL Medical Electronics, we're committed to bringing the joy of sound to people with hearing loss. As a Software Project Manager, you'll play a crucial role in our Research & Development team, overseeing the creation and coordination of user stories for our web, mobile, and desktop applications.Your ResponsibilitiesCollaborate...


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  • Data Analyst

    vor 1 Monat


    Innsbruck, Tirol, Österreich MED-EL Vollzeit

    Job DescriptionWe are seeking a highly skilled Statistician (m/f/d) to join our team at MED-EL. As a key member of our clinical research team, you will be responsible for analyzing clinical data to support the development of manuscripts and reports for federal regulatory agencies.Key ResponsibilitiesData Analysis: Utilize statistical techniques to analyze...

  • Data Analyst

    vor 2 Monaten


    Innsbruck, Tirol, Österreich MED-EL Vollzeit

    Job DescriptionWe are seeking a highly skilled Statistician (m/f/d) to join our team at MED-EL. As a statistician, you will play a crucial role in analyzing clinical data for manuscripts and reports to federal regulatory agencies.Key ResponsibilitiesData Analysis: Utilize statistical techniques to analyze clinical data and provide detailed analysis results...

Regulatory Compliance Expert

vor 2 Monaten


Innsbruck, Tirol, Österreich MED-EL Medical Electronics Vollzeit

About MED-EL Medical Electronics
MED-EL is a prominent developer of cutting-edge medical technologies aimed at addressing various forms of hearing impairment.

Our distinctive range of implantable auditory solutions has positively impacted the lives of countless individuals across more than 140 nations globally. With our main office located in Innsbruck, Austria, MED-EL proudly employs over 2,800 dedicated professionals worldwide.

Position Overview
The Regulatory Affairs Specialist will play a crucial role in ensuring compliance with industry regulations and standards. This position involves:

  • Conducting thorough assessments of regulatory requirements for medical devices.
  • Collaborating with cross-functional teams to facilitate product approvals.
  • Maintaining up-to-date knowledge of regulatory changes and trends.
  • Preparing and submitting necessary documentation to regulatory bodies.

We are committed to fostering an environment that values innovation and excellence in the field of medical technology.