Regulatory Affairs Associate

vor 4 Wochen


Innsbruck, Tirol, Österreich MED-EL Vollzeit
Job Summary

We are seeking a highly skilled Regulatory Affairs Associate to join our team at MED-EL. The successful candidate will be responsible for regulatory dossier compilation and submission, as well as developing regulatory assessment and submission strategies.

Key Responsibilities
  • Compile and submit regulatory dossiers to ensure compliance with regulatory requirements
  • Develop and implement regulatory assessment and submission strategies to support business objectives
  • Gather and analyze regulatory intelligence to inform business decisions
  • Manage informational lists and databases to support regulatory compliance
  • Communicate with sales teams to ensure regulatory requirements are met
Requirements
  • Written and verbal fluency in English
  • Proficient in using PC and MS applications software
  • Attention to detail and excellent organizational skills
  • Strong orientation to teamwork and goals accomplishment
Benefits
  • Central location
  • Employee discounts
  • Flexible hours
  • International environment
  • Onboarding
  • Workplace well-being
Salary and Benefits

Salary will be determined based on professional experience. The formal minimum salary according to Collective Bargaining Agreement is € 33,235.30 for fulltime 38.5 hours/week.

How to Apply

Please apply in English.



  • Innsbruck, Tirol, Österreich MED-EL Vollzeit

    Regulatory Affairs RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our team at MED-EL. The successful candidate will be responsible for regulatory dossier compilation and submission, as well as regulatory assessment and submission strategy development.Your Key ResponsibilitiesCompile and submit regulatory dossiersDevelop and...


  • Innsbruck, Tirol, Österreich MED-EL Vollzeit

    Regulatory Affairs RoleWe are seeking a skilled Regulatory Affairs Specialist to join our team at MED-EL.Key Responsibilities:Compile and submit regulatory dossiersDevelop regulatory assessment and submission strategiesGather regulatory intelligenceManage informational lists and databasesCommunicate with sales teamsYour ProfileRequirements:Fluency in English...


  • Innsbruck, Tirol, Österreich Novartis Farmacéutica Vollzeit

    About the Role:We are seeking a highly skilled Associate Director Engineering to lead technical development and life-cycle management in cross-functional teams for easy-to-use, safe, and robust products as Medical Device Expert.Key Responsibilities:Lead technical development and life-cycle management in cross-functional teams for easy-to-use, safe, and...


  • Innsbruck, Tirol, Österreich MED-EL Vollzeit

    Job DescriptionWe are seeking a highly skilled Post-Market Surveillance Specialist to join our team at MED-EL. As a key member of our regulatory affairs department, you will play a crucial role in ensuring the safety and quality of our medical devices.Key Responsibilities:Perform Post-Market Surveillance: Conduct regular monitoring of our medical devices to...


  • Innsbruck, Tirol, Österreich X-Therma GmbH Vollzeit

    X-Therma GmbH is a fast-paced and innovative company from San Francisco with a hardware R&D branch in Innsbruck, Austria. We are developing groundbreaking technology to improve modern medicine and save countless lives. With our subzero storage and transport solutions, we are enabling global access to organ transplants as well as cell and gene therapy...


  • Innsbruck, Österreich Leonhard Lang GmbH Vollzeit

    Leonhard Lang GmbH Präsenz / Mobil Berufserfahrung (Senior Level) Qualitätsmanagement, Qualitätssicherung Vollzeit Jahresgehalt: 53.200 EUR **WIR SETZEN IMPULSE**: - Seit 1983 entwickelt, produziert und vertreibt Leonhard Lang Medizinprodukte, wie Elektrodensysteme und Zubehör für EKG, Elektrochirurgie, Defibrillation, Stimulation sowie Gele und...


  • Innsbruck, Österreich MED−EL Elektromedizinische Geräte Gesellschaft m.b.H. Vollzeit

    Your Tasks- Regulatory dossier compilation and submission - Regulatory assessment and submission strategy development - Regulatory itelligence gathering - Management of informational lists and databases - Sales area communications - Your Profile- Written and verbal fluency in English - Attention to detail and excellent organizational skills - Strong...


  • Innsbruck, Österreich MED-EL Vollzeit

    Regulatory dossier compilation and submission Regulatory assessment and submission strategy development Regulatory itelligence gathering Management of informational lists and databases Sales area communications Your Profile Written and verbal fluency in English Proficient using PC and MS applications software Attention to detail and...


  • Innsbruck, Österreich X-Therma GmbH Vollzeit

    X-Therma is a fast-moving and innovative startup from San Francisco with an office and hardware R&D branch in Innsbruck, Austria. We are developing breakthrough technology to improve modern medicine and save billions of lives. With our subzero storage and transport solutions, we are enabling global access to organ transplants as well as cell and gene therapy...


  • Innsbruck, Österreich X-Therma GmbH Vollzeit

    X-Therma is a fast-moving and innovative startup from San Francisco with an office and hardware R&D branch in Innsbruck, Austria. We are developing breakthrough technology to improve modern medicine and save billions of lives. With our subzero storage and transport solutions, we are enabling global access to organ transplants as well as cell and gene therapy...


  • Innsbruck, Österreich Innerspace GmbH Vollzeit

    As an important part of a small team, you will have the opportunity to support our company on its way to quality excellence. Through your meticulous and accurate way of working, you will own the product documentation structure and you will be responsible for creating comprehensive and understandable documentation. In your role, you will form an essential...


  • Innsbruck, Österreich Business Beat Innerspace MAD MADiscover Miviso Vollzeit

    **Role Description**: As an important part of a small team, you will have the opportunity to support our company on its way to quality excellence. Through your meticulous and accurate way of working, you will own the product documentation structure and you will be responsible for creating comprehensive and understandable documentation. In your role, you will...