MED-EL

Regulatory Affairs Specialist (m/f)

RA_1_1907

Innsbruck, Österreich

Main Tasks

  • Lead, organize and support submissions to Notified Body
  • Support preparation of regulatory submissions, licence renewals and registrations to international authorities
  • Organize and maintain regulatory documentation and data files to meet regulatory requirements
  • Provide regulatory input to product development, product changes and manufacturing changes

 

Requirements

  • Master’s degree is required, preferably in a legal, science or engineering discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
  • At least 2 years medical device or regulatory affairs work experience is strongly preferred, graduates with any biomedical related experience e.g. in pharma industries, clinical research or health technology assessment are also welcome
  • Excellent English (spoken and written) is required, German native speaker or excellent German
  • Eager to learn, attention to detail, proven problem solving & organizing skills as well as a collaborative personality

 

 

Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is EUR 36,154.72

 

We offer a challenging opportunity in a multinational work environment with English as our company language. We look forward to receiving your application at jobs.medel.com

 

 

 

 

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