Specialist, Regulatory Affairs (m/f/d)
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Specialist, Regulatory Affairs (m/f/d)
Regulatory Affairs
Innsbruck, Austria
- Support and organize submissions to Notified Body
- Support and organize submissions, license renewals and registrations to international authorities
- Organize and maintain regulatory documentation to meet regulatory requirements
- Provide regulatory input to product development, product changes and manufacturing changes
- Education and/or experience equivalent to a Master’s degree preferably in a legal, science or engineering discipline, with a health science or biomedical component e.g. HTA, public health, clinical research, regulatory affairs
- 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, excellent/native German is preferred
Please apply in English!
Central Location
Employee Discounts
Flexible Hours
International Environment
Onboarding
Workplace Well-Being
Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is € 38,855.04.
If you have any questions please contact Ms. Caroline Schenk.
MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 130 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,300 employees around the world.
Want to join a company that helps bring the joy of sound to people with hearing loss? Apply now!
Social Media
Read user stories on the MED-EL Blog
Chat with users on the HearPeers Forum
Contact
MED-EL Medical Electronics
Headquarters
Fürstenweg 77a
6020 Innsbruck, Austria
Tel +43 5 7788 7788
jobs.medel.com
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