Create, edit, and proofread clinical evaluations to assess the safety and performance of a range of MED-EL products, in accordance with applicable regulations
Acquire in-depth knowledge of MED EL products
Conduct literature reviews to identify clinical data relevant to regulatory submissions
Collate and analyze clinical data from clinical trials, scientific literature, product testing, and post-market experience
Collaborate with other departments within MED EL and with external partners
Your Profile
Master’s degree or higher degree (University, FH) in Life or Natural Sciences, Healthcare or Medicine, Engineering or Technical Sciences
Demonstrable scientific writing experience
Experience with Regulatory Affairs is desirable
Excellent verbal and written communication skills in English; German is a plus
Demonstrated understanding of, and enthusiasm for, scientific work and clinical research
Please apply in English!
Your Benefits
Central Location
Employee Discounts
Flexible Hours
International Environment
Onboarding
Workplace Well-Being
Further Information
Minimum Salary: Annual gross salary from € 57,785.7,5 based on professional qualification and experience.
Earliest Entry Date: This position is to be filled immediately.
Temporary Position: This position is limited until 30-Nov-2027.
Your Contact Person: If you have any questions please contact Marina Engl.
About MED-EL: 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 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,800 employees around the world.
Want to join a company that helps bring the joy of sound to people with hearing loss? Apply now!