Your Tasks

• Planning, coordination, and management of clinical evaluation activities while ensuring compliance with regulatory requirements and internal quality standards
• Research, compilation, and analysis of clinical data from studies, tests, scientific literature, and post-market experience
• Preparation, review, and verification of clinical evaluation reports and related documentation to assess the safety and performance of MED-EL products in accordance with applicable regulations
• Continuous development and expansion of in-depth knowledge of the MED-EL product portfolio and its clinical application Close interdisciplinary collaboration with internal departments and external partners

Your Profile

• Master’s degree or higher degree (University, FH) in Life Sciences, Natural Sciences, Healthcare, Medicine, Engineering or Technical Sciences
• Proven experience in scientific writing
• Experience with Regulatory Affairs is a plus
• Excellent communication skills in English, both written and spoken; German skills are desirable
• Understanding of, and enthusiasm for scientific working, medical technology, and clinical research

Your Benefits

• Central Location
• Employee Discounts
• Flexible Hours
• Internatonal Enviroment
• Onboarding
• Workplace Well- Being

Further information

Minimum Salary

Salary will be determined based on professional experience; the Formal minimum salary according to Collectice Bargaining Agreement is € 47,810.14.

Earliest Entry Date

This position is to be filled immediately.

Your Contact Person

Marina Engl