Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
6020 Hötting - Österreich
Umweltwissenschaftler/in
Arbeit
Vollzeit
ab 16.01.2026
Beschreibung
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... weiter lesen
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... weiter lesen
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
Permanent full-time post 38,5 hours per week, flexible working time model with core working hours, details will be discussed in a personal interview.
Want to join a company that helps bring the joy of sound to people with hearing loss? Apply now!
https://jobs.medel.com/EN/open-position/RDCE_12601/online
A personal interview is only possible after prior invitation from the HR department.
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
Permanent full-time post 38,5 hours per week, flexible working time model with core working hours, details will be discussed in a personal interview.
Want to join a company that helps bring the joy of sound to people with hearing loss? Apply now!
https://jobs.medel.com/EN/open-position/RDCE_12601/online
A personal interview is only possible after prior invitation from the HR department.
Ref-Nr.: 8743328
Aktualisiert:
17.01.2026
Quelle: Bundesagentur für Arbeit
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
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