Regulatory Affairs Specialist


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Regulatory Affairs Specialist

Your tasks
Ensure accurate and timely reporting to authorities in compliance to SOP`s, MEDDEVs, ISO 14155, 93/42/EEC and international and local laws for medical device adverse event reporting and vigilance reporting
Maintain country specific adverse event and vigilance requirements
Create responses to general requests/queries regarding vigilance and reporting
Support the submission related activities for new and ongoing product submissions
Your profile
Bachelor degree
Minimum 3 years' experience in Regulatory Affairs
Detail-oriented person with experience in working in a highly regulated environment
Excellent interpersonal communication (oral and written)
Ability to work in an interdisciplinary team
Fluent in German and English
Our offer
We can offer you a new challenge, with interesting tasks and much more - including an open corporate culture, flat hierarchies, support for further training and development, opportunities to take on responsibility, an excellent range of foods, sports and cultural facilities, attractive employment conditions, and flexible working time models in various roles.

Maryline Schelcher, Human Resources Manager, is looking forward to receiving your complete application (cover letter, cv, references and certificates) via our online job application platform.

For this vacancy only direct applications will be considered.
Sonova AG
Laubisrütistrasse 28
CH-8712 Stäfa
+41 58 928 01 01