We, SIS MEDICAL AG, a leading and fast growing innovative company in the field of minimally invasive coronary interventions are continuously looking for motivated professionals in order to provide best quality and top performing products to the market.
To support our strong growth, we develop our site.
To strengthen our Quality Assurance and Regulatory Affairs Group in Frauenfeld, we are looking for a solution oriented and creative personality as
Quality Assurance or Regulatory Affairs Specialist (m/f)
Worldwide registrations of class I and III medical devices
Assembly and maintenance of the worldwide registration documentation (STED, CSDT), provision of notarized and legalized documents
Collaboration with our distributors for submission in the respective countries
Assure seamless transition from MDD 93/42/EEC to MDR
Regulatory and quality projects (e.g. MDR, UDI) according to requirements in the target territories
Degree in technical or natural sciences or business administration background; at least Applied Sciences University level
5 years of experience in medical device industry, in Regulatory Affairs, Design Assurance or Quality Assurance
Proficiency in MS Office applications
German and English orally and in writing: C2 level
We offer a working culture, which is based on collegiality, performance and cooperation in a young, well-established and innovative organization with a lot of pioneering spirit. Apart from challenging and varied tasks in an international setting, we offer diverse development possibilities in our dynamic and growing team.
Share with us the passion for excelling performance in the Medtech industry and forward your complete set of application documentation to:
SIS Medical AG Frau Janina Seitz Office Administrator Hungerbüelstrasse 12a 8500 Frauenfeld