Would you like to work for a company who has made it its mission to make a contribution to improving human living conditions? With more than 3,600 employees worldwide Eppendorf is a leading Life Sciences company. We develop and distribute devices, consumables and services for use in laboratories worldwide. Our daily work is characterized by our principle: Collaborate on new ideas. Would you like to test the latest premium products independently and contribute to their design? At Eppendorf you will be developing continuously in your area of expertise and you will have access to modern technical equipment and excellent working conditions. You are also motivated by scientific expertise? Then apply now!
You are the contact person for internal and external regulatory inquiries for your area of responsibility.
You continuously gather, analyze, assess and communicate global regulatory market requirements.
You coordinate and execute registrations and certifications (including communication with authorities)
You drive the global implementation of regulatory requirements.
You have successfully completed a master degree in natural science or engineering and have profound working experience in the field of regulatory affairs.
You are experienced in international, regulatory environments (e.g. medical devices, IVD, product safety) and you understand and apply the requirements from QM-Systems ISO 13485 and ISO 9001.
You worked in an international organization in the medical-device or laboratory industry.
You are fluent in German and English.
We really appreciate our employees and their performance. This is why we offer an attractive salary.
You will also have the opportunity to work from home - in a way that suits your personal situation best.
By working for us you will make a meaningful contribution to improving human living conditions.
At our locations in Hamburg, Leipzig and Oldenburg i.H. you can also benefit from a subsidized lunch in the company restaurant.