Internship for medical regulatory affairs / part time (f/m) Vacancy No: DE-02
As a member of Osmunda Group, our Berlin office has been engaged to assist the European medical Device and pharmaceutical manufacturer with regulatory and clinical affairs in Asian countries. We are looking for a team member willing to bring commitments and grow with us.
We offer a responsible position in a fast growing company with the great opportunity for self-development. A full-time position can be offered after the internship with an excellent performance.
You are responsible for assisting the administration management related to the projects, promoting and representing the company in various conferences, medical translations for professional documents and maintaining client relations by consulting the client with regulatory and clinical knowledge.
You are approaching or have a medical-related academic degree. Any working experience in pre-clinical or clinical environment is preferred. Alternatively, any regulatory or quality management experience in medical device or pharmaceutical industry is very welcomed.
You are highly motivated and a quick learner to adjust to different projects with a good priority management in timelines and work.
You are fluent in English. Ability of speaking and writing in German and Chinese is a big advance.
Please send your application and CV in English (please also in Chinese if you can) by email quoting the vacancy number to email@example.com.