Meissner Str. 191
0351 25999 420
Specialist Regulatory Affairs (medical devices) (w/m/d)
Freelance or part/full-time, temporary position (parental leave replacement), effective immediately.
What will you do?
You will ensure a smooth flow of processes in the Regulatory Affairs division:
You will be in charge of the technical documentation and design dossiers of our medical devices class III.
You support the area of the change management process by processing change requests
You are responsible for the registration and approval of our products in the countries requested by our customers.
Who are you?
You have successfully completed your technical or scientific studies (or comparable training in the field)
You have acquired a sound knowledge of quality management and the relevant laws and standards
You have already gained professional experience in the field of regulatory affairs and quality management
You have a distinctive goal-oriented way of working and enjoy working in a team
You are communicative and speak or write a confident English
You are confident in using MS Office programs (such as Word, Excel, PowerPoint, Outlook)
You are confident in dealing with culture-specific differences
Who do you contact?
Please submit your informative documents preferably by email to Frau Tauchert.