Jobs

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.

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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

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Who do you contact?

Please submit your informative documents preferably by email to Frau Tauchert.

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