Regulatory Specialist

3 weeks ago


Beijing, Beijing, China TÜV Rheinland Full time

Job Description

As a Regulatory Specialist at TÜV Rheinland, you will be responsible for classifying and judging medical devices according to the MDR regulation. Your tasks will include checking the completeness of technical documents, preparing audit documents, and following up on audit projects.

Requirements

To succeed in this role, you will need a Master's degree in a relevant field, fluent English skills, and at least 4 years of working experience. You should also be able to learn quickly, communicate effectively, and demonstrate strong responsibility.



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