Medical Device Classification Specialist

1 month ago


Beijing, Beijing, China TÜV Rheinland Full time

Job Description

As a Medical Device Classification Specialist at TÜV Rheinland, you will be responsible for classifying medical devices according to the MDR regulation and making rule judgments. Your tasks will include checking the completeness of technical documents, preparing audit documents, and following up on audit projects while arranging project schedules.

Key Responsibilities:

1. Classify medical devices according to MDR regulation and make rule judgments.

2. Check the completeness of technical documents for medical devices.

3. Prepare audit documents, including sampling plans and audit programs.

4. Follow up on audit projects and arrange project schedules.

Requirements:

1. Master's degree in a science-related field.

2. Fluent English reading, listening, and speaking skills (CET 6 level or higher).

3. At least 4 years of working experience.

4. Strong learning and communication skills.

5. Strong sense of responsibility.



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