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Job Description
- Prepare documentation needed to CE certify a specific range of products.
- Responsible for international registration for this range of products by supplying all the documents needed.
Job Requirements
- Minimum 5 years of experience, Experience with ISO13485 , Medical device CE certification, preparing technical files. Familiar with medical device classification and testing as biocompatibility testing, ….etc
- A good similar experience in Pharmaceutical industry is also considerable.
