面議(經常性薪資達4萬元或以上) 台北市大安區 1年工作經驗 4天前更新
•Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.
•Independently interacts and builds partnerships with competent authorities (TFDA, and other regulatory agencies.
•Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
•Providing advice and support to the project team for regulatory or technical aspects of the projects.
•Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
•Other duties as assigned
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