全職
大學以上
面議（經常性薪資達 4 萬元或以上）
•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
At Qualtech, we recognize the value of each member’s contribution to the reputation of our organization. Be part of a multidisciplinary team who takes pride at achieving excellence in all aspects of their work.
Join us and discover a work experience where diverse ideas are met with enthusiasm, and where you can learn and grow to your full potential in healthcare industry. That‘s why we strive to foster teamwork and innovation, encouraging professional growth and fulfillment.
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注意！福利項目可能依不同職缺有所不同，實際職缺福利請依面試時與公司面談結果為準
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