A global Medical Device provider actively involved in developing, manufacturing and marketing intensive care products.

職務說明

• Reports to Group CEO
• Oversee the strategic direction, preparation and progress of regulatory agency and notified body submissions
• Organize and lead the knowledge construction of existing and emerging regulations, standards, or guidance documents.
• Serve as a management representative for regulatory agency, notified body and customer audits.

理想的應徵者

• Extensive knowledge in TFDA, FDA and CE regulations
• RA experience in Medical Device is a must
• Logical and willing to take on challenge to transform the business
• Fluent in English and Mandarin

福利待遇

Global scope, competitive bonus

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