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Deputy Manager ofRegulatoryAffairs Responsibilities: 1. Ensure regulatory compliance; pay close attention to the changes in medical devices regulations; improve internal regulation system accordingly. 2. Maintain close liaison with regulatory project team and other stakeholders; disseminate regulatory information to leadership and relevant people such as R&D, sales, marketing, QA, customers and overseas colleagues. 3. Responsible for product registration and internal regulation system maintenance. 4. Ensure all changed local working progress is timely following the quality and safety relevant variations. 5. Assure compliance of raw materials and finished product with regulation. 6. Manage client complaints from a regulation point of view. Requirements: 1. Bachelor degree or higher; major in law, medicine and pharmacy or related. 2. Minimum 5 years experience in regulatory affairs. 3. Very understanding of regulatory environment in China. 4. Experience in international registration would be beneficial. 5. Worked for medical devices manufacturing industry would be beneficial. 6. Good project management skill and can work in a team. 7. Fluent in Chinese & English
本公司为世界500强企业,二类有源医疗设备(输液泵/注射泵相关),年薪19-25万
有意者可联系QQ417924374 或发送简历至abo18@foxmail.com
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