{"id":105655,"date":"2021-12-23T14:29:05","date_gmt":"2021-12-23T14:29:05","guid":{"rendered":"http:\/\/eyedeal.com\/job-opening\/ra-director\/"},"modified":"2022-02-11T04:06:41","modified_gmt":"2022-02-10T20:06:41","slug":"ra-director","status":"publish","type":"job-opening","link":"https:\/\/www.eyedeal.com\/en\/job-opening\/ra-director\/","title":{"rendered":"RA Director"},"content":{"rendered":"<h3><span class=\"font-673513 font-555555\" style=\"color: #4b4b4b;\">Responsibilities<\/span><\/h3>\n<ol>\n<li>Responsible for the research and transformation of domestic and foreign medical device registration technical standards, and responsible for the entire process of product pipeline registration;<\/li>\n<li>Lead the work related to the approval of innovative medical devices<\/li>\n<li>Responsible for organizing expert consultation meetings and evaluation meetings<\/li>\n<li>Responsible for the testing\/inspection work related to the company&#8217;s product registration<\/li>\n<li>Organizing and coordinating the registration-related work such as quality system and clinical trials<\/li>\n<\/ol>\n<h3><span style=\"color: #4b4b4b;\">Requirements<\/span><\/h3>\n<ol>\n<li>Possess a doctoral degree in bioengineering, chemistry, polymer materials and other related majors<\/li>\n<li>More than two years of relevant work experience in three types of implanted medical devices (such as cardiac stents\/pacemakers\/vascular stents\/orthopedic implant products, etc.)<\/li>\n<li>Familiar with domestic and EU, FDA, ASEAN, Japan, Canada and other major international regional medical device registration procedures<\/li>\n<li>Familiar with relevant regulations and standards for medical devices, and have good writing skills in both Chinese and English<\/li>\n<\/ol>\n","protected":false},"featured_media":0,"template":"","yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v19.1 - 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