Huadong Medicine Co., Ltd 华东医药-- Domestic Registered 国内注册岗
More detailed job description(Chinese) can be found via Liepin’s 2019 Fall Recruitment Job Fair at http://liepinoverseas.com/2019fall-careerfair/?utm_source=us-cc&utm_medium=us-cc&utm_campaign=2019fall
Interested students with following positions could either apply those information by clicking the link or send their resume + applied position (in the mail title) to recruiter_boston@liepin.com
Collected resumes will be directly deliver to the HR department, no pre-assessment test needed
Company Information
Established in 1993, Huadong Medicine Co.,Ltd specializes in the production and sales of antibiotic, Chinese patent medicine, synthetic drug, genetic engineering drugs, as well as wholesale business of Chinese and western medicine, Chinese herbal medicines, medical apparatus and instruments. The company is a large comprehensive listed pharmaceutical company integrated with pharmaceutical R&D, pharmaceutical industry, pharmaceutical distribution, retail, pharmaceutical logistics, and undertakes the task of special drug storage of the state, provincial and municipal governments. The company successfully issued 50 million A-shares on the Shenzhen stock exchange in December 1999. ( Stock abbreviation: Huadong Medicine; stock code: 000963). At present, the registered capital of the company is 14.58 million yuan. The company and its main subsidiaries have more than 8,000 employees. In 2017, the company realized operating revenue of 27.832 billion yuan. Net profit attributable to shareholders of listed companies was 1.480 billion yuan.
Management department技术管理部-- Domestic registered 国内注册岗
Job requirements:
· Master and above;
· Biology, pharmacy, pharmaceutical analysis, medical policy, and regulatory research-related majors
Job responsibility:
· Carry out collection and analysis of domestic policies and regulations, and provide support for the company's R&D product registration process
· Complete the application for the online products arranged by the supervisor, including cases NMPA approval or the provincial bureau
· Complete re-registration at the expiration of the validity period of the drug approval number issued by NMPA
· R&D project management
· Follow up and coordinate the work in the project management, supplementary application or re-registration process
· Assist the registration supervisor in completing the review and proofreading of the registration information of the new drug