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广东省高水平新型研发机构
State Key Laboratory of Ophthalmology (Research Center for Non clinical Evaluation of Ophthalmic Drugs)
Key Laboratory of Non Clinical Evaluation of Drugs in Guangdong Province
炎症与免疫相关疾病教育部基础研究创新中心
创新药物评价与研究广东省工程研究中心
Guangdong Innovative Drug Evaluation and Research Engineering Technology Research Center
Guangdong Provincial Engineering Technology Research Center for Ophthalmic Drug Creation and Evaluation
One stop public service platform for research, development and evaluation of cell and gene therapy drugs in Guangdong-Hong Kong-Macao Greater Bay Area
Non clinical Evaluation Center for Traditional Chinese Medicine, National Research Center for Modernization of Traditional Chinese Medicine
广东省企业技术中心
Key technology platform for research and evaluation of chiral drugs
Innovative drug research and molecular imaging technology and product research technology platform
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Key technology platform for pharmacokinetics research
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研究类岗位
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岗位职责
贯彻执行GLP法规中质量管理相关要求,翻译、研究、培训国内外相关法规标准;
对试验方案、实施过程及总结报告进行审查和检查;
协助组织安排对质量体系的检查和稽查;
持续完善质量体系建设。
岗位要求
有较强的分析问题及执行能力,具备良好的沟通技巧、工作认真、细致,拥有良好的团队合作精神。
本科及以上学历,具有药学日语、药学英语、药事管理、医疗器械、食品、化妆品等相关专业背景。
有药品或生物制药QA工作经验,参与质量体系建立及管理经验者优先。
日语1级,有医药背景、翻译经验优先。
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