Guangzhou General Pharmaceutical Research Institute Co.,Ltd


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Latest information

Latest information

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神经生物学科研人员
神经生物学科研人员
2024-01-31

岗位职责:
1)负责犬神经退行性疾病、精神疾病表型评价平台搭建与研究工作;
2)犬认知与行为评价;
3)负责项目申请、实施与验收等
4)参与资源库日常科研工作
任职要求:
1)学历:研究生
2)专业:神经生物学

邮箱地址:renliziyuan@gpri.com.cn
联系电话:020-66284063
联系人:叶小姐

  • 计算机管理员

    岗位职责:
    1、负责网络及其设备的维护、管理、故障排除等日常工作,确保网络日常的正常运作;
    2、解决排除各种软硬件故障,做好记录,定期制作系统运行报告;
    4、维护数据中心,对系统数据进行备份。
    负责非临中心计算系统的管理,包括维护、运行、定期检查等工作。
    任职要求:本科及以上,有在GLP机构计算机相关工作经验优先考虑。

    邮箱地址:renliziyuan@gpri.com.cn
    联系电话:020-66284063
    联系人:叶小姐

    2024-01-31

  • 专题负责人

    岗位职责:
    1、组织开展新药研发、临床前及临床生物样本检测项目工作;
    2、根据标准及相关要求书写实验方案和总结报告;
    3、使用液质联用仪等分析仪器进行定性分析或含量测定,分析数据并对仪器进行常规维护。
    任职要求:
    1、熟悉生物分析基本流程,具备优秀的实验技能,熟练操作液质联用仪;
    2、应届毕业生或一年以上相关工作经验均可。

    邮箱地址:renliziyuan@gpri.com.cn
    联系电话:020-66284063
    联系人:叶小姐

    2024-01-31

  • 兽医(动物医学)

    岗位职责:
    1. 监控中心Beagle犬的的饲养管理及兽医日常护理;
    2. 负责Beagle犬的疾病的预防、监测、诊断和处置工作;
    3. 负责Beagle犬的质量检测;
    4. 负责生产繁育设施的管理;
    5. 协助Beagle犬的销售出库等相关工作。
    任职要求:
    1、本科及以上学历,动物医学、临床兽医学专业
    2、有宠物医院工作经历者优先考虑

    邮箱地址:renliziyuan@gpri.com.cn
    联系电话:020-66284063
    联系人:叶小姐

    2024-01-31

  • 动物营养

    岗位职责:
    1)负责不同生长阶段犬只营养需求研究
    2)负责犬饲料配方研究
    3)负责繁殖性能营养方面的研究,配种前-妊娠中的体况控制
    4)负责项目申请、实施与验收等
    5)参与资源库日常科研工作
    任职要求:
    1)学历:研究生
    2)专业:动物营养与饲料科学
    3)工作年限:不限
    4)具有从事饲料配方工作经历优先
    5)具有饲料营养对畜禽生长、繁殖研究经历者优先。

    邮箱地址:renliziyuan@gpri.com.cn
    联系电话:020-66284063
    联系人:叶小姐

    2024-01-31

  • 神经生物学科研人员

    岗位职责:
    1)负责犬神经退行性疾病、精神疾病表型评价平台搭建与研究工作;
    2)犬认知与行为评价;
    3)负责项目申请、实施与验收等
    4)参与资源库日常科研工作
    任职要求:
    1)学历:研究生
    2)专业:神经生物学

    邮箱地址:renliziyuan@gpri.com.cn
    联系电话:020-66284063
    联系人:叶小姐

    2024-01-31

  • 分子育种

    岗位职责:
    1)负责研究种群遗传质量监测、遗传育种等
    2)协助种犬选育、系谱管理等工作
    3)负责项目申请、实施与验收等
    4)参与资源库日常科研工作
    任职要求:
    1)学历:研究生
    2)专业:动物遗传育种
    3)工作年限:不限
    4)英语等级:英语六级
    5)掌握生物信息学、分子育种、数量遗传学技术
    6)有育种经历

    邮箱地址:renliziyuan@gpri.com.cn
    联系电话:020-66284063
    联系人:叶小姐

    邮箱地址:gyzy_rl@126.com
    联系电话:020-66284063

    2024-01-31

Company profile

Company profile

Guangzhou General Pharmaceutical Research Institute Co.,Ltd

Guangzhou General Pharmaceutical Research Institute Co.,Ltd

Guangzhou General Pharmaceutical Research Institute Co.,Ltd. (hereinafter referred to as the “Research Institute”) was formerly known as Guangzhou Pharmaceutical Industry Research Institute. It was established in 1972 and was originally a comprehensive medical research institution of Guangzhou Science and Technology Bureau. In 2000, it entered the whole system. Guangyao Group, in July 2015, the entire equity was injected into Guangyao Baiyunshan Group. After more than 40 years of development, the Research Institute has become a new research and development institution with complete disciplines, talents, outstanding features, strong innovation capabilities and integrated industrialization in South China. It is also the first batch of new R&D institutions in Guangdong Province and Guangdong Province Science and Technology Services. Top 100 enterprises, Guangdong Province honest demonstration enterprises, Guangzhou Science and Technology Innovation Little Giant Enterprise, Guangzhou Pharmaceutical Industry Intellectual Property Advantage Enterprise, Guangzhou Science and Technology Service Industry Model Enterprise.

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Research and development Center

Research and development Center

Drug Non-Clinical Evaluation Development Center
Drug Non-Clinical Evaluation Development Center

The Drug Non-Clinical Evaluation Research Center (National Key Laboratory of New Drug Safety Evaluation of Guangzhou) is the technical platform for drug R&D and safety evaluation established by the National Pharmaceutical Research Institute of Guangzhou Pharmaceutical Industry Co., Ltd. (hereinafter referred to as the “Center”). The center has a long history of GLP qualifications. As early as 1997, it began to set up a GLP laboratory--"National Ninth Five-Year Plan Project----------------------------------------------------- It became one of the first research institutes for the evaluation of new drug safety in the "1035 Project" in China; in September 2004, it passed the GLP certification of CFDA and became the first institution to pass GLP certification in South China; in 2010, it passed the international AAALAC certification, which is the South China region. The first institution to pass AAALAC certification is the first institution in South China to receive both

Laboratory Animal Research and Development Center
Laboratory Animal Research and Development Center

The National Canine Experimental Animal Seed Center (hereinafter referred to as the “Center”) is the only national canine experimental animal seed center approved by the Ministry of Science and Technology in June 2010 (Guo Ke Fa Cai [2010] No. 267), which is affiliated to Guangzhou Medical Research Institute. Hospital Co., Ltd. Founded in 1983, the center is a professional research institute for experimental Beagle dog resources with a long history, pure source, standardized management and leading level. It has been committed to the preservation, breeding, research and development of germplasm resources, and is a domestic experimental animal breeding institution. , research institutes, new drug research and development institutions and customs provide high-quality breeding dogs, research dogs, teaching dogs and quarantine dogs and other series of public welfare services.

Biological Sample Analysis and Detection Center
Biological Sample Analysis and Detection Center

Based on the GLP management system, the biological sample testing center is a third-party public service platform for providing standardized biological sample testing services. Center based on perfect quality management system and the GLP research for many years, equipped with complete facilities and international advanced equipment, USES the industry recognized biological analysis in laboratory information management system of Watson LIMS ™ to manage laboratory, its internal management, experiment method to form and content completely accords with the specification of GLP and 21 CFR PART11, provides a safe and reliable data for laboratory management; The center is dedicated to the analysis and testing of biological samples. It can develop, verify and apply a variety of analytical methods for testing, and provide professional technical services from a scientific and regulatory perspective.

Drug Screening Research and Development Center
Drug Screening Research and Development Center

Drug screening and research and development center has been committed to technology research, chiral synthesis and separation, and all kinds of controlled release technology research and industrialization of research, have many years of research, tracking progress abroad, successfully developed a number of three kinds of new chemical API, and achieved a lot slow controlled release and other preparations of the new drug certificate and production approval, has the first-class national new drug research and the ability of quality standards, quality first in a series of dozens of agents and the quality of scientific research subject, accumulated a wealth of experience.

Technical service

▲ Carry out new drug research and development for enterprises, including innovative drugs, generic drugs, high-end preparations, secondary development of famous and excellent Chinese patent drugs and other businesses. ▲ Provide safety evaluation and pharmacodynamic evaluation services in line with domestic and foreign standards and application requirements, including single multiple administration toxicity test, reproductive toxicity test, genetic toxicity test, local toxicity test, immunogenicity test, safety pharmacological test, toxicokinetic test, pharmacodynamic test, pharmacodynamic evaluation, etc. ▲ It has the only third-party public service platform for biological sample testing in south China with GLP qualification and quality assessment by the ministry of health, which can provide high-level biological sample testing technology services in line with domestic and international application requirements, and its quality system is in line with international standards. ▲ It has t

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Technical service

Qualification certification

GLP certification, international AAALAC accredited Beagle Dog and Monkey Research Center (DMRC), National Key Laboratory of New Drug Safety Evaluation Research, National Canine Experimental Animal Seed Center, South China New Drug Safety Evaluation Center

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Qualification certification