杭州招聘

1. 负责仪器设备的采购申请、验收、维修及其计量检定（送检）工作，制定仪器设备的检定、维修计划；
2. 学习有关仪器设备管理文件，结合本机构的实际情况，制定实施细则及规定并组织相关培训；
3. 负责计量工作计划的编制和实施；
4. 负责组织仪器设备的维修和备品配件的管理工作；
5. 负责仪器设备台帐的制定，及时更新仪器设备状态，及时贴换相应标签；
6. 负责实验室（仓库之外）的物料盘库；
7. 组织安全教育和培训；

任职条件：

1、生物医学、生物工程、医学检验等相关生物学专业大专及以上学历；

2、具备良好的规划、控制、协调、管理能力；

3、熟悉实验室常用设备的使用和维护；

4、熟练各种常用办公软件

5、工作认真踏实，富有责任心。

Amador Bioscience strives to provide global-standard laboratory, clinical research, strategy consulting and regulatory filing services to biopharmaceutical companies. The laboratory services focus on PK/PD/ADA assay development and sample analysis. Amador clinical research unit specializes in innovative clinical development strategy and protocol design, and initiation and monitoring of clinical studies in China and US. In addition to R&D strategy and regulatory pathway, our consulting services perform global-standard data analysis and generate submission-ready study reports. We have successfully supported CTD filings in China and US.

With profound academic background and rich experience in R&D services in the biopharmaceutical industry, AmadorBio is a global clinical research team of pharmacologists, statisticians, bioanalytical scientists, translational & clinical scientists, medical scientists, clinical trial management experts, data management experts, quality assurance auditors, clinical trial managers and regulatory specialists. (40% of PhD, MD and PharmD, 35% of MS). AmadorBio provides professional services for more than 20 leading biopharmaceutical companies from early research and development, clinical development to regulatory submission in China and US.

AmadorBio operates in biotech hubs: San Francisco Bay Area, USA and Shanghai-Hangzhou-Suzhou region, China, providing comprehensive solutions complied with global standards and government drug inspection regulations in China and US.

The mission of Amador is to provide global-standard services facilitating the development of novel biotherapeutics.

    安渡生物致力于为生物医药公司提供全球标准的实验室、临床研究、策略咨询和监管申报服务。实验室服务专注于PK/PD/ADA方法学开发验证和样本分析。安渡生物的临床研究中心专注于为美国和中国的生物医药公司提供创新的临床研究开发策略、方案设计、启动和监查的专业服务。我们的咨询服务除研发策略和监管服务外，还可提供全球标准的数据分析并生成完备的申请报告。我们在中国和美国成功地支持了多家医药公司的CTD申请。

    安渡生物是一支具有资深学术背景、行业研发服务经验丰富的临床研究团队，拥有临床药理、数理统计、生物分析、转化科学、医学、临床运营、数据管理、质量保证审核、项目管理以及监管申报各方面专家，其中博士(PhD, MD, PharmD)占40%，硕士占35%。安渡团队致力于支持从临床前到临床各个阶段的药物开发计划。目前我们为20余家中美生物制药公司提供从早期研发，临床开发到监管申报等多个项目的专业服务。

    安渡生物在美国旧金山湾区和中国长三角地区设有办公室和实验室，提供涵盖中美及符合国际标准和政府药检规范的全方位解决方案。

    安渡生物的使命：提供全球标准的服务，促进新型生物药物开发。