• 电话: +86 21 63862192
  • 邮箱: info@alphabiopharma.com
  • 上海: 黄浦区太仓路233号新茂大厦504-508室
  • 北京: 朝阳区光华路9号世贸商业中心4号楼天阶大厦2512室

人才理念

组织能力指的是团队整体发挥的战斗力

  • 深植于组织内部
而非个人,有可持续性

    深植于组织内部
    而非个人,有可持续性

  • 为客户创造价值

    为客户创造价值

  • 明显超越竞争对手

    明显超越竞争对手

组织能力要聚焦,优秀的公司往往在两三个方面展示出众所周知的组织能力;组织能力还要清晰界定,这样团队才能集中精力和资源来关注、开发这样的能力。

  • 员工思维

    员工思维

    员工是否展现与组织能力匹配的价值观、 行为和投入度?

  • 员工能力

    员工能力

    员工是否具备组织能力行为和投入度?

  • 员工治理

    员工治理

    公司是否提供有效的管理支持和资源容许员工充分发挥所长?

打造组织能力的三个维度

打造组织能力的三个维度,必须符合两个原则:
一是平衡,即三个能力要一样强;
二是匹配,三个支柱的重点必须与所需的组织能力协调。
打造组织能力的三个维度

员工风采

icon
icon
ICON

icon
icon

员工发展与培训

  • 新员工培训

    新员工培训
  • 通用管理技能培训

    通用管理技能培训
  • 专业技能培训

    专业技能培训

培训方式

  • 现场培训现场培训
  • 在线直播课程在线直播课程
  • 午餐分享会午餐分享会
  • 线下培训沙龙
线下培训沙龙

员工福利

  • 福利年假
    福利年假
  • 带薪病假
    带薪病假
  • 商业保险
    商业保险
  • 年度旅游
    年度旅游
  • 年度体检
    年度体检
  • 生日会
    生日会
  • 下午茶
    下午茶
  • 节日福利
    节日福利
  • 团队建设
    团队建设
  • 员工班车#
    员工班车
  • 员工住宿#
    员工住宿
  • 福利午餐#
    福利午餐

出现icon为工厂员工专享福利

icon

招聘信息

临床药理副总监

  • 工作地点:上海
  • 发布时间:2021-09-27
  • 招聘人数:1人
点击收起

岗位描述

1. With experience managing data, writing and reviewing clinical pharmacology/PK reports and regulatory
submissions dossier and responding to regulatory queries.
2. Conducts clinical pharmacology studies in line with product development strategies, regulatory
requirement and scientifically sensible; Collaborate with the investigator sites, investigators, CRO or other
Partners and ensure high quality standards of their deliverables.
3. Serves as clinical pharmacology expert in the assigned project team; leads the study design and
coordinates pharmacokinetic / DMPK related elements for projects.
4. Manage PKPD analysis for understanding of PKPD relationship for drug effect and dose selection.
5. Oversees PK, PK/PD and DMPK biopharmaceutical analyses performed with a variety of tools and
approaches.
6. Identify potential risks and provide mitigation strategies from DMPK perspective.
7. Review and ensure PK or PD analysis plan and report in phase I, II and III .
8. Representing the clinical pharmacology during the Communication with HA.
9. Assists with managing timelines and budgets to ensure efficient execution of clinical pharmacology
studies

任职要求

1. Advanced training with a degree of Master, PhD, PharmD or MD.
2. 5-8 year's industry experience with investigation of drug metabolism, transporters, and biotransformations of therapeutics.
3. Knowledge of bioanalytical expertise, PK, metabolism, drug interactions, and regulatory requirements.
上传简历
文件大小不超过3mb

验证工程师/主管

  • 工作地点:上海
  • 发布时间:2021-09-27
  • 招聘人数:1人
点击收起

岗位描述

1. Responsible to establish the validation process and procedure in the company.
2. Responsible for the organization and coordination of the implementation process of validation and verification for plant, facility, equipment, process, cleaning procedure.
3. Responsible for organizing the risk assessment related to verification and validation;
4. Responsible for the preparation and review of the verification documents;
5. Responsible for technical guidance and training of relevant skills and knowledge in the verification process; 7.Responsible for the organization and implementation of revalidation work to ensure the continuity of validation status. 8. Responsible for the validation or qualification of analysis method, process validation, clean validation etc,.if needed.

任职要求

1. At least bachela degree.
2. Major in bioengineering, pharmacy, etc.
3. Experience in new biopharmatical plant validation.
4. Proficient in the knowledge of regulation include but not limited to the GMP 2010, ASTM E2500 etc,.
5. 3-5 years in GMP certification and quality management
上传简历
文件大小不超过3mb

质量经理

  • 工作地点:上海
  • 发布时间:2021-09-27
  • 招聘人数:1人
点击收起

岗位描述

Establish and continuously improve the assigned quality systems in line with the regulatory expectation as the system owners

Product Quality Assurance
1.Ensure the compliance of quality relevant tasks (e.g., Deviation, change management , CAPA follow up, etc.)
2.Act as QA representative in the project, and perform QA operational tasks timely. 3.Responsible for the release of the material.
4.New supplier qualification and management
5.Execute the random tasks assigned by QA head.

任职要求

1. At least bachela degree.
2. Major in bioengineering, pharmacy, etc.
3. Experience in Cell therapy project is preferred.
4. At least 5 years QA working experience in GxP system as well as experience in working on an international level.
上传简历
文件大小不超过3mb