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We respect talent, and the simple and open atmosphere allows everyone to actively innovate and strive for the health of humanity. Here, everyone can come up with their own ideas at any time and even contribute new ideas as a team. Talent strategy is our long-term strategy. The growth and development of talent is our responsibility. We provide dual-channel career opportunities in R & D and management to achieve your creativity and help you achieve your career goals.

You are welcome to join, participate and contribute to the vigorous development of Genetron Health as China's leading precision oncology company. 

Senior Director / GM
Company:Genetron Health,Inc
Department:
Work place:Gaithersburg, Maryland, USA
Recruitment:1
Education:
Job type:Full Time
Release time: 08- 28
Working years:
(Sr.)Director,BD
Company:Genetron Health,Inc
Department:
Work place:Gaithersburg, Maryland, USA
Recruitment:1
Education:
Job type:Full Time
Release time: 08- 28
Working years:5 years

Sr. Director/Director, Business Development

Genetron Health is a leading and fast-growing precision oncology company that is committed to providing a one-stop, multi-scenario genomic profiling solutions in areas including early cancer screening, diagnosis and monitoring as well as biopharmaceutical services. It has successfully developed seven NMPA-approved clinical sequencing platforms and gene assays. Partnering over 500 hospitals along with several pharmaceutical companies and research institutions, Genetron Health has built an extensive proprietary genomic database to deliver comprehensive genomic testing services. In China, the company has one R&D center, two manufacturing facilities and five clinical laboratories in Beijing (CLIA-certified and CAP-accredited), Shanghai, Hangzhou, Chongqing and Guangzhou. Its world-class team of scientists has also published many research papers in prestigious scientific journals worldwide.

The company is opening a new R&D center and a CLIA lab in Gaithersburg, Maryland, USA with the following exciting opportunities. Genetron Health Inc offers a family friend work environment, competitive compensation package including paid leave, health/dental insurance, 401(k) with company matching contribution, and annual cash/stock incentive awards.  Genetron Health Inc. is an equal employment opportunity employer, and does not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. 

Job Overview:

The Sr. Director/Director, Business Development is responsible for the new business development and clinical testing functions for the US/global Business Unit(s), focusing on the early detection of cancer and cross-border pharma services.

Primary Responsibilities:

Provide strategic leadership and direct oversight of technology R&D/licensing, business development, in vitro diagnostics (IVD) product development and clinical testing services aligned with the GHI mission

Identify strategic opportunities to build a sustainable and profitable business in compliance with federal laws and local regulations and consistent with corporate goals.

Education, Experience & Skills:

·Bachelor's Degree or equivalent; MBA or advanced degree in Life Sciences is preferred

>5 years working experience in industry with a proven track record of providing strategic oversight for business development

Well-developed organizational and interpersonal skills

Finely honed written and verbal communication skills, underpinned by the ability to present clear instructions/directions to teams within the organization and external audiences

(Sr.) Scientist, Assay Development
Company:Genetron Health,Inc
Department:
Work place:Gaithersburg, Maryland, USA
Recruitment:1
Education:
Job type:Full Time
Release time: 08- 28
Working years:3 years

Senior Scientist/Scientist, Assay Development 


Genetron Health is a leading and fast-growing precision oncology company that is committed to providing a one-stop, multi-scenario genomic profiling solutions in areas including early cancer screening, diagnosis and monitoring as well as biopharmaceutical services. It has successfully developed seven NMPA-approved clinical sequencing platforms and gene assays. Partnering over 500 hospitals along with several pharmaceutical companies and research institutions, Genetron Health has built an extensive proprietary genomic database to deliver comprehensive genomic testing services. In China, the company has one R&D center, two manufacturing facilities and five clinical laboratories in Beijing (CLIA-certified and CAP-accredited), Shanghai, Hangzhou, Chongqing and Guangzhou. Its world-class team of scientists has also published many research papers in prestigious scientific journals worldwide.

The company is opening a new R&D center and a CLIA lab in Gaithersburg, Maryland, USA with the following exciting opportunities. Genetron Health Inc offers a family friend work environment, competitive compensation package including paid leave, health/dental insurance, 401(k) with company matching contribution, and annual cash/stock incentive awards.  Genetron Health Inc. is an equal employment opportunity employer, and does not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. 

The Senior Scientist/Scientist is responsible for biomarker discovery, assay development, analytical and clinical validation of in vitro diagnostics in the areas of early cancer detections and cross-border pharma services.


Primary Responsibilities:


Lead multidisciplinary scientific teams in product development programs and projects, coordinating between stakeholders (e.g., Regulatory, Quality, Clinical, Commercial etc), with direct oversight of the teams responsible for biomarker discovery, assay development, analytical and clinical validation of in vitro diagnostics

Lead the Research and Development team to drive discovery and development of diagnosis assays and products, characterize and evaluate assay performance, perform complex analysis of large genomic data sets.

Plan, implement and supervise discovery, preclinical and clinical validation studies to ensure study  deliverables are met according to specified timelines, budgets, quality and resources

Ensure best-practices for research and data integrity standards are integrated in research and development strategies;

Present project updates, data analysis, and experimental conclusions at technical meetings.


Education, Experience & Skills:


Master or PhD in computational biology, bioinformatics, statistics, biological sciences, cancer biology, genetics, genomics, computer science, physics, engineering, or equivalent preparation and experience.


>3 years of relevant experience in positions of increasing responsibility preferred


Effective written and verbal communication skills.


Ability to multitask as needed in a complex environment.


CLIA Laboratory Supervisor
Company:Genetron Health,Inc
Department:
Work place:Gaithersburg, Maryland, USA
Recruitment:1
Education:
Job type:Full Time
Release time: 08- 28
Working years:3 years


Genetron Health is a leading and fast-growing precision oncology company that is committed to providing a one-stop, multi-scenario genomic profiling solutions in areas including early cancer screening, diagnosis and monitoring as well as biopharmaceutical services. It has successfully developed seven NMPA-approved clinical sequencing platforms and gene assays. Partnering over 500 hospitals along with several pharmaceutical companies and research institutions, Genetron Health has built an extensive proprietary genomic database to deliver comprehensive genomic testing services. In China, the company has one R&D center, two manufacturing facilities and five clinical laboratories in Beijing (CLIA-certified and CAP-accredited), Shanghai, Hangzhou, Chongqing and Guangzhou. Its world-class team of scientists has also published many research papers in prestigious scientific journals worldwide. 

The company is opening a new R&D center and a CLIA lab in Gaithersburg, Maryland, USA with the following exciting opportunities. Genetron Health Inc offers a family friend work environment, competitive compensation package including paid leave, health/dental insurance, 401(k) with company matching contribution, and annual cash/stock incentive awards.  Genetron Health Inc. is an equal employment opportunity employer, and does not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.  


Position Overview:

The CLIA Laboratory Supervisor is in charge of the daily operations of the CLIA laboratory that is expected to provide timely testing as requested and accurate results as required. The Supervisor should always utilize excellent customer service skills for both internal and external customer services. A deep and thorough understanding of testing principles, Quality Control, and teamwork are essential. A positive and professional interpersonal style with a strong commitment to the team effort is mandatory.

Specific Responsibilities:

Supervises clinical testing and daily operations of the CLIA laboratory consistently according to established standard operating procedures as described in procedure manuals, quality control specifications and workflow guidelines

Responsible for completion of any special projects, process improvements or new method introduction at the request of the Lab Director

Ensures that all workflow processes are completed within acceptable time frames. Monitors TAT report to ensure timely reporting of the results

Responsible for the maintenance and organization of all documentation generated by the laboratory or by instrumentation such as QC, calibrations, etc

Understands and observes all confidentiality and HIPAA provisions

Recognizes and conveys to management any departmental improvements necessary

Responsible for all equipment in assigned areas of work

Assist and guide technologists with all problems, initiate resolution of errors, document discrepancies, perform troubleshooting on all instruments trained on and resolve all errors and other problems

Independently perform diagnostic testing with accuracy, precision, and efficiency following established SOPs. Report diagnostic data in compliance with policies, SOPs, and turn-around-time schedules

Constantly reviewing current procedures and coordinate changes, with director’s approval, in order to implement procedures that will facilitate more accurate and timely reporting of results.

Ability to perform laboratory calculations.

Ability to look beyond daily functions to implement higher standards through evaluation and education

Recognize and resolve all QC discrepancies and assist other technologists, if needed, with resolution of QC discrepancies when necessary

Perform and document all routine and periodic maintenance according to instrument guidelines and established SOP's.

Be able to recognize instrument malfunction and independently troubleshoot instrument, assay, and/or analytical problems to prevent delays in patient testing and initiate service calls when necessary

Communicate all problems, instrument malfunctions, etc. to Lab Director

Adjusts work assignments to meet the needs of the section/laboratory, when instruments are down, reduced staffing, or areas are slow

Understand QC concepts, identify problems, and implements corrective action

Perform all bench, kit, and assay QC. Make sure when QC or kit reagents change that the QA/QC coordinator is notified, and the change is documented

Perform, monitor, and maintain daily QC, QA, all appropriate maintenance log sheets, discrepancy logs, and maintenance records

Monitor and document the temperature dependent equipment on Temperature QC log sheets, equipment maintenance log sheets, discrepancy logs, calibration logs, and general work performance logs

Assumes other duties as assigned by management.


CLIA Lab Technologists
Company:Genetron Health,Inc
Department:
Work place:Gaithersburg, Maryland, USA
Recruitment:1
Education:
Job type:Full Time
Release time: 08- 28
Working years:1 years

CLIA Laboratory Technologists 

Genetron Health is a leading and fast-growing precision oncology company that is committed to providing a one-stop, multi-scenario genomic profiling solutions in areas including early cancer screening, diagnosis and monitoring as well as biopharmaceutical services. It has successfully developed seven NMPA-approved clinical sequencing platforms and gene assays. Partnering over 500 hospitals along with several pharmaceutical companies and research institutions, Genetron Health has built an extensive proprietary genomic database to deliver comprehensive genomic testing services. In China, the company has one R&D center, two manufacturing facilities and five clinical laboratories in Beijing (CLIA-certified and CAP-accredited), Shanghai, Hangzhou, Chongqing and Guangzhou. Its world-class team of scientists has also published many research papers in prestigious scientific journals worldwide.

The company is opening a new R&D center and a CLIA lab in Gaithersburg, Maryland, USA with the following exciting opportunities. Genetron Health Inc offers a family friend work environment, competitive compensation package including paid leave, health/dental insurance, 401(k) with company matching contribution, and annual cash/stock incentive awards.  Genetron Health Inc. is an equal employment opportunity employer, and does not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. 

Position Overview:

The CLIA Laboratory Technologist provides accurate and timely testing and results for use in the diagnosis and treatment of disease. A deep understanding of testing principles, Quality Control, and teamwork are essential. A positive and professional interpersonal behavior with a strong commitment to the team effort is mandatory.

Specific Responsibilities:

• Performs testing consistently according to established standard operating procedures as described in procedure manuals, quality control specifications and workflow guidelines

• Responsible for the completion of any special projects, process improvements or new method introduction at the request of the supervisor

• Ensures that all workflow processes are completed within acceptable time frames. Monitors TAT report to ensure timely reporting of the results

• Responsible for the maintenance and organization of all documentation generated by the laboratory or by instrumentation such as QC, calibrations, etc

• Responsible for all equipment in assigned areas of work

• Performs processing, result entry, and quality control for all specimens

• Independently perform diagnostic testing with accuracy, precision, and efficiency following established SOPs. Report diagnostic data in compliance with policies, SOPs, and turn-around-time schedules

• Perform and document all routine and periodic maintenance according to instrument guidelines and established SOP's

• Monitor/evaluate temperature dependent equipment. Document any problems on a QC deviation form and ensure follow-up to rectify the issue

• Be able to recognize instrument malfunction and notify supervisor

• Communicate all problems, instrument malfunctions, etc. to supervisor

• Adjusts work assignments to meet the needs of the section/laboratory, when instruments are down, reduced staffing or workload

• Perform, monitor, and maintain daily QC, QA, all appropriate maintenance log sheets, discrepancy logs, and maintenance records

• Daily checking of Quality Control from other areas where trained

• Document the following: temperature dependent equipment on Temperature QC log sheets, document equipment maintenance log sheets, discrepancy logs, calibration logs, and general work performance logs.

• Assumes other duties as assigned by management.

Education and Experience:

• Bachelor or Master Degree in a biological or physical science field from an accredited university. ASCP qualifications or equivalent preferred.

销售代表
Company:北京泛生子基因科技有限公司
Department:销售部
Work place:北京,上海,南京,合肥
Recruitment:0
Education:大专及以上
Job type:全职
Release time: 05- 19
Working years:1-3年


岗位概述:

依据公司整体营销目标及营销策略,完成公司分配的区域销售任务。


岗位职责:

1. 协助城市经理负责本区域市场的开发工作,了解本区域同类产品的销售形式及竞争品牌的经销状况,完成公司分配的区域销售任务

2. 建立并完善客户档案,与客户建立长期合作关系

3. 开发区域经销商,协助区域经销商制定价格、渠道、促销策略

4. 配合商务同事及时完成财务对账及催回款

5. 领导交办的其他工作


任职要求:

1. 大专以上学历

2. 年龄28岁左右

3. 地区的体检中心或类似机构

4. 二年以上一线地推开发工作经验,美团、大众点评、携程、去哪儿优先

5. 开拓能力强,承压性强,有上进心,敢于挑战高薪



资质申报主管(广州)
Company:北京泛生子基因科技有限公司
Department:检验所
Work place:广州
Recruitment:0
Education:
Job type:全职
Release time: 08- 01
Working years:

岗位概述:

负责对接广州实验室装修、执业许可证申请及PCR实验室的准入批复等事宜。

四、主要职责
一、职责描述:全面负责检验所日常资质的申请和维护
1、根据检验所的标准规范及相应的法规要求申请必修的资质,包括医疗机构执业许可证的申报、PCR实验室的准入批复、检验所校验、生物安全备案、环评(污水、废气、医疗废物)等的申请和关系维护。
二、职责描述: 全面负责检验所PT和EQA的工作
1、确保公司各检验所的PT和EQA申请的正常运行,回报结果的准确性
2、及时的跟进各检验所项目的进展,及结果的检测情况
3、针对不符合项进行整改反馈
三、职责描述:协助检验所质量体系的建设,体系维护
1、协助编写自己工作相关的SOP、填写记录
2、配合各种外部机构的认证及内审和现场评审
四、职责描述: 资质项目的前瞻性
1、对已申报的政府项目保持密切跟踪,能够随时收集汇总项目执行过程中阶段性确认材料,能够担负政府项目审核及结项的统筹工作;关注行业内资质申报的影响,并结合公司实际需要,主动积极的查阅相关资料,评估申报必要性,确认是否申请。
任职资格:
五、任职资格
教育:本科及以上学历
专业:医学、生物等相关专业
职称/资格证书:英语4级及以上
专业经验:有2年以上NGS行业项目申报or实验室操作or对外政府关系维护经验;优秀的文字表达能力,能够独立撰写项目申报材料和项目报告;有申请医学检验所、年检、PCR实验室准入等经验者优先考虑
管理经验 :有2年以上的资质申报经验
计算机技能:熟悉办公软件,操作过文控系统、采购、OA系统等
岗位知识:阅读能力强,能很好的解读相应的标准规范文件和法规文件
能力素质:有良好的沟通表达及协调能力,细心负责,踏实认真


体外诊断工艺工程师
Company:北京泛生子基因科技有限公司
Department:
Work place:北京
Recruitment:0
Education:大专及以上
Job type:全职
Release time: 05- 19
Working years:1-3年


负责组织实施全线外诊断试剂产品、LDT新产品的工艺验证、工艺转化、试剂生产,严格执行质量标准和验证方案操作规程,严把质量关,以保证企业品牌战略的实施。做好产品质量的控制工作,对产品质量做到时刻监督、改进和优化,对发生的问题采取积极有效的解决措施。负责指导研发部门输出产品技术文件并加以验证等工作。


岗位职责:

1. 负责公司体外诊断试剂产品的工艺验证、工艺转化;

2. 负责公司LDT新产品的性能验证、质量控制;

3. 制定工作流程和计划,协调相关部门的资源,保证项目按计划完成;

4. 制定新产品的验证计划,开展验证实验,对总结验证结果,编制验证报告;

5. 负责转化以后投入临床使用的LDT产品定期进行质量的控制;

6. 协助注册产品申报注册任务,配合体考;

7. 负责实验室日常管理,包括物料管理、仪器设备维护与管理。

8. 指导研发部门输出产品技术文件并加以验证等。


任职要求:

1. 医学检测、生物技术、分析化学、微生物学等相关专业,本科以上学历;

2. 1年以上诊断试剂行业验证岗位工作经验,经历过产品体系考核或ISO13485认证经验者优先;

3. 有较好的实验操作基础,熟悉基因测序仪、数字PCR仪、实时荧光定量PCR仪、分光光度计、pH计、天平等仪器的使用和维护者优先;

4. 熟悉医疗器械相关的政策和法规;

5. 具有一定的英文水平,良好的英文读写能力;

6. 良好的语言表达及沟通能力;

7. 有较强的责任心,具有良好的团队合作精神及专业素质;

8. 工作中能够吃苦耐劳,可以忍受一定的工作压力。


生产经理/主管
Company:
Department:质量及注册部
Work place:北京
Recruitment:0
Education:本科
Job type:全职
Release time: 08- 01
Working years:5年以上

岗位职责:

1. 全面负责医疗器械体外诊断试剂产品的生产管理工作;

2. 负责生产质量管理体系建立与实施;

3. 参与生产质量体系文件的制定、修改、升级;

4. 负责政府机关和监督管理部门的关系维护;

5. 负责组织产品质量问题调查工作;

6. 负责公司外审的准备和接待工作;

7. 负责组织体外诊断试剂的工艺转化;

8. 负责组织体外诊断试剂生产人员培训;

9.负责制定年度、季度、月度生产计划制定,并负责实施;

9. 负责合格供应商的评审工作;

10.负责ISO13485\ISO9001和生产质量管理体系考核工作;


岗位要求:

1. 本科以上学历,医学检测、生物技术、生物工程、医药等相关专业;

2. 熟悉医疗器械相关的政策和法规,尤其是医疗器械生产质量管理规范相关的法规;

3. 五年以上医疗器械体外诊断试剂生产、注册或质量等工作经历者优先;

4. 具备三年以上医疗器械体外诊断试剂生产管理经验;

5. 具有一定的英文水平,良好的英文读写能力;

6. 有较强的责任心,具有良好的团队合作精神及专业素质;

7. 良好的语言表达及沟通能力,亲和力强;

8. 具备良好的组织能力和协调能力;

9. 工作中能够吃苦耐劳,可以忍受一定的工作压力;

10. 有三类医疗器械体外诊断试剂ISO9001\ISO13485和体考工作经验。


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北京泛生子基因科技有限公司
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    Genetron Health Technologies Inc.

    6 Davis Drive. Research Triangle Park. North Carolina. U.S.A

    Tel: +1 919 964 3638


    Tel:4000-996-336

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    Tel:4000-996-336

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    Tel:4000-996-336

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