[天津]杰科（天津）生物医药2018校园招聘

发布时间：2017-11-14
工作地点：天津
信息来源：天津科技大学-宣讲会
职位类型：全职
职位描述
（泰达中校区）杰科（天津）生物医药有限公司

发布时间：2017-11-20

时间：11月20日 十三周 星期一 14:00-15:30
地点：泰达中校区 5-211

公司简介：

杰科（天津）生物医药有限公司（简称：杰科生物）是一家中美合资，从事生物制剂的研发及生产的生物药物公司。坐落于天津滨海新区中新生态城。公司正在天津滨海新区中新生态城建设包括研发、中试、质控、行政及GMP生产等功能的大型生产基地，并且从国内外招聘优秀人才，组建研发及生产顶尖团队。公司正在建设的是中国规模最大之一的生物药物生产基地，其研发、生产及质量控制等设施均达到欧美设计建造标准。第一期工程已开工，将在三年内投产运行。在未来十年内，杰科生物预计共建设10条生产线，满足10多个生物药物的大规模GMP生产，达到1500-2000人的规模。公司产品包括单克隆抗体、抗体融合蛋白、细胞因子、重组蛋白或DNA疫苗等。

公司的管理及研发团队是由以留美科学家朱建伟博士为核心的一批具有全球视野的科研专家和管理精英组成。高级科学家研发团队的累计SCI论文达到200篇以上。管理团队具备有质量管理、财务管理、行政管理、产品研发、新技术开发、分析方法开发、技术转移、法律事务、公共关系、商务开发、以及运行事务等综合能力。管理团队的成员在美国和中国成功研发50个以上不同类型的生物药物，包括重组疫苗，免疫毒素，重组细胞因子药物，治疗用单克隆抗体及融合蛋白，质粒DNA疫苗，多种病毒载体的抗肿瘤药物等，具备丰富的生物医药企业创新研发，质量管理及生产运行的经验。

招聘岗位：

Biopharmaceutical Upstream Process Engineer

Job responsibilities:

(1) Responsible for large-scale culture of E.coli and CHO cell, including inoculation and stepwise fermentation, according to the production instruction to control the process parameter.

(2) Operation of 3L, 30L and 300L fermentor and related equipment according GLP/GMP requirements.

(3) Write and revise SOP, batch record and other technical documentation as necessary.

(4) Effective communication of data/results through written documentation and oral presentations.

(5) Accountable for completing the assigned tasks and communicate results in a timely manner.

(4) Perform other duties as assigned by department manager. .

Basic requirements:

(1) Master degree inFermentation Engineering or Bio-engineering or Bio-chemistry.

(2) Knowledge and experience in fermentation process development and/or manufacturing for protein therapeutics products.

(3) Extensive experience of E.coli/CHO cell culture and fermentation equipment.

4) Good written and oral communication skills in English.

(5) Must be able to write effectively as demonstrated through authorship of batch records, SOPs and technical reports.

(6) Strong team work and communication skill.

(7) Ability to work independently, with minimal supervision, and to manage multiple projects at one time.

(8) Eager and quick to learn, self-driven and motivated.

2. Biopharmaceutical Purification Process Engineer

Job responsibilities:

(1) Responsible for purification process development of antibody drugs, recombinant protein drugs and other biopharmaceuticals.

(2) Assist department manager to resolve the technical problems about technology transfer, scale-up and production, improve and optimize the production process.

(3) Write and revise SOP, batch record and other technical documentation as necessary.

(4) Effective communication of data/results through written documentation and oral presentations.

(5) Accountable for completing the assigned tasks and communicate results in a timely manner.

(4) Perform other duties as assigned by department manager. .

Basic requirements:

(1) Master degree inFermentation Engineering or Bio-engineering or Bio-chemistry.

(2) Knowledge and experience in downstream purification process development and/or manufacturing for protein therapeutics products

(3) Familiar with downstream purification unit operations, such as chromatography, ultrafiltration, depth filtration, etc.

(4) Experience with scale-up, process improvement and optimization.

(5) Must have a ability to read, write and speak English.

(6) Must be able to write effectively as demonstrated through authorship of batch records, SOPs and technical reports.

(7) Strong team work and communication skill.

(8) Ability to work independently, with minimal supervision, and to manage multiple projects at one time.

(9) Eager and quick to learn, self-driven and motivated.

Analytical Associate Scientist

Job summary:

The qualified candidate will join the Analytical Department to enable the optimization, development, validation and application of analytical methods to characterize the identity and purity of biotherapeutics.

Job responsibilities:

Develop and optimize analytical methods for characterization of biotherapeutics in pre-clinical and

clinical stages.

Write Standard Operation Procedure (SOP)

(3) Develop analytical methods for intermediates as part of PAT (Process Analytical Technology)

(4) Involved in analytical method transfer from other companies.

(5) Perform all experiments under applicable safety and regulatory compliances.

(6) Generate high quality results in support of analytical testing of growing drug pipeline.

(7) Document data/results according to applicable compliances, such as GMP.

(8) Effective communication of data/results through written documentation and oral presentations.

(9) Accountable for completing the assigned tasks and communicate results in a timely manner.

Basic requirements:

(1) A master degree with 5 years or a Ph.D.

(2) Strong hands-on experience in HPLC (SEC, IEX, RP), LC-MS (peptide mapping and N-linked glycan) and CE (cIEF and CE-SDS).

(3) Ability to work independently and to manage multiple projects at one time.

(4) Good written and oral communication skills in English.

(5) Eager and quick to learn, self-driven and motivated.

Analytical Senior Scientist (Analytical Dept.)

Job responsibilities:

Develop and optimize analytical methods for characterization of biotherapeutics in pre-clinical and clinical stages.

Write Standard Operation Procedure (SOP)

Develop analytical methods for intermediates as part of PAT (Process Analytical Technology)

Involved in analytical method transfer from other companies.

Perform all experiments under applicable safety and regulatory compliances.

Generate high quality results in support of analytical testing of growing drug pipeline.

Document data/results according to applicable compliances, such as GMP.

Effective communication of data/results through written documentation and oral presentations.

Accountable for completing the assigned tasks and communicate results in a timely manner.

Basic requirements:

A master degree with 5 years or a Ph.D. with 2 years of experience in analytical science or equivalent within a biopharmaceutical industry.

Strong hands-on experience in HPLC (SEC, IEX, RP), LC-MS (peptide mapping and N-linked glycan) and CE (cIEF and CE-SDS).

Ability to work independently and to manage multiple projects at one time.

Good written and oral communication skills in English.

Eager and quick to learn, self-driven and motivated.

5. 生物药理化分析检验工程师

岗位职责：

负责生物药理化分析工作，完成所需要的检验工作

负责生物药理化分析方法的开发和工艺研发过程中样品的分析以及起草分析方法开发报告

负责按GMP要求书写检验记录及相关记录

起草相关的SOPs

负责分析方法的验证和确认

负责DS和DP检验以及稳定性样品分析

负责仪器设备的定期维护保养，对实验设备清洁整理

任职要求：

大学本科或硕士学历，药物分析、生物学、化学等相关专业背景

能熟练使用水份滴定仪，紫外分光光度计，HPLC，CE-SDS，CIEF等理化检验仪器

能独立解决常见检验问题

耐心细致，具有良好的归纳整理能力，条理性强，高效且能同时完成多项任务。

有良好的沟通能力和团队合作精神

生物药生化分析检验工程师

岗位职责：

负责生物药生化分析工作，完成所需要的检验工作包括DNA、HCP、ProteinA等的分析

负责生物药生化分析方法的开发和工艺研发过程中样品的分析以及起草分析方法开发报告

负责按GMP要求书写检验记录及相关记录

起草相关的SOPs

负责分析方法的验证和确认

负责DS和DP检验以及稳定性样品分析

负责仪器设备的定期维护保养，对实验设备清洁整理

任职要求：

大学本科或硕士学历，药物分析、生物学、化学等相关专业背景

能熟练使用qPCR、酶标仪等检验仪器

精通ELISA和药物活性分析

能独立解决常见检验问题

耐心细致，具有良好的归纳整理能力，条理性强，高效且能同时完成多项任务。

有良好的沟通能力和团队合作精神

微生物检验

岗位职责：

负责生物药生产和开发阶段的样品检测，包括但不限于内毒素、微生物限度、无菌检测。

负责实验室和生产车间洁净区的环境监控。

负责生物药微生物分析方法的开发和样品的分析以及起草分析方法开发报告

负责按GMP要求书写检验记录及相关记录

起草相关的SOPs

负责分析方法的验证和确认

负责DS和DP检验以及稳定性样品分析

负责仪器设备的定期维护保养，对实验设备清洁整理

任职要求：

大学本科或硕士学历，药物分析、生物学、微生物等相关专业背景

能熟练使用浮游菌采样仪和粒子计数器等检验仪器

能独立解决常见检验问题

耐心细致，具有良好的归纳整理能力，条理性强，高效且能同时完成多项任务

有良好的沟通能力和团队合作精神

报名方式：

请将您的简历以如下方式发送至我公司：

主题： 校园招聘 姓名

发送邮箱：recruit@

面试流程：

杰科生物在收到简历后，将于48小时内进行逐一处理。经过初选的简历，会以邮件形式通知初选结果及相关电话面试安排。关于后续的统一面试安排，会另行邮件通知。

咨询电话： 022 5900 2008