丁香人才 > 职位招聘 >医药公司/药店/医疗器械招聘 >上海医药公司/药店/医疗器械招聘 >FLEX FACTORY TRAINING MANAGER招聘

FLEX FACTORY TRAINING MANAGER

GE通用电气(中国)医疗集团 2016-12-10发布 2017-01-20截止
  • 学历要求: 不限
  • 外语要求: 不限
  • 年龄要求: 不限
  • 专业要求: 不限
  • 工作年限: 不限
  • 月薪范围: 面议
  • 职位性质: 全职
  • 工作地点: 上海市
  • 职称要求: 不限
  • 招聘人数: 若干

职位描述


Role Summary/Purpose: The Flex Factory Training Manager has a broad range of responsibilities that include, but not limited to, analyzing training needs, designing, developing and implementing technical courses to ensure customer (in/external) needs are met. Work cross functionally with various GEHC teams to integrate new product training into the Flex Factory technical training curriculum. In addition, he/she will also provide application support in the form of process development, consulting, and or instructor.
Essential Responsibilities:
- Supports global flex factory training and building initiatives that supports Enterprise Solutions.

- This individual will collaborate with multiple stakeholders to identify and prioritize training and business requirements that are translated to user and functional requirements to develop training systems.

- Provide on-site customer training on Flex Factory equipment and automation

- Provide in-house and customer site training on individual pieces of equipment as needed.

- Assists in new product development, provides market application support and product demonstrations as needed.

- Support Bio-manufacturing Services and Fast Trak scientists with bench top to large scale client projects

- Responsible for the development, creation, delivery and facilitation of Flex Factory training program.

- Support the design, development and execution of (Flex Factory & Fast Trak) standard and custom technical user training courses that follow a structured process to be delivered through varying methods (classroom, lab, e-learning, etc.)

- Leadership in area of expertise to move projects forward

- Conducting and building scientific application trainings for Flex Factory and Fast Trak on key tops such as (Monoclonal Antibodies (MAb's), vaccines, recombinant proteins, plasma fractionation)

Quality Specific Goals:

- Awareness of and compliance with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position

- Complete all planned Quality & Compliance training within the defined deadlines

- Identify and report any quality or compliance concerns and take immediate corrective action as required
Qualifications/Requirements:
- Technical competence in either upstream bioprocessing (especially mammalian cell culture) or purification, with exposure to the other

- Experience as a hands-on operator in a GMP biomanufacturing operation

- A strong interpersonal skillset, including good technical communications and an ability to uphold GE company values during customer interactions

- Working knowledge of Excel, Word and PowerPoint, Outlook

- Bachelor's Degree in Biology, Chemistry, Chemical Engineering or related discipline or Bachelor’s Degree and 1 year experience within technical discipline or equivalent (defined as High School Diploma/GED/Biotech training program and 3 years progressive experience within bioprocess-related positions)

- Must be able to travel internationally without restrictions

- Must be able to sustain up to 50% travel, including multi-week assignments

- Demonstrated good presentation skills
Additional Eligibility Qualifications:
Desired Characteristics:
- At least one year of hands-on GMP manufacturing experience
- Expertise in bioreactor operation and cell culture or chromatography and tangential flow filtration
- Experience in any of the following areas is beneficial: field service, bioprocess development, customer service, training, facility start-up
- Experience with one of the following platforms: Wonderware ArchestrA, Emerson Delta V, Allen-Bradley SLC/PLC, Panel View, RSView32, Intellution/iFix, Siemens PLC Step 7, WinCC control system, Rockwell RSLogix 5000 software or equivalent.
- Strong industrial experience in purification of biomolecules (upstream, downstream, technology transfer, validation, process development, biomanufacturing
- Deep scientific understanding of principles and theory behind unit operations for processing biologicals with knowledge in principles of scale up, validation, disposable, hybrid and traditional set ups and GMP manufacturing
- Able to operate in a high pace environment with frequent changes


Job Segments: Curriculum, Biotech, Training, Chemical Research, Biology, Education, Science, Operations, Engineering

联系人: Zhang Fan

地    址:北京市经济技术开发区永昌北路1号

GE 医疗集团隶属于GE(通用电气)公司,为全世界提供开创医疗护理新时代的革新性医疗技术和服务。GE医疗集团在医学成像、信息技术、医疗诊断、患者监护系统、药物研发、生物制药技术、卓越运营和整体运营解决方案等领域拥有广泛的专业技术,能够帮助客户以更低的成本为全世界更多的人提供更优质的服务。GE医疗集团还和医疗行业领袖加强合作,全力支持全球政策的发展,助力打造成功的、可持续的医疗体系。

GE医疗集团总部设在英国,员工分布于全球100 多个国家和地区,致力于为医疗专业人士和患者服务。

2009 年5 月,GE在全球启动“健康创想”战略。根据该战略,GE 承诺在六年内投资 ...详情

单位概况

GE通用电气(中国)医疗集团
近两周应聘简历处理率:36%
医疗设备/器械
医药企业 其他
1000~9999人
北京市经济技术开发区永昌北路1号
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