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GE通用电气(中国)医疗集团 2017-08-23 更新 2017-11-11 截止



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

- This individual will collaborate with multiple stakeholders toidentify and prioritize training and business requirements that aretranslated to user and functional requirements to develop trainingsystems.

- Provide on-site customer training on Flex Factory equipment andautomation

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

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

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

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

- Support the design, development and execution of (Flex Factory &Fast Trak) standard and custom technical user training courses thatfollow 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 FlexFactory 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, QualityManagement System, Quality Management Policy, Quality Goals, andapplicable laws and regulations as they apply to this job type/position

- Complete all planned Quality & Compliance training within thedefined deadlines

- Identify and report any quality or compliance concerns and takeimmediate corrective action as required
- Technical competence in either upstream bioprocessing (especiallymammalian 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 technicalcommunications and an ability to uphold GE company values duringcustomer interactions

- Working knowledge of Excel, Word and PowerPoint, Outlook

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

- Must be able to travel internationally without restrictions

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

- 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 chromatographyand 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, RockwellRSLogix 5000 software or equivalent.
- Strong industrial experience in purification of biomolecules(upstream, downstream, technology transfer, validation, processdevelopment, biomanufacturing
- Deep scientific understanding of principles and theory behind unitoperations for processing biologicals with knowledge in principles ofscale up, validation, disposable, hybrid and traditional set ups and GMPmanufacturing
- Able to operate in a high pace environment with frequent changes

Job Segments: Curriculum, Biotech, Training, Chemical Research, Biology,Education, Science, Operations, Engineering
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Zhang Fan fan.zhang1@ge.com



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