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发表于 2005-1-10 13:57:34
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Senior System Quality Engineer
电子邮箱:hr-sh-kt@kodak.com
发布日期:2005-01-06 工作地点:上海市
招聘人数:1 薪水范围:面议
接受简历语言:中文和英文
职位描述:
Description:
In this position you will be part of a team responsible for designing, implementing and testing software modules & tools for Kodak Health Imaging Mammography Computer Aided Detection (CAD) products.
Responsibilities:
1. Development and Verification Phase:
·Review requirements and give feedback to assure that requirements are verifiable.
·Develop test plans, test procedures, test reports.
·Coordinate Defect Review meeting, prepare list of defects need to be reviewed during the defect meeting, create meeting agenda and minutes.
·Conduct product, performance and reliability testing.
·Update Requirements Traceability Metrics.
·Review Beta Trade Trial Plan (including Clinical protocol or Beta Test Plan/procedure).
·Measure product quality (with Six Sigma level, SWMLE)
2. Validation Phase
·Review Beta test plan, Manufacturing Test Plan, User manual, Service Manual
·Perform Product Regression test before first customer ship
·Develop Test Summary Report
3. Finished Product-Shipping phase (after gate 3)
·Support Technical Call Center (TSC), Service Engineering customer escalation investigation, implementation and closure.
·Monitor and manage Customer calls (escalation, Complaints, Incident Report, Potential Reportable Event)
·Track and measure product quality including trending
Minimum Requirements:
·MS or BS/BA degree in Computer Engineering or Computer Science with at least three years in software engineering or software quality engineering.
·Medium to strong knowledge and experience with . .NET, C#, C++, Java in Windows XP, Win 2000.
·Understanding of some Object-Oriented methodologies
·Experience with Development, Configuration Management and Change Tracking tools like DOORS, ClearCase, DDTS or ClearQuest.
·Familiar with IHE framework, DICOM, & HL 7 standards
·Experience with TCP/IP networking
·Experience with multi-threading client server design and implementation
·Excellent written and oral communication skills
·Ability to quickly learn new applications and new technology
·Ability to work independently and in teams
·Ability to work productively on multiple projects
·Excellent problem solving skills
·Commitment to meet corporate objectives and product schedules
·Familiar with US Food and Drugs Administration (FDA) 21 Code of Federal Regulations for Medical Device and Quality System Records requirements
·Familiar with ISO 13485 |
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