*Position: QA Tester with Clinical Background* *Location: Norwood, MA*
*Duration: 6+ Months* *Key SOFTWARE TEST Responsibilities* Performs software verification and validation activities as a part of the overall software development process for medical diagnostics instruments. The primary responsibilities of the software test engineer are to: · Verify through testing or inspection that the product functionality meets the software requirements · Design, develop, and execute software tests to verify design meets documented requirements · Plan and implement configuration of physical setup of equipment · Create/track software defects in the defect tracking database and verify closure of defects · Report passed and failed requirements to the test team lead, the project team, and the department manager · Communicate task status to the test team lead and manager · Interact with other test and development personnel on a project · Manage own priorities effectively · Multitask effectively on and across projects · Communicate effectively one on one as well as in groups at both high and low concept levels · Ability to travel to domestic and international locations. *Knowledge and Skills* Must have knowledge of how software verification / validation activities integrated within a software development process. The senior software test engineer required skills include: · Perform web site testing using various browsers (such as Internet Explorer, Chrome, and Firefox) on various operating systems (such as Apple and Windows) · Experience with testing a wireless environment · Black-box, performance, stress and load testing, as required by the project · Designing and developing software tests from requirements and design documentation · Performing manual testing, and possibly automated testing, of product features · Providing documented evidence of test execution · Risk management (project, technical, and hazard) · Proficiency in Microsoft Word and Excel · Ability to comprehend software design documents · Ability to peer-review software requirements and design documents. · Ability to create manual tests for complex software modules from requirement and design documents · Ability to define estimate and track progress of tasks and communicate project status · Ability to create Requirements Trace documentation · Ability to perform reviews of manual, and possibly automated, tests · Ability to determine resource utilization · Ability to work effectively both alone and as part of a team · Strong writing, presentation, and general communication skills · Ability to handle a variety of tasks and juggle multiple assignments Knowledge and skill of any of the following items is a plus: · Experience with Microsoft Test Manager · FDA Design Control regulations and associated standards and guidances · Microsoft Team Foundation Server scripting, particularly in the area of build automation · Automated testing tools, such as Microsoft Coded UI · Automated web testing tools · Experience with testing medical devices · Experience on an Agile/Scrum team · Database fundamentals · Communication protocols · Network monitoring · Computer system performance monitoring · Various programming languages, such as C#, C ++, C or Visual Basic · Communication protocols, such as LIS 3, HL7 · Chemistry · Calculated Parameters for reported analytes · Statistical Data Analysis · Project management experience · Strong organizational and administrative skills *Experience* · BS/MS in Computer Science or Engineering, or 5-8 years of successful experience in a related field and the successful demonstration of Key Responsibilities, Knowledge and skills as presented above. *Thanks & Regards,* *Md Faisal Zahid* Technical Recruiter Technology Resource Group Inc. 3736 Hillsdale Court Santa Clara, CA 95051 Office : *408-709-1760 Ext: 906*, Direct: *408-834-4157* E mail id: *fai...@tresourceinc.com* <fai...@tresourceinc.com> | :*g-talk: ausafleo ym: ausafleo* *Fax:* *408-884-2409 * *www.tresourceinc.com* <http://www.tresourceinc.com/> *Disclaimer: *This e-mail contains PRIVILEGED AND CONFIDENTIAL INFORMATION intended solely for the use of the addressee(s). 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