*Quality Analyst [Medical Instruments]* *Location: Boston, MA*
*Type: Contract Opportunity* *Responsibilities* Performs software verification and validation activities as part of the overall software engineering process for medical diagnostics instruments. The primary responsibilities of the software test engineer are to: • Design, develop, and execute software tests to verify that design implementation meets documented requirements • Plan and implement configuration of physical setup of equipment • Create/track software defect records 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 and software quality to the test team lead and manager • Interact with other personnel on a project • Manage own priorities effectively • Multitask effectively on and across projects, when required • 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: • Performing black-box, performance, stress and load testing, as required by the project • Designing and developing software tests from software requirements and specification documentation • Providing documented evidence of test execution • Participating in risk management activities (project, technical, and hazard) • Proficiency in Microsoft Word and Excel • Ability to comprehend software specification documents • Ability to peer-review software requirements and specification documents. • Ability to create tests for complex software modules from software requirements and specification 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 • Possesses strong writing, presentation, and general communication skills *Knowledge and skill of any of the following items is a plus: * • FDA Design Control regulations, and associated standards and guidance’s • Microsoft Team Foundation Server scripting • Automated testing tools • Experience with testing medical devices • Experience on an Agile/Scrum team • ASTQB Certification (or the equivalent) • 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, POCT1A • 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. • An appropriate advanced degree may be substituted for experience, where applicable. *Thanks & Regards,* *Soumya Ranjan* *Scalable Systems* Tel:* +1 732-743-8519* Email me at: *[email protected] <[email protected]>* Visit us at www.scalable-systems.com -- You received this message because you are subscribed to "rtc-linux". Membership options at http://groups.google.com/group/rtc-linux . Please read http://groups.google.com/group/rtc-linux/web/checklist before submitting a driver. --- You received this message because you are subscribed to the Google Groups "rtc-linux" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. For more options, visit https://groups.google.com/d/optout.
