US-CA-SanDiego: Sr Software Quality Engineer To apply for this position, please visit this Website. http://sqa.fyicenter.com/jobs/99667875_Sr_Software_Quality_Engineer.html To see other opportunities, please visit http://sqa.fyicenter.com Date: 11-Jul-2011
Sr Software Quality Engineer All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities. Required Skills: -Must possess and teach fundamental understanding of quality philosophies, principles, methods, tools, standards, organizational and team dynamics, interpersonal relationships, and professional ethics. -Must possess and teach an understanding of software quality management principles and demonstrate a comprehensive knowledge of developing and implementing software quality programs, to include tracking, analyzing, reporting, problem resolution, and training. -Must possess knowledge of software development and maintenance processes and methods. -Must possess a basic understanding of project management principles and techniques as they relate to software project planning, implementation, and tracking. -Must have a thorough understanding of software inspection, testing, verification, and validation. -Must have a basic understanding of how and when to perform software audits including audit planning, approaches, types, analyses, reporting results, and follow-up. -Must possess a basic understanding of the configuration management process to include planning, configuration identification, configuration control, change management, status accounting, and reporting. Required Background • Experience with Software Verification and Validation Methodologies • Experience with FDA Regulations CFR 820 and Part 11 • Experience with ISO13485/QSR. Preferred Educational Background: • BS/BA or equivalent in Engineering, Biological/Life Sciences, Chemistry or related field required. • Graduate degree preferred. Preferred Experiential Background: • 7+ years relevant experience required. • Experience conducting compliance audits, microbiological testing, immunological testing or optical scanning. • Experience with FDA Regulations CFR 820 and Part 11 • Experience with ISO13485/QSR. • Excellent attention to detail, well organized and able to work independently and in teams. • Excellent interpersonal, verbal and written communication skills. • Knowledge and skills typically acquired through previous positions in fast-paced corporate environments which involved responsibility for similar work. Thank you, Team SQAFYI - Software QA Resource FYI http://sqa.fyicenter.com -- You received this message because you are subscribed to the Google Groups "Software Quality Assurance Center" group. To post to this group, send email to [email protected]. To unsubscribe from this group, send email to [email protected]. For more options, visit this group at http://groups.google.com/group/software_qa_center?hl=en.
