US-CA-SanDiego: Software Quality Manager To apply for this position, please visit this Website. http://sqa.fyicenter.com/jobs/99664719_Software_Quality_Manager.html To see other opportunities, please visit http://sqa.fyicenter.com Date: 02-Mar-2012
Manager, Software Quality • Provide quality guidance and leadership to Product Development Core Teams in the planning and execution of design & development activities including Software Lifecycle requirements (e.g. software testing, verification and validation, and risk management activities, etc.) needed to accomplish project objectives and deliverables • Review/Approve validation plans/protocols/reports, software requirements, traceability matrices, test summary reports, software changes • Assess, create and implement new methods, techniques, and evaluation criteria for identifying risks involving software applications, solving problems and implementing corrective actions • Develop and implement product quality plans, documents and systems by creating procedures, product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members • Provide Quality Engineering support for current and new software product development through manufacturing, service and product obsolescence. • Support Quality Department activities which may include employee training, performance of internal/external quality audits, and system software implementation NOTES: Employer will assist with relocation costs. Additional Salary Information: Competitive Salary, Stock Options, Bonus • Bachelor's Degree in Computer Science, Engineering or related technical field required • 5+ years of work experience in software design and software quality assurance • Minimum three years experience with In Vitro Diagnostic-Medical Device/ Instrumentation / Software • Experience with software-hardware interfaces including writing and executing test plans related to software-hardware combined products • Prefer experience with one or more of: JAVA, C++, R-script, Perl- script, Labview, Subversion, and IBM-DOORS • Working experience in design and validation processes including generation of detailed specifications and requirements addressing regulatory compliance requirements/guidelines (US-FDA, European Council Directives, Canada, Japan, etc.), industry standards (AAMI, IEEE, etc.) and international standards (ISO, IEC, etc.) • Demonstrated leadership skills / abilities to create, implement and achieve business goals through cross-functional teams and staff • Professional certification is desirable (i.e. SQA-Software Quality Assurance, CQM-Certified Quality Manager) 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.
