HI Hope you are doing great!! Please find the requirement below , If you find yourself comfortable with the requirement please reply back with your updated resume and I will get back to you or I would really appreciate if you can give me a call back at my contact number
*804-859-7510. You can add me on G'talk : chetan.ramy You can add me on YM : chetan_ramy Position: Validation Engineer Location:* *Sylmar, CA or Plano, TX.* *Duration: 4+Months Interview Mode: Phone then Skype Visa :: USC ,GC and EAD only* This Candidate will be responsible for the vailidation of software tools. They will write test plans and test reports. They will investigate issues, define behaviors, and help lead other clinical systems engineers in execution of work. They will validate designs and products. They are accountable for applying an expert understanding of clinical applications, customer needs to be addressed, behaviors, and architect solutions to streamline product development in addition to ensuring product quality. They will ensure the logical and systematic conversion of customer requirements and performance requirements into total systems solutions that acknowledge technical, schedule, and cost constraints. They will perform technical planning and performance evaluation studies, conduct technology assessment activities, analyze system integration issues, generate initial baseline interface specifications, estimate cost and risk, and evaluate customer satisfaction through testing (alpha and beta), analysis and studies. They will assure that quality of services meets or exceeds internal customer requirements. * Bachelors Degree in Biomedical Engineering, Electrical Engineering, a related field, or equivalent * Minimum of five+ years of work experience in medical product development * Product development experience especially dealing with definition and validation * Matlab expertise * Semcad experience OR HFSS (high frequency structural simulator) OR CFT Microstudio OR EMP Pro OR Elite Marketing Pro * Demonstrated ability to effectively integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs. * Must have the demonstrated ability to understand and comply with applicable U.S. Food & Drug Administration (FDA) regulations *Plusses* * MRI knowledge * Professional certification or designation such as International Board of Heart Rhythm Examiners (IBHRE). Thanks and Regards, *Chetan Singh* | Sr. Technical Recruiter | -- You received this message because you are subscribed to the Google Groups "Business_Intelligence" group. To unsubscribe from this group and stop receiving emails from it, send an email to business_intelligence+unsubscr...@googlegroups.com. To post to this group, send email to business_intelligence@googlegroups.com. Visit this group at http://groups.google.com/group/business_intelligence. For more options, visit https://groups.google.com/groups/opt_out.
