*Greetings!* **
Our Direct Client has an urgent requirement for *"Validation Engineer (w) Medical Device" *for their long term project in *"Minneapolis, MN".*....Please submit resumes at - *[email protected] * * * *Title: *Validation Engineer (w) Medical Device Exp *Location:* Minneapolis, MN *Duration: *6+ Months * Job Description* *Skills:* ** · 5 - 7 years of experience in Medical Devices Industry · Medical Devices manufacturing Industry experience along with the indepth knowledge in FDA / ISO requirements- such as ISO 13485/IEC 62304/ISO 14971 and FDA part 820. · Experience in Systems Design of Patient Monitoring devices / ultrasound scanners / infusion pumps etc · Certified Internal Auditor per ISO requirements · Experience with conventional inspection and measurement equipment · Analytical ability in problem solving · Develop Design Input, Output, verification and Validation plan for Design Function · Develop and execute Verification and validation protocols based on system requirements · Develop and initiate sampling procedures and statistical process control methods *Warm Regards,* ** *Viduthalai Selvan (Vidu)* *First Tek, Inc.* *Direct:* 732-328-2287 *[email protected]* | *www.first-tek.com* *Ranked 31st on Deloitte 2008 NY, NJ, CT Technology Fast 50* *A 2007 Inc 500 winner for 2004-2006* *A 2007 NJ Finest winner for 2004-2006* *Ranked 4th on Deloitte 2007 Technology Fast 50 for 2002-2006*** -- You received this message because you are subscribed to the Google Groups "SAP Workflow" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/sap-workflow. For more options, visit https://groups.google.com/groups/opt_out.
