Hello All, Please go through the job description and let me know your interest. Please revert me with your updated resume Email id : *[email protected] <[email protected]>,[email protected] <[email protected]>*
*Position:- **Medical Regulatory and Verification Engineer * *Location:- Addison, TX* *Duration:- 6+ Months* *Looking for US Citizen only.* *Job Description:- * 6 - 8 Years.As a member of product development teams, represents the QA function for Product Design throughout all stages of the Product Development Process. Develops:- *Design FMEAs- House of Quality / QFD- Product Specifications- DOE- Measurement Systems Analysis / Test Methods*- Capability Analysis- Tolerance Analysis- Quality inspection procedures, including sampling plans- Customer Input analysis- Risk Management Plans Ensures proper development of product specifications (to insure good capability and life cycle stability). Supports Design Validation from protocol development, to testing, to a completed final report. Responsible for Design Verification activities from protocol development, to testing, to a completed final report. Develops the plan for Measurement Systems Analysis and works with the Quality Engineers to develop and improve on the measurement systems at the suppliers/manufacturing facilities/R&D centers. -- *Thanks and Regards,* Rahul Kumar Technical Recruiter - Talent Management Group ll IT-SCIENT ll Phone: 510.870.5023|| Fax: 877.701.4872 || Email Id: *[email protected] <[email protected]>* || Web: www.itscient.com -- You received this message because you are subscribed to the Google Groups "SAP BASIS" 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-basis. For more options, visit https://groups.google.com/d/optout.
