Hello All, Please go through the job description and let me know your interest. Please revert me with your updated resume Email id : *rku...@itscient.com <rahul.si...@itscient.com>,rahulkumar.itsci...@gmail.com <rahulkumar.itsci...@gmail.com>*
*Position:- Validation Engineer or ** Manufacturing Process Engineer* *Location:- Minneapolis, MN* *Duration:- 6+ Months* *Job Description:- * *Experience 7- 8 years.* *Graduate in Mechanical or biomedical Engineering or related field.* Experience in Manufacturing Process Validation, CAPA, FMEA. Experience in any quality management systems, quality records Devices or implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Familiarity with quality improvement tools, including statistical methods and control plans. Experience with FDA 21 CFR Part 820 compliance & ISO 13485 + 14971 Standards. *Key Skills and Tools:* GD&T, ability to read prints, Pro E, Solidworks Gage R&R studies, Minitab analysis IQ/OQ/PQ/EQ, TMV. ECR/ ECN creation, review PDM/ PLM tools - Enovia, Factory works, CAD, DXF files, Trackwise, Agile etc ISO 13485, design control processes. -- *Thanks and Regards,* Rahul Kumar Technical Recruiter - Talent Management Group ll IT-SCIENT ll Phone: 510.870.5023|| Fax: 877.701.4872 || Email Id: *rku...@itscient.com <rahulkumar.itsci...@gmail.com>* || 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 sap-basis+unsubscr...@googlegroups.com. To post to this group, send email to sap-basis@googlegroups.com. Visit this group at http://groups.google.com/group/sap-basis. For more options, visit https://groups.google.com/d/optout.
