-- Dear folks,
Please share good resource for below mention position; *Please share resume at [email protected] <[email protected]>* *MEDTRONIC* *Memphis, TN. 38132* *Quality Engineer* *12+ months* *$40/hr * *Primary responsibility will be to handle quality engineering duties associated with products design/manufacturing transfer, establish appropriate measurement system analysis, lead risk assessment and support manufacturing process validations and controls. * *Keys: Engineering Degree, GD&T, Process Validations, SPC, Medical Device exp- Risk Mgt/Risk assessment* •Prior experience in product mechanical evaluation & testing and GD&T. •Prior experience in the application of production and process controls including process validation, process control plans and statistical process control. •Prior experience with quality systems (product design through manufacturing) in a mature industry that has stringent quality regulations. •Prior experience in the medical device industry •Knowledge of CFR 21 Part 820 (QSR), ISO 13485, ISO 14971, CMDCAS, MDD 93/42, PAL, and other domestic and international regulations that may apply •A quality engineering certification from the American Society for Quality other qualifying organization is preferred. Examples include the CQE, CRE, etc. . Other duties may be assigned. Engineering Drawings/Specifications (GD&T) • Review drawings to evaluate quality requirements including correct application of geometric dimension and tolerance, proper use of engineering, process and material specifications, and identification of key characteristics for inspection plans and methods. Recommend revisions to assure design requirements are specified in the appropriate detail and clarity to provide a successful design transfer. Review and approve engineering change requests. Review product verification and validation plans and approve reports. Production and Process Controls • Apply the quality toolset including FMEA, IQ, OQ, PQ, GR&R/measurement system analysis, control plans, process verification/validation plans, validation protocol development, Cpk, Cp, SPC, hard gaging applications, computer-based inspection methods, operator work instructions, DOE, process data analysis, and DMAIC. • Assist manufacturing sites with the interpretation of quality requirements including verification/validation planning and execution, first production run requirements, and problem resolution *Regards,* *Monajir Khan* *Techwire Solutions, Inc* IT Recruiter 101 Hudson St, Suite 2100, Jersey City, NJ 07302, USA Phone: 609-353-5706 || [email protected] || || Gtalk: [email protected] || Yahoo: [email protected] || Web : *www.techwiresol.com* <http://www.techwiresol.com/> *Office Locations: New Jersey || California || Washington || New Delhi || Noida || Pune || Hyderabad ||* Disclaimer: Under Bills.1618 Title III passed by the 105th U.S. Congress this mail cannot be considered Spam as long as we include contact information. To be removed from our mailing list please reply to *[email protected] <[email protected]>* with the word "REMOVE" in your subject line -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" 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/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
