Hi, Kindly give reply to vino...@beyondtekit.com
This is my direct client opening for *Quality Engineer -2 - Memphis, TN.This is a 6+ Months contract* position. *The client is looking for only LOCAL candidates. * *Job Description:* *SUMMARY:* Responsible for concurrent quality engineering activities. Participates in external and internal quality audits. *ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.* · Participates in design control projects providing quality engineering support. · Serves as the independent reviewer on all assigned projects ensuring that design history files comply with company policies and governmental regulations. · Reviews drawings to evaluate quality requirements including: correct application of geometric dimensioning and tolerancing, proper use of process and material specifications, and key characteristics for inspection plans and gauging techniques. · Recommends revisions to assure design requirements are specified in the appropriate detail to provide a successful design transfer. · Reviews and approves engineering change requests. Develops inspection techniques that include identification of characteristics, sampling plans, and gauging. · Recommends gauging techniques including gauge work instructions – assures gauges provide repeatable and reproducible results through the use of statistical techniques. · Uses quality tools to implement improvements including: process flowcharting, pareto analysis, correlation and regression analysis, significance tests, design of experiments, statistical process control, gauge repeatability and reproducibility, and trend analysis techniques. · Assists suppliers with the interpretation of quality requirements. · Develops control plans that identify inspection characteristics, gauging techniques, and sampling requirements. · Works with suppliers to resolve conflicts and recommends revisions as required. · Assists the design control project team with the development of essential design control deliverable including, but not limited to: complaint analysis on similar products, risk analysis, failure mode and effects analysis, essential requirements checklist, and design verification / validation. · Assists with the development of protocols to ensure processes and products are validated with the appropriate level of confidence. · Assists in internal and external quality audits and inspections. · Provides support to other Global Quality projects as needed. *EDUCATION and/or EXPERIENCE: * · *Requires GD&T/ Print reading and understanding, read and understand design requirements, metrology experience, report technical information (Must have)* · Bachelor's degree in mechanical or biomedical engineering and 1-3 years related work experience · CQE, CRE, etc. desired. · Prior experience in the medical device industry preferred. · Knowledge of CFR 21 Part 820 (QSR), ISO 13485, CMDCAS, MDD 93/42, PAL, and other domestic and international regulations that may apply. · Experience in mechanical evaluation or testing. *OTHER SKILLS and ABILITIES: * · Superior written and oral communication skills. · CQE or other quality certification preferred. · Overnight travel (up to 25%) may be required. *Please complete the following skills-matrix and send back with your updated resume.*** Full Name: Degree Major: Total IT Experience: Total Quality Engineer exp: Total exp of *GD&T/ Print reading and understanding, read and understand design requirements:** please specify* Total *metrology exp, report technical information: please specify* Total exp in CQE, CRE, etc: please specify Total exp in the medical device industry: Total exp of CFR 21 Part 820 (QSR): Total exp in ISO 13485, CMDCAS, MDD 93/42, PAL, and other domestic and international regulations: please specify Total exp in mechanical evaluation or testing: Do you hold CQE certification or equivalent? Y/N Are willing to Overnight travel (up to 25%)?Y/N Hourly Rate: Whether is it C2C/1099/W2? If 1099, specify the corporate name: Day Phone #: Evening Phone #: Cell Phone #: Availability: Current City/State: Have you applied recently for this requirement earlier through any one else? Y/N *Thanks & Regards,* * * *Vinoth* (* 714-857-2002 **x** **810* 7* 714-364-9705* *vino...@beyondtekit.com* *www.beyondtekit.com*** IM: vinodth_beyondtekit *http://www.linkedin.com/in/vinothsamuel* --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "zilliontechnologies" group. To post to this group, send email to zilliontechnologies@googlegroups.com To unsubscribe from this group, send email to zilliontechnologies+unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/zilliontechnologies?hl=en -~----------~----~----~----~------~----~------~--~---
