*please send your resumes at [email protected]*
** <[email protected]> *Manufacturing Engineer,* *Wallingford,CT,* *6+ Months* * * *Your Responsibilities:* Provide process development and design for manufacture talent to the Manufacturing Engineering organization. Design, develop, validate and implement manufacturing processes and equipment used during the manufacture of medical devices by performing the following duties: · Work with design and procurement teams early in the development cycle, provide DFM, DFA input to insure resulting designs meet cost and manufacturability targets · Develop, evaluate, and improve manufacturing assembly and test methods to insure consistent quality and efficient manufacture of products. · Design, build and validate manual and automated assembly/test fixtures for production of new and existing products, for the purpose of reduced assembly/test time and improved product quality. · Work with design engineering during product development; provide input to improve the manufacture, test and cost of new and existing products. · Responsible for the transfer of new product designs into remote manufacturing facilities and contracting manufacturing environments. · Provide technical oversight and support to sustain production for products manufactured at remote manufacturing locations including the resolution of 1st and 2nd tier supplier issues. · Identify opportunities for cost reduction. Implement process and product improvements to achieve cost reduction goals. · Develop and perform process validation for manufactured product and associated assembly equipment, test equipment and processes. Including the development of protocols, procedures and reports necessary for a comprehensive validation. · Oversee the procurement of material and the manufacturing processes for pilot production runs. · Evaluate engineering change requests to determine effects on existing processes and that they are suitable and practical for manufacturing. *Your Profile:* · Minimum 10 years work experience with a keen understanding of medical device manufacturing process design, tooling and equipment design. · Understanding of Lean Manufacturing, six sigma, APQP, PFMEA, and DOE desired. · Direct experience in equipment and process validation. · Thorough knowledge of ISO and FDA requirements highly desired. *Thanks & Regards,* *Pramod Reddy Kotha* *Astir IT Solutions, Inc.* Off: 732-694-6000*730 *Fax:* 973-215-2191 *Email:**[email protected]* Yahoo: *recruiter.pramod Gtalk: pramodreddy.astirit* *LinkedIn:* http://www.linkedin.com/pub/pramod-recruiter/38/693/a89 * **50 Cragwood Rd, Suite # 219, South Plainfield, NJ 07080 ** www.astirit.com* <http://www.astirit.com/>* * *2007-2009 NJ Finest *||* 2007-2009 INC 500 Company *|| *NJBIZ - Business of the Year 2006 Finalist* This e-mail communication is intended solely for the exclusive and confidential use of the individual(s) to which it was addressed. Unless expressly stated otherwise, the information contained herein, including any attachment is the confidential and privileged information of Astir IT Solutions, Inc. Any disclosure, reproduction, distribution by or to any person other than the intended recipient is strictly prohibited. If you have received this e-mail communication in error, please notify the sender immediately and destroy this e-mail and any copies that may exist. -- You received this message because you are subscribed to the Google Groups "OracleD2K" group. To post to this group, send email to [email protected]. To unsubscribe from this group, send email to [email protected]. For more options, visit this group at http://groups.google.com/group/oracled2k?hl=en.
