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Mechanical Engineer - Supplier/Medical Device/Quality
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Posted:
14 Oct 2009
Apply Deadline:
11 Jan 2010
Location:
Northridge, CA, USA
IMMEDIATE OPPORTUNITY in Northern Los Angeles CA for a Mechanical and a Quality Engineer to work with a Worldwide Manufacturer of Medical Equipment. These are contract positions.
Responsibilities:
-> Establish and successfully execute our supplier management and development plans which will align to overall business objectives
-> Communication of Clients expectations for continuous improvements and providing leadership for improving the supplier relationship through supplier improvement conference calls, and supplier partnership meetings and effectively provide feedback and work w
-> Develops product and process improvements
-> Perform thorough supplier audits and assessments of their processes and QMS and drives improvement
-> Improve the cost of quality of parts, processes and products
-> Assist in performing Failure Analysis and inspection techniques on supplier materials
Requirements:
-> Graduate Degree in Engineering Required Quality or Reliability Certification for Quality Engineer Preferred Emphasis in Engineering Materials A DEFINITE PLUS
-> FIVE YEARS MINIMUM Strong work Experience in Medical Device Manufacturing Industry
-> Create Material Inspection Instructions to support Receiving Inspection and align the inspections methods between suppliers and company
-> Demonstrated knowledge of national and international requirements and standards such as FDA QSR Part 820, ISO 14971, ISO 13485, ISO 9001, CMDCAS/CMDR and others
Benefits:
-> Paid Vacation
-> 401K
-> Health Insurance, and more...
-> Travel
Questions you will be asked:
• Do you have a GRADUATE Degree In Engineering, preferably Mechanical with Quality Control or Reliability Certification. Any Additional education or certification. Black Belt is a Definite Plus.
• Describe your experience and knowledge of national and international requirements and standards such as FDA QSR Part 820, ISO 14971, ISO 13485, ISO 9001, CMDCAS-CMDR and others. Required Describe.
• Describe your experience with performing thorough supplier audits and assessments of their processes and QMS and drives improvement. When and Where Describe - REQUIRED
• Do you have experience with leading and executing Supplier Quality programs, and supporting other cross functional departments to meet their objectives in acquiring highest quality materials and systems (parts, sub-systems, final assembly, outsourced products, audits, etc.) from suppliers that meet the material requirements. Required Describe.
Related Words: mechanical engineer, mechanical engineering, bsme, quality assurance, quality, qa, qc, statistical process control, spc, total quality management, tqm, process analyst, inspection, iso, taquchi, sampling theory, six sigma, six-sigma, 6 sigma, 6-sigma, sigma black belt, sigma black belts, master black belts, six sigma, six-sigma, 6 sigma, 6-sigma, sigma black belt, sigma black belts, master black belts, black belt, master blackbelt, master blackbelts, manufacturing engineer, fda qsr part 820, iso 14971, iso 13485, iso 9001, cmdcas/cmdr
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