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Quality Engineer - Quality/Manufacturing/Documentation
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Posted:
25 Jul 2008
Apply Deadline:
22 Oct 2008
Location:
Jacksonville, FL, USA
QUALITY ENGINEER - Worldwide Manufacturer of Medical Equipment has an IMMEDIATE opening in the state of FLORIDA for a Quality Engineer. This is a contract position. A Four-year Degree in Engineering and minimum THREE years relevant experience in a high tech manufacturing environment is required. Individual will partner with Mfg. Engineering to assist in developing test methods, equipment acquisition for new product testing, validations/qualifications, statistical analysis of data for significance, and other documented requirements for quality objectives. Participates in new product development, and establish quality and reliability expectancy of the finished product. Identifies, applies, and updates engineering and technical standards requirements for devices, including standards compliance in product design, manufacture, and labeling. Also, will participate in Business Team operations to approve testing of all new product designs, design test parameters for R&D, Operations and QA, conduct reliability assessments, monitor design developments for maintaining quality compliance and assists in software engineering, testing, and validation. Additional certifications ASQC, Design Controls, DHF, and Engineering Documentation, QS, 21CFR-GMP/QSR, 29/40 CFR, title 8, and NRC Compliance are helpful. There is minimal travel up to 20%. Salary based on range of qualifications, depth of experience, and education. Comprehensive Benefits. Local candidates only or those willing to relocate on their own.
Questions you will be asked:
• Do you have a BS or advanced degree in Engineering? Where and When. Any additional education or certification? Where and When.
• Describe your 3 years relevant experience in a high tech manufacturing environment providing assistance in developing test methods, equipment acquisition for new product testing, validations-qualifications.
• Describe your experience with participating in Business Team operations to approve testing of all new product designs, design test parameters for R&D, Operations and QA, conduct reliability assessments, monitor design developments for maintaining quality compliance and assists in software engineering, testing, and validation.
Related Words: process control, lean, business systems, process improvement, process efficiency, work flow, workflow, information flow, process flow, reengineering, re-engineering, process design, process redesign, process analyst, business requirements, it requirements, it requirement, business consulting, business needs, needs assessment, business processes, mechanical engineer, mechanical engineering, bsme, manufacturing engineer, mechanical engineer, mechanical engineering, bsme, manufacturing engineer, industrial engineer, rehabilitation, blue cross, physician, therapy, hmo, hbo, medaphis, first data, rtpm, pi historian servers, pi process book, pi data links, realtime performance management, osi software, business systems, process improvement, process efficiency, work flow, workflow, information flow, process flow, reengineering, re-engineering, process design, process redesign, process analyst, business requirements, it requirements, it requirement, business consulting, business needs, needs assessment, business processes, healthcare, process improvement, data analysis., quality assurance, quality, qa, qc, statistical process control, spc, total quality management, tqm, process analyst, inspection, inspection, iso, taquchi, sampling theory
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