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Quality Assurance Coordinator, Kitchener Ontario, Oct. 9, 2009

Quality Assurance Coordinator

V.P of Operations with one of the largest medical manufactures in the world is looking for a quality control individual that can work independently and be able to provide technical support and services to his management team in the development of production methods, facilities and systems,planning, estimating, measuring and scheduling of work at their facility in Kitchener Ontario.

The is a permanent position and includes full benefits, three weeks holidays and six paid company floater days.

Main Duties:
*Develop and conduct production, inventory and quality assurance programs in accordance with their head office in Europe
*Help in the design plant layouts and production facilities
*Develop and carry out work studies and related programs that have an immediate impact on production quality,costs and customer satisfaction
*Collect and compile operational or experimental data and assist in the development of estimates, schedules, specifications and reports
*Collect and analyze data and samples in support of quality assurance programs

Requirements
*Willing to be hands-on with company products and on the manufacturing floor with all levels of staff
*Experience with Lean manufacturing and Kaizen
*Six Sigma Green Belt required with at least 3+ years experience (approx 10 projects completed)
*Post Secondary Graduate in Mathematics, Statistics
*Working knowledge of Accounting is an asset

Please contact:
ashleywesley@me.com
519-766-4933

Sr. Quality Engineer, Newark, DE Area, Oct. 9, 2009

SR. QUALITY ENGINEER - NEWARK, DE AREA

SENIOR QUALITY ENGINEER TO $110K

Seeking Senior Quality Engineer with at least 8 years of experience in the bio-tech/ medical device industry. Your responsibilities will include leading
internal/ external quality audits, implementing process improvements and quality management systems, personnel training, statistical analysis, and validation reviews. This is an immediate need!

Qualifications include a BS Degree in Engineering (or related field) with 8+ years of quality assurance experience in the medical device or bio-tech
industry. Background with Lean or Six Sigma is preferred. CQE or CQA is a plus.

SEND A COPY OF YOUR RESUME TO:
Karl Martinez
LIBERTY PERSONNEL SERVICES, INC.
E-MAIL: km@libertyjobs.com
PHONE: (610) 941-6300 ext.129
FAX: (610) 941-2424


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