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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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