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Six Sigma Black Belt, Columbia, MO and Bentonville, AR.  April 11, 2010


Six Sigma Black Belt needed in Columbia, MO and Bentonville, AR to work in a food manufacturing facility.
If interested send an e-mail to mybizexcel@gmail.com

Quality Engineer (MetroWest).  April 11, 2010


Quality Engineer (MetroWest)

Our client is an established provider of manufacturing services to the medical device industry with a long track record of stability and growth.

Overview:
A minimum of five years of medical device experience and a 4 year degree is required. ASQ CQE or SSBB certification preferred. Quality systems (QSR 21 CFR

Part 820) and ISO13485 expertise required. Technical degree in an engineering or related discipline such as computer science or statistics is preferred. Well versed in statistical techniques and data analysis and expertise using one or more statistical software packages (Minitab, Stat-Pro, Statistica, etc.) is required. Excellent written and verbal communication skills required. This opportunity requires a high energy candidate looking to help lead a customer focused continuous improvement mentality.

This position requires previous experience supporting product development teams and/or supporting continuous improvement efforts for products in production.

Well versed in acceptance sampling and process capability/process control. Support validation requirements definition and execution (IQ, OQ, PQ), test method definition, root cause analysis, gage R&R and measurement systems analysis (MSA).

Previous experience and expertise in structured problem solving and root cause analysis. Participate in or lead corrective action initiatives. Define,
remediate or optimize processes in compliance with QSR’s and organizational needs.

Please submit resume to: sbennett@biomedicalsearchconsultants.com

For more information, please visit www.biomedicalsearchconsultants.com

Quality Engineer, Dallas, Texas.  April 11, 2010


Dallas, Texas Quality Engineer Up tp 80k

Local Candidates only or candidates that can move on a small lump sum.
Fortune 250 client that has generated incredible profits over the last several years is looking to fill a Key role in their organization. The client continued to perform during the recent recession when most were struggling. This company is recognized as being one of the best run companies in America! The mission critical role is for a Quality Engineer that will take this plants Quality to the next level.  They only hire "A" players that are very dynamic, bring a bunch of passion, enthusiasm, and desire to succeed in their current roles.

OVERVIEW OF ROLE:
As Quality Engineer, you will develop, implement and sustain the systems required to assure the delivery of products and services that will meet and exceed our customer’s total quality requirements. Serve as a subject matter expert in the application of total quality activities that result in achieving customer

satisfaction, continuous improvement in processes, and reduced total cost. Manage Lean tools and disciplines throughout the operations, supporting kaizen efforts and vendor interface in problem resolution and product improvements.

RESPONSIBILITIES:
Establish systems to monitor performance on quality metrics.
Research and evaluate data to identify root causes and propose/implement solutions.
Proactively identify product/process deficiencies using the 8D/Root Cause Countermeasure process.
Work closely with Buyer/Planners to evaluate/improve supplier quality levels.
Develops/performs DOEs for problem solving needs.
Implement SPC/control plans to assure process capability.
Perform gage R&R.
Facilitate problem solving and lead cross-functional teams in warranty reduction.
Key role in implementing measures to the improve end-of-line quality.
Key role in assisting in qualification of new supplier selection process.
Participate on New Product Introduction teams.

REQUIREMENTS:
BS Degree in a related field. (Engineering background preferred)
Sound understanding of statistics/SPC/process capabilities, gage R&R/measurement systems, and of Six Sigma principles.
Experience in lean manufacturing

Quality Engineer, Millipore, Jaffrey, NH.  April 11, 2010


Millipore (NYSE: MIL) is a Life Science leader providing cutting-edge technologies, tools and services for bioscience research and biopharmaceutical
manufacturing. Since its founding in 1954, Millipore has expanded its capabilities through strategic acquisitions, targeted capital investments, and organic growth.

Today we offer an extensive portfolio of products and services in: Life Sciences, Drug Discovery and Development, Lab Filtration, Lab Water, Upstream
Bioprocessing, Downstream Bioprocessing and Process Monitoring.organizations. Millipore’s major manufacturing centers are based in Molsheim, France, Cork, Ireland and Jaffrey, New Hampshire.

POSITION SUMMARY: This individual will be responsible for effective and consistent quality systems. S (He) will support and provide guidance to the efforts and products manufactured at the Jaffrey NH facility of Millipore.

KEY RESPONSIBILITIES:
• Senior level position requires complete understanding and application of FDA GMP and ISO 9001:2008 principles, concepts and practices.
• Develops solutions to a variety of complex problems
• Designs, implements and continually evaluates quality assurance and/or control methods and systems.
• Designs methods and processes for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Conducts quality assurance tests, performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do
not meet required standards and specifications.
• May conduct vendor visits to ensure quality.
• Develops standards and procedures to provide quality guidance and methods.

QUALIFICATIONS & EXPERIENCE:
• 5 years minimum in FDA regulated industry (pharmaceutical, biotechnology or medical device)
• ASQ Certified Quality Engineer (CQE)
• Minitab, Infinity QS SPC software (or statistical software equivalent) proficiency.
• Lean Six Sigma program/project implementation; green belt or black belt certification a plus.
• ASQ Certified Quality Auditor (CQA) or Pharmaceutical GMP Professional (CPGP) a plus

EDUCATION: Bachelors of Science degree in Biology, Pharmacy, Life Sciences or Engineering or related field.

There is limited relocation assistance.

To apply send a resume to nancy_beaumont@millipore.com


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