US: Quality Engineer
To apply for this position, please visit this Website.
http://sqa.fyicenter.com/jobs/99657448_Quality_Engineer.html
To see other opportunities, please visit http://sqa.fyicenter.com
Date: 12-Sep-2013
Quality Engineer
* Responsible for all operational quality aspects associated with product manufacture and release.
* Responsible for the successful validation and qualification of process and raw material changes.
* Investigate Quality problems associated with the production department and implement effective corrective and preventive measures
* Drive/support & implement continuous improvement projects with the operations team using Process Excellence lean/six sigma tools.
* Ensures the pertinent corporate quality and regulatory standards are attained.
* Maintains strong communication with internal and external stakeholders.
* Participates / supports the Internal and External Audit Programme.
* Participate in teams to help make necessary improvements and changes to all process related issues in the production department
* Identify and implement continuous improvements in conjunction with the operations team.
* 3 years minimum in FDA regulated industry (pharmaceutical, biotechnology or medical device) * 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
Thank you,
Team SQAFYI - Software QA Resource FYI
http://sqa.fyicenter.com
-- To apply for this position, please visit this Website.
http://sqa.fyicenter.com/jobs/99657448_Quality_Engineer.html
To see other opportunities, please visit http://sqa.fyicenter.com
Date: 12-Sep-2013
Quality Engineer
* Responsible for all operational quality aspects associated with product manufacture and release.
* Responsible for the successful validation and qualification of process and raw material changes.
* Investigate Quality problems associated with the production department and implement effective corrective and preventive measures
* Drive/support & implement continuous improvement projects with the operations team using Process Excellence lean/six sigma tools.
* Ensures the pertinent corporate quality and regulatory standards are attained.
* Maintains strong communication with internal and external stakeholders.
* Participates / supports the Internal and External Audit Programme.
* Participate in teams to help make necessary improvements and changes to all process related issues in the production department
* Identify and implement continuous improvements in conjunction with the operations team.
* 3 years minimum in FDA regulated industry (pharmaceutical, biotechnology or medical device) * 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
Thank you,
Team SQAFYI - Software QA Resource FYI
http://sqa.fyicenter.com
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