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Knowledge of SPC, FMEA, DOE, RCA, GDT Sound knowledge of quality management systems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc.
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Statistical knowledge and techniques e.g. root cause analysis tools, Design of Experiments (DOE), Sampling Plans, Statistical Process Control (SPC), Process and Product Understanding (PPU), and Lean Manufacturing.
$77,502 - $94,725 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Solid Quality Engineering background with deep knowledge and detailed understanding of process control, SPC methodologies, reporting and when to use, DOE approaches and quality management system.
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Other important knowledge/experience areas include: Six Sigma, management technical staff, OSHA required programs for chemical safety & hygiene, SDS requirements, use of statistical tools (SPC, DOE, etc.
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Familiarity with, or ability to learn various statistical and quality methodologies including but not limited to Statistical Process Control (SPC), Statistical Quality Control (SQC), 5S, 8D, Failure Mode and Effects Analysis (FMEA), Root Cause Analysis, Gage Repeatability and Reproducibility (R&R), and Design of Experiments (DOE.
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Knowledge and application of statistical techniques, SPC, DOE, and problem-solving tools. 7+ years of demonstrated experience in medical device companySolid experience in crafting reports and delivering results in cross-functional group settingsDemonstrated strong client service skills, teamwork, and collaborationDemonstrated planning and multitasking skills to improve productivityDemonstrated commitment to open and clear communication, team building, and quality.
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Ability to use standard manufacturing measurement tools and equipment (SPC, GD&T, DOE, Gage R&R, statistical analysis). We are seeking a highly motivated and skilled Quality Engineer that will lead and facilitate the implementation of quality initiatives and their continual improvement.
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SPC, Linear Regression, DOE, Process Capability, Process Capability, Hypothesis Testing. ASQ Certified Quality Engineer is a plus. Audits production processes, raw materials or suppliers/vendors to ensure that established quality standards are met.
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Strong quantitative process development skills including (p)FMEA, tolerance analysis, DoE, SPC, GR&R, and Cpk/Cp. The Quality Manager supports the development and execution of a holistic quality program in collaboration with CAIRE’s global headquarters operations located in Ball Ground, GA. The Quality Manager leads a team of quality professionals that drives key processes within Quality Engineering, Supplier Quality Engineering, Incoming Inspection, Metrology, and Radiology.
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Ability to apply SPC, DOE, Lean/Six Sigma, mathematics and statistics to solve complex manufacturing process problems. Execution of test protocols in conjunction with production supervision, quality engineering and direct labor personnel.
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Train, Mentor and develop technicians and peers to be skilled experts in the application of Quality tools (SPC, DOE, Centerlining Process, Control Plans, Problem Solving, etc. Audit facility for compliance with GMP standards and maintain plant in compliance with corporate quality requirements.
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Implement prevention-based quality tools and mindset – Quality as a superordinate value, lead FMEA failure mode effects analysis (in the design phase of NPI and process development), Process Controls like SPC, DOE design of experiments, measurement of process capability, Poke-Yoke to engineer out potential failure modes, reduction of process drift to reduce sources of variation and to drive uniformity of process outcomes.
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Leads investigations, corrective actions, continuous improvement projects, and process capability improvements (FMEA, root cause analysis, process mapping, Six Sigma, SPC, DOE, etc.) The Principal Quality Engineering Independently supports the most complex projects, collaborating with other quality, engineering, and manufacturing operations functions to ensure the quality aspects of validation and qualification activities, performing various types of analysis and generating and reviewing internal investigations, CAPAs, and change controls.
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Experience with Design of Experiments (DOE) and Statistical Process Control (SPC), with preferred Lean Six Sigma or Black/Green Belt certification. Accumulated experience of 5-8 years in supplier development, quality, process engineering, or product development essential.
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Must be proficient in the use of analytical tools, such as DOE, SPC, 8-D, 5 Why, etc and techniques to analyze data, train others and participate in teams and find solutions to problems.
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