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Possess continuous improvement experience with emphasis in the laboratory information management and deployment of LEAN/Six Sigma, analytical methods and manufacturing process development for polymeric materials.
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Use quality-by-design approach for improved yields, reproducibility and process improvement. + Experienced in leading process improvement projects with the goal of enhancing robustness for commercial manufacturing.
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Background in organic-polymer synthesis and characterization, biocompatible polymers, peptides and lipid-protein-conjugates, oligonucleotides, structure-property relationships, formulation and process development, small & large molecules, analytical separations, isolation and identification of impurities.
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Creative technical skills that lead to innovative approaches to the development process. Expertise in the conception, formulation, optimization, automation, processing, characterization and manufacture of a unique silicone polymer composition of a specialty medical device including analytical chemical testing including gas and liquid chromatography, gel permeation chromatography (SEC), UV/Vis, FTIR, viscosity testing.
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Analysis of silicone raw materials, intermediate formulation mixes and final formulations using various state-of-the-art analytical techniques including but not limited to GPC, HPLC, GC, rheometer, UV-vis and others.
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Any of the following: Professional Facilitation Training and/or Certificate, Project Management Training, Curriculum Development Training, Lean/Six Sigma Green Belt, Organizational Behavior Training, and/or Team Development Training.
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Lean Six-sigma Green Belt preferred. Application of Lean Six-Sigma principles is the recommended approach. We are looking for a strong operations leader to sponsor and lead the end-to-end transformation of the quality control process.
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Utilize extensive knowledge of polymer chemistry principles for materials selection/management, formulation processes to enhance the scalability and quality of the lens material. Be hands-on and responsible for providing technical leadership and direction for scaling up and tech-transfer including interaction with external vendors.
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Hands-on Ph. D. chemist with 10+ years proven industry experience in identification, development and commercialization of innovative market driven technologies including pharmaceuticals and medical devices.
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Serve as the technical lead and core team member on projects and interact with global clinical, manufacturing, production, quality, regulatory, project management, legal, claims and strategy and marketing personnel.
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Process improvement experience in a recognized methodology (Lean Six Sigma, CMMI, ISO) + Coordinate with accounting and finance departments in administering subcontract invoicing and payments, job cost management, contract audit/filing, and closeout process.
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The Regional Continuous Improvement Manager will also teach and apply Lean Six Sigma principles to achieve self-sustaining processes. 3+ years' work experience in Lean Six Sigma continuous improvement activities and financial calculation of savings, budget forecasting, ROI calculation and ration analysis.
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Lean manufacturing/six sigma/statistical analysis ; Six Sigma Green Belt a plus. Responsibilities include project management, process improvement, leading cross-functional teams, manufacturing timelines, and continuous improvement.
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Lean) Six Sigma Green Belt. Problem solving, analytical, and process improvement skills / experience. The Supplier Quality Engineer drives customer satisfaction and continual improvement in accomplishing ESA's strategic plan through monitoring, managing and resolving issues related to Supplier quality performance.
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Minimum of 2 years experience leading operational excellence and/or continuous improvement initiatives in a process manufacturing environment or other relevant experience. Creative and change-oriented Continuous Improvement process skills.
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continuous improvement lean six sigma green process control jobs Company: Luxottica
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