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HPLC, UPLC, GC, ICP-MS analysis of raw materials, finished product, and stability samples. Physical testing, chemical, or microbiological analysis of raw materials, finished products, stability and special samples.
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Provide guidance to small group of laboratory chemists who are responsible for conducting analysis of raw and in process materials utilizing HPLC, GC, and wet chemistry techniques.
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Performs chemical analysis using established procedures and operates analytical instruments and apparatus for the chemical evaluation of samples from the C-M melt shop, customers, raw material vendors, and non-routine samples as assigned.
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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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Utilize extensive knowledge of polymer chemistry principles for materials selection/management, formulation processes to enhance the scalability and quality of the lens material. + 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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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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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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Perform QC/QA analysis on raw materials or final products using instrumentation such as pH meter, Densitometer, HPLC, ICP and other techniques. Receive and log incoming raw materials or final products to schedule for analysis.
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The Quality Control Chemist performs analytical testing of raw materials, in-process, finished products following protocols and procedures (SOP's) and company policies. Support other senior staff Chemist in sample analysis for QC/QA or R&D activities.
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Maintain housekeeping in the Stillyard Area and Boiler Room to tour condition, including, but not limited to, picking up and properly disposing of all trash, grounds keeping, clean up and properly dispose of all raw materials and products from leaks and spills in a timely manner.
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Perform analysis using HPLC/UV-Visible spectrophotometer for raw materials, finished products, and stability samples. Perform wet analysis for raw materials and finished products, including Loss on Drying, Viscosity, pH, and water content.
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Essential Functions: Perform physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs.
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Develop key metrics and analysis around product mix and pricing, inventory levels, production capacity and raw materials. 3 to 10 years experience in oil and gas industry with significant OCTG (Oil Country Tubular Goods) procurement and supply chain background.
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The Quality Control organization responsibilities include bioanalytical, chemical, microbiological, and in vivo testing of raw materials, in-process materials and finished products.
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Under the general supervision of the Quality Assurance Manager and Quality Control Supervisor, the QC Technician controls the release of all raw materials used in making TPU and tests all intermediate and finished product on the site.
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