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Our facility in Burnet, TX is seeking a Continuous Improvement Project (CIP) Scientist with advanced knowledge of analytical chemistry and techniques applied to the characterization of complex mixtures.
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Assurance, Analytical Development, Quality Control Specialist I (KLIMS), Analytical Operations. QC Analytical labs. Supervisor, Quality Control Analytical page is loaded. QC Analytical laboratory.
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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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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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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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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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Effective analytical and problem-solving skills with the ability to apply creative solutions to challenges. Utilize extensive knowledge of polymer chemistry principles for materials selection/management, formulation processes to enhance the scalability and quality of the lens material.
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Be hands-on and responsible for providing technical leadership and direction for scaling up and tech-transfer including interaction with external vendors. 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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Develop and manage world-wide supplier relationship, sourcing and supply chain for Research & Development projects and commercialization of the finished products. Extensive experience working in a GLP laboratory / facility environment.
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Conceptualize, design, and develop innovations in Vision Care in alignment with the strategic business goals of Bausch & Lomb. Project, resource, strategy and budget planning and interaction/negotiation with business partners, due diligence, licensing.
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We have a significant global research, development, manufacturing, and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.
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Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the worldfrom the moment of birth through every phase of life.
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As required by New York State's pay transparency bill, Bausch + Lomb provides a good faith minimum and maximum salary range of compensation for roles that can or will be performed, in New York State. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives.
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Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Accurate record keeping both electronically and in a laboratory notebook.
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Title: analytical scientist Company: The American Society Of Pharmacognosy
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