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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. + 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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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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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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Be hands-on and responsible for providing technical leadership and direction for scaling up and tech-transfer including interaction with external vendors. Credentials / Required Skills:+ 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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Broad experience in protein conjugation chemistry, formulation, conjugate purification, and characterization is highly desired. Ph. D. in organic chemistry and 1-3 years of experience working in an industry setting (or postdoc equivalent) is required.
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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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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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Understanding of the basic principles of protein chemistry and/or drug product process is required. The job entails experimental work on various aspects of Drug Product characterization, including formulation development, safety risk assessment of excipients as well as process reagents, extractables and leachables, in use compatibility studies for intravenous and subcutaneous administration, process development to support drug product manufacturing support, particulates testing.
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Conceptualize, design, and develop innovations in Vision Care in alignment with the strategic business goals of Bausch & Lomb. 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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GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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PhD in chemistry or related science with 2+ years industrial experience in protein characterization in the biotechnology and/or pharmaceutical space. Perform protein therapeutics characterization test in support of molecular assessment and formulation development.
$35 - $50 an hourFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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A strong technical background encompassing protein chemistry, analytical development, and formulation development is required. The incumbent in this role will support the formulation development of protein biologics from early development through commercialization, with a specific focus on neurotoxins for therapeutics and aesthetic use.
$78Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Identify relative risk of protein adsorption and degradation under various formulation conditions using analytical techniques, such as: quartz crystal microbalance with dissipation (QCM-D); size exclusion chromatography (SEC); particle characterization (micro-flow imaging); and ion-exchange chromatography (IEX.
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Reporting to and partnering with the CEO, this role will lead a team of talented research scientists in Cancer Biology, Protein Therapeutics, Analytical Development, Pharmaceutical Chemistry, Formulation Development, Process Development and CMC Leadership for our Nemvaleukin alfa, IL-12 and IL-18 R&D programs.
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