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Set technical direction for research and development projects for the design, development, and commercialization of new functional inorganic materials. Develop new technologies that provide the basis for product development and commercialization of new products in new promising and rapidly growing application areas.
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They will be leading a large team of Research, Commercialization, & Quality Engineers tasked with developing and/or improving current and future dsm-firmenich Biomedical products/processes. Senior Manufacturing Engineer Exton, PAOn-SiteThe Senior Manufacturing Engineer will provide technical leadership, machine design, and processing expertise towards the process development, scale up, and commercialization for new and existing product lines.
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Additionally, the Senior Flavorist promotes the commercialization of flavors with QA/production and supports on any challenges in the flavor manufacturing plant. An in depth understanding of ingredients and technology along with their impact on product taste and functionalitySkilled in catalog of flavor raw materials and functionality, processing methodsExperienced in commercialization of flavors in production, QA release and trouble shooting.
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As they expand their operations, working towards further clinical trials and ultimate commercialization, they're looking for a hands-on Senior Process Engineer to help manage their primary lab-based activities – syntheses, manufacturing, characterization, process optimization and scaleup.
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Job Overview: Manager - Category Commercialization, Allied Partners The Manager of Category Commercialization, Allied Partners is responsible for leading the commercialization of select Keurig Dr Pepper (KDP) beverage brands across liquid refreshment beverage categories, for Allied partner brands.
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It is the division's leader in sterile product and process development, responsible for late-stage commercialization activities including process scale up, technology transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations.
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Establishes and validates platform engineering and scientific models for sterile product and process commercialization. The Associate Principal Scientist is an experienced drug product commercialization scientist/engineer, accountable for end-to-end leadership for these key activities within the Sterile Drug Product Commercialization department.
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Biologics Analytical Research and Development (BARD) is responsible for the development of analytical strategies to support drug development and commercialization efforts throughout the product development lifecycle.
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The Bioproduct Research and Development organization strives to deliver creative medicines to patients through the development and commercialization of insulins, monoclonal antibodies, novel therapeutic proteins, peptides, oligonucleotide therapies and gene therapy modalities.
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This role also involves process scale-up and technology transfer of manufacturing related workflows to Contract Development and Manufacturing Organizations (CDMOs) or Regeneron based manufacturing suites to ensure timely and reliable entrance to the clinic through product commercialization.
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Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and ODH, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities.
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Assume full scientific HEOR strategic support of commercialization activities including the facilitation of achieving and maintaining market access and growing the market. The VP, HEOR Strategy, Neuroscience & Eye Care is accountable for the execution of strategic plans for all AbbVie Neuroscience & Eye Care products to obtain and maintain market access, favorable pricing and optimal formulary status, and ensuring that the strategic plans are consistently relevant to product development and the marketplace.
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Astellas Institute for Regenerative Medicine (AIRM) is a wholly owned subsidiary of Astellas Pharma Inc and focused on the development and commercialization of stem cell and regenerative medicine therapies.
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Fifteen (15) years of experience in Regulatory Affairs and Quality experience in the biotechnology, medical devices, or pharmaceutical industry with increasing responsibility (including interfacing with FDA and other regulatory agencies in development and commercialization of new medical technologies.
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ConnectiveRx was formed in 2015 by bringing together the industry-leading business of PSKW, PDR/LDM, Careform (2017) and The Macaluso Group (2018) to advance our technology-driven expertise in providing state-of-the-art commercialization solutions.
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commercialization job Title: platform manager Company: Genomatica
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