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Process Engineer Position Summary:Catalent Pharma Solutions is Chelsea, MA is hiring a Process Engineer who is responsible for assisting senior engineering staff in the design and implementation of manufacturing processes, instrumentation and equipment for clinical and commercial manufacturing.
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As the Strategic Sourcing Manufacturing & Supply Director for Cell and Gene Therapy (CGT), you will be a part of a fast-growing and innovative organization at the company's world headquarters in Boston, MA. The department is committed to a trusting and collaborative culture where we value growth and development.
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Sourcing Strategy Development - Develop and execute sourcing strategies for raw materials used in cell and gene therapy manufacturing. Market Analysis - Stay informed about market trends, supplier capabilities, and emerging technologies related to raw materials for cell and gene therapy manufacturing.
$214,800 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Lead Tech Transfer of processes to the Pilot Plant and Manufacturing. Process development may be directed to either batch or continuous manufacturing. Work closely with process Industrialization and New Technology Engineering team to design and implement model predictive control strategies for drug substance manufacturing processes.
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As a senior member of the team, youwill be responsible for leading the development of innovative CMC regulatory strategies and the preparation and submission of high quality CMC sections of INDs and CTAs, in close collaboration with regulatory team members, our in house CMC and Quality teams, contract manufacturing organizations, external experts and global health authorities.
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Director/Sr. Director - Process DevelopmentGreater Boston Area Competitive Compensation + excellent bonus/benefitsDuties and Responsibilities:Lead all process development activities (cell culture/banking/development, fermentation, protein purification, tech transfers)Oversee internal(in-house) and external vendors (domestic & international CDMOs)Work cross-functionally with CMC & Manufacturing leaders such as Analytical, Drug Product, QA/QC, Manufacturing, Supply Chain, etc.
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Its end-to-end value chain presence encompasses onshore and offshore wind turbine design, manufacturing, installation, as well as cutting-edge service solutions. Its end-to-end value chain presence encompasses onshore and offshore wind turbine design, manufacturing, installation, as well as cutting-edge service solutions.
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Carestream is a worldwide provider of medical imaging systems and solutions; x-ray imaging systems for non-destructive testing; manufacturing of film and precision contract coating services for a wide range of industrial, medical, electronic and other applications-all backed by a global service and support network.
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The Role Veeva Vault, our cloud-based content management and collaboration solution, is used by our customers to manage content-centric processes across key departments within a life sciences company, including clinical trials, quality management, manufacturing, regulatory, sales, and marketing.
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This position leads various teams within FMI, directing quality personnel working with manufacturing and IVD operations teams within the Quality System Program, including manufacturing process review, batch release of products, IVD assay validation and verification, manufacturing material acceptance, device non-conformance and CAPA investigation.
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The incumbent will provide Automation support to the daily operations, continuous improvement, and projects for the Pilot Plant, Bulk Manufacturing, Filling, Assembly, Packaging, Utilities, Facilities, and other DCS and PLC Automated Equipment and Control Systems in a GMP regulated environment.
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The Fraunhofer USA Center for Manufacturing Innovation (CMI) in Boston, MA is part of Fraunhofer USA, a 501 (c) (3) non-profit contract R&D organization. Fraunhofer USA - Center for Manufacturing Innovation.
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Provides GMP Quality Assurance oversight of AVEO products manufactured at Contract Development Manufacturing Organizations (CDMOs). AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development.
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10+ years of professional experience in facilities operations, preferably in semiconductor, manufacturing, biomedical science facilities, or similar environments. 5-8+ years of professional experience in facilities operations, preferably in semiconductor, manufacturing, biomedical science facilities, or similar environments.
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Veeva Vault, our cloud-based content management and collaboration solution, is used by our customers to manage content-centric processes across key departments within a life sciences company, including clinical trials, quality management, manufacturing, regulatory, sales, and marketing.
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manufacturing job Title: ambulatory Company: Christus Health in Quincy, MA
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