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In health, we focus on areas like medical countermeasures, advanced therapeutics, regenerative medicine, cell and gene therapies, biologics manufacturing, natural products, APIs and KSMs, enzymes, biocatalysis, and microbiome therapy to support national health security and public health initiatives.
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Machine Learning | Semiconductor Manufacturing | AI | Electrical Engineering | Automation | MLOps | Java | C. Lead the development and deployment of machine learning algorithms for semiconductor manufacturing challenges.
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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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E.g. Allen Bradley, Siemens and CODESYS systems- Experience with the designs of complex, automated material handling equipment, packaging technologies, or systems including robotics (FANUC, ABB, UR) and high-speed manufacturing.
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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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Experience in technology transfer to Contract Development and Manufacturing Organizations (CDMOs) for both non-Good Manufacturing Practices (non-GMP) and Good Manufacturing Practices (GMP) manufacturing, encompassing cell line development, process development, and scale-up.
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Serve as the Quality SME on the Chemistry, Manufacturing, and Controls (CMC) Governance teams covering Analytical Development, Process Development, Technical Operations, and Supply Chain topics for technical transfers, new product introduction, clinical trial and commercial products to assure a compliant strategy is developed, executed and maintained.
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You will define and execute process development and tech transfer activities to enable iPSC expansion and differentiation in GMP manufacturing throughout the product lifecycle. You will be responsible for leading and growing a high performing team and responsible for the process development and external manufacturing to support their Cell Therapy Pipeline (iPSC.
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This position shall actively monitor and report the deadlines, bottlenecks, and manufacturing schedule to help the project and export cable package reach the offshore wind project milestones and ensure that equipment, materials, and components arrive at the right place, at the right time, in the right conditions with the right documentation fulfilled.
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Collaborate with interdisciplinary teams to develop and optimize vector manufacturing processes for gene therapy applications. Preferred: Experience with manual or automated operation of AKTA systems (UNICORN software.
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Strong cross-functional experience and extensive domain knowledge of Oracle Cloud SCM modules (Inventory Management, Cost Management, Procurement Management, Demand Planning, Supply Planning, Product Information Management, Warehouse Management) and good understanding of supporting ERP Manufacturing & Quality Management Cloud modules.
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Interface with construction and manufacturing teams to ensure faithful and profitable execution of VBC projects. Works closely with VBC / Manufacturing Project Managers on project specific items.
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Our products can be seen on structures from parking garages and mixed-use buildings to single-family homes and high-rises, and are also used in the modular, residential window and door, industrial and manufacturing markets.
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We're looking for a few different interns in the Product Supply space:Instrumentation Engineer Laser Process EngineerThe group collaborates across the organization including Research & Development for new product design and Manufacturing for ongoing production in our global manufacturing centers.
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Provide Quality guidance and be accountable for the continuous development, execution and administration of a GxP Quality System meeting all compliance requirements with respect to Good Laboratory Practices (GLP), Good Clinical Practices (GCP) and Good Manufacturing Practices (GMP.
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manufacturing job Title: software eng in Boston, KS, Nevada
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