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Certifications such as CQE from ASQ, Six Sigma Green Belt, certified Quality Systems Auditor highly preferred. Minimum 3 years of experience in Quality, Supplier Quality, or Manufacturing, in the automotive, aviation, or medical device industries or a combination of both Supplier Quality and Internal Plant quality development.
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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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Partner with Quality to implement and manage phase appropriate systems/processes/procedures to meet cGMP manufacturing requirements against regulatory standards in various regions (US/EU/etc.
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Playing a critical role as the subject matter expert (SME) and project lead of Pharmaceutical Development within CMC function, the position will be responsible for pre-formulation studies, formulation and process development, drug delivery design, optimization, scale-up and manufacturing in support of Revolution Medicines pipeline compound development and clinical programs.
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Initiates programs to identify improvements for process reliability, manufacturing yield, product quality, efficiency, and customer service, including reducing operational costs such as labor, materials, energy, and processes.
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Provide analytical support for clinical-scale non-GMP IND-enabling manufacturing operations, including qualification of in-process and release methods and assist in tech transfer in support of GMP manufacturing and release of clinical material.
$140,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Novity, a spin-out from Xerox’s Palo Alto Research Center (PARC), brings truly predictive maintenance (PdM) technology to the industrial manufacturing sector to reduce costly unplanned downtime.
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Our products and services cover a range of industries, including semiconductor manufacturing tools, satellite propulsion, aerospace applications, medical devices, lighting, environmental applications, and academic research.
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Redwood City, CA / Technology Development Manufacturing Sciences & Technology / Contract Adverum is looking for a Manager/Associate Director, Pilot Process Development (PPD), Downstream, to join the Manufacturing Sciences and Technology (MSAT) team at our Redwood City, CA office.
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Work cross-functionally with design, NPI, quality and reliability, manufacturing teams and support new technology integration into products. Perform package design for AI/ML and networking applications custom Si with single-chip/multi-chip and SiP/module packaging, design feasibility studies and analyses to ensure good manufacturing at ODM.Participates early on Si/package/PCB/system co-design, and ODM SMT manufacturing work in product development design reviews providing feedback on manufacturability and helps incorporate latest technology advancements and design rules.
$170,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Out client is looking for a highly skilled, motivated, and creative analytical scientist to join their Vaccine Product Development organization as Scientist I within Protein Development and Clinical Manufacturing.
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We love our environment: We have the only LEED certified paint manufacturing facility in the World! Positions supervised by the Assistant Store Manager may include; Counter Sales, Equipment Repair, Tint Room, Wallcovering, and Warehouse (Shipping and Receiving.
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PhD in Biochemistry, Molecular Biology, Biology or related subject with 0-5 years of analytical experience in the cell and gene therapy manufacturing field. BS in Biochemistry, Molecular Biology, Biology or related subject with 10-15 years of analytical experience in the cell and gene therapy manufacturing field OR.
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Manage manufacturing activities for viral vector and cell therapy, including cGMP aseptic qualification, in support of manufacturing and formulation of viral vectors as drug substance and of cell therapeutics as drug products.
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Experience in tech transfer and process characterization methods, manufacturing under cGMP, validation, and process comparability in a regulated environment. CARGO's founders are pioneers and world-class experts in CAR T-cell therapy, and its team has significant experience and success developing, manufacturing, launching and commercializing oncology and cell therapy products.
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manufacturing six sigma jobs Title: quality engineer in San Mateo, CA
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