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Broad experience in hardware manufacturing: assembly, integration, instrumentation, cleaning, non-destructive testing, leak testing, final acceptance testing of integrated hardware, fabrication, machining, etc.
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3 years' experience of Quality Assurance oversight of aseptic manufacturing and all production stage batch record review and disposition. Full lifecycle review and disposition of parenteral manufacturing Batch Records (Formulation, Filling, Inspection, & Packaging) for Media Fills and Drug Product.
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Overview: The Microcircuit Emulation Center at SRI International (formerly Sarnoff Corporation) is looking for a Wafer Fab Integration Engineer to support the manufacturing of microcircuits (integrated circuits) on-site at our Princeton, NJ office.
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Keywords: GMP, GLP, GXP, GCP, batch record management, batch record review, full-process manufacturing, cell therapy, deviations, junior role, maintenance, calibration, FDA, EMA, biopharmaceuticals, quality assurance, QA.
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Lead batch disposition activities, including review of manufacturing batch records, QC test records, audit trails, and assembly of batch release package. The ideal candidate will have both early and commercial stage-experience, including applicable contract manufacturing, cell therapy, and viral vector experience.
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At least 5 years of experience in CMP and other device manufacturing techniques (Electroplating, Liftoff, Photolithography, etc.) The responsibilities consist of but not limited to: wafer data review and disposition; create & modify recipes and set up APC on various CMP tools; communicate to the primary process/metrology/integration engineers and production line; understand the application & reliability of metrology tools such as AFM, topography, SEM/FIB/TEM, etc.
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Job DescriptionJob DescriptionThe CompanyScorpius BioManufacturing is a boutique biologics CDMO providing cGMP manufacturing, bioanalytical, and process development services for protein modalities.
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This includes, but is not limited to, raw materials, vector, supplier quality, audits and inspections, training, quality systems, quality operations, quality control, contract testing labs, and contract manufacturing organizations.
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Coordinate the introduction of production from design, to supplier, or in-house fabrication, into the manufacturing environment, oversee assembly of machined and fabricated components, and integration/inspection of assemblies, and disposition of non-conformances.
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Reporting to our Senior Manager, Quality Assurance CMC, this position is responsible for managing, reviewing, and approving quality documents from Contract Manufacturing Organizations and Contract Testing Laboratories for manufacturing, testing, validation, and disposition of clinical and commercial products for human use.
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The 2nd shift Quality Inspector is responsible for quality assurance and quality manufacturing functions such as generating certificate of compliance, inspection and testing, disposition of product, incoming inspection, in-process and final inspection, review of DHRs (device history records.
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Knowledge of electro-mechanical assembly manufacturing control and quality problem-solving tools, i.e., 8D, corrective/ preventive action, FMEA. 3 years plus experience in quality, engineering, electro-mechanical product manufacturing, or supplier quality management.
$61,213 - $107,122 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Contract Manufacturing Manager will interact with and support Marketing & Sales as well as all other functional departments including Operations, Logistics, Demand Planning, Quality, Research & Development, Procurement, and Finance across within the Post Consumer Brands business unit and across Post Holdings.
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Assist/Direct with product inspection and disposition in Manufacturing, raw material inspection and disposition, work instructions, gage instructions, pack instructions, sorting activities, PPAP activities, Gauge R&R, layout inspection, capability studies, and handling dispositions of returns.
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Located in our Elizabethtown, KY plant, you will be a Health, Safety, & Environmental Manager for our manufacturing facility. Manage all requirements related to chemical management including chemical approvals, GHS complaint labeling, employee training, and proper disposition.
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