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Join Adecco's team in Bothell, WA as an Electro-Mechanical Assembler and seize exciting opportunities!
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Experience with commercial scale manufacturing support for mammalian cell culture, aseptic final product filling/kitting/ labeling, liquid media manufacturing (vials, bags, bottles) and/or analytical reagent (e.g. endotoxin detection assay) manufacture, current Good Manufacturing Practices, US/EU regulations, and supervision.
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Create and modify PCBA design packages and electrical component specifications, including but not limited to electrical circuit schematics, PCBA manufacturing specification packages, and wire harness / cable assembly specifications for products currently in production phase.
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Define, develop, validate, release and refine PCBA and system test programs and related documentation for internal use, and by international manufacturing partners. The Manufacturing Test Engineer II shall develop and maintain test software, hardware, processes, and procedures as required for the production testing of medical electrical components and systems, and ceramic crystal transducers, in an FDA regulated environment.
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Draw on experience with: Lean Six Sigma, automation Delta V, manufacturing execution systems (MES), data analytics, process modelling, and statistical analysis, aseptic operations, validation to set strategic direction for the site, including leadership of process improvement activity, capacity increases and introduction of the clinical pipeline into the site to deliver on pivotal and commercial launch responsibilities.
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The MES Recipe Engineer and Validation Specialist role will deliver electronic batch record (EBR) configuration and validation in the Emerson Syncade Manufacturing Execution System (MES). Experience with cell therapy or other biopharmaceutical manufacturing.
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Collaborate with Manufacturing, Supply Chain, Quality, Facilities and Tech Transfer departments, capturing and documenting detailed requirements. Perform application support duties for the manufacturing execution system (MES) as needed.
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Our client, Thermo Fisher is seeking a Manufacturing Operator to join their team. Job Title: Manufacturing Operator. Minimum 1 years of directly applicable experience as an Electro-Mechanical assembler.
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Experience with manufacturing equipment and processesBroad background in surface science, materials engineering, and precision assembly techniques desired. Three to five years’ experience in process development in the manufacturing of devices (preferably medical) requiring a high degree of traceability and documentation.
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The Manufacturing Lab Technician is responsible for supporting the production of reagents used in various NanoString Analysis Systems, for example, nCounter and GeoMx. The role requires learning and performing both manual and automated production processes for the manufacturing of raw, intermediate, and final reagents needed for the multiplexed detection and the quantification of many different types of target molecules from biological samples.
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Performs general and/or more complex manufacturing formulation batch production record reviews and approval in support of product release in accordance with specifications and SOPs. Knowledge of biotech product manufacturing.
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Perform preventative maintenance work on equipment such as steam boilers, HVAC systems, pumps, pneumatic valves, fire sprinkler systems, compressed air/vacuum systems and other utility systems and equipment supporting the facility and manufacturing areas.
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Analyzes and recommends product design changes including packaging design for ease of manufacturing, cost reduction and quality improvement. Education & Experience Bachelor's degree (B.S.) in Industrial/ Manufacturing or Mechanical Engineering required Minimum of 4 years related experience in Manufacturing Engineering or Industrial Engineering Training in LEAN Manufacturing and Six Sigma preferred.
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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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The Quality Assurance (QA) Associate Director (AD) will be responsible for leading multiple shifts and two sites (Bothell and Seattle), who are involved in the daily activities of manufacturing, assessing and releasing drug products at the Bothell site, and providing quality oversight of Viral Vector Determination Team at Seattle (Dexter.
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manufacturing job Company: Eclaro in Bothell, Peoria, Arizona
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