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15 years of experience in pharmaceutical manufacturing operations in Cell Therapy Manufacturing and/or Biochemical Manufacturing, manufacturing science and technology, manufacturing systems, and/or quality assurance with at least 6 years in senior management positions.
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Since integrating into Lundbeck in October 2019, Lu-SBP has supported commercial launch of Lundbeck's first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes.
$31.25 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The work will be highly collaborative and provides support to and engagement in Speak Up Event Review Committee (ERC), supported by agreements between Boeing, Labor Union(s), and the FAA. Provide staffing/support of Speak Up triage meetings and fact-finding efforts, and support IRT (Issue Review Team) investigations of Ethics cases requiring technical knowledge/expertise in manufacturing and quality processes & systems.
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The position will directly report to a Downstream lead and assist in downstream process development and tech transfer to GMP manufacturing facility. Establish relevant process transfer document and cGMP documents to support successful implementation of process technology in clinical/commercial manufacturing operations including Standard Operating Procedures (SOP) draft and review.
$90,000 - $120,000 a yearExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Associate Director Business Process Optimization & Systems is part of the Cell Therapy External Manufacturing (ExM) organization and reports to the Sr. Director Global Business Process & Supplier Digital Strategy.
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Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. The Quality Assurance Specialist position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant (Jump.
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Expertise in demand management processes, problem solving, lean principles, business practices and SAP/ Rapid Response systems. Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status.
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Six Sigma Green or Black Belt training and certification. Comfort and experience in lean manufacturing. Modern Hydrogen has an immediate opening for a Senior Manufacturing Engineer to develop our Design for Manufacturability / Design for Assembly (DFM/DFA) competencies.
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Our nationwide network of over 3,000 partner manufacturing facilities enables us to maintain consistently fast lead times while offering a broad array of capabilities, including CNC machining, 3D printing, sheet metal fabrication, injection molding, and urethane casting.
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Possess a Six Sigma Green Belt. CSCP is responsible for strategic sourcing, customer demand forecasting, capacity planning and management, supply chain planning and execution, capacity provisioning, and decommissioning and dispositioning of datacenter assets worldwide.
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Knowledge of Quality Assurance methodologies, Lean Manufacturing Principles, and Statistical Analysis is a plus. RPI, a global leader in print-on demand, is currently seeking a Product Manufacturing Engineer to drive manufacturing improvements and assure consistency across all locations throughproduct implementations, process improvement, quality assurance methods, and manufacturing standards management.
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Discover More About DNRP : Visit our website, explore an interactive map of our recent accomplishments and check us out at Facebook, X (formerly Twitter), LinkedIn, TikTok, Instagram, YouTube and Keeping King County Green News.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Deep expertise and industry experience in cell therapy process development principals including DOE and experience with current technologies in PSC process development and manufacturing, particularly scalable stem cell culture systems such as bioreactors.
$290,000 - $340,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum.
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Leading a diverse team of scientists involved in purification process development, characterization, and validation, including technology transfer to cGMP manufacturing for hybrid and continuous processes.
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green belt lean manufacturing jobs in Kirkland, WA
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