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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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The successful candidate will apply their expertise in small molecule process development and manufacturing towards a variety of modalities in the Immunome pipeline including antibody drug conjugates, radiopharmaceuticals.
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Summary:As a Sr. Manufacturing Associate, you will provide manufacturing engineering and process development support for critical and proprietary processes used in the manufacture of medical ultrasound transducers.
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Education & ExperienceBachelor of Science degree in Mechanical, Automation, Manufacturing or Mechatronics Engineering. This role provides the opportunity to work within the Network Solutions Business Unit of Leviton Manufacturing Company Inc. ResponsibilitiesDevelop concepts and detailed designs for complex mechanical mechanisms that manufacture, inspect and validate products using CAD software.
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Certification in lean manufacturing (Ex. IASSC Sig Sigma Black/Green Belt, SME Lean Gold, etc) Understanding of Lean Manufacturing concepts and methods. Minimum 10 years' experience in manufacturing and distribution, preferable with an industrial OEM.
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The Principal Scientist will be a foundational member within the Delivery & Device team, with the opportunity to work in a dynamic cross-functional environment (clinical, development, commercial, manufacturing) and establish the core capabilities of delivery science at Seagen.
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Manufacturing Test Engineer II - Bothell, WA. 2-3 years demonstrated experience in a working in a manufacturing environment. Exposure to Orcad, PADS or other schematic and PCB layout-related software tools.
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PURPOSE AND SCOPE OF POSITION (Position Summary): 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.
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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.
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Acara Solutions has been providing staffing services to medical device, aerospace and other advanced manufacturing firms for 65 years. Our medical device client in Bothell, WA is looking for a Senior Strategic Sourcing Manager to join their organization.
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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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System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
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Strong working knowledge of cGMP regulations and Regulatory Agency requirements applicable to biologics and cell therapy manufacturing. The Director, QC is a key member of the Quality Control Leadership Team responsible for the design, implementation, and continuous improvement of all processes/systems in support of the Quality Control testing program at the Bothell Cell Therapy manufacturing site.
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Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. At Bristol Myers Squibb we are reimagining the future of cell therapy.
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Experience in the biotech and/or pharmaceutical manufacturing industry preferred. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and technologies, as well as customized services for the scale-up and cGMP manufacturing of protein-based therapeutics.
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manufacturing job Company: System One in Bothell, Peoria, Arizona
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