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Experience must include 6 months in each of the following: mechanical engineering; MES; 5S; Kaizen; Six Sigma; Quality Tools; Lean manufacturing; VSM; PFMEA; and Computer-Aided Design (CAD) software.
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Learn how to operate the bio-pharmaceutical manufacturing equipment such as: incubators, stainless steel and disposable single-use bioreactors, depth filtration skids, LN2 dewars, chromatography skids, single-use mixers, centrifuges, cleaning/sanitization of equipment, washers, autoclaves, environmental monitoring cleaning verification sampling, tanks and in-process testing instruments.
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The qualified individual will bring experience in relevant analytical technologies, such as ELISA, SRID, Luminex, or BLI. The position will perform in-process testing, as needed, to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification.
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Working knowledge of principles and applications associated with manufacturing operations including SPC, Six Sigma, 5S, SMED and Lean Manufacturing. Evaluate manufacturing processes by designing and conducting research, applying knowledge of product design, fabrication, assembly, tooling, and materials.
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Lead lab-scale cell culture or purification experimentation to troubleshoot manufacturing issues or support new product introduction. Technical aptitude, a passion for science and a keen interest in pharmaceutical manufacturing.
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At Thomas, we're revolutionizing the manufacturing industry with our cutting-edge omni-channel growth marketing strategies. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity.
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Manage a team of Manufacturing Associates in Protein Purification conducting purification operations including chromatography, filtration, titration, and column packing and unpacking. The Manager/Sr. Manager, Protein Purification Manufacturing is responsible for leading, planning and driving the execution of manufacturing production operations in the Protein Purification area of cGMP manufacturing.
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Qwaltec is looking for a Senior Mission Operations Engineer to support the NASA Goddard Space Flight Center (GSFC) On-Orbit Servicing, Assembly and Manufacturing 1 (OSAM-1) mission under the Ground System and Mission Operations 3 (GSMO-3) contract.
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Minimum 5 years of work experience in clinical or commercial biologics or cell therapy manufacturing under cGMP. Join us at AstraZeneca as an Associate Director Digital Manufacturing Systems at our cell therapy facility in Rockville, Maryland, the newest addition to our global supply network.
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The Field Service Technician will be working to maintain and troubleshooting sophisticated mechanical equipment integral to water purification, and delivering top-tier water solutions for critical water systems in various industries, including pharmaceuticals, life sciences, industrial power, electronics, and manufacturing.
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MasTec's Clean Energy and Infrastructure Group (CE&I) is a $4 billion annual revenue business unit that provides construction services for industrial facilities; building products manufacturers, power generation facilities, manufacturing plants; solar, wind, and thermal energy plants; buildings, and infrastructure.
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Identify, develop and implement Manufacturing and Process Safety Programs designed to address site-specific requirements in cGMP and non-GMP areas within Development and Manufacturing. Provide support and guidance to the Development and Manufacturing Leadership Team on scheduled shutdowns and equipment changeovers, as well as Project Managers on Capital Projects.
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Serve as bioprocess SME that provides technical oversight in support of IND filling and to ensure that clinical manufacturing is successfully executed per schedule. Independently author technical reports of studies, protocols, SOP and risk assessments to enable technology transfer, manufacturing and IND activities.
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Our systems are used in a variety of industries including aerospace, shipbuilding, heavy equipment manufacturing, machine tool, energy and construction verticals. At the corporate headquarters in Rockville, MD, we are currently seeking to add to the team an Instrumentation Engineer.
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Interacts with Regulatory Affairs, and Manufacturing to ensure that regulatory submissions meet domestic and international standards and regulatory requirements. Collaborates with manufacturing, clinical and regulatory groups to ensure site quality.
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manufacturing job Title: picker Company: Ryder in Gaithersburg, MD
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