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0-2+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish.
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Qwaltec is looking for a Flight Operations Team Lead to support the NASA Goddard Space Flight Center (GSFC) On-Orbit Servicing, Assembly and Manufacturing (OSAM-1) Mission under the Ground System and Mission Operations (GSMO-3) contract.
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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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The Electro-Mechanical Technician will be responsible for the rapid manufacturing of sub-assemblies and finished systems. 2+ years’ experience in manufacturing or research and development (R&D.
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Follow manufacturing guidelines and procedures. Leidos currently has an opening for an Electro-Mechanical Technician to work in our Ladson, SC facility. Solder wires, PCBA’s, and components. We provide automated threat detection for weapons, narcotics, explosives, contraband, and undeclared goods, as well as nuclear and radioactive materials, by leveraging industry leading screening technologies, AI/ML capabilities and advanced biometric tools.
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The Operations Manager will lead all aspects of a multi-product (Cell Therapy, & Single Use Assemblies/Final Fill Solutions) operation at the Life Sciences Manufacturing Facility in Gaithersburg, MD.
$154,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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In addition to manufacturing duties, the candidate will support process development in creating production processes for new synthetic biology-based cellular medicines. The ideal candidate will have hands-on experience in biotech manufacturing, a solid understanding of bioprocess engineering, and a commitment to maintaining high-quality standards.
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Members of the PPS function work closely with other development functions and manufacturing sciences to develop and transfer clinical and commercial purification processes. The position resides in the Purification Process Sciences group (PPS) within the Bioprocess Development R&D (BPD) department.
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Columbia Care is one of the largest and most experienced cultivators, manufacturers and providers of cannabis products and related services, with licenses in 18 U.S. jurisdictions and the EU. Columbia Care operates 130 facilities including 99 dispensaries and 31 cultivation and manufacturing facilities, including those under development.
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Serves on team projects (i.e. qualifications, investigation) in the role of testing support and initiation of investigationResponsible for completing laboratory housekeeping to ensure safety and complianceIdentifies areas for improvement or gaps in both safety and compliance (ZAPs/ZIPs)Effectively communicates issues/hurdles to supervisor and/or managerSupports GSK site initiatives and departmental goalsJob requires gowning into GMP manufacturing spaces to collect samples.
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They will work with an EPCM team but, as project managers, should also be competent in project execution, including but not limited to: Change Management Project Controls (Risk, Schedule & Cost Engineering) Engineering Design and Quality Management Resource Management Contractor Management Construction Safety Management GxP Fundamentals (Documentation, Manufacturing, etc.
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Individual with experience must have knowledge of unit operations typically used in biotech and vaccine manufacturing such as bulk manufacturing, downstream operations, formulation, steaming (SIP) and cleaning (CIP.
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In this role, you will be responsible for the oversight of the Quality Risk Management, CQV, CSV programs for the Cell Therapy operation of the Rockville Manufacturing Center (RMC) facility. Accountabilities:As the Associate Director of Quality Engineering, you will provide leadership, direction and mentoring to ensure that the QE organization is successful in meeting the quality and manufacturing objectives in support of site goals.
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In this role, you will serve in a deputy program manager capacity as a trusted agent directly supporting client program managers, acting to support all aspects of planning, management, and execution of a growing defense R&D and manufacturing program.
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Conduct clinical research studies involving administration of investigational products according to the principles of current Good Clinical Practices (cGCP), Good Laboratory Practices (cGLP), and Good Manufacturing Practices (cGMP) and in accordance with all relevant host nation, US Federal, Department of Defense (DoD) and Army regulations and policies.
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manufacturing job Company: Ey in Rockville, MD
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