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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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Collaborate across Process Development, Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs, Finance and Technical Development for successful commercialization of late-stage portfolio.
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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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PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. Perform and support troubleshooting activities related to manufacturing and laboratory equipment and building utilities, such as mechanical, HVAC, electrical, and plumbing.
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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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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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This position is responsible for directing all aspects of CMC (Chemistry, Manufacturing and Controls) for pharmaceutical drugs and agents as well as the analytical work associated with that CMC across all of the small molecule projects within Pharma Cinq and, potentially, gene therapy projects.
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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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The individual in this role will report to the Vice President, Advanced Manufacturing Technologies and will partner with other USP business leaders and organizations, including Pharmatech Associates, Global Biologics, and Global and Federal Practice, to coordinate companywide AMT Biologics efforts.
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TTI is a world-class leader in design, manufacturing and marketing of power tools and accessories, outdoor product equipment, and floor care products. Our brands include Milwaukee®, AEG®, Ryobi®, Hart ®, Oreck®, Hoover®, Dirt Devil® and Vax.
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May require 10+ year in the in DoD program and/or materials management and in production manufacturing operation utilizing MRP/ERP depending upon the job discipline. Experience in finance, contracting, export regulations, engineering, logistics, manufacturing and supply chain management.
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10 years of experience in facilities management and engineering, with at least 5 years in a leadership role within a biopharmaceutical, CDMO, or gene therapy manufacturing environment. Familiarity with automation, process control, and HVAC systems tailored to biologics manufacturing.
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For Eyes is part of EssilorLuxottica, a global leader in the design, manufacturing, and distribution of ophthalmic lenses, frames, and sunglasses. BASIC QUALIFICATIONS Doctor of Optometry Commitment to quality patient care Knowledge of current Optometric theory & technology Strong communicator & listener Problem solving ability Solid Organization skills Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements.
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The Senior Materials Management Coordinator will work with the Associate Director of Materials Management in managing day-to-day activities surrounding Material Management, including but not limited to the Material Planning, purchasing, receiving, shipping, storage, maintenance, and consumption of raw materials for the GMP Manufacturing, Process Development and Research Grade Production team.
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manufacturing job Company: Horizon Therapeutics in Rockville, MD
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