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ElevateBio is looking for a Cell Therapy Manager, QA Operations to join their growing Quality Group at our BaseCamp facility in Waltham, MA. In this role, the Manager will be primarily responsible for providing Quality oversight over execution of clinical cell and gene therapy manufacturing for cGMP compliance through on the production floor interactions, review and approval of batch related documents, and events.
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The Manager is a hands-on manager that can organize and lead a team of QC personnel, support and execute QC testing, and contribute significantly to overall Quality Control strategy The ideal candidate will have experience working in a GMP QC laboratory setting, experience with cell and gene therapy test methodologies, compendial safety testing and enjoy a fast-paced, collaborative, and vibrant startup culture.
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Experience developing quality control plans, supplier quality audits, failure analysis, and root cause corrective actions. 2 or more years of related experience in Manufacturing and/or Quality Engineering.
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The Manager, Quality Control has responsibility for actively overseeing cGMP quality control activities associated with development and commercialization of the company’s small-molecule assets.
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Entrada is seeking a Director, GCP/GLP Quality to manage GCP and GLP quality assurance activities. Works across all levels in the organization to deliver GCP/GLP Quality compliance.
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The Sr Manager, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as varied vendors supporting Clinical Studies.
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Assist the Department Head or General Manager with maintaining compliance with Preventative Maintenance and Deep Cleaning Programs through the daily and/or weekly inspection of rooms with the Housekeeping Manager and Property Engineer.
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The Project Controls Manager has responsibility for the overall financial reporting and forecasting, change management, scheduling, document control, and project administration. Skanska is searching for a dynamic Project Controls Manager.
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The Facility Quality Manager will be responsible for ensuring the compliance of the quality systems, manufacturing processes and associated records for adherence to Nestle Health Science.
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2-3 years in a healthcare specialty required; experience in apheresis, cell therapy/ stem cell transplantation, bone marrow transplant, hem/onc, laboratory medicine, and/or regulatory compliance/quality assurance preferred.
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As part of the Clinical Operations organization, and within the Clinical Data Management team, the Senior Manager, Clinical Data Management is a critical role to ensuring the highest quality clinical trial data is available to support company objectives and claims.
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The CLIA Quality Manager will collaborate with direct and/or delegated authority to ensure the CLIA Quality Management Systems (QMS) are effective and compliant with applicable requirements, provide leadership and guidance re: CLIA and associated regulations, and support the Lab Director and leadership in maintaining audit readiness.
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Knowledge of hotel operations, including marketing plans, security and safety programs, personnel and labor relations, preparation of business plans, repairs, maintenance, budget forecasting, quality assurance programs, hospitality law, and long-range planning.
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Apply today and shift your career into drive for tomorrow as a Car Sales Finance Manager ! The Car Sales Finance Manager is responsible for managing retail business including sales, finance and sales team.
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Develop and apply rigorous standards and processes to quality control the raw material, intermediate processes, and the entire workflow in nucleic acid analyses and nucleic acid assay development so that valid conclusions could be drawn.
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Title: quality manager Company: Lighthouse Professional Services in Waltham, MA
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