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Experience being responsible for quality control of all scientific data generated within the Nonclinical Pharmacology group. This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group within GNAT unit of client.
$32 an hourExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Record and review GMP data, monitor and evaluate QC systems and equipment, recommend improvements to procedures, and revise GMP documentation as required. Oversee and continuously improve FDA / regulatory compliant Quality System for QC laboratory system.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The position requires knowledge of quality systems, statistical tools, lean six sigma methodologies, process capability, and understanding of control plans and process flow. The Senior Appliance Quality Engineer responsible for taking our Appliance products to the next level of quality, reliability, serviceability, and attribute leadership by using DFx tools and processes.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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This is a hands-on systems/data analysis and project management role, that collaborates with the business users, technical teams, and vendors for solution implementation projects. In this role, you will be a subject matter expert for business processes, workflows, systems, and data.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Oversee the implementation and monitoring all tracking systems related to data reporting requirements. Rehab Systems Management Provides supervision in all areas of the Day Hab Systems reporting standards to ensure organizational compliance with all DMA, DDS regulations.
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In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
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The Scientist, Analytical Development & Quality Control is responsible for analytical development, feasibility, method qualification, routine, and stability testing of antibody drug conjugates and intermediates.
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The Senior Analyst / Scientist will work cross-functionally with others in Quality Control, Analytical Development teams, Quality Assurance, and Manufacturing, as needed. The Senior Analyst/ Scientist, Quality Control Chemistry, will support external laboratory testing and internal study protocol design, study report review and IND support as needed.
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Establish vision and strategies for CMC Regulatory and CMC Quality Assurance and Quality Control, ensuring proper integration with Global Regulatory and Clinical Quality leadership and business systems.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Assurance Change Specialist based onsite in our Tewksbury, MA facility. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Manage CMC aspects of tech transfer, manufacturing and distribution by routinely interfacing with other departments, such as Commercial, Clinical, Regulatory, Quality Assurance and Quality Control.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Must have strong knowledge of biologics and small molecules manufacturing, materials management, quality control, quality assurance and CMC regulatory requirements. Responsible for all aspects drug substance including conjugation process development, validation, characterization, scale-up, tech transfer, analytical method qualification, specifications, release and stability testing.
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Assess change controls for impact to validated computer systems and participate in corrective and preventive actions (CAPA) and other Quality Management System (QMS) activities. systems, laboratory systems and other systems supporting clinical manufacturing or quality processes.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Leadership in areas of Lean Manufacturing, KAIZEN, ISO quality systems, innovation, and current systems technology. Preferred: Experience with Lean Manufacturing and ISO quality systems.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Posted job title: Travel CT Tech - Cat Scan Technologist. Travel CT Tech, CT Technologist Contract, Travel CT Tech, Allied Health Travel Positions, Travel Medical Imaging Jobs, Imaging Technologist Travel Assignments, Travel, Contract, Assignment, Traveling CT Tech Assignment, CT Tech, Contract CT Tech, CT Tech, CT, Healthcare.
$2,857.49 a weekPart-timeExpandApply NowActive JobUpdated 9 days ago
quality tech systems jobs Title: senior data scientist in Bedford, MA
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