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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.
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Experience with the use of quality systems and tools (for example, CAPA, Six Sigma methodology, change control, Statistical Analysis, Control Plans, and document management.
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CFS is seeking an experienced Quality Inspector to lead inspection and test activities for the SPARC project. Commonwealth Fusion Systems (CFS) has the fastest, lowest cost path to commercial fusion energy.
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At least 1 professional security management or risk management certification: Certified Information Systems Security Professional (CISSP), Certified Information Security Manager (CISM), Certified Informations Systems Auditor (CISA), Certified Risk & Information Systems Control (CRISC), Certified Information Privacy Professional (CIPP) or Open FAIR Certified.
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The Lead of Quality Control and Analytical Development is responsible for managing a team that provides quality oversight in support of clinical and commercial operations and analytical development of early and late-stage clinical products.
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Participate in project kick-off teams improving quality aspects of product introduction, and have a fundamental understanding of quality systems, SPC, and control plans. Support quality improvement efforts, Internal Auditing and Continuous Improvement initiatives.
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Proficiency in Model-Based-Design principles and best practices within the MATLAB/Simulink environment, coupled with extensive experience using MATLAB/Simulink toolboxes for control systems design, signal processing, and embedded C/C.
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Experience in troubleshooting support of electric distribution operations using control room computer systems assets, remote switching and/or dispatching of electrical distribution equipment via SCADA, preferred.
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The QA Supervisor will manage the quality of raw material, in-process material and finished product, ensuring the existing product manufacturing procedures, GMP, HACCP, weight control and other quality control procedures are followed and are updated when necessary.
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Rehab Systems Management Provides supervision in all areas of the Day Hab Systems reporting standards to ensure organizational compliance with all DMA, DDS regulations. He/she will coordinate all aspects of the Day Hab Systems reporting standards to ensure organizational compliance with all DMA and DDS regulations and have the ability to teach others and provide constructive feedback and supervision.
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Assist peers with demand work orders and alarm responses via control systems. Experience in the building controls industry, experience with building control and monitoring systems preferably in a Medical Center environment.
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The Alloy Global Bioanalytics group provides bioanalytical support to all Alloy activities, including assay development, quality control, and high-throughput characterization of antibodies, TCRs, TCR mimics, and other modalities.
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Harvard is part of a collaborative consortium of researchers that includes NYU, UCSF, Mt. Sinai School of Medicine, the Institute for Systems Biology, and the Army Center for Environmental Health Research.
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Job Title: Quality Systems Engineering Manager. Experience in semiconductor or electronics manufacturing industry in the functional areas like Quality Management Systems and audits.
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quality control systems jobs Title: senior scientist in Woburn, MA
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