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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 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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CFS is seeking an experienced Quality Inspector to lead inspection and test activities for the SPARC project. To that end, CFS has assembled a team of leaders in tough tech, fusion science, and manufacturing with a track record of rapid execution.
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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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Collaborate with cross-functional teams, including the CDMO joint project team, Obsidian Process and Analytical Development, Quality Assurance, Quality Control, and Regulatory to assure effective tech transfers and start-up of new manufacturing processes according to agreed upon timelines in support of business objectives.
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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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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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Pay Information $3,062 per week About The Position MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality CT Tech for a contract with one of our top healthcare clients.
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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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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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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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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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quality control tech systems jobs Title: senior data scientist in Lexington, MA
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