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Duties include ASSB electrodes manufacturing process development, scale up manufacturability development, design and execution of cell builds and analysis/interpretation of results vs. Work with multiple R&D teams to select materials and design processes for optimization and manufacturing of cells for next generation all solid-state batteries.
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In financial crimes risk management, Quantifind's solution uniquely combines internal financial institution data with public domain data to assess risk in the context of Know Your Customer (KYC), Customer Due Diligence (CDD), Fraud Risk Management, and Anti-Money Laundering (AML) processes.
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The Senior Manager, Manufacturing Technical Operations (MTO) is responsible for managing compliance related Quality records including, but not limited to, Deviations, CAPA’s, Change Controls, Risk Assessments and Analytical and Quality Control Investigations supporting Biopharma Cell and Gene Therapy (CGT) in Boston, Cambridge, and Providence.
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This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). As a Cyber Risk Principal Associate within the Governance and Risk division, you see security as an innovation enabler and differentiator, not a step in the compliance process.
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Full command of Microsoft Word, Excel and PowerPoint along with related financial services software including S&P CapitalIQ, S&P Leveraged Commentary, Advantage Data, Bloomberg, Thomson One, Thomson Loan Pricing Connector, FactSet, etc.
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PhaseForward Inform, Oracle Clinical and/or other clinical data management software desirable;General software skills: MS Access, MS Word, MS Excel, MS Project, Visio, familiarity with medical coding dictionaries, especially MedDRA and WHODRUG.Experience applying best practices in clinical data management programming in the clinical trial environment, including requirements definition and QC plansKnowledge of GCP and other regulations.
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Reporting to the Vice President of Clinical Operations, the Trial Master File (TMF) Associate Director / Director serves a key role, working across the organization for the execution of TMF Operations processes and strategy.
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Extensive knowledge of current game titles, as well as movies and other visual arts, to use as reference for crafting and communicating original ideas. Work across disciplines with engineers, artists, sound designers, and production to shepherd 3Cs systems and mechanics through the production pipeline, from initial conception to shipping.
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Collaborate with other departments, such as Marketing, Finance and Artistic Planning to optimize overall sales performance and streamline processes. This role is responsible for rigorous data analysis and insight development; application of those insights to the seasonal programming and financial planning processes; and development of ticket pricing, revenue budgets and forecasts.
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REQUIRED: Masters in Public Health or in another Social Science discipline is desired OR a Bachelor's degree required with a minimum of five (5) years work experience in healthcare clinical research operations.
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Strong grasp of electrochemistry, chemical engineering, and materials science fundamentals. The role will focus on electrochemical characterization techniques, design and/or fabrication of electrochemical components, operating electrochemical reactors and systems,as well as physical and chemical characterization.
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The Director, Digital Employee experience will lead team of IT Support engineers and desktop tooling teams to design and deliver digital experience to PTC employees. Partner with Service Management on the design and execution of ITIL processes.
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Collaborate with our design engineers to apply DFMAT, APQP, and Lean manufacturing strategies starting at the design of hardware through build and delivery. Provide direction to both manufacturing engineers and technicians on a production floor for the assembly and integration of a variety of opto-mechanical and electrical assemblies.
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Lead and manage multiple drug discovery projects, overseeing the entire drug development process from target identification to preclinical development. Deep understanding of the drug discovery process, including target identification, hit-to-lead optimization, and preclinical development.
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Work within an interdisciplinary team of molecular biologists, computational biologists, software engineers, and scientific leaders focused on developing diagnostic products using massively parallel sequencing of tumor genomic DNA and RNA.
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