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Ability to scope and integrate control frameworks and regulatory requirements into enterprise controls and advise on control design to meet cybersecurity risk and compliance needs.
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Assist in regulatory compliance and keep abreast of new developments, techniques and materials as they come about, and insure adherence to proper infection control protocol. Working at UB comes with benefits that exceed salary alone.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Our nearly 1,500 technical and engineering experts have direct industry experience in industrial automation, control system integration, facility and process engineering, architecture, construction management, regulatory compliance, enterprise technology and other consulting services.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Uploading and entering information in a Clinical Trial Management System, eSource Data System, e-Regulatory System, and/or Document Control/Learning Management System. MN Urology is seeking a Summer Clinical Research Intern.
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Ensures that application development and production support processes and practices are compliant with corporate and regulatory standards (both domestic and international). Administers change control process for zero defect system development.
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Regulatory, PCQI, HACCP, SQF, GMPs, food microbiology) Manage Pepperidge Farm QA documentation including creating new documents, revising existing documents, determining training needs, overseeing the approval and distribution processes, maintaining document control database and coordinating document reviews.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Designing, reviewing, and modifying regulatory and advanced regulatory control loops and regulatory loop tuning, alarm and point configuration and console operator HMI graphics.
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Along with the Assistant Director, Medicare Advantage Operations, the Program Manager is responsible for program management activities impacting the functional areas within the span of control of the Assistant Director including but not limited to initiation, planning, development, and monitoring of program implementations and day to day operations performance monitoring in order to ensure timeliness and compliance.
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ComJob Summary:Fully own clinical-related technical writing for medical device regulatory projects (CER, MDD/ MDR compliant format, literature review and analysis) and support clinical projects including study reports and manuscripts.
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Experience in peptide method development, characterization, and analytical control strategy, especially having mass spectroscopy (MS) experience. Support project team lead to author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents.
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SummaryThe Compliance Analyst III – Global Control Room will partner with other members of the team to support the Firm's Information Barrier Program and provide regulatory guidance to key business partners, including, but not limited to, investment banking and research.
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The Document Control Specialist. compliance with all regulatory requirements, including FDA, cGMP, and other industry standards. continuous improvement initiatives related to the document control process.
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Assists the team leader in all aspects of daily operations including profitability, expense control, buying, merchandising, labor, regulatory compliance and special projects as assigned.
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Knowledge of operational support functions such as logistics, procurement, contracts, equipment maintenance, quality assurance-related process control systems, safety programs related to industrial operations, and environmental regulations as applied to support functions.
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Under limited supervision and general direction, you will support the assurance programs responsible for evaluating, assisting with delivery, and reporting results of our cybersecurity regulatory and contractual requirements in addition to supporting the issues management service a responsible for treatment plan consulting, remediation effort progress reporting, and closure validation for findings that result from application assessment and control testing conducted by teams.
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