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Responsible for Attending progress review meetings with the Project Controls Manager to facilitate timely and accurate recording of progress into the Project Schedule and project reports. Strong knowledge and awareness of governing HSE management plans and exercise the responsibilities contained in these plans, and model safety leadership to the project team, including project safety statistics (AI / MTI / LTI.
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Analyze, model, document process and procedures, and recommend solutions for efficiency improvements in support of HSPD , NERC CIP, DOE personnel security, information security, and OPM program requirements.
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Tentatively Wednesday & Thursday)Requirements Bachelor's degree Basic familiarity with Microsoft Office 5-8 years of related contract management experience Strong attention to detail, responsiveness, and timeliness in work Experience with document review, editing, and formatting.
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Regulatory Document Review – Virology section (IND, BLA) for accuracy of test results. · Define business operation model for the virology lab (i.e. capacity planning, activity scheduling, sample projection, and metrics.
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5+ years of experience conducting the following activities: Business requirements gathering, fit-gap analysis, functional process design, system configuration, system testing (INT,UAT) and solution delivery, customer support, process document creations and review, working with onsite and offshore delivery model.
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Create, document, review and approve journal entries (e.g., journal upload, general ledger queries). Careers with Optum offer flexible work arrangements and individuals who live and work in the Republic of Ireland will have the opportunity to split their monthly work hours between our Letterkenny and telecommuting from a home-based office in a hybrid work model.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Review and document work products to ensure compliance with funding requirements, including document submittal checklist, plans and specifications review, bid document review, executed contract review, user charge methodology and drinking water model use ordinance review, and other checklists as necessary for project management.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Set up and maintain structures to manage the work of the team (using the systems, tools, and standards provided) including, but not limited to, engineering management, contract management, document control, testing, and accurate and timely cost and schedule reporting to ensure the highest quality practices are embedded in all aspects of engineering and project management.
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Advise case teams regarding legal technology and workflow design appropriate for all phases of the eDiscovery Reference Model (EDRM), including forensics collection, document review, and trial presentation.
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Review/Staff acquisition/requirements documents (, ICD/CDD, ADM/APB, TEMPs and test plans, ILS/ISP, and Rapid Prototyping Requirements Document). Review DT/OT products; monitor test results; participate in DRB; resolve/track DRs. Provide IOC/FOC and Ops Acceptance recommendations.
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Responsible for review of study documentation for Trial Master File (TMF) quality for sponsor and/or CRO. The Clinical Document Lead (CDL) is responsible for the high-level QC of the eTMF and for all work completed by the Clinical Document Specialist (CDS) Team. As a senior employee, the CDL is involved in helping to mentor and train new employees with direction from the CDTM. The CDL is also r sponsible for reporting on deadlines to the Project Manager and Client when needed.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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A minimum of one year in a supervisor-level position or two years of industry-related experience, including a solid understanding of the data processing, litigation support and document review processes, is required; experience in collaborating across shifts is desired.
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Familiarity with the eDiscovery industry – Electronic Discovery Reference Model (EDRM), technology, global legal framework, and competitive landscape – is strongly preferred. ·Supervise, guide, and lead team members by acting as a role model, coaching for performance, allocating work, and providing technical guidance and training to all team members.
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O Work with stake holders to understand and document requirementso Develop specification, design, and test resultso Review test cases and validate test resultso Conduct reviews of requirements, design, Code Required Skills: o 4-8 years of experience in Model Based Development using MATLAB-Simulink preferably for automotive, off highway and agriculture machineryo Knowledge is pneumatic and hydraulics controls and controls strategyo Familiar with Code generation for targets, and experienced in C/C.
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They will document and present model validation findings to model owners and developers and will interface with key stakeholders, regulators, and internal auditors to discuss the justification and reasoning behind various validation and review findings.
Full-timeExpandApply NowActive JobUpdated 10 days ago
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