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Experience in the configuration and setup of ECM document imaging, document management, document import processing, workflow, electronic forms (html, unity) and reporting modules.
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However, it does not encompass all tasks that may be carried out by the Document Management Specialist. We are seeking to fill a Document Management Specialist position! Must be proficient in the use of Microsoft Office programs (including Word, Excel, and PowerPoint), Google suite (Gmail, Google drive, Google docs, Google sheets, Google sites), and Adobe Acrobat Pro for ad hoc projects and document management needs.
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The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
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Title: Document Specialist Location: Cranbury, NJ Schedule: M-F Full Time Type: Direct Hire Responsibilities The Document Specialist is responsible for maintaining all production and quality related documents according to the SQF & FDA requirements.
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Document patient’s daily participation and progress on progress note in an accurate and timely fashion and obtain the co-signature of the OTR. Ensure MD orders are obtained for treatments, re-certifications, and discharges.
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Commercial building inspection ~ fire safety ~ industrial safety ~ environmental safety ~ construction work ~ customer service ~ online reporting and document handling ~ ability to travel approximately a 50-mile radius.
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Provide application/technical support for an EDMS (Electronic Document Management System) called Document Control & Archiving (part of the Syncade Suite) by Emerson Process Management. Provide application/technical support for an EDMS (Electronic Document Management System) called Document Control & Archiving (part of the Syncade Suite) by Emerson Process Management.
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Demonstrated proficiency in the use and understanding of computer software (e.g., word processing, graphics, document management). Publications Manager / Medical Writer MUST HAVE: •An MS, MD, or PhD in a Life Science or a PharmD required.
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The Sample Management Technician will receive and document samples and chains of custody (COCs) to check integrity of all aspects of the sample receipt. The Sample Management Technician's primary responsibility is to enter sample IDs and required tests from the chains of custody (COCs) into LIMS in a complete and accurate manner.
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Document estimates and invoices, both in writing and on provided smartphone. Journeyman Plumber If job security, top pay, excellent benefits, and career advancement representing a well-known national brand are what you're looking for, Roto-Rooter is the company for you.
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Review both promotional and internal materials for clarity and accuracy using Veeva PromoMats, our document management system. Understanding of Microsoft Office, SharePoint, Adobe/PDF software and the ability to learn document management systems.
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Years of experience as a trademark paralegal preferred. Conducts preliminary analysis of basic trademark and copyright issues and makes recommendations to in-house counsel regarding such matters.
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The BA/ScrumMaster will work with business/data science stakeholders to gather requirements, document processes, write user stories, epics, acceptance criteria, allocate resources and manage Jira board.
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Ensure document submitted for MLR Review align with FDA submission standards. Capture live comments from MLR Advisors in Veeva PromoMats. Complete an editorial review of promotional and internal materials for accuracy, quality, and compliance.
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Position Summary The Corporate Paralegal role is a dynamic position reporting to the Associate Legal Counsel supporting the Rocket Legal Function and Business Development team, involving frequent interaction and collaboration with company leadership and external partners.
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document job Title: paralegal in Princeton, NJ
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