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Document Control Coordinates document and data control with the Director of Regulatory Affairs and Document Control Specialist, including creation / review / update of controlled documents and product specification.
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Through accelerated learning, in-depth training and practical experience, the Retirement Plan Specialist will quickly grow from document review to administering basic plans. You’ll review documents submitted by our clients, proactively keep clients updated on progress and help client understand the year end reporting documents necessary to complete government filings, including the annual 5500 return.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Under the direction of the QA Document Control Supervisor, the QA Specialist – Document Control, will control the movement, filing, archiving, and securing of all documents with the objective of ensuring compliance to company policies and procedures.
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The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone achievements, participate in developing regulatory strategy, prioritize submissions with operating plans as well as ensuring alignment with KOD in countries (e.g., OUS, [the globe minus US, EU, Canada.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Perform visual and/or document review/release of component products. Areas of focus are sustaining Quality Management System (QMS) processes, process improvement, quality control inspections, and document control.
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Participate in providing guidance and feedback to business unit regulatory teams on registration requirements for new and renewal registrations, product and process changes, and review of labeling content.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The QA Document Control Specialist is responsible for maintaining the document and record control systems to meet Quality Management System requirements and is responsible for coordinating the issuance, revision, review and approval of SOP’s and other documents.
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The Litigation Support Specialist is part of a dedicated team that supports the collection, processing, review, analysis, production, and presentation of electronically stored information (ESI) across the office.
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The Loan Post Close Specialist II is responsible for the post-closing review of Consumer, Commercial and Specialty loans to ensure all document and perfection requirements have been met and that the bank's position and security interest has been satisfied following Bank policy and procedures.
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Support the review, vetting, and approval of acquisition documents such as an Acquisition Strategy Document (ASD), Request for Proposals (RFP) and Statement of Work (SOW). The Acquisition Specialist/Program Management Expert shall provide program planning and acquisition support to SAF/SQSC and serves as prime consultant to the organization on highly significant matters relating to policies, programs, capabilities, and long-range goals and objectives.
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EHS Document Reviews: Review existing EHS program documentation and update as needed. Document the results of the inspections and track corrective actions to closure. Safety Committee: Lead safety committee meetings, document safety meeting minutes including corrective actions.
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Document Quality Control Specialist. They use a computer to review the files and identify errors such as double feeds, checks, notary documents, and missing or incorrect barcodes.
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Settlement and custody, document preparation and review, records management, and trust system maintenance. Assists in business unit's compliance with applicable laws, regulations, regulatory requirements and Bank policies and procedures, including but not limited to those related to Fair Banking, Anti-Money Laundering laws and regulations, Bank Secrecy Act and USA PATRIOT Act.
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. Provide CSV & validation Production and Project support to S12 MES Next Gen. Complete all tasks required per the Change Management Process for S12 MES Next Gen SOP and in compliance with CSV and related SOPs. Review the summary reports from testing/validation to ensure all issues are resolved and approved.
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Key collaborator working closely with site personnel and Clinical Supply QMS Redesign Team to ensure successful implementation of new QMS by assisting with project-specific tasks, including but not limited to, project support, document management, documentation review, technical editing, meeting coordination and facilitation, training, onboarding, and other administrative tasks.
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