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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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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.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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.
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Areas of focus are sustaining Quality Management System (QMS) processes, process improvement, quality control inspections, and document control. Support document control functions of change control by ensuring that records are readily available, properly defined, categorized, maintained, and implemented according to the document type.
ExpandApply NowActive JobUpdated 8 days 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 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.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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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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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment." Associate Director, QA Training & Document Control. Assist with cross-training of Document Control personnel and customers to ensure adherence with procedures.
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Negotiate full suite of trading agreements including, but not limited to, ISDA Master Agreements and Credit Support Annexes, stock loan, prime brokerage agreements, listed derivative trading agreements, OTC clearing agreements, tri-party control agreements, master confirm agreements, confidentiality agreements, electronic trading agreements and other trading-related agreements.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Managing the overall integrity of the Project Budget and Forecast in accordance with the approved Baseline Developing and maintaining detailed technical quantity-based performance metrics Leading Change Management Meeting to identify change and risk exposure Manage the project schedules including critical path activities and review schedule float for schedule slippages Ability to analyze cost and schedule performance and document variances utilizing Earned Value Management (EVM) principles.
$118,500 - $213,500 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This role coordinates document control transactions, site record retention, calibration and inspection activities. Complete document control transactions. In addition, the Quality Specialist will facilitate Customer complaint investigations, assist in audit coordination, support supplier quality and customer assessments and support risk management activities where appropriate.
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The Quality Assurance Document Control Specialist is a quality focused individual who ensures documentation and record keeping processes conform to cGMP and regulatory requirements as well as Bell International Laboratories approved procedures and output documents are accurate.
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Provide guidance and supervision to the Document Coordinator and/or Document Specialist in Land information management and the control of related documents, records, and reports.
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Strong knowledge of quality systems (Quality Planning, Management Review, Internal Audit, CAPA, Document Controls, etc.) Liaise and communicate with Quality assurance, Quality control, Validation department in regard to any changes or improvements in QMS or regular day to day duties.
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