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Familiarity with MES infrastructure, HP ALM, Electronic Document Management Systems, Change Management Systems, and middleware WebMethods preferred. Familiarity with MES infrastructure, HP ALM, Electronic Document Management Systems, Change Management Systems, and middleware WebMethods preferred.
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Innova Solutions is immediately hiring for a QA Associate Specialist - Document Control. The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
$28 - $32 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The companys portfolio includes reliable and eco-friendly MFPs and printers, as well as business applications and consultative services which enable customers to optimize and manage their document workflow, reaching new heights of efficiency.
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Clinical Document Governance Management (CDGM) is accountable for strategy and delivery of clinical document management (CDM) systems, processes, standards and operations of CDM services (including Trial Master File management (TMF), clinical submission readiness, record retention and archiving, Good Documentation Practice capability build) across Novartis globally.
$118,400 - $177,600 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Deep understanding of drug development process, international drug approval procedures and standards (e.g., ICH-E3, ICH-E6, eCTD) and industry-wide standards in clinical document management (e.g., DIA TMF reference model.
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Complete AML/KYC verification services, including support document validation and screenings. Complete subscription document review and processing. The candidate will maintain the fund administration system used to manage all investor records, handle investor queries, process investor capital activity, support investor AML/KYC validations, interface with clients as well as manage multiple client deliverables ensuring superior client service and delivery.
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Conducting discovery, including depositions, document review, and expert witness preparation. A law firm located in Parsippany is seeking a Mid to Senior Litigation Associate Attorney. The Mid to Senior Litigation Associate Attorney will handle substantive and client-facing assignments, gaining valuable experience and professional growth opportunities in a collaborative environment.
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. With advanced technical document writing and time management skills, including ability to prioritize and manage expectations.
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Test Equipment Console layout, ITA Design, Electrical/Mechanical Drafting, 3D Design and Modeling, Configuration Management Practices, Knowledge of Mil/ASME/ISO Standards, machining /manufacturing processes, materials/finishes, thermal calculations/management, Design Review preparation, estimation, and technical presentation package/document development.
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Assisting with patent litigation matters, including document review and preparation of legal filings. Assisting with patent litigation matters, including document review and preparation of legal filings.
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If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of Cell Therapy as we strive to put more patients on the path to a cure.
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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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To thrive in this role, you should have ten-plus years of experience in architecture, design, and building a scalable target state architecture for data processing-based on document content including PII/CII handling, policy-based hierarchy rules and Metadata tagging.
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Position Summary:The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client's Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review, and system reporting.
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Immediate need for a talented Manufacturing Systems Validation Specialist. Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR part 11 electronic records and electronic signatures, and good documentation practices with the ALCOA+ principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles.
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document job in East Hanover, NJ
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