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Evaluate, procure, administer, and manage security tools and supporting vendor services, including but not limited to password managers, phishing threat management, firewalls, intrusion detection/prevention systems (IDS/IPS), endpoint management, endpoint detection and response (EDR), managed detection and response (MDR), antivirus, document management, and Security Information and Event Management (SIEM) solutions.
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Must have hands-on familiarity with a variety of computer applications, including word processing, databases (such as document review and file management systems), spreadsheets, and imaging.
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This job may involve working in areas such as Investigations, Information Governance and Electronic Discovery (eDiscovery) related to the collection of computer and digital data, digital forensics, cyber investigations, data management, privacy and security, document review consulting, and engagement project management as part of a rotational program that provides exposure to all parts of the business.
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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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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the BMS Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System) Generate document management system reports for Quality Council metric reporting.
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Some technical writing skill set and be able to critically review documents while effectively inputting and expressing Quality principles Position Reports to Jenna Walker – Associate Director, QA Training & Document Control Education: Bachelor’s degree or equivalent Key Requirements and Technology Experience: Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment.
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Supports the cGMP Document Control operations for the Client Cell Therapy organization, including the document approvals, document change control process, periodic review and system reporting.
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APPLICATION PROCEDURE: Please provide, via email to villa-hiring@thevilla.org, items listed below (preferably in one PDF document): A cover letter detailing interest in and readiness for the role, addressed to Dr. Liz Willis, Head of School.
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Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment. 2+ years of Document Control & Reporting Experience, Some technical writing skill set including the ability to critically review documents while effectively inputting and expressing Quality principles.
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Some technical writing skill set and be able to critically review documents while effectively inputting and expressing Quality principles Position Reports to Jenna Walker - Associate Director, QA Training & Document Control Education: Bachelor's degree or equivalent Experience Basic Qualifications: Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment.
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Week 4: Mid-point check-in, complete documentation outline, with sub-chapters pending additional interviews and document review. Documentation of the marketing budget management process, including transfers, allocations, and true-ups.
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Maintaining food safety and quality by reporting all food safety risks or quality issues to QA and plant management immediately and hold all at risk products for management review.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations, including the document approvals, document change control process, periodic review and system reporting.
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JOB DESCRIPTION: 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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document review management jobs in Seattle, WA
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