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Manage, onboard, and lead the General Contractor BMS Lead(s), the Control Systems Integrator (CSI) and Electrical and Installation (E&I) controls contractor throughout all phases of the project, while developing program efficiency improvements and incorporating lessons learned to ensure a safe, robust, reliable and functional controls system that adheres to Facebook’s design and quality requirements.
$143,000 - $199,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Develops and deploys the quality systems (e.g., management review, CAPA, design control, process control) that ensure products conform to defined requirements. Change Management, Supplier Quality, Non-Conformance investigations, Complaint management, and Document Control.
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Maintaining current and accurate records on internal and client database and document control systems. Managing the project budget, project financial tracking and reporting, and project close-out - Managing the inspection and acceptance work performed by vendors and company resources, including the quality of services, equipment and materials, engineering documents, and other required project deliverables.
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As a Project Manager II, you will manage the cost, quality, and schedule of wireless infrastructure projects for new site builds and for modifications to existing facilities. You have a track record of completing work with a high level of quality.
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The QA Documentation Specialist is responsible for developing, implementing, and maintaining end-to-end Quality Assurance document systems at Chemical Guys. We manufacture our auto-detailing chemicals right here in Carson, CA and this is a great opportunity to grow and work alongside our both our quality (QA/QC) and manufacturing teams.
$21 - $30Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provide governance and improve the effectiveness of the management system by managing the use of global tools (e.g., customer complaints, KPIs, scorecards, Intelex, root cause methods, corrective and preventive action methods, document control systems), managing internal and external audits, and conducting on-going management review.
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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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This will be achieved by leveraging an understanding of best practices in Quality Management & Document Control systems, tools and concepts that drive a culture of Quality working in close partnership with our engineering and operations teams.
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Position Summary: As a Quality Systems Manager, you will play a pivotal role in our FDA regulated manufacturing facility. Supervise the Document Control program, including change control and metrics.
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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) Position Reports to Jenna Walker Associate Director, QA Training & Document Control.
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Take a leadership role in quality decisions by supporting change control processes, CAPA systems, deviation processes, nonconforming material processes, customer complaints, supplier approvals, material receiving, internal audit processes and document control.
$60,000 - $80,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment. " Assist with cross-training of Document Control personnel and customers to ensure adherence with procedures.
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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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Be responsible for all area logbooks, ensuring current versions are in use, log books are completed/signed off, and logbooks are reviewed and returned to Quality Assurance Document Control.
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Job Title : Quality Assurance Document Control (QADC) Associate Specialist. Leading Pharmaceutical company looking for an experienced QA Document Control Specialist.
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