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Processes include Deviation Investigations, Corrective Action / Preventive Action (CAPA), Complaints, Change Control, Quality Risk Management, Documentation, Training, Audits & Inspections.
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REQUIRES: Master’s or equivalent in Computer Science/Applications, Information Technology, Business Management/Administration or Electronics Engineering + 1 year experience as Software Quality Engineer, Software Quality Assurance Analyst, Test Engineer, Quality/Product Test Professional or related.
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As a Data Quality Specialist, Data Management & Governance Chief Data Office, you will join a team of change agents who specialize in ensuring that data is secure and protected, accessible, understood, of known quality, and can be effectively used in support of business goals.
$134,100 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This is Hybrid opportunity in NYC. Looking for: SME in Quality Management Initiatives Must have HEDIS (3 years experience) SQL background Management skills - will manage a team of 4 Hybrid role - 3 days in the office.
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Seek opportunities for simplification and efficiency across the GxP Quality Performance Management landscape. + Support quality performance management related integration efforts.
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Experience in using CMMS software Blue Mountain Regulatory Asset Management (BMRAM) Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world.
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Build, deploy and reinforce learning tools and materials to support quality event management capability development. In support of the quality management system module leads maintain records of issues, enhancement requests and support the implementation of system changes.
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Ensures required quality procedures are established including CAPA, Non-Conforming Product, Risk Management, Post-market-surveillance, Purchasing Controls, Management Review, Traceability, Employee Controls, Post market management, Change Control, Advisory Notifications, Supplier compliance and others as coordinated within the Quality team and with other cross-functional departments.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Author, review and approve Quality Management System (QMS) documents. " Regularly review the process (trends metrics, trends observations, right first time (RFT), Design, optimization) for their effectiveness and provide feedback to the Quality management team for action and remediation.
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Capture and report on Quality data and metrics for management review and other organizational forums. The Quality Systems Manager will be responsible for providing day-to-day support to ExM Operations on Quality Systems that enable business objectives to be achieved.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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O Author, review, and approve Quality Management System (QMS) documents. o Capture and report on Quality data and metrics for management review and other organizational forums.
$45.24 an hourExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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This role involves managing all aspects of the Quality Management System, from the receipt of raw materials and finished goods to the manufacturing, handling, storage, and distribution of dietary supplements, in accordance with established GMP requirements.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The Quality Systems Manager will act as end-to-end Local Process Owner of one or more Quality Systems used within Global External Manufacturing. The Quality Systems Manager is responsible for implementing, supporting and monitoring the effectiveness of the Quality Systems and Training within the Global External Manufacturing (ExM) organization.
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Act as team lead for coordinator of work associated with complaints, change control, deviation, CAPA and document management in the applicable ExM location. Our client, a leading pharmaceutical company, is hiring a Quality Manager, on a contract basis.
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Responsibilities The Quality Assurance Specialist for Small molecule is responsible for management of deviations and customer complaints including coordination, review / approval of deviations and complaint investigations.
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quality management jobs Title: quality in Iselin, NJ
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