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On-Site : work five days per week on-site with ad hoc flexibility. Hybrid-Eligible or On-Site Eligible. The Director GMP Quality Operations is responsible for the quality oversight of operations of the manufacturing site for the manufacture of Cell Product, including management of direct reports and defining daily priorities to execute the team's responsibilities.
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Previous experience on a Site Leadership Team or R&D Leadership Team is strongly preferredHybrid-Eligible RolesIn this Hybrid-Eligible role, you can choose to be designated as: Hybrid: work remotely up to two days per week; or select On-Site: work five days per week on-site with ad hoc flexibility.
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On-Site and work 5 days per week with ad hoc flexibility; This position focuses not just on the “what” but the “how”, ensuring phase appropriate quality compliance. Facilitate and support CDMO/CMO, Vertex site, and country office inspections across the VCGT network.
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Coordinate with the site Superintendent on all quality issues. The QA/QC Engineer will be responsible for the daily operations on-site of all quality expectations reaching the Shawmut standard for the project which includes the product and the installation.
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Professional On-Site Development/training Programs + Summer Hours + Flexible Schedule / Hybrid Schedule + Paid Architect Licensure & Certifications Exams + Wedding Pay + Freaky Fridays + Charitable Match Program + Market Leading Wellness Health and Welfare Benefits and more.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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On-Site designated role, you will work five days per week on-site with ad hoc flexibility. The Operational Quality Associate Director Cell and Gene coordinates or executes activities on multiple complex projects and takes a role in the design and execution of new projects.
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This position will be responsible for all SQA activities on major features of the UST web application. The Department of Revenue is rewriting its Underground Storage Tank Program (UST) web site from the ground up.
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Assist in general quality activities including control of quality records, monitoring quality objectives at all levels, implementing, monitoring, and maintaining the BMS, evaluation/disposition of non-conformances, audits (on-site and internal), implementation, and support of the navigator operating system.
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We're seeking an Automation Engineer for Field Quality to perform critical inspections, repairs, and quality control activities at various sites across the continental US. This role combines technical aptitude with hands-on problem-solving, requiring travel and the ability to work flexible hours, including overnight shifts.
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Develop and maintain a compliance monitoring system and schedule for each ABCD Head Start center, including conducting regular site visits, implementing continuous quality improvement plans for facilities, and tracking progress made on each quality metric.
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Ensure all activities related to maintaining computer systems and equipment within the site QMS follow national/international GxPs as well as 21 CFR Part 11, Annex 11, Annex 15, CLIA and GAMPs. Direct hands-on experience with local/international GxP regulations and industry guidance(FDA, EPA, EU, ICH, USP, ASTM and ISO.
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