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Make disposition on all raw materials, components and finished products as directed by the Quality Systems Manager. The Quality Systems Supervisor will assist in the direction and maintenance of all daily operations of the Quality Assurance/Quality Control department at a Kleen Test Products location.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Reporting to our Senior Manager, Quality Assurance CMC, this position is responsible for managing, reviewing, and approving quality documents from Contract Manufacturing Organizations and Contract Testing Laboratories for manufacturing, testing, validation, and disposition of clinical and commercial products for human use.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Hourly QA Team Lead will be responsible for the development and implementation of quality assurance practices and procedures within the site. Quality Assurance Team Lead.
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Demonstrated expertise in Regulations & quality systems (e.g., product disposition, Deviations/CAPA, Change Control, Audits, Supplier Management, Project Management, Validation, etc.) Senior Manager, Quality Assurance.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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3 years' experience of Quality Assurance oversight of aseptic manufacturing and all production stage batch record review and disposition. Extensive knowledge of regulations and quality processes involving product disposition.
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8 years of GMP quality assurance experience in the pharmaceutical, biologics or health industry as Quality Assurance Manager, Lead, Specialist or similar role; 10 years of GMP quality assurance experience in the pharmaceutical, biologics or health industry as Quality Assurance Manager, Lead, Specialist or similar role;OR.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Moderna is seeking a Specialist of Clinical Quality Assurance Quality Operations responsible for cGMP batch disposition and oversight for Clinical products manufactured at Moderna, Inc. This position will be based in our Clinical Manufacturing sites at Burlington.
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Located in Germantown, MD Project Enhancement Corporation (PEC) is a technical services business focused onproviding Project Management and specialized consulting services in the areas of nuclear safety, worker safety and health,emergency management, incident response, quality assurance, environment as well as materials andfacilities disposition within the DOE/NNSA and commercial power industry.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Contribute to the maintenance and reporting of metrics related to batch record review and product disposition in support of the Management Review. Author, review, and approve standard operating procedures (SOPs), quality policy documents, and laboratory/batch records.
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Collaborate with Quality Assurance to provide oversight and direction related to product safety incidents and negotiate disposition and related payments / penalties. The Contract Manufacturing Manager will interact with and support Marketing & Sales as well as all other functional departments including Operations, Logistics, Demand Planning, Quality, Research & Development, Procurement, and Finance across within the Post Consumer Brands business unit and across Post Holdings.
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4 - 5 years directly related experience in production & quality assurance (electro-mechanical assembly experience preferred) Participate in Material Review Board (MRB) to review and disposition nonconformities and to work with Supplier Quality Engineering to coordinate supplier corrective actions.
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Reports to the Senior Manager of Quality Assurance Operations, and may manage personnel both directly and/or through subordinate supervisors, including of overlapping shifts. Astellas is announcing a Quality Assurance Operations Manager opportunity at their Astellas Institute for Regenerative Medicine (AIRM) site in Westborough, MA.
Full-timeExpandUpdated 26 days ago - UpvoteDownvoteShare Job
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Understanding cell culture, cryopreservation, purification, aseptic processing or lab technique, Packaging, Shop floor quality, batch review, or disposition preferred. Work with site functional teams, including manufacturing, engineering, warehouse, and quality assurance to gather user requirements for recipe development.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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10 years of GMP quality assurance experience in the pharmaceutical, biologics or health industry as Quality Assurance Manager, Lead, Specialist or similar role; Associate Director, Quality Assurance GMP at MorphoSys US will report directly to MorphoSys’ Head of Global QA Operations.
ExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Must be able to work as a team player with Operations Associates/Facilitators, Engineers, Planning, and Quality Assurance/Quality Control Associates across multiple business partners and provide a high degree of customer service.
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disposition quality assurance jobs
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