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This individual will support quality control activities related to custom raw material manufacture for RNA and AAV gene therapy products conducted both internally and at various contract manufacturing organization (CMO) sites.
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The ISO Quality Specialist will be responsible for development, implementation, and maintenance the organization's Quality Management System for non-GMP products. The primary responsibility of the Quality Specialist is to maintain the adherence to quality standards for non-GMP products.
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Quality certifications like ASQ Six Sigma Green Belt or Black Belt, CQE, etc. Job Title: Quality Systems Engineering Manager. Excellent knowledge of Quality Management System (QMS) in high volume semiconductor, or electronics manufacturing environment.
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This individual will support method development, validation, and quality control activities conducted at Sarepta Andover in compliance with cGMP regulations. Support troubleshooting and optimization of cell and molecular assays, including assay development & validations in accordance with cGMP regulations.
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Experience with the use of quality systems and tools (for example, CAPA, Six Sigma methodology, change control, Statistical Analysis, Control Plans, and document management) Manager, Quality Systems Engineering - Medical Products page is loaded.
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Participate in project kick-off teams improving quality aspects of product introduction, and have a fundamental understanding of quality systems, SPC, and control plans. Support quality improvement efforts, Internal Auditing and Continuous Improvement initiatives.
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The Supplier Quality Engineer develops and implements quality plans, metrics, programs, and procedures using quality control statistics, lean manufacturing concepts, and analyses.
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Support Manufacturing, Quality Control and Assay Development by shadowing the process and providing beneficial feedback and knowledge on the process. Collaborate with Manufacturing, Assay Development, Engineering, Technical Support, and Quality Control groups to support resolution of complex issues.
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Must have: A Bachelor of Science degree in Electrical/Control Engineering, Mechanical Engineering, Chemical Engineering, or Computer Science 10+ Years Work Experience Ignition & Rockwell Relevant regulatory requirements of the life science industry such as cGMP, 21 CFR Part 11, etc.
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You will work with a team that includes the nursing staff, Mental Health Tech, Emergency Services Providers, and Psychiatric Nurse Practitioner to provide high quality compassionate care for patients in crisis.
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A Quality NDT Technician performs systems checks and calibration, nondestructive tests, and evaluations for acceptance or rejection determinations according to written instructions and recording of results.
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Ability to serve as Software Quality organizational spokesperson to other functions. Software Quality Engineering (SWQE), within Engineering Sustainment Quality Assurance (ESQA), provides solutions and services to the business.
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Comply with all current Good Manufacturing Practices (cGMP) requirements to ensure products are consistently produced and controlled according to the Quality Management System (QMS). You will assemble a range of components into finished goods across one or more production lines ensuring standard documentation, quality, and production rates are met under the direction of the Production Team Leader/Supervisors.
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Quality Technician Process Inspector needed for an opportunity with SOC's client to work in Wilmington, Massachusetts. Work closely with the program team to ensure quality standards are consistently met and maintained.
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We provide advisory and technical services to help clients cleanup and close contaminated sites and surplus operational facilities and restore them for reuse, plan and permit new facilities, address critical climate change issues, restore habitats and water quality, protect natural and cultural resources, maintain compliance, and cost effectively manage residuals and wastes.
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cgmp quality jobs Company: Randstad Usa in Lowell, MA
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