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Cambridge Isotope Laboratories (CIL) has an outstanding opportunity for a Quality Assurance Specialist I to join the team responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components based onsite in our Tewksbury, MA location.
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Adhere to all requirements for IAC accreditation including quality assurance reviews. Perform quality control procedures to ensure that the ultrasound equipment operates at optimal levels and manage a preventive maintenance program for ultrasound equipment.
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KEYWORDS: RMF, Risk Management Framework, ICD, Information Assurance, IA, IAO, IAT, IAM, A&A, A+, Network+, Security+, Non-classified Internet Protocol Router Network (NIPRNet),Secret Internet Protocol Router Network (SIPRNet), DISA Security Technical Implementation Guides (STIGs), CISSP, CASP.
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Drive continued efficiency improvements through the effective use of metrics, 5S, and the PPI process Recommend and implement changes in manufacturing procedures to improve product quality and production efficiency.
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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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The Quality Assurance Engineer II is a strong contributor to the design and development of Sloan's growing product portfolio and continuous improvement initiatives while also working in a highly collaborative team to customize existing products to meet customer requests and support the core business.
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Proficiency in using data management tools and platforms, such as data cataloging software(e.g., Collibra, Alation), data quality tools (e.g., Informatica, Talend), and data governance platforms (e.g., IBM Data Governance, SAP Data Intelligence.
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Ability to manage and coordinate personnel, as well as organize and drive performance of the quality assurance system. Minimum of 5+ years of progressive Quality experience working in regulated environment preferably in the field of biotechnology, biopharma, and/or cell/gene therapy (deep experience with GLP or GCP preferred.
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Currently possess or the ability to attain; NETTCP Quality Assurance Technologist, and USACE Construction Quality Manager Certification. Through his vision, drive and commitment to Safety, Quality and Excellence, the organization, now encompassing various companies throughout the United States is a leader in the heavy civil construction and paving industries.
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The Quality Control Documentation Specialist is responsible for performing the data review for the release of regulated and/or non-regulated materials including raw materials, in-process and finished products undergeneral supervision and in accordance with standard operating procedures (SOPs.
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The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development.
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Supplier Quality Engineer. Medtronic is seeking multiple hires to join the Supplier Quality Engineering team at our Affera manufacturing site in Billerica, MA. The Supplier Quality Engineers will be responsible for ensuring the quality and compliance of products and materials sourced from suppliers.
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As new products are introduced, the Senior Associate, Quality Assurance (Warehouse Operation) will support the onboarding of GMP materials through participation in risk assessments, Material Review Board, generation of specifications, master data review and supplier qualification activities.
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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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quality assurance jobs Title: quality assurance intern Company: Deloitte in Tewksbury, MA
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