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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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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 Assurance Lead for the cross-functional CMC Sub-Teams. The Director, CMC QA will report to the Executive Director of CMC QA and be responsible for maintaining strategic responsibility over QA Operations, developing and implementing Ultragenyx CMC Quality approach for assigned Gene Therapy programs, and working with colleagues to improve processes utilized to ensure product quality.
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The Manual QA Engineer position will report directly to the QA Manager on the Quality Assurance Team. This is a full-time remote position. The Manual QA Engineer will work on a development team to advocate quality in the software development lifecycle; create detailed test plans and procedures based on business requirements and product specifications; execute scenarios and test scripts to test functionality of the company’s web based and desktop software products; perform ad hoc and manually scripted testing.
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Job Summary Job Description • Serves as a key contributor to understanding process effects on diverse materials used in high volume electronics manufacturing, via analysis work conducted in the Quality Assurance and Reliability Analytical Lab. • Works with a multi-disciplinary team of engineers to identify and understand physics of failure and failure mechanisms, while issuing and advising corrective actions and recommendations.
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What You’ll Do: Reporting to the Lead Clinical Research Associate, the CRA II/Sr. CRA will perform quality and compliant Investigator site monitoring and relationship-driven Investigator site management in line with MapLight’s SOPs, our Mission, Vision, and Values, as well as industry quality and regulatory best practices (ICH GCP.
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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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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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Sr. Quality Engineer. This involves the development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS, RTU), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client's facility.
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Utilize extensive knowledge of polymer chemistry principles for materials selection/management, formulation processes to enhance the scalability and quality of the lens material. Serve as the technical lead and core team member on projects and interact with global clinical, manufacturing, production, quality, regulatory, project management, legal, claims and strategy and marketing personnel.
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Organize and manage Quality Assurance function(s) in close cooperation with customers and the Company’s Management team as a member of the Operational Management Team. Certified Manager of Quality/Organizational Excellence preferred.
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The Quality Control Analyst will work within the QC team, testing gene therapy products utilizing cell-based assays (Potency assay) in support of clinical and commercial lot release and stability activities.
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Job Description No recruiters please The Quality Manager is responsible for leading the manufacturing Quality group at AVI. This is a collaborative position working closely with Operations to support production management and production initiatives while ensuring compliance with AVIs Quality Management System (QMS) and FDA Quality System Regulation (QSR) requirements.
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Keeps the management well informed of pond maintenance needs including cleaning, water quality concerns, and repairs. The Pond comprises 16 of the 62 acres in the Park. The Pond offers a spacious sunbathing area, recreational swimming, shaded picnic grounds, children's playground area, volleyball net, sailboat, canoe, stand up paddle board and kayak rentals, bathrooms, showers, and a concession stand.
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Our Company Founded in 1956, Williams-Sonoma, Inc. is the premier specialty retailer of high-quality products for the kitchen and home in the United States. Our corporate values that guide our actions and decisions are our People First culture, customers, quality, shareholders, integrity, and corporate responsibility.
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quality assurance jobs Title: quality assurance intern Company: Department Of Defense in Tewksbury, MA
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