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Review raw data, protocols, reports, and CoA/CoTs for release and stability of RNA based products (HPLC, GC, KF) and AAV based gene therapy products (e.g. qPCR, ELISA, SDS-PAGE, Sanger sequencing, UV spectrophotometry) generated internally as well as at the vendor sites.
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Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I, that will be primarily focused on wet chemistry, based onsite in our Andover, MA facility. The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw materials, in-process and finished formulations under general supervision and in accordance with standard operating procedures (SOPs.
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The individual will also assist in managing quality events, data trending, and review of quality documents originated at the testing laboratory at Sarepta. The individual will devise, troubleshoot, and validate cell-based assays to assess the critical quality attributes of AAV gene therapy products including potency and infectivity.
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Quality certifications like ASQ Six Sigma Green Belt or Black Belt, CQE, etc. Job Title: Quality Systems Engineering Manager Job Description:This position will require engagement across departments, ADI manufacturing sites, leading cross-functional audit teams, Quality Systems deployment and standardizing BKMs across ADI sites globally.
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Conducts Data Analysis and prepares metrics detailing field product quality. Works with staff as necessary to enhance data capture and analysis in support of internal and external quality improvement and reporting efforts.
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Implement machine learning and natural-language-processing (NLP) methodologies to train and deploy data-scientific models that improve, support and streamline the work of the quality engineering (QE) teams at Red Hat.*Telecommuting permitted: work may be performed within normal commuting distance from the Red Hat, Inc. office in Westford, MA.What You Will Do:Design roadmaps and write python scripts, develop python scripts and maintain high quality standards to deploy the model into production.
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Identify and measure software quality attributes, metrics, and data. 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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Identify supplier escapes/issues and ensure proper containment and backflow to the Supplier Quality Management team. We are seeking a Hardware Quality Engineer with hands-on hardware quality experience to become a key part of Operations Quality - Advanced Electronic Assembly Team. Here at Raytheon, our Operations Quality Team assures product and process quality with an emphasis on Product Compliance, Customer Satisfaction and Continuous Improvement.
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Quality Technician Process Inspector needed for an opportunity with SOC's client to work in Wilmington, Massachusetts. Review and interpret engineering drawings, CAD data, and specifications to determine inspection requirements.
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The Supplier Quality Engineer is responsible for the overall supplier quality of specific suppliers, contract manufacturers and material commodities within Brooks. Experience driving standard quality and statistical methods, problem solving methods, process capability methods, sampling methods, fixturing/gaging principles and destructive and nondestructive testing methods at suppliers.
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QA Technician will assist Quality Assurance Supervisor and Manager in ensuring compliance with all Manufacturing Quality and Food Safety Policies and Guidelines. The Quality Assurance Technician must be able to interact across interdepartmental boundaries in a professional, pro-active manner, avoid conflicts and exemplify a collaborative spirit.
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Engage in the overall Project Lifecycle Methodology to inform appropriate data quality and testing considerations are part of the process. Our Engineering organization is looking for a Director to lead Software Test and Software Quality Assurance (SQA.
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The Quality Engineering subjects are Risk Management, Test Method Validation (TMV), Statistics, Reliability Engineering, Process Validation (PV). Participate in the New Product Development (NPI) and design changes, Design History File (DHF) and Device Master Record (DMR) reviews meetings and fully understand the design control process and Quality Engineering.
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Author and review SOP changes; participate in change controls, CAPAs and other quality systems. Work independently and as a team player with quality and attention to detail. Promote and actively demonstrate the Lantheus values of Accountability, Quality, Efficiency, Customer Service, Collaboration, and Safety, as well as appropriate workplace behaviors and professionalism, including respect, flexibility, and a positive attitude toward work and others.
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Basic computer skills, including data entry and Microsoft Office applications. Data Collection : Record detailed observations, data, and results accurately. Strong attention to detail and accuracy in conducting experiments and recording data.
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Title: data quality Company: Proactive Strategies in Lowell, MA
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