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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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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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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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Contributor to various QA Quality Program functions when needed (e.g. Deviation, CAPA, Supplier Management, Customer Complaints, biennial review, internal/external auditing, risk management, non-conformances, product returns, raw material review and release, etc.
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Six Sigma, Lean and / or American Society for Quality (ASQ) Certification (CQE, CQM/OE, CSQE, CQA, CRE, etc.) Typically requires Bachelor of Science degree in Engineering, Science, Technology, or Math and a minimum of 8 years of Quality Engineering, Manufacturing engineering, Supplier Management or related field.
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Identify and measure software quality attributes, metrics, and data. Ability to serve as Software Quality organizational spokesperson to other functions. We have an immediate need for a Principal Software Systems Quality Engineer to support the Land & Air Defense Systems (LADS) Strategic Business Unit (SBU.
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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 person hired for the position of Quality Inspector Level II is responsible for following documented procedures for inspection of Thermoplastic composite molded products under minimal supervision, as well may be required to assist in the disposition of material under the guidance of the Production Supervisor, Manufacturing Engineer and or Quality Supervisor.
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Provides consultation, design, and development services, requiring data collection and presentation, reports, and other specialized documents for clinical quality improvement and regulatory compliance.
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Provides quality compliance oversight of Pharmacovigilance (PV) to ensure Adverse Event, complaint management and post market surveillance are executed compliantly and in a timely manner. Oversees the management of the Quality Systems & Compliance team supporting product quality complaints, post market surveillance, Annual Product Quality Reports, field alerts, recalls, internal audit program, inspection readiness and external audits / inspections, Compliance Surveillance, Quality metrics, and Quality Management Review (QMR.
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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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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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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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Summary:Client is looking for a Data Engineer to join the Quality, Technology and Strategy organization. Responsibilities: Work on complex finance and supply chain data sources from Oracle EBS (E-Business Suite) and Agile PLM(Product Lifecycle Management) systems along with secondary sources like Coupa.
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Performs Supplier Quality Engineering assignments requiring interactions with Suppliers to perform QMS audits, process audits and material issue resolution\. Performs Quality Management Systems assignments requiring AS9100 System auditing, root cause and corrective action analysis and Performs Receiving and In\-Process Inspection assignments 10% of the time requiring product verification, documentation validation, and associated systems transactions.
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Title: data quality Company: Proactive Strategies in Andover, MA
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