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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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Enters charges and reviews patient record for billing accuracy performing quality checks on ICD-10 and CPT codes and other related information in order to streamline the billing process per practice protocols.
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Process non-stock listed items into the Defense Logistics Agency (DLA) system. Support the configuration control function to include receipt, dissemination, processing, tracking, and providing recommendation for the final disposition of Advanced Change Study Notices, ECPs, Requests for Deviation/Request for Waiver, Deficiency Reports (DRs), Airworthiness Directive Notes, Service Actions, Service Bulletins, Aircraft Service Changes, Notices of Deficiency, and Quality Control Plans (QCPs.
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With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen.
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With over 20 years of experience, travel contracts in all 50 states and internationally, and many industry awards and recognitions, Premier Healthcare Professionals focuses on quality, not quantity.
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The Quality Engineering subjects are Risk Management, Test Method Validation (TMV), Statistics, Reliability Engineering, Process Validation (PV). PURPOSE AND SCOPE 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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Sets up and operates plastic extrusion equipment to manufacture miniature, precision tubing to established quality standards in order to meet production demands. Knows process of screw and tool design, resin characteristics, temperature control, automated feedback loops, and ancillary downstream equipment such as burst testers and slickers.
$54,000 a yearExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Main Duties and Responsibilities:Develop and direct the implementation of changes to Process Control, Quality Control and Quality Assurance procedures to improve product quality, reliability, yield and cost effectiveness.
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A documented record of delivering reliability engineering information which adds value to management’s decision making process is required. Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
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The Quality Manager (textile/leather manufacturing) will lead Quality Assurance efforts by identifying key quality factors, coordinating teams to implement preventative measures, and ensuring product consistency through process validation and corrective actions.
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Utilize Six Sigma / Lean Manufacturing principles and appropriate tools to drive continuous improvement of key operational measures (e.g., yield, velocity, takt time, cost, inventory, nonconformances) to enhance product and process quality.
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Innova Solutions is immediately hiring for a Quality Assurance Associate. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures.
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Experience with supporting circuit card assembly production floor, (process and/or quality focus). Provide Operations Engineering support to the Circuit Card Assembly Factory located in Andover, MA. Primary responsibilities will be to support the Operation of SMT Process lines, which includes automated and programable equipment, for multiple products.
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These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
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Requirements: Master's degree in Regulatory Affairs, Engineering, Life Sciences, or closely related technical discipline (willing to accept foreign education equivalent) and five (5) years of experience as a Regulatory Affairs Specialist or experience executing the complete lifecycle of product registrations before national and international regulatory agencies, including documenting internal processes for quality control, and coordinating post-market surveillance and reporting activities.
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quality process jobs in Tewksbury, MA
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