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Monitor compliance with the Company QMS. Prior experience with close tolerance machining and inspection in an ISO certified manufacturing environment required. Inspect and test parts at receiving, in-process and final inspection points using calibrated hand tools and CMM, and document results on inspection records.
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Minimum of 5 years’ experience related to quality assurance, lean manufacturing, regulatory compliance, and Six Sigma manufacturing in a manufacturing environment; previous direct leadership experience preferred.
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Facilitate in the development of documents, and update documents pertaining to lab procedures and product manufacturing to maintain cGMP and ISO compliance, and increase efficiency. Complete all work in compliance with established cGMP, FDA, OSHA, USDA, EPA, ISO and Quality System regulations, as applicable, to assure output meets established quality and regulatory specifications.
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The Mfg Lab Technician performs laboratory activities in the manufacturing lab including Buffer and antibody manufacturing. The technician follows the manufacturing schedule to complete required tasks and is responsible for following standard operating procedures involving basic laboratory techniques, calculations, material measurements operation of laboratory equipment and record keeping as necessary.
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Description: Lockheed Martin is seeking a Supplier Quality Engineer for a position based in Grand Prairie, TX to provide support to the M270 Fleet Expansion Program in data collection, analysis and presentation in Supplier and Manufacturing areas of Quality.
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The Quality & Document Specialist will serve as the primary handler of our company's ISO and Documentation Programs. Understanding of IPC Manufacturing Guidelines (not required, but recommended.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Field Underwriting in one of the following programs - Construction, Forest Products, Manufacturing, or Oil Gas. Evaluate, quote, and negotiate prices on applications from new and renewal customers and requests for changes in policies which requires an understanding of statutory requirements, ISO, company and NCCI coverage forms and endorsements and commercial line reference materials, including Best's Underwriting Guide.
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Preferably an experienced ISO Auditor. Knowledge in either Supplier Quality, Quality or Manufacturing Engineering, gained preferably within a medical device environment. Preferably an experienced ISO Auditor.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Our clients range from Class-A Office Buildings, Luxury Residential Properties, Distilleries, Fortune 500 Companies, Financial Institutions, Telecommunications, Manufacturing/Industrial Factories, Hospitals and many others.
$18 - $20Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Company DescriptionAero Controls is an FAA, EASA, and ISO certified Part 145 Repair Station headquartered in Auburn, WA. /r/n/r/nFounded in 1984, Aero Controls has built a reputation based on quality products and services while specializing in repairs/overhaul, component sales, aircraft dismantlement, and consignment management.
$25 - $30 an hourFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Experience preferred in operations and/or in advanced manufacturing engineering and facilities management. Ensure all projects comply with known cGMP standards such as ISO, NOM, YY.Good understanding of Clean Room design and operation, ISO standards, and validations.
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You will operate under 5S & Lean Manufacturing principles following ISO standards. As a Formulation Technician with IDEXX, you will perform small and large-scale bulk processing, manufacturing and filtration for experimental and commercial diagnostic products, as well as operate laboratory instrumentation.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Minimum 5 years manufacturing work experience and/or 1 year as Maintenance Technician II, with experience & training to include: Allen Bradley PLC (SLC-500 and/or PLC5) Eurotherm Drive (590-690 Series) Process Control & Instrumentation (temperature, flow, pressure, level, etc.
$85,000 - $115,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Practical experience in application of ISO standards and regulatory requirements within the In Vitro Diagnostic and/or Medical Device space (MDSAP, EU, and US regulatory requirements desired, additional geographies a plus.
$127,000 - $174,700 a yearExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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In liaison with the supplier quality team, execute and ensure that the components and raw materials meet all specified standards in order to enable continuity for manufacturing. Participate as internal auditor to verify compliance to ISO processes, procedures, and work instructions; issue corrective actions as required.
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