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Will train Quality team members on Inspections, Document Control, GMP compliance, etc. Medical Device manufacturer in eastern TN has immediate need for a Quality Manager with strong experience in FDregulated manufacturing environment.
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The Quality Manager will ensure compliance with FDA regulations in addition to managing the Quality Lab. Knowledge of CAPAs and root cause analysis is important. This company is growing and adding new equipment, so the Quality Manager will be involved in Validations for new equipment and processes.
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The Quality Manager is also heavily involved in customer interaction. Qualified candidates will have BS degree along with at least 3 years Quality management experience. ASQ certifications are a plus.
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Their efforts ensure that work submitted by transcriptionists and delivered to clients meet quality standards through transcript review and transcriptionist support. Overview: Quality Assurance Representatives utilize professional legal transcription skills and knowledge to contribute to the oversight of the quality management program.
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Quality Inspectors are responsible for packaging materials, loading finished product onto conveyors. Inspects product to ensure we meet quality specifications on work orders. Inspects components continually during the production process to determine and maintain high quality and reliability of products.
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As an Air Quality Senior Project Manager/Principal for Civil & Environmental Consultants, Inc. (CEC) in our Knoxville, Tennessee office you will lead air permitting and regulatory compliance programs for private-sector clients with complex technical/regulatory issues in the manufacturing, oil & gas, power, and mining industry consulting groups.
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The Quality Control Analyst is responsible for reviewing Medical Disability Examination (“MDE”) reports and Disability Benefits Questionnaires (“DBQs”) generated by medical providers for veterans evaluated on behalf of the Department of Veterans Affairs (the “VA.
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The Quality Manager will ensure compliance with FDA regulations in addition to managing the Quality Lab. The Quality Manager will ensure compliance with FDA regulations in addition to managing the Quality Lab.
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Must have prior experience with FDA audits, regulatory agency interaction, and ISO certification processes. Relocation Assistance is available. This is a well-established corporation with multiple sites in the U.S. Excellent opportunity to join a company launching several new products that will expand their market share.
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Performs quality reviews of Appeals cases closed through APS using Appeals Quality Standards and Attributes (AQSA). Interprets and applies AQSA using the Appeals Quality Measurement Standards Guideline.
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Quality Tech will perform routine lab tests including: receiving inspection, gage calibration, final inspection, and any customer specific testing and document requirements. Support to maintain the Quality Policy and Fulton Bellows QMS.
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If you are passionate about quality and compliance in pharmaceutical manufacturing and possess the necessary skills and qualifications, we invite you to apply for the Batch Record Reviewer position at Tjoapack.
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Quality Manager- Medical Device Manufacturing. Quality Manager- Medical Device Manufacturing. Location: Knoxville, TN area.
$100,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Performs periodic sampling of products as they are being bottled/canned to ensure continuous meeting of standards including product quality, fill levels, labeling, freshness dating, and container integrity.
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Perform periodic assessment of the effectiveness of the loan quality control functions within the business lines utilizing approved testing matrices. Title: Internal Quality Control Specialist.
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Title: quality Company: Gw Plastics in Knoxville, TN
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