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Manage and lead the Mission Assurance team of quality engineers supporting the Lynnwood & Poulsbo sites. Actively oversee the implementation of Mission Assurance goals and objectives and support Quality Engineering & Control business rhythms.
$87,100 - $157,450 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the BMS Jump site, including the coordination, issuance, reconciliation, and management of production labels and records.
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Job Overview: As a Quality Assurance Specialist, you'll be responsible for maintaining and enhancing our Quality Management System (QMS). As a Quality Assurance Specialist, you'll play a vital role in upholding our commitment to quality and making a positive impact on patient care.
$40 - $43 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Extensive experience in Quality Assurance processes. Experience with use of complex Root Cause Analysis (RCA) tools and methodologies, research techniques and methodologies like six sigma and Kaizen to improve process/product quality is a plus.
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Primarily responsibilities will include creating and modifying standard operating procedures, Quality Assurance (QA) product release, administration of change management and document control processes, and auditing.
$62,000 - $85,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Other duites as assigned by managerEducation:•B.S. in any ScienceExperience / Knowledge Desired:•A minimum of 3 years of experience in pharmaceutical Quality Assurance, with direct experience in Quality Management Systems.
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Provide Quality on-the-floor oversight including quality walk-throughs of the production, testing and warehouse locations to ensure practices fully adhere to cGMP.Provides technical knowledge and guidance towards GMP compliance during triage/troubleshooting activities.
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The Quality Assurance Representative follows Best Practices to support approved compliance policies and procedures. Our Vacation Ownership business line includes Club Wyndham, WorldMark by Wyndham, Margaritaville Vacation Club, Accor Vacation Club and the brand new Sports Illustrated Resorts.
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A minimum of 3 years of experience in pharmaceutical Quality Assurance, with direct experience in Quality Management Systems. QMS Deviation and CAPA phase tracking and due date monitoring. Advance Smartsheet Dashboard Creation.
$80 - $88ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Education: B.S. in any Science Experience / Knowledge Desired: A minimum of 3 years of experience in pharmaceutical Quality Assurance, with direct experience in Quality Management Systems. Veeva experience preferred) Advanced Excel knowledge and proficiency.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Jump site, including the document change control process, issuance and reconciliation of batch records, batch related forms, product labels, and management of archival and retention of GMP records.
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JOB TITLE: Quality Assurance Specialist. Veeva experience preferred) 401k Retirement Savings Plan administered by Merrill Lynch. Deviation Trending Program administrator. Ensure adherence to deviation and CAPA due dates and extension process.
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The Quality Assurance Specialist position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant (Jump). If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
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Compile slides and assemble presentations, schedule logistics, meeting facilitation, and author meeting minutes. Investigation & CAPA Review Board Administrator. Compile, contextualize, evaluate, and present Quality Systems data and metrics.
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Work cross-functionally to determine remedial actions to reduce recurrence and implement effective CAPAs∯*∯ Deviation Trend Review Board logistics, preparation, facilitation, and meeting minutes. Author quarterly deviation trend report.
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Title: assurance Company: Supplay in Lynnwood, WA
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