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Direct and promote the use of diagnostic and predictive quality and continuous improvement tools and techniques including (SPC, statistical analysis, Lean, six-sigma). Provide leadership and direction to Incoming Inspection, In-process Inspection, Supplier Quality, Manufacturing Quality Engineering, Customer Quality Assurance, and Calibration Teams.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Collaborate with Quality Director and QA Manager on policies, goals and objectives, expansion of the QMS, and resources needed to meet expectations. As a Quality Control Manager, you will report to the Quality Director and develop a team of approximately 10 to 15 QC analysts.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Working under the guidance of the Director of Quality Assurance and Compliance, the Quality Assurance and Compliance Specialist will be responsible for ensuring quality assurance and compliance with a strong emphasis on Good Laboratory Practice (GLP) standards within the vivarium facility.
$80,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Knowledge of Macintosh and PC related software, Microsoft Excel, FileMaker Pro. Knowledge of Master Control or other document control/quality management software. Minimum of 6-8 years’ experience as quality assurance auditor/technician in biological sciences or pharmaceutical science.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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You will be part of a dynamic organization of engineers, scientists and quality specialists developing a novel intradermal biosensor technology. Quality Engineering Certification, Software Quality Engineering Certification (e.g., ASQ CQE, ASQ CSQE.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. If you are a UCSD student, you may be eligible for the UC San Diego Division of Biological Sciences Co-Op Program.
Part-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays.
$27.4 an hourFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Bachelor of Arts/Bachelor of Science in a related discipline and 10-12 years of experience in quality assurance or compliance supporting GMP, GCP, GLP operations in a pharmaceutical company, or the equivalent combination of education and experience.
$285,608 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The QC Lead for the BioLegend’s Quality Control department will lead a QC team responsible for the testing of such products as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays.
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The Research Billing Quality Review Analyst oversees comprehensive audits of accounts with research charges submitted post-claim to Medicare, Medi-Cal, and Commercial insurance payers, as well as post-statement invoicing for research studies.
$66.67 an hourFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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JOB TITLE: Quality Control Inspector. REPORTS TO: Quality Assurance Manager. Essential Job Requirements: Produce/create electronic/handwritten Quality Assurance documentation as Objective Quality Evidence for work performed throughout the preservation process.
Part-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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130902 Research Billing Quality Review Analyst - Hybrid. In addition to conducting audits, the Research Billing Quality Review Analyst synthesizes regulations and industry publications, assisting in the development of training materials and other departmental guidance documents.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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The Senior Manager of Drug Safety & Pharmacovigilance (PV) Quality, is a key role and is responsible for oversight of Drug Safety & PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program within the Quality Assurance department.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Job Description BAE Systems is seeking a Quality Inspector IV to support at the San Diego Ship Repair yard. Typically requires a high school diploma and four (4) years shipboard experience in Quality Assurance, or the overall equivalent.
$100,540 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Track key production metrics and compiling and presenting regular reports, with content and cadence specified by the Director of Manufacturing and Supply Chain / Quality Systems Manager. Own manufacturing and quality assessment of consumable products from raw materials as directed by the Director of Manufacturing and Supply Chain / Quality Systems Manager.
$75,000 a yearExpandApply NowActive JobUpdated 14 days ago
quality job in San Diego, Parkville, Maryland
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