• Exela Pharma Sciences, LLC (Lenoir, NC)
    The QA Specialist II - Engineering/ Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other ... in identifying potential issues and communicating with the Engineering and Validation departments. Job Responsibilities Perform Quality review/approval of URS,… more
    HireLifeScience (02/08/24)
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  • Novo Nordisk Inc. (Durham, NC)
    QA presence & process confirmation on shop floor. Relationships Manager, Quality Assurance . Essential Functions Ensures site compliance with Regulations, ISO ... shop floor. Handles release of raw materials & provides quality oversight, review & approval of validation ...components/raw material, batch records, change control requests, deviations & validation documents Performs QA presence & process… more
    HireLifeScience (04/24/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …compliance with specifications and procedures Releases product based on Quality Assurance record review and approval by QA Manager Performs regular internal ... and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch...leading international regulatory agency preferred As applicable, experience with Quality Assurance oversight and support for all… more
    HireLifeScience (03/20/24)
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  • Novo Nordisk Inc. (Durham, NC)
    QA presence & process confirmation on shop floor. Relationships Manager, Quality Assurance . Essential Functions Ensures site compliance with Regulations, ISO ... degree as appropriate Minimum of one (1) year of QA and/or cGMP related experience required, preferably in the...device industry General knowledge of Batch Review Processes (BRP), validation processes and Quality Management Systems (QMS)… more
    HireLifeScience (04/24/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …our next generation of cutting-edge medications. We are looking for multiple levels QA Specialists (I-IV) What we offer you: Leading pay and annual performance bonus ... in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting… more
    HireLifeScience (02/29/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …setting with quality and operations counterparts that include Manufacturing Operations, Quality Assurance , Engineering and Validation , Quality ... seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team...is required. Minimum of 4 years of experience in Quality Assurance related to manufacturing is required… more
    HireLifeScience (03/13/24)
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  • Aequor (Seattle, WA)
    …communication - Experience working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP ... of cGMPs and domestic regulatory requirements. Knowledge of manufacturing quality (manufacturing, packaging, facilities, critical systems, validation , etc.).… more
    HireLifeScience (04/03/24)
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  • QA Validation Specialist

    Regeneron Pharmaceuticals (East Greenbush, NY)
    …you must hold a BS/BA in Engineering, Chemistry, or Life Sciences and: + Associate QA Validation Specialist : 0-2 years of relevant experience + QA ... Validation Specialist : 2+ years of relevant experience + Sr. QA Validation Specialist : 5+ years of relevant experience May substitute proven… more
    Regeneron Pharmaceuticals (04/27/24)
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  • QA Validation Specialist

    Regeneron Pharmaceuticals (East Greenbush, NY)
    Validation department at Regeneron is adding to their team! The ** QA Validation Specialist - External Partners** coordinates the equipment, systems, ... Sciences and the following minimum amounts of experience required for each level: + Associate QA Validation Specialist : 0-2 years + QA Validation more
    Regeneron Pharmaceuticals (04/24/24)
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  • QA Validation Specialist

    Regeneron Pharmaceuticals (Troy, NY)
    …and implement company manufacturing standards policies and procedures. The day to day of a QA Validation Specialist could include, but are not limited to, ... or Life Sciences and the following years of relevant experience for each level: + Assoc. QA Validation Specialist : 0 - 2 years + QA Validation more
    Regeneron Pharmaceuticals (04/24/24)
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  • Validation Specialist

    Unither Pharmaceuticals (Rochester, NY)
    Validation Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify ... , QC laboratories and Tech Services to provide a high degree of assurance that all qualification/ validation activities, where appropriate, are completed. … more
    Unither Pharmaceuticals (03/28/24)
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  • Coordination of Benefits Validation

    LA Care Health Plan (Los Angeles, CA)
    Coordination of Benefits Validation Specialist II Job Category: Administrative, HR, Business Professionals Department: Claims Integrity Location: Los Angeles, ... that purpose. Job Summary The Coordination of Benefits (COB) Validation Specialist ensures the accurate coordination of...address discrepancies and ensure accurate billing and reimbursement. (15%) Quality Assurance - Conduct quality more
    LA Care Health Plan (04/27/24)
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  • Sr. Validation Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    Sr. Validation Specialist , Pharmaceuticals- Monroe, NC (MULTIPLE-POSITIONS AVAILABLE) Department: Validation Location: Monroe, NC START YOUR APPLICATION ... (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req\_id=3032926&source=3032926-CJB-0) Glenmark is actively seeking a Senior Validation Specialist to join the growing team… more
    Glenmark Pharmaceuticals Inc., USA (04/12/24)
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  • FEMA PA CRC Document Validation

    iParametrics LLC (Alpharetta, GA)
    FEMA Public Assistance Document Validation Specialist We are seeking a highly qualified and detail-oriented professional to join our team as a FEMA Public ... Assistance Document Validation Specialist . In this crucial role, you...validated documents, communications, and any corrective actions taken. + Quality Assurance - Implement quality more
    iParametrics LLC (04/24/24)
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  • Quality Specialist - Development…

    Unither Pharmaceuticals (Rochester, NY)
    …Your role Reporting to the Quality Assurance Manager, The Quality Specialist (Development and Validation ) assists and supports the organization ... Quality Specialist - Development & Validation Who...the Specialist will work directly with customer quality assurance and technical teams. Effective &… more
    Unither Pharmaceuticals (03/24/24)
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  • QA Validation Specialist

    Insight Global (Rensselaer, NY)
    Job Description A large pharmaceutical client is looking for a Data Entry specialist to join the team in Albany, NY. This candidate should have a background in ... science or statistics and have experience working in a regulated setting. They will be responsible for gathering various log books and compiling the data within Excel. They will be writing quarterly reports on their findings and expected to ensure all data is… more
    Insight Global (04/17/24)
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  • Revenue Tax Specialist 3 (Data…

    Louisiana Department of State Civil Service (Baton Rouge, LA)
    …tasks workflow of the Data Validation team to maximize efficiency. + Conduct quality assurance reviews of tasks completed by other team members within the ... monitoring outstanding tasks to ensure assignments are completed promptly and efficiently, performing quality assurance reviews of work completed by lower level … more
    Louisiana Department of State Civil Service (04/23/24)
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  • Specialist Quality Assurance

    Abbott (Buffalo Grove, IL)
    …mothers, female executives, and scientists. **The Opportunity** + Analyze quality standards for components, materials or services.Apply measures, sampling methods, ... testing methodology and other procedures that ensure that quality standards are met. + Apply quality principles, analyzes quality records, prepares reports… more
    Abbott (03/29/24)
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  • Specialist , Manufacturing Systems…

    Bristol Myers Squibb (Summit, NJ)
    …better place than here at BMS with our Cell Therapy team. The ** Specialist ** works cross-functionally to execute validation activities and prepare validation ... integrity supporting ALCOA+ principles throughout the CSV lifecycle. The Specialist will be responsible for ensuring the validation... documentation. + Work with BO, MES IT, and QA to ensure that the site validation more
    Bristol Myers Squibb (04/26/24)
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  • Data Validation Technical Lead

    CalSTRS (Sacramento, CA)
    …the following skills:** + Experienced in being a subject matter expert in data validation , quality assurance and ability to analyze complex problems, draw ... technical expert, demonstrating a depth of expertise on data conversion quality assurance activities. The incumbent will also collaborate with other… more
    CalSTRS (04/27/24)
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