• Novo Nordisk Inc. (West Lebanon, IN)
    …and procedures Releases product based on Quality Assurance record review and approval by QA Manager Performs regular internal audits of NNUSBPI ... position has QA signature authority on the review of individual batch records, supporting test...leading international regulatory agency preferred As applicable, experience with Quality Assurance oversight and support for all… more
    HireLifeScience (05/09/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …on Quality Assurance record review and approval by Manager, Quality Assurance Review and assess Corrective and Preventive Actions Reviews and ... position has QA signature authority on the review of individual batch records, supporting test...pharmaceutical or biotechnology company with one (1) year direct Quality Assurance experience Knowledge, Skills, and Abilities:… more
    HireLifeScience (05/09/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support ... records. Will be a QA presence on the manufacturing floor. Relationships Reports to:...or a leading international regulatory agency preferred Experience with Quality Assurance oversight and support for all… more
    HireLifeScience (05/09/24)
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  • Aequor (Bothell, WA)
    …skills include- strong cross-functional experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role ... a regulated cGMP environment. The primary focus of the QA Specialist role will be to support...or cell therapy manufacturing is preferred. Hands-on experience with batch record review and product disposition is… more
    HireLifeScience (05/03/24)
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  • Novo Nordisk Inc. (Durham, NC)
    …potential? Join Team Novo Nordisk and help us make what matters. The Position Performs quality review & approval of Batch Production Records (BPRs), Change ... QA presence & process confirmation on shop floor. Relationships Manager, Quality Assurance . Essential Functions Ensures site compliance with Regulations, ISO… more
    HireLifeScience (04/24/24)
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  • Catalent (Manassas, VA)
    POSITION SUMMARYThe Quality Assurance Specialist I is responsible for inspection and verification of the products and production processes along all the ... from receiving to dispatching. To ensure adherence to company quality standards procedures and policies. Inform the QA...cGMP and execute corrective actions when needed. Assist the Quality Assurance team with special projects as… more
    HireLifeScience (05/10/24)
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  • Catalent (Manassas, VA)
    …work with complex formulations to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for ... to company quality standards. Communicate any deviations to management. Assist the Quality Assurance team with special projects as required. Comply with SQF,… more
    HireLifeScience (04/16/24)
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  • Catalent (Manassas, VA)
    Quality System documentation. Communicate any deviations to management. Assist the Quality Assurance team with special projects as required. Comply with SQF, ... soft chews for nutritional supplements and nutraceuticals, as well as small batch lozenges. With extensive development and manufacturing expertise and a wide range… more
    HireLifeScience (04/16/24)
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  • Spectraforce Technologies Inc (Bothell, WA)
    Title: Quality Assurance Specialist (Pharma ONLY - NON IT JOB) Duration: 06 Months Location: Bothell, WA *Schedule- 9:00pm - 7:30am, Sun - Wed** **Top ... skills include- strong cross-functional experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role… more
    JobGet (05/03/24)
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  • Integrated Resources, Inc (Bothell, WA)
    …SOPs, procedures, edits, and annotations within EDMS experience The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document ... Job Title: QA Document Control Labelling Specialist Location:...technical writing skill set and be able to critically review documents while effectively inputting and expressing Quality more
    JobGet (05/10/24)
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  • Integrated Resources, Inc (Bothell, WA)
    …skills include- strong cross-functional experience, strong interpersonal skills Job Description: . The Quality Assurance Specialist position plays a key role ... regulated cGMP environment. . The primary focus of the QA Specialist role will be to support...cell therapy manufacturing are preferred. * Hands-on experience with batch record review and product disposition is… more
    JobGet (05/03/24)
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  • Dexian - DISYS (Bothell, WA)
    …skills include- strong cross-functional experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role ... a regulated cGMP environment. The primary focus of the QA Specialist role will be to support...cell therapy manufacturing is preferred. * Hands-on experience with batch record review and product disposition is… more
    JobGet (05/07/24)
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  • Integrated Resources, Inc (Smyrna, GA)
    Job Title: Quality Administrative Specialist Location: Smyrna, GA [Hybrid role- 2 days onsite, 3 days remote] Duration: 06 Months on W2 (Temp to hire) JOB ... cGXPs with local/International regulatory requirements and global standard operating procedures. o Quality Management Review o Quality System Monitoring o… more
    JobGet (05/03/24)
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  • QA Specialist ( Batch Record…

    Regeneron Pharmaceuticals (Rensselaer, NY)
    We are currently looking to fill a Quality Assurance Specialist position. This position performs activities supporting dispositioning product and/or raw ... materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs,...amount of relevant experience for each level: + Associate QA Specialist - 2+ years + … more
    Regeneron Pharmaceuticals (04/24/24)
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  • QA Specialist II - Batch

    Actalent (Foster City, CA)
    …routine work, general instructions on new assignments. Skills: batch record review , Quality assurance , standard operating procedure, glp, gmp environment ... Description: Executes batch record review Performs a wide...requirements. Participates in developing Standard Operating Procedures to ensure quality objectives are met. Maintains programs and processes to… more
    Actalent (04/30/24)
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  • QA Specialist II - Batch

    Actalent (Foster City, CA)
    …all aspects of producing quality products. Skills: batch record review , Quality assurance , standard operating procedure, glp, gmp environment ... requirements. Participates in developing Standard Operating Procedures to ensure quality objectives are met. Maintains programs and processes to...* 2+ years of experience relevant to job description. QA / batch record review more
    Actalent (05/02/24)
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  • QA Specialist ( Batch

    Regeneron Pharmaceuticals (Troy, NY)
    We are currently looking to fill a Quality Assurance Specialist ( Batch Disposition) position. This position performs activities supporting dispositioning ... product and/or raw materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs,...amount of relevant experience for each level: + Associate QA Specialist - 2+ years + … more
    Regeneron Pharmaceuticals (04/24/24)
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  • Quality Assurance Specialist

    Integra LifeSciences (Cordova, TN)
    …headway to help improve outcomes. **JOB DESCRIPTION** The Specialist , Quality Assurance ( QA ) is responsible for batch record release, donor record/ ... data entry, auditing, and investigations. The Specialist , QA is responsible for quality assurance...+ Perform quality reviews of donor and batch records + Review and analyze test… more
    Integra LifeSciences (04/16/24)
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  • Specialist , Quality

    Bristol Myers Squibb (Bothell, WA)
    …patients, there's no better place than here at BMS with our Cell Therapy team. The Quality Assurance Specialist position plays a key role in supporting the ... a regulated cGMP environment. The primary focus of the QA Specialist role will be to support...- Wednesday, 9 pm - 7:30 am **Responsibilities:** + Review executed batch records to ensure compliance… more
    Bristol Myers Squibb (05/01/24)
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  • Principal Specialist , Quality

    Editas Medicine (Cambridge, MA)
    …life science and 8+/6+ years respectively of relevant industry experience in Quality Assurance in a Pharmaceutical/Biotech GMP environment. + Experience ... and facility start-up, floor operations, MBR and SOP generation/revision, record review , controlled document generation, batch release, training, materials… more
    Editas Medicine (04/26/24)
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