• Legend Biotech USA, Inc. (Raritan, NJ)
    …as protocol and reports from development. Support the implementation of manufacturing and process improvement strategies through cell therapy manufacturing ... knowledge and expertise of cell and gene therapy processes and/or process technologies. They will...and implementation of new manufacturing technologies. Ensure successful manufacturing process comparability and process validation more
    HireLifeScience (05/09/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …with responsibilities for providing quality oversight over the production of personalized cell therapy to support both clinical and commercial requirements in ... aseptic manufacturing facility, preferably in quality assurance,manufacturing compliance, clinical quality, or cell therapy . A minimum of 2 years of experience… more
    HireLifeScience (05/08/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …Experience in supporting cell -based products is a plus Strong knowledge of cell therapy process preferred Experience in cGMP regulatory body audits ... , equipment, and associated deviations and investigations within a cell therapy manufacturing plant to support both...and protocol driven activities such as tech transfer and process validation Provides guidance on industry best… more
    HireLifeScience (04/25/24)
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  • Insmed Incorporated (San Diego, CA)
    …and process development teams to develop, qualify/validate AAV gene therapy cell -based biological potency assays, protein chemistry assays, and molecular ... is seeking a Scientist, QC with broad knowledge and expertise in cell -based potency assays, molecular biology assays, and chemical/biochemical assays as applied to… more
    HireLifeScience (05/11/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …Proficient in the use of quality systems such as SAP. Experience working with cell therapy is preferred Knowledge of cGMP regulations and FDA/EU guidance related ... diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous… more
    HireLifeScience (03/13/24)
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  • Aequor (Libertyville, IL)
    …Project/Domain Overview : Libertyville is Client vector manufacturing facility part of the Cell therapy network. Client will be implementing next generation IT ... and proactively control costs to stay within budget. Follow change control process .Portfolio Financial and Reporting: Support Site IT lead and Global IT PMO… more
    HireLifeScience (05/11/24)
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  • Dexian - DISYS (Summit, NJ)
    … requirements and good documentation practices. * Experience in the qualification of cell therapy equipment a plus * Advanced knowledge of pharmaceutical, ... Title - Equipment Validation EngineerDuration- 06 monthsLocation- Summit, NJPay range- $75.00...Validation Engineer supports the successful implementation of various process /lab equipment at multi-use sites through interaction with internal… more
    JobGet (05/08/24)
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  • On-Board Companies (Bothell, WA)
    …MS Windows Server and SQL server also a plus.* Experience with cell therapy or other biopharmaceutical manufacturing. Other highly regulated industries ... through design reviews and user acceptance testing during the development and validation process .* Perform and communicate planning, development, peer review,… more
    JobGet (04/30/24)
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  • WuXi AppTec (Philadelphia, PA)
    WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to ... Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to… more
    JobGet (05/17/24)
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  • Sunrise Systems Inc (Seattle, WA)
    …Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document ... change control process , periodic review and system reporting. Experience Basic Qualifications: Minimum of 1 year of relevant document control experience in a… more
    JobGet (05/12/24)
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  • Associate Director, Quality Engineering,…

    Bristol Myers Squibb (Devens, MA)
    …for start-up and ongoing operations of the Devens Cell Therapy Facility, including commissioning, qualification, and validation (CQV), computer systems ... validation (CSV), process validation , and change control. **Key Responsibilities** + Directs the...+ Directs the QA oversight of commissioning, qualification, and validation activities required for cell therapy more
    Bristol Myers Squibb (05/15/24)
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  • Quality Manager, Stem Cell Transplant…

    UT Health San Antonio (San Antonio, TX)
    …support the collections, manufacturing, testing and release of clinical and investigational cell therapy products. + Prepares quarterly quality reports and ... Quality Manager, Stem Cell Transplant & Cellular Therapy (Multispecialty...recipients and donors, through audits, assessments and reporting of process and outcome measures, quality improvement activities, and investigations… more
    UT Health San Antonio (04/11/24)
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  • PS Cell Therapy Tech I

    University of Utah (Salt Lake City, UT)
    Details **Open Date** 04/24/2024 **Requisition Number** PRN38365B **Job Title** PS Cell Therapy Tech I **Working Title** PS Cell Therapy Tech I **Job ... Weekend/Holidays) **VP Area** U of U Health - Academics **Department** 01601 - Cell Therapy /Regenerative Med **Location** Campus **City** Salt Lake City, UT… more
    University of Utah (04/25/24)
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  • Associate Director, Cell Therapy Lab…

    J&J Family of Companies (Malvern, PA)
    Associate Director, Cell Therapy Lab Automation - 2406182172W **Description** Janssen Research & Development, LLC. is recruiting for an Associate Director, ... Cell Therapy Laboratory Automation that can be...Analytical Development (AD) Biologics group supports method development and validation , process and formulation development, release, and… more
    J&J Family of Companies (04/22/24)
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  • Lab Technician - Cell Therapy

    Actalent (Waltham, MA)
    …safe manner. * Adheres to all cGMPs, compliance/regulatory mandates and quality requirements. Skills: cell therapy , t cell , GMP, batch record, batch record ... appropriate production documentation. * Maintains cleanliness and orderliness of process area. * Ensures production area is stocked with...review, biologics, tcr, validation , manufacturing technician, Lab Technician, Laboratory Technician, … more
    Actalent (05/11/24)
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  • Senior Associate Scientist - Translational…

    Bristol Myers Squibb (Seattle, WA)
    …day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy , this is work that transforms the lives of patients, and ... industry experience to join our Translational Research department in the Cancer Immunology and Cell Therapy Thematic Research Center (CI CT TRC). As a subject… more
    Bristol Myers Squibb (05/11/24)
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  • Manager, Quality Engineering and Validation

    Bristol Myers Squibb (Bothell, WA)
    …to patients, there's no better place than here at BMS with our Cell Therapy team. The Quality Engineering and Validation (QEV) team at BMS is responsible for ... optimizing a production line to the latest breakthroughs in cell therapy , this is work that transforms...site automation (MES, DeltaV, InfoBatch, PI System, etc.), maintenance, process validation and engineering documents, test protocols,… more
    Bristol Myers Squibb (05/18/24)
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  • Senior Validation Engineer I (Aseptic…

    Bristol Myers Squibb (Bothell, WA)
    …day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy , this is work that transforms the lives of patients, and ... Engineer I, Validation is responsible for supporting the production of personalized cell therapy products for clinical and commercial supply at the BMS… more
    Bristol Myers Squibb (05/18/24)
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  • Laboratory Process Validation

    BioBridge Global (San Antonio, TX)
    …bridge critical medical industry needs with innovative solutions. Job Title: Laboratory Process Validation Associate, Research & Development Revision: 0000 Job ... **Major Duties and Responsibilities** Essential Tasks Develops, or revises equipment/assay/ process validation plan documents. Develops or revises production… more
    BioBridge Global (05/10/24)
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  • Senior Manager Validation , Engineering…

    Bristol Myers Squibb (Bothell, WA)
    …day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy , this is work that transforms the lives of patients, and ... , Engineering and Technology is responsible for supporting the production of personalized cell therapy products for both global clinical trials and commercial… more
    Bristol Myers Squibb (05/12/24)
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