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Acts as a drug product process development technical expert to provide swift and innovative solutions to complex challenges in formulation, filtration, filling (vials/syringes/devices) and lyophilization of parenteral products.
$48 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Transferrable Industry backgrounds: Drug substance/ pharma / chemical/ oil refinery/ mechanical. (Transferrable Industry backgrounds: Drug substance/ pharma / chemical/ oil refinery/ mechanical.
$35 - $54ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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In support of Amgens mission to serve patients, the Development Product Engineering Organization at Amgen is a diverse team responsible for identification, development, commercialization, and continuous improvement of drug delivery technologies to optimize the patient experience for Amgens portfolio of therapeutic products.
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The Engineer will apply cell culture and/or purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology.
$42 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Engineer will apply cell culture and purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in both stainless and single-use formats.
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Knowledge of drug substance cell culture/harvest bioprocessing and/or knowledge of downstream bioprocessing (chromatography, filtration, buffer compounding) This Senior Associate Manufacturing position is within Amgen Thousand Oaks Drug Substance Supply (Manufacturing) organization and will be focused on lifecycle management of existing products and NPI continuous improvement initiatives for cell culture, harvest, and purification operations.
$107,310 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Provides process development expertise for commercial drug product processing in specific areas such as Sterile processing, Process Characterization, Tech Transfer and Validation. 5+ years of drug product process development experience in the pharmaceuticals/biotechnology industry.
TemporaryExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience with automation (Delta V) is a plus, as well as experience with computer programming (SQL / VBA / PLC), drug substance systems, and/or chromatography, filtration, single-use and stainless steel product trains, and various mixers.
$41.06 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support commercial drug product manufacturing operations with technical evaluation of NC/CAPA and technology transfer. 10+ years of drug product process development experience in the pharmaceuticals/biotechnology industry.
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Albertsons Companies is a leading food and drug retailer in the United States. The Company operates stores across 34 states and the District of Columbia with 24 banners including Albertsons, Safeway, Vons, Jewel-Osco, Shaw's, Acme, Tom Thumb, Randalls, United Supermarkets, Pavilions, Star Market, Haggen, Carrs, Kings Food Markets and Balducci's Food Lovers Market.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience in leading the design and implementation of clinical pharmacology and biopharmaceutics studies including bioequivalence, bio-comparability, drug-drug interaction, special population, ethnic sensitivity, ADME and pediatric studies and integrating results into regulatory filings, and product labels.
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Biologics/ drug substance purification experience required (Chromatography, filtration, UFDF unit ops) Knowledge of purification processes/equipment; scale-up factors, process deviations, quality attributes.
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Description Job Title: Drug Substance SupervisorLocation: Thousand Oaks, CAAbout the role:The Drub Substance (DS) Supervisor oversees manufacturing operations while maintaining compliance with environmental, health and safety (EHS) guidelines, current good manufacturing practices (CGMPs) and any other regulation that could apply.
$132,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Supports commercial drug product manufacturing operations with technical evaluation of NC/CAPA and technology transfer. Strong knowledge of Quality systems, Drug Product Manufacturing and Validation.
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Designs clinical pharmacology components of drug development project clinical plans and provides clinical pharmacology expertise to project teams including plan, design and oversight of clinical pharmacology studies.
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drug job in Moorpark, CA
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