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Understanding the healthcare delivery system including: buy & bill, specialty pharmacy, distribution models, medical device and/or biologics experience is strongly preferredBuild and execute business plans for top markets within their geographyAdditional commercial function experience a plus (i.e. sales training, marketing, managed markets, sales/business analytics, etc.
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Minimum of 5 years’ experience with mass spectrometry, liquid chromatography, and other analytical techniques for analysis of biologics. At least 3 years hands-on experience with mass spectrometry analysis of biologics and related sample preparation workflows.
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RN to work in a team environment (RNs, MAs, PAs, MDs) to administer ordered infusion(s) (i.e. Blood products, Chemotherapy/Biologics, Research Medications, Gene Therapies, Cell Infusion, draw labs, access IV/CVC, change CVC caps/dressing, give Factor, subQ/IM injections, provide patient/family education, and provide return appointment schedule to family.
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Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives.
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The U.S. Food and Drug Administration (FDA) has accepted for review ImmunityBio’s resubmission of its Biologics License Application (BLA) for N-803, a first-in-class IL-15 superagonist, plus Bacillus Calmette-Guérin (BCG) for the treatment of BCG-unresponsive non-muscle-invasive bladder cancer carcinoma in situ (CIS) with or without Ta or T1 disease, and has set a user fee goal date (PDUFA date) of April 23, 2024.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Bachelors degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with a minimum of 2-4 years of experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Working knowledge of GMP, quality systems and regulatory requirements (21 CRF Part 11/210/211/600/610), practices/principles. Experience with cell therapy manufacturing. Perform quality investigations of manufacturing Deviations, GMP and Quality System issues, non-conforming materials, and CAPA, as needed.
$100 - $125Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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VTI Life Sciences strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries.
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This position supports the California Department of Public Health’s (CDPH) mission and strategic plan by ensuring quality standards in clinical and public health laboratories, tissue and blood banks, the production of biologics, and laboratory scientists through licensing, examination, inspection, education, and proficiency testing.
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The U.S. Food and Drug Administration (FDA) has accepted for review ImmunityBio's resubmission of its Biologics License Application (BLA) for N-803, a first-in-class IL-15 superagonist, plus Bacillus Calmette-Guerin (BCG) for the treatment of BCG-unresponsive non-muscle-invasive bladder cancer carcinoma in situ (CIS) with or without Ta or T1 disease, and has set a user fee goal date (PDUFA date) of April 23, 2024.
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Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals. The manufacturing technician is an integral part of the overall process required to convert human plasma to injectable protein therapies.
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Knowledge of Fill Finish and Biologics production environments preferred. Mantell Associates is currently partnered with a fully integrated CDMO with global sites, who are seeking a Senior Quality Engineer to provide experienced QA support from product development through cGMP clinical and commercial production.
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We are looking to staff a highly motivated Validation Specialist/ Engineer 1 responsible for delivering commissioning, qualification, and validation (CQV) services related to equipment, instruments, and systems for clients in the biotech/pharmaceutical / medical device industry.
$66,000 - $85,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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5+ years of specialty/rare disease/biologics sales experience, neurology strongly preferred. As part of that team, the Territory Business Manager (TBM) for the Neurology Franchise will drive demand generation through a focused approach on healthcare professionals, academic institutions, and specialty pharmacy/infusion providers.
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BS in Mechanical/Biomedical/Industrial Engineering is required with 10+ years or equivalent experience in engineering in a life science, pharmaceutical, medical device, and/or biologics setting required.
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biologics job in Torrance, CA
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