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We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform.
$50 hourlyFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Lead Reagent Manufacturing Associate will interact with multiple teams including the Clinical Operations, Technology Development, Process Engineering, Supply Chain, and Quality groups.
$143,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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You will collaborate closely with multiple teams across Process Development, Analytical Development, Regulatory Affairs, Quality and Manufacturing. Summary: The Bioprocess Development Associate will develop and optimize protein and protein-conjugate manufacturing processes.
$85,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong background in biologics development and manufacturing, with expertise in raw materials selection, characterization, and process optimization. Promotes scientific innovation and technology adoption to enhance material assessment for process development and manufacturing efficiency.
$230,230ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Associate Director of Radiopharmaceutical Process Development will be executing the CMC development plan and IND enabling activities, leading to the clinical manufacturing of the Drug Product.
$185,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are seeking a highly motivated, attentive, and self-driven candidate to join our team, Biologics Pre-Pivotal Formulation and Process Development, as a Senior Research Associate I. Once onboarded, the successful candidate will contribute in developing formulation and drug product processes for innovative molecules to support toxicology and early clinical stage studies.
$120,120 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work in close cooperation with CMC and Quality Assurance to ensure timely manufacturing, packaging, labeling, and shipping of supplies for the clinical trials. Knowledge of the drug development process, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
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Manufacturing Science and Technology (MSAT) is responsible for successfully and seamlessly transitioning the vaccine process from Process Development to Commercial, developing and executing technical launch and commercialization strategy, continuously improving process robustness through to end of lifecycle, and ensuring best possible patient outcomes while creating value for the enterprise.
$197,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Working understanding of analytical tools used in process development (DSC, TGA, DVS, HPLC, NMR, KF, PLM, XRPD). Experience in tech transfer, scale-up, manufacturing on multikilogram scale, and working in GMP environment.
ExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Writes and/or reviews protocols, purification development reports, batch records, standard operating procedures, and other technical reports in support of manufacturing and process tech transfer.
$240,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Protein Characterization Associate Scientist III will report to Director-level personnel in Assay Development to support Quality Control, Process Development, and other CMC departments. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.
$138,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Manufacturing Associate will work with other manufacturing associates and engineers to implement and validate new processes and procedures, troubleshoot equipment, and optimize overall system performance.
$90,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Downstream Process Development group is responsible for critical drug development functions such as: development of robust downstream processes, technology transfer and scale-up to contract manufacturing facilities, and technical support and overseeing of manufacturing at contract manufacturing facilities.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Perform various manufacturing tasks such as operating, troubleshooting, sterilizing, maintaining, preparing, and cleaning of various process equipment such as stirred-tank bioreactors, media/buffer solutions, disc stack centrifuges, homogenizer, dryer, TFF skid, chromatography systems, parts washers, and CIP systems, under the guidelines of established SOPs and cGMP regulations.
$80,000 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Partner closely with the CMC, Regulatory, and Quality teams to ensure smooth transition from process validation to routine commercial manufacturing. Manage the Global Supply Review (GSR) process specifically ensuring no impact to global supply, closely managing routine manufacturing for API & Drug Product & Packaging.
Full-timeExpandApply NowActive JobUpdated 1 month ago
process manufacturing associate jobs in San Mateo, CA
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