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As a Technician I, GMP Manufacturing - Upstream you will play a critical role in the production and cultivation of AAV-based gene therapy products in compliance with current Good Manufacturing Practices (cGMP) regulations.
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Serve as primary internal support technician for FAS and Technical Sales Specialist for the installation, validation training and troubleshooting of automated, single-use equipment for biopharma and cell/gene therapy customers.
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Strategic Sourcing Associate Director, Cell and Gene Therapy Raw Materials (hybrid) page is loaded. Minimum of 7-10 years of experience in strategic sourcing, procurement, or supply chain management, with a focus on raw materials for Cell and Gene therapy or biologic in the pharmaceutical or biotechnology industry.
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Conduct nonclinical development activities (pharmacology and toxicology) for IND-enablement of gene therapy products. Maintain current understanding of gene therapy field, as well as the scientific literature related to specific drug discovery projects.
$170,704 - $183,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Lead Maintenance Planner and Scheduler (Gene Therapy Program) As Lead Lab Maintenance Planner and Scheduler, you will be responsible for providing support of the Vector Laboratory's equipment and instrumentation asset maintenance, calibration, and spare parts program at the Discovery Labs (DL) in King of Prussia, PA. The assets to be managed include general and advanced laboratory equipment and instrumentation used to manufacture and characterize biopharmaceuticals.
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ElevateBio is looking for a Cell Therapy Manager, QA Operations to join their growing Quality Group at our BaseCamp facility in Waltham, MA. In this role, the Manager will be primarily responsible for providing Quality oversight over execution of clinical cell and gene therapy manufacturing for cGMP compliance through on the production floor interactions, review and approval of batch related documents, and events.
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Familiar knowledge of GLP and GMP requirements as they pertain to protein and gene therapy process development and Quality Control (QC) testing is a plus. Leads the activities associated with the development and execution of methods relevant to protein and gene therapy products for analytical development in a Research and Development environment.
$125,700 - $182,250 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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When you join us at Thermo Fisher Scientific, you'll be part of an experienced, driven team that shares your passion for exploration and discovery. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.
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Here at Kelonia Therapeutics, we aren’t just a preclinical company; we’re trailblazers in viral engineering, pushing the boundaries of in vivo lentiviral gene and cell therapy. At Kelonia, we've gathered a group of pioneers in cell and gene therapy to lead our journey, with extraordinary scientific founders at the helm, providing the cutting-edge technology that sets us apart.
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Keywords: Regulatory, IND, CTA, SharePoint, Gene Therapy, Cell Therapy, Biotechnology, FDA, Pharmaceutical, Regulatory Submission. Piper Companies is currently seeking a Sr. Regulatory Operations Specialist to support a growing and innovative cell and gene therapy company in Philadelphia, PA (Hybrid Schedule.
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A Research Associate to support our therapeutic gene therapy discovery efforts using our proprietary CNS-targeted LNP platform and the CasPlus gene editing system, while also helping the team manage the laboratory.
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Conduct preventive maintenance of surface testing equipment, flare stacks, fluid tanks, and generators. Perform maintenance operations mechanical in nature including turning wrenches, motor valves, rebuilding regulators, BPRs, flanges, and dump controllers.
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Lead analytical development and quality control for AAV gene therapy, small molecules, antisense oligonucleotides, mRNA and protein therapeutics. Modalities include AAV gene therapy, small molecules, antisense oligonucleotides, mRNA and protein therapeutics.
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Taking Care of Our Customers : Performing preventative maintenance services and basic equipment inspections on equipment. Titan Machinery is adding a Lube/Fluid Technician to our team.
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As Gene Therapy Manufacturing Supervisor, you will play a critical role in helping to establish REGENXBIO s first internal GMP BDS and FDP clinical and commercial AAV gene therapy manufacturing capability.
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gene therapy equipment maintenance technician jobs Company: Thermo Fisher Scientific
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