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The Associate Director- Cell Therapy Sales, Operations, & Mid/Long-Term Supply Planning is a key contributor to a GSC organization that leads and drives business critical business processes of Sales, & Operations Planning (monthly), detailed monthly drug product planning/scheduling activities (monthly), and Long-Term Supply & Capacity Planning (semi-annually.
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Roto-Rooter is a great place to work, providing excellent pay, flexible work schedules and top benefits for our outside sales representative team. Conduct territory sales visits offering our excavation or water restoration services.
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The Stability Senior Scientist reports to the Senior Principal Scientist or Associate Director of GBS and is responsible for end-to-end oversight of product stability programs. The Stability Senior Scientist reports to the Senior Principal Scientist or Associate Director of GBS and is responsible for end-to-end oversight of product stability programs.
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Title: Senior Research Associate. Perform enzymatic assays, ex vivo sample processing, and various molecular biology techniques including flow cytometry, western blot, and ELISA. Hands-on experience with cell culture and standard molecular biology assays, including enzymatic assays, flow cytometry, and western blot.
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The AS&T Associate Scientist is responsible for lifecycle management of analytical testing methods for Century's genetically-engineered cell therapy products in support of clinical manufacturing.
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Service-oriented with strong face-to-face sales skills. BlueTriton Brands, Inc. (“BlueTriton”) is a water and beverage company in North America that produces and distributes a portfolio of brands of spring water, purified water, and other beverages, which include Poland Spring®, Deer Park®, Ozarka®, Ice Mountain®, Zephyrhills®, Arrowhead®, Origin™, Saratoga®, AC+ION®, Pure Life®, B’EAU®, and Splash Refresher.
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Our sales and store support teams, also known as clerks in the grocery world, play an important part in ensuring our stores are clean, organized, and shoppable so that our customers can find exactly what they need to keep their families healthy and fed.
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Specifically, the candidate will support the development and optimization of pre-clinical and clinical assays for neutrophil-mediated diseases by assisting with cell culture, in vitro and ex vivo assays, and molecular biology assays.
$68,000 - $90,467 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The CMC Regulatory Associate Director, Biologics is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses & background packages (including participating/leading HA meetings); and/or post-approval submissions.
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The Edibles Associate provides on-site support to the production areas within a cannabis cultivation facility. As a Edibles Associate, you are responsible for supporting the manufacturing of cannabis infused edibles and assembling and packaging products for distribution.
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The TLL will work closely, and within approved SOPs, with other field professionals, including but not limited to the National Sales Director and Regional Managers, in addition to home office-based colleagues in Marketing, Medical Affairs, Sales, and Market Access.
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Biologics development GxP laboratory seeks a hard-working, results-focused Research & Development (R&D) scientist with experience in protein analysis to bring a world-class R&D Biologics portfolio to market.
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The Pharmacokinetics, Dynamics, and Metabolism (PKDM) department at Sanofi contributes to the safe and effective therapeutic treatment of each patient by applying appropriate pharmacokinetic (PK) and pharmacodynamic (PD) principles to drug development and accelerating the process, where possible.
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Name: Stability Associate Scientist. Use computer software/programs: Microsoft Office applications, SAP, LIMS, Quality Management System (e.g. TrackWise or Veeva), JMP, etc. Review/approve creation/modifications to Master Stability Protocols (MSP) and Study-Specific Protocols (SSP), batch-specific enrollment documentation, and LIMS stability studies.
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Job Title: Stability Associate Scientist. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a pharmaceutical manufacturing facility.
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Title: sales associate Company: Fuyao Glass America in Somerset, NJ
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