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Perform routine analytical tests (e.g., SEC, CE, ICIEF, Protein A) to support the upstream and downstream process development. Analytical Development Scientist. This position involves performing routine analytical tests to support process development, transferring analytical methods to the QC department, and assisting in the development of analytical methods for biologic drugs.
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Novo Nordisk is seeking a highly motivated analytical support specialist to join the Analytical Development team in Boulder, CO. The candidate will be responsible for various analytical laboratory activities including but not limited to: method development and transfer of methods for oligonucleotide intermediates (IPC's) as well as drug substance and drug product release within a nonGMP lab.
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Title: Analytical Development Analyst. Support the development and transfer of analytical methods of biologics drugs (including monoclonal antibodies, bispecific antibodies, ADC.
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The Sr Analytical Development Scientist is primarily responsible for supporting the team during all assay development activities including those required for a regulated environment, as well as participating in the sampling and testing using those analytical tools.
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Perform analytical tests to support process development and transfer analytical methods to QC department. Proficient in analytical chemistry or biology background, skilled in analyzing biological drug products (monoclonal antibodies, bispecific antibodies, ADCs) analysis methods, including but not limited to HPLC, UPLC, CE, Elisa.
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As a bench scientist, independently support the development, validation, assessment and execution of one or more analytical methods e.g. real time PCR (vg titer, residual DNA, residual plasmid DNA), digital droplet PCR, ELISA (capsid titer and residual protein), plaque assay, TCID50 (infectious titer), agarose gel electrophoresis, SDS-PAGE, CE-SDS, HPLC, immunoblotting, immunocytochemistry, analytical ultracentrifugation etc.
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Oversee all analytical development activities in compliance with International Conference on Harmonization (ICH) guidelines to support characterization of raw materials. The Director, Analytical Development (AD) is responsible for setting strategy for the analytical development function and executing the strategy to meet all applicable regulatory guidance.
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Analytical Engineer Associate capable of performing analysis using tools such as; FTIR, thermal analytical methods (DSC, TGA, TMA), chromatography, and other ASTM, ISO, and IPC test methodologies in a Materials Laboratory setting.
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Technical lead of analytical method development for nucleic acids, lipids, & lipid nanoparticles as part of development of FL85 platform, product, process, and formulations. FL85 is seeking a Director of Analytical Development to join our team to lead development of assays focused on CMC development of products based on FL85’s novel technology platform.
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The individual, reporting to the Head of Analytical Development, will lead the method development and qualification of (cell-based) potency and other bioassays in house and support technical transfer to and sample testing at CDMO. The successful candidate will collaborate with other functional teams in Lilly Cambridge and Indianapolis sites and contribute to a variety of assay activities in a highly collaborative environment.
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In this role, you will be responsible for timely development of analytical methods supporting process development and qualification of methods for Quality Control for release and stability testing in compliance with Agenus Quality Systems.
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Harness your mastery in Analytical Tech Transfer, Validation, HPLC, Spectroscopy, Stress Testing, and other specialized analytical development techniques. Develop and execute a visionary analytical development strategy aligned with mission and goals, driving the firm closer to commercialization.
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The Analytical Sciences Technician is responsible for the regulatory and scientific conduct of method development and validation for gene and cell therapy. Moving forward we will combine continuous improvement and innovation to become the preferred preclinical CRO in the industry, by working in partnership with our clients, and leveraging state of the art technologies and platforms we will enable our customers to accelerate and improve the product development cycle, from concept to commercial.
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Reporting to the Associate Director of Analytical Development, the Scientist will be responsible for the development of biophysical and analytical chemistry methods to further gene therapy products throughout clinical development, as well as performing BLenabling characterization studies.
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Catalent San Diego focuses on bringing client drug compounds from discovery to the clinic with services that include analytical development, preformulation testing, formulation development, GMP manufacturing and stability storage and testing.
$17 - $20 an hourPart-timeExpandApply NowActive JobUpdated 2 days ago
Title: analytical development Company: Zeichner Risk Analytics Zra
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