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Perform cGMP analytical testing (bioassay, flow cytometry, qPCR, ELISA, and UPLC) We seek an experienced Analyst, QC Bioassay / Biochemistry to support establishing new commercial-level in-house GMP testing laboratories performing release and stability testing for multiple stages of our gene therapy and immune oncology products.
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CONSIDERED EXPERIENCE INCLUDES: Field Service Technician Calibration Tech Validation BioLab Automated Robotic Multichannel Pipetting & Multiplex Microplate Autoloaders Sampler Readers Immunoassay Bioassay Electrochemiluminescence Detection Tabletop Laboratory Instruments CCD Optics Micropumps Mechatronics Proprietary Software #DiedreMoire #JobSearch #JobHunt #JobOpening #Hiring #Job #Jobs #Careers #Employment #jobposting #biotechjobs #FieldServiceJobs #LabTechnicianJobs.
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Scientific Director - Bioassay (Bioproducts Research & Development) page is loaded. Scientific Director - Bioassay (Bioproducts Research & Development) Assess and evaluate new technologies suitable for bioassay development.
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The CTL Bioassay Developer develops, evaluates, and transfers complex laboratory tests and cell processing methodologies from translational research into the clinical laboratory providing intellectual and scientific expertise to support and conduct complex clinical research in cellular therapy.
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Bioassay Laboratory, Biorepository, Biosafety Level -3 Lab, Data Management. Bioassay Laboratory, Biorepository, Biosafety Level -3 Lab, Data Management. computational chemistry or computeraided drug designing from a.
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In depth knowledge of common analytical techniques used in the bio-pharmaceutical industry such as iCIEF, UPLC, CE, Bioassay, ELISA, LC-MS etc., including method. The Senior Principal Scientist will serve as the point of a contact for BMS on the technical leadership for a multitude of products or major brands (Biologics) for the Global Quality Analytical Science & Technology organization.
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At least 1 year of experience within the biopharmaceutical or pharmaceutical industry preferably in ELISA or cell-based bioassay field. ELISA, cell-based bioassay, analytical test, bioassay, GMP, Trackwise, SAP, 5S, large molecule bioassay, analytical technique.
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The Associate Director, QC Cell Culture and Bioassay will be responsible for overseeing a testing laboratory charged with the execution of all GMP bioassay testing (release and stability) related to Sarepta' s Gene Therapy pipeline.
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The Nuclear and Radiochemistry Group supports both operational missions and R&D efforts in bioassay, nuclear forensics, nuclear nonproliferation, safeguards, treaty monitoring, and weapons programs.
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Collaborate with Analytical Development to generate and approve protocols, reports, and other technical documents required for the qualification and transfer of bioassay methods. This individual will join the Quality Control Bioassay team supporting the GMP manufacturing facilities in Redmond, WA and Seattle, WA. The role is responsible for conducting routine/non-routine testing and analysis of GMP product using methods such as ELISAs, qPCR, and cell-based assays at both Washington state facilities.
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Experience in TLD, OSL, Accuscan gamma detection system, bioassay, internal and external dosimetry. Experience in TLD, OSL, Accuscan gamma detection system, bioassay, internal and external dosimetry.
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As a Bioassay Scientist you are responsible for performing techniques within a laboratory environment, compliant with regulations including cGMP and GLP. Responsible for bioassay troubleshooting and continuous improvement initiatives.
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Job Title: Quality Analyst I, Bioassay Location: Union City, GA Job Type: Temp-to-Hire, Full-Time Shift: On-Site, Options below: Tue.-Sat.: 12am-8am Wed-Sun: 9pm-5am Thur-Mon: 9pm-5am Sat-Wed: 12am-8am Salary: $25/hour (DOE) + Kelly Standard Benefits Job Description: The Quality Analyst I, Bioassay, will be responsible for performing daily lab operations with the assigned functional area related various assays for qualifying raw materials and reagents as well as complete other assigned duties.
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Support all operations of the Bioassay labs including the ordering supplies and maintaining laboratory equipment and lab spaces. Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on Bioassay related matters.
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BS./M.S. in relevant scientific discipline with a minimum of 5 – 8 years of direct CMC bioassay development experience in biotech/biopharma or Ph. D. with 2+ years of directly relevant experience.
$121,000 - $158,000 a yearExpandApply NowActive JobUpdated 2 days ago
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