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Upon establishment of the laboratory and program, this position will utilize a wide range of analytical and radiochemical analyses to support the advancement and release of novel targeted radiopharmaceuticals from the R&D phase through clinical development to GMP commercial radiopharmaceutical production.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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5+ years of laboratory experience in molecular and cell biology, immunoassay, protein chemistry, or other bioassay techniques required. The Field Application Scientist will provide technical support to customers related to the ACROBiosystems GMP product line.
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Your primary responsibilities as a QC Analyst will revolve around providing meticulous support for in-process control (IPC) laboratory operations and conducting testing of raw materials. QC Analyst I requires a minimum of 2 years of hands-on lab experience with at least two analytical technology platforms, one of which must be HPLC; 2+ years GMP experience; and a Bachelor's degree in chemistry, physics, engineering, or related scientific discipline, with documented hands-on analytical experience in coursework.
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The Microbiology Manager is also responsible for the development, implementation, and compliance of activities in the microbiology laboratory area to meet production goals, quality, and cost objectives.
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
$90,000 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated 1 days ago - UpvoteDownvoteShare Job
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Knowledge of biologics manufacturing, bioassays, biochemistry, biostatistics and experience within a GMP testing laboratory. As our new Analytical Technology Specialist, you will support the operations of the Bioassay Laboratory conducting Cell-Based Potency Assay (CBPA) testing of product release, stability and investigation lots.
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Manage the analytical testing of products (in-process, for information, and release) Review the testing schedule with the QC Supervisor Perform day to day analytical testing activities in GMP QC lab to support the on-time release and periodic testing of biological drug products using complex instrumentation and laboratory equipment’s per regulatory/quality policies.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Will primarily focus on the facilitation of routine calibration, maintenance and repairs of GMP manufacturing and laboratory equipment to ensure a continued state of regulatory compliance and continuity of clinical manufacturing operations.
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Certification/Licensure: AALAS certification at the Assistant Laboratory Animal Technician level (ALAT) The pay for this position is $23.00 - $25.00 per hour. About Insourcing Solutions Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment.
$23 - $25 an hourFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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The Facility & Reliability Engineer will also support the successful operation of facility, laboratory, and business functions at multi-use GMP sites within Bristol Myers Squibb, Summit West Cell Therapy Operations, through interaction with internal customers and external service providers.
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Facilitation of process equipment commissioning and qualification, routine calibration, maintenance, and repairs of GMP manufacturing and laboratory equipment to ensure a continued state of.
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The role is a key member of the site and winemaking leadership teams supporting all goals and objectives ensuring delivery of the highest level of wine quality, accountability, adherence to ISO, GMP programs and employee engagement.
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Tech transfer to CMO and scale-up of chemistry, including supporting GMP manufacture. We are seeking a highly motivated process research and development chemist with a proven record of sustained laboratory achievement and innovation to join our growing CMC group at ORIC Pharmaceuticals.
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The Associate Director/Director of Laboratory Quality Assurance provides Quality Assurance lab oversight of a GMP analytical testing and process development laboratory for the testing and development of gene therapy Adeno-associated viruses (AAV.
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Quality check, quality inspection, gmp, quality assurance, Quality control, Laboratory. quality check, quality inspection, gmp ,quality assurance. 2+ years of GMP experience.
$54,080 - $57,200 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago
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