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QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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IQVIA MedTech is a fast-growing business focused on delivering fit for purpose solutions to the medical device and in vitro diagnostics industry. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
$200,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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You have demonstrated knowledge of in vitro diagnostics and biotechnology device manufacturing and experience establishing and maintaining robust validation and process control strategies with Strong Lean Six Sigma or alternate continuous improvement skills for root cause analysis.
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This is an onsite laboratory-based role in preclinical formulations R&D for the intracellular delivery of RNA. The successful candidate will create novel nanoparticles comprising nucleic acids, lipids, polymers and peptides, perform physical-chemical characterizations, and conduct in-vivo / in-vitro studies.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
$65,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Previous experience with Computer System Validation (CSV) and experience with System Development Life Cycle of automated computer systems within biopharmaceutical environments. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
$65,000 a yearFull-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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The Associate Technician Quality Assurance Engineering of Beckman Coulter Diagnostics is responsible for full range of Instrument PM and quality control test (raw materials and in-vitro diagnostic (IVD) reagents used in clinical chemistry laboratories.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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We are seeking an exceptional individual with industry experience in antibody development for a Senior Platform Scientist role to lead the development of in single chain antibody fragments (scFvs) on Protillion's high-throughput protein engineering platform via novel in vitro translation methods.
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By joining Bio-Techne, San Marcos you’ll join a proven leader in the Manufacturing of In-Vitro Diagnostics. Position Summary: As an Equipment Technician, you will operate and maintain the on-site lyophilization, filling and capping equipment as well as perform preventative maintenance and routine maintenance on equipment.
$75,600 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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5+ years in a manufacturing environment, including experience with production processes, equipment, and materials used in biotech production, specifically with lateral flow assays and other in vitro diagnostic products.
$90,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum of 7-10 years Regulatory Affairs experience in Pharmaceutical, Biologics, In vitro diagnostics, or Medical Devices. Thermo Fisher is seeking a Regulatory Affairs professional to join the area of molecular diagnostics to lead the Bio-Sciences Division Regulatory Affairs team in North America.
$177,200 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Basic knowledge of regulatory requirements for in vitro diagnostic and medical device products. The Clinical Research Associate holds an essential position within clinical operations function of the Global Clinical Affairs team to ensure adherence to Good Clinical Practice (GCP) and department standard operating procedures.
$95,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
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