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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.
$105,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - 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 11 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 Today - 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 Today - 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.
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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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Thermo Fisher is hiring a Sr Regulatory Affairs Manager for in vitro diagnostics. They will provide support to In-Vitro Diagnostic core teams and can work in Carlsbad, CA. The manager will handle regulatory activities including drafting and reviewing sPMA’s, pre-submissions, and other filings.
$154,700 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago
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