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The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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Platform through lentivirus vector design, in vitro function assay, and assay development of virus. vector design, virus packaging, immune cell isolation and expansion, multi-color flow cytometry.
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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application. QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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Experience in the performance of in vitro assays with clinical materials and the use of LIMS. Duties will also include the preparation of bacterial and tissue culture growth media, the preparation of bacterial isolates and tissue culture cell lines for cryogenic storage, the propagation of tissue cultures from cryogenic storage, and monitoring HL60 cells by FACS. Assistance with other assays such as ELISA / MSD and serological assays for the characterization of bacteria is possible.
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Experience programming in Excel Visual Basic, Access, LabView, C-Sharp or MATLAB plus. Knowledge of Pro-E (preferred) or Solidworks a plus. Experience in statistical analysis, spectroscopy application or Imaging Sensors is a plus.
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Assists PLM’s and applications with in-house (e.g., Raman Boot Camp) and outside events (e.g., workshops/seminars at customer sites) Capturing revenue through upselling and cross-selling accessories, services, contracts and more to existing customers through ServiceMax. This is to be done via cold calls, prospecting, and emails, etc.
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Our client, a world leader in Pharmaceuticals & In-Vitro Diagnostics (IVD), is looking for a "Senior Lab Technician". Knowledge in oligonucleotide synthesis and PCR technology is desirable. Performing oligonucleotide synthesis and characterization by following detailed instructions outlined in production batch records and SOPs.
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The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. Eurofins 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.
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A minimum of five (5) years experience in medical device, IVD (in-vitro diagnostics), and/or pharmaceutical experience required. The Manager of Quality Operations leads a team of quality specialists and ensures that product is produced that meets design specifications, quality system requirements, and regulatory requirements.
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The OpportunityQuidelOrtho 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.
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The function supports in vitro diagnostics regulatory affairs, including companion diagnostics, in support of Johnson & Johnson therapeutic product development. In partnership with the diagnostic test provider, handle the timely coordination, compilation, and submission of investigational and new in vitro diagnostic medical device applications to the regulatory authorities with an emphasis on North America and the European Union.
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The Company develops, manufactures, and markets in-vitro diagnostics (IVD) tests. Must have a law degree from an accredited and recognized university. The Company develops, manufactures, and markets in-vitro diagnostics (IVD) tests.
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Research experience in molecular and cellular biology including experience with culturing and handling of cells and tissues, in vitro biochemical (e.g. ELISA, enzymatic activity) and molecular (e.g. QPCR) assays is required.
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In vivo study design and assay development. The candidate will be able to contribute to developing in vivo cell therapy. Experience: >3 years’ post-graduate experience in human immunology, virology or lentivector gene therapy, 1-3 years of.
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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.
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vitro job in Somerset, NJ
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