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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.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Experience with optical spectroscopies such as Raman and PL is a plus. Is the primary point of contact for our Customer Spectroscopy customers, Field Service Engineers & global affiliates. BS in Electrical Engineering, Electrical Engineering Technology or physical science, equivalent military education.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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At least three years of experience working in regulatory affairs roles on CDx projects within the in vitro diagnostic industry. The Regulatory Affairs Manager will create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compilation, facility registrations, special projects and strategy to drive market growth worldwide.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Collaborate with Regulatory Operations to compile and review regulatory submissions for completeness and quality. LET ME WIN, BUT IF I CANNOT WIN, LET ME BE BRAVE IN THE ATTEMPT – Motto of the Special Olympics.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Plans and prepares regulatory submissions (510(k), PMA, Technical Files and other regulatory documentation) for product approvals/clearances required by the US FDA and international government agencies, including requisite pre-submissions and post-market approval reports with moderate supervision.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Spectrometers, diffraction gratings, miniaturized motor assembly, ESD sensitive opto-sensors. Use of epoxy resins, glues, and small machines. Cleaning and assembling high precision optical and mechanical components such as.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Identify and draft necessary SOPs and/or Working Practices for Regulatory Affairs. A minimum of 4 years in IVD Regulatory Affairs with direct experience in preparing regulatory submissions including IDEs, 510(k)s and/or PMAs is required.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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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.
$100,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Preferred Work Experience: At least three years of experience working in regulatory affairs roles on CDx projects within the in vitro diagnostic industry. Preferred Work Experience: At least three years of experience working in regulatory affairs roles on CDx projects within the in vitro diagnostic industry.
$1 - $2ExpandApply NowActive JobUpdated 6 days ago
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