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Bachelor of Science Degree in the Biological Sciences, Bioengineering or Chemistry with a combination of education and experience performing biochemistry, molecular biology, microbiology, and chemistry.
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Performs pre-analytical, analytical and post-analytical phase testing of all complexities as defined by Clinical Laboratory Improvement Act/Amendment (CLIA) to include specialized tests and analysis in one or more areas of clinical laboratory such as Hematology, Microbiology, Clinical Chemistry, Urinalysis, Immunohematology, Serology, Parasitology and chemical and morphological examinations to obtain data for use in diagnosis and recording laboratory test results.
$63.52 - $68.72 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Description:Responsible for a variety of high-complexity, clinical laboratory testing in Chemistry, Hematology, Microbiology and Blood Bank. Perform QC/QA procedures, preventive maintenance and test validation.
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Experience in risk management, tech transfer, validation, analytics, and microbiology and/or chemistry, within a GMP environment. Bachelors of Science in Chemistry, Microbiology, Engineering.
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Minimum Requirements: · BS or MS in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline · 3 years experience supporting cGMP manufacturing (specifically within validation, engineering, technical services/MSAT, operations, quality assurance, etc.
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Medical device sterilization validation experience (may include steam, EO, gamma, e-beam, and low- temperature modalities) The Senior Validation Engineer will conduct cleaning, disinfection, and sterilization validation testing on-site or in cooperation with external laboratories to support domestic and international regulatory submissions.
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The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.
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Medical Technologist II requires licensure and experience in Blood Bank or Microbiology and at least one other Lab section. Up to $15,000 Sign On Bonus available based on experiencePosition Summary:Precisely and accurately performs and evaluates a variety of technical procedures in Blood Bank or Microbiology and at least one other Lab section/location based on State licensure and experience.
$15,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provides expertise to sterilization, validation and microbiological methods and processes related to IGT Devices products designed and manufactured, as well as products purchased. You're the right fit if: You've acquired 5+ years of experience in Quality Operations in the medical device industry specifically in a sterilization and microbiology function.
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Demonstrates an understanding of quality concepts such as: cost of quality, analytical metrics and / or statistics, trending, quality planning, validation, CAPA and problem solving. Bachelor’s degree in related science field, or equivalent work experience (Microbiology, Chemistry, Biology, Physics) preferred.
$66,500 - $95,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform lab work: HPLC, TOC, LAL, bench testing, Analytical chemistry analysis and microbiology (cross training) according to written procedures. Chemistry, hplc, method validation. Method validation/method Transfer.
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Bachelor’s degree with a major in Biology, Microbiology, or related Life Science. The Quality Control Environmental Monitoring Associate I is responsible for performing sampling and testing in support of manufacturing and validation activities, under the direction of a Supervisor or higher.
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Conduct testing following SOPs using LCMS, HPLC, UV/Vis, Wet Bench chemistry,Raman spectroscopy, pH as well as Microbiology and Environmental testing such as Endotoxin , Bioburden, and others. With its foundations in engineering disciplines, the company’s platforms vertically integrate proprietary hardware, software, bioinformatics, chemistries, and molecular biology to advance basic research, target validation, and clinical trials.
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This individual will join the Quality Control management team supporting the GMP manufacturing facilities in Redmond, WA and Seattle, WA. As the QC Microbiology Manger, you will be responsible for the daily oversight for the QC Microbiology lab operations in support of routine GMP operations, method transfer, validation and method lifecycle activities at Just-Evotec.
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Prepares, reviews and executes validation projects for heat-sensitive devices using vaporized hydrogen peroxide gas sterilization techniques. Must have a thorough knowledge of cGMP and regulatory requirements for validation of equipment and computerized systems in the biopharmaceutical or pharmaceutical industry.
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