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Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Review genomics data from NGS, Sanger, and MLPA assays, to facilitate high quality molecular genetics testing.
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Maintain appropriate documentation of compliance with CLIA regulations. Report malfunction of medical equipment to Office Coordinator/Practice Manager. Keep inventory of medical supplies and reports them to Office Coordinator/Practice Manager for reorder.
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This individual will foster collaborations between ABS Operations, R&D, Manufacturing, and Akoya’s IVD Program Management Team to ensure the highest possible quality outcomes, while focusing on the implementation and daily maintenance of a Quality Management System (QMS) in a CLIA, GLP and GCP setting.
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Maintain a clean and safe work area as well as practice safe work habits in accordance to current Materials and Services Management, Human Resources, Employee Health and Safety, OSHA, CLIA, etc.
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Ensuring regulatory compliance with OSHA guidelines, CLIA regulations, HIPAA medical privacy guidelines. Ensuring regulatory compliance with OSHA guidelines, CLIA regulations, HIPAA medical privacy guidelines.
$20 an hourPart-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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A variety of molecular genetics techniques are used to include Next Generation Sequencing, real-time PCR, Sanger Sequencing, and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy, and Fragile X syndrome to name just a few.
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