[ref. b87450518] Genomic Technologist II (Molecular Pathology) - Plainfield

apartmentNational Coalition Of Healthcare Recruiters placePlainfield descriptionPermanent calendar_month 

Only QUALIFIED Healthcare Professionals accepted) Technologist/Technician - Need a new job? I've got great news for you. I have a Genomic Technologist II (Molecular Pathology) position available north of Plainfield, New Hampshire!

Details
  • Full-time
  • Shift: Day with weekend rotation
  • Opportunities for growth
  • Full, comprehensive benefits package (PTO, health insurance, life insurance, 401k, etc)
Requirements
  • Bachelor's degree
  • ASCP certification required
  • Minimum of 2 years experience with multiple clinical genomics platforms (as outlined above).
  • Moderate proficiency in Microsoft EXCEL, Microsoft PowerPoint, and Microsoft Word
  • Minimum of 2 years experience with various QC principles and analysis in a clinial laboratory (ex. CLSI Standards.)
  • Minimum of 2 years experience with routine and preventative maintenance, operation, and trouble shooting for technical and software related issues.
  • Detail-oriented, well-organized.
  • Advanced written and verbal communication.
Job Summary
  • Can perform and train on a variety of genomics testing including but not limited to nucleic acid isolation, PCR (end point, real-time, droplet digital), chromosome microarray, molecular infectious disease testing, Sanger sequencing, Next Generation Sequencing, RFLP, and familiarity with molecular automated platforms
  • Participates in validation of clinical testing and development of new clinical assays to be run in the Clinical Genomics and Advanced Technology Lab.
  • Maintains quality control|quality assurance as designated by the genomics Lead.
  • Analyzes, reports, and troubleshoots data generated from cinical genomics technologies and assays such as but not limited to NGS, PCR, FISH, karyotyping, RFLP analysis.
  • Has proficiency with both the LIS and EMR.
  • Communicates well in oral and written fashion.
  • Writes and reviews all applicable laboratory SOPs.
  • Responsible for analysis of clinical testing proficiency samples to be reported to regulatory agencies (i.e., CAP Surveys).
  • Performs other duties as required or assigned.

Click apply or email your resume to leah@ka-recruiting.com| call or text 617-746-2751!

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