Genomic Technologist II (Molecular Pathology)National Coalition of Healthcare Recruiters • Plainfield, New Jersey, United States
Genomic Technologist II (Molecular Pathology)
National Coalition of Healthcare Recruiters
- Plainfield, New Jersey, United States
- Plainfield, New Jersey, United States
Über
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!
Sprachkenntnisse
- English
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