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Genomic Technologist II; Molecular Pathology

Job in Meriden, Sullivan County, New Hampshire, 03770, USA
Listing for: K.A. Recruiting
Full Time position
Listed on 2026-03-01
Job specializations:
  • Healthcare
    Medical Technologist & Lab Technician, Clinical Research, Medical Science
Job Description & How to Apply Below
Position: Genomic Technologist II (Molecular Pathology)
Location: Meriden

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 clinical 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 / call or text !

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