Genomic Technologist II (Molecular Pathology)

Genomic Technologist II (Molecular Pathology) (Employer Name Not Available)

Occupation:

Radiologic Technologists and Technicians

Location:

Plainfield, NH

• 03781 Positions available: 1 Job #: 2371150

Source:

National Coalition of Healthcare Recruiters

Posted:

08/30/2025

Web Site:

www.nchcr.com

Job Type:

Regular, Full Time (30 Hours or More) Job Requirements and Properties Work Onsite Full Time Schedule Full Time Job Type Regular Job Description Help for Partial Job Description. (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!