Position: Full-time Molecular Genomic Specialist I
Location: Clinical Lab Building on UPMC Presbyterian’s Oakland Campus
Schedule: Monday – Friday, Daylight Hours (No Weekends or Holidays)

The Molecular and Genomic Pathology Laboratory (MGP) is a cutting-edge, state-of-the-art clinical laboratory focused on providing exceptional patient care in the fields of inherited diseases, hematological malignancies, and solid tumors. We utilize advanced molecular testing platforms and informatics techniques, including next-generation sequencing (NGS), to deliver high-quality, precise diagnostic results.

Why Join Us?
At MGP, we offer a dynamic and supportive environment where your expertise is valued. You’ll enjoy a rewarding career with opportunities to work on a diverse range of responsibilities while continually developing your skills. Our collaborative culture encourages teamwork, and each team member contributes their unique strengths to advance the mission of the lab.

If you’re ready to join a forward-thinking team dedicated to excellence in patient care, apply today to become part of the MGP Lab team!

UPMC is currently offering a generous sign-on bonus of $15,000 for those who qualify!

Responsibilities:

Independently perform clinical testing in accordance with established SOPs. Process all clinical, QC and PT specimens through clinical workflow. Demonstrate high-level problem-solving skills and analytical abilities to successfully perform laboratory testing. Accurately record relevant data and values in case folders and internal databases. Process samples meticulously to avoid cross-contamination. Meet established turn-around-time deadlines for clinical testing. Maintain expertise in or knowledge of molecular biology techniques, including but not limited to: nucleic acid isolation, nucleic acid quantitation, PCR/RT-PCR/qPCR, Sanger sequencing, LOH, methylation analysis, MassARRAY MALDI-TOF, next-generation sequencing, etc. Effectively communicate with other laboratory members including lab leadership. Maintain track of technical and professional development, including but not limited to attendance at seminars/webinars and participation in educational programs and activities. Identify critical, abnormal and/or unacceptable results and follow-up according to established protocol. Document all corrective action and follow-up with lead and/or supervisor. Adhere to established laboratory and hospital policies and good clinical laboratory practice in areas of procedures, quality control, quality assurance and safety and compliance. Operate, perform routine maintenance on, and calibrate all laboratory equipment as required. Identify problems with instrumentation, methodology, specimens, and/or supplies and follow-up according to established protocols. Maintain proficiency in appropriate Laboratory Information Management Systems (LIMS). Appropriately use automated and/or liquid handling machines for clinical testing. Accurately and precisely analyze molecular assay results for final interpretation by medical staff.