Description

• The Assistant Director will support the UPMC Clinical Genomics Laboratory (UCGL) at UPMC Magee Women's Hospital, a laboratory performing prenatal, constitutional, and oncology molecular testing.
• UCGL provides comprehensive services including whole exome sequencing, disease specific genomic panels, hereditary cancer screening, carrier screening, and pharmacogenomic analysis using advanced technologies such as next generation sequencing (NGS).
• The Assistant Director will contribute to technical leadership, compliance oversight, case sign out, assay development, client consultation, and education/training, while also holding a faculty appointment at the University of Pittsburgh.
• Evaluate and report clinical genetics and genomics cases, including carrier screening, Sanger sequencing, quantitative RT PCR, and NGS.
• Provide technical and compliance oversight for the clinical genomics laboratory; review and approve procedures and QA/QI plans with the CLIA/CAP Lab Director.
• Assist in developing, validating, implementing, and maintaining laboratory procedures.
• Ensure ongoing compliance with CLIA, CAP, and other regulatory requirements.
• Collaborate with UPMC and University of Pittsburgh partners, including UPMC Children's Hospital, on service development and business planning.
• Consult with clinicians and clients regarding test selection and result interpretation.
• Maintain active ABMGG certification and remain up to date with advances in genetics and molecular genomics.

• Participate in research aligned with the clinical and public health missions of UPMC and the University of Pittsburgh.
• Collaborate with faculty and researchers across the institution.
• Contribute to teaching at undergraduate and graduate levels; provide training to laboratory staff, students, residents, and fellows.
• Publish in peer reviewed journals and present at professional conferences.

• PhD, MD, or DO in Clinical Laboratory Science, Genetics, Molecular Biology, or related field.
• ABMGG board certified or board eligible in Laboratory Genetics and Genomics or Clinical Molecular Genetics.
• Minimum 3 years clinical laboratory experience.
• Expertise in exome/genome analysis and interpretation of sequence and CNV data from NGS.
• Excellent written and oral communication skills.
• Demonstrated problem solving and operational leadership.
• Proficiency with LIMS and genomic data analysis tools.