OMICS Laboratory Lead/Manager II
Title: OMICS Laboratory Manager II
Location: Onsite, Pittsburgh, PA 15219
Type: 6-month contract to hire
Hours: 8AM-5PM
Start: January
Overview:
Join as a Laboratory Manager II to monitor personnel and workflow in the area. Track and monitor QA/QC in conjunction with other laboratory leadership. Oversee laboratory throughput metrics and workflow optimization, ensuring balanced workloads, adherence to deadlines, and high data fidelity under time-sensitive conditions.
Responsibilities
- Manages daily laboratory operations of a division, department, function, or program, including conducting and overseeing quality assurance and quality control.
- Perform clinical testing in accordance with established SOPs. Maintain oversight of all clinical testing.
- Maintain clinical workflow for area to meet established quality and TAT, including technologist and bench schedule, status of cases (STAT, special request, etc).
- Maintain competency for all benches in area. Rotate regularly through clinical workflow.
- Be able to step in and help clinical work when necessary.
- Troubleshoot problematic cases, including when to repeat case and when to cancel testing.
- Act as point-person for communication with vendors regarding problems with instruments and/or software.
- Update SOPs, as needed, to maintain current accurate procedure documentation.
- With support and guidance from laboratory leadership and Medical Director, oversee supplemental validations and implementation of procedural changes.
- Write-up all supplemental validations and compile supporting data.
- Oversee training of technologists, including new hires and cross training of current technologists.
- Monitor and assess competency for all area technologists.
- Adhere to CAP and other regulatory agency regulations for competency assessment. Monitor Proficiency Testing for assays in area. Track all results for concordance and document as appropriate.
- Work with MGP QA and lab leadership and Medical Director as needed for preparation for inspections. Complete performance reviews for all area Molecular Genomic Specialists.
- Monitor and approve reagent/supply orders for area. Act as liaison for daily happenings in clinical workflow between technologists and laboratory leadership.
- Track area technologist indirect hours (MRS). Work with laboratory leadership including Medical Director for ideas for, validation of and implementation of development projects.
- Maintain track of technical and professional development, including but not limited to attendance at seminars/webinars and participation in educational programs and activities.
- Oversee sample triage, barcoding, and data integrity across all omics workflows.
- Ensure consistent application of CAP/CLIA-compliant procedures for sample tracking, storage, and LIMS documentation across genomic, proteomic, metabolomic, and lipidomic assays.
- Coordinate operation, scheduling, and maintenance of high-throughput automation platforms (Eppendorf, Tecan, Hamilton) and analytical instruments (Orbitrap Exploris, Stellar, SomaLogic, iScan).
- Provide mentorship and cross-training on multi-omics sample preparation, instrument workflows, and data tracking protocols to ensure consistency and scalability across teams.
- Lead validation and process harmonization for new assays across omics platforms.
- Collaborate with QA and regulatory teams to maintain CAP/CLIA readiness and audit documentation.
- Bachelor’s degree required
- Minimum of 3 years of relevant experience in a high-volume, complex clinical or research laboratory setting
- Advanced Excel skills
- Proficient in molecular biology techniques, including Illumina NGS Next-Generation Sequencing, PCR, library preparation, and barcoding
- Troubleshooting, mentoring and QC review experience
- Experience with laboratory automation and robotic systems, such as Hamilton instruments and automated liquid handlers
#LI-MD2 Ref: #558-Scientific
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