General Laboratory Supervisor

Position Summary

We are seeking a qualified and experienced Technical Supervisor for a CLIA-certified High Complexity Laboratory. The Technical Supervisor will provide technical oversight of laboratory testing, ensure compliance with CLIA, CAP and state regulatory requirements, and support the implementation and maintenance of a robust Quality Management System.

Key Responsibilities

• Perform all high-complexity laboratory testing, data review and reporting.
• Monitor quality control, proficiency testing, and quality assurance activities.
• Investigate testing discrepancies, QC failures, proficiency testing events, and implement corrective actions.
• Ensure compliance with CLIA, CAP, state regulations.
• Review and approve validation and verification studies for new tests, instruments, and methodologies.
• Develop, review, and approve laboratory SOPs, policies, and technical procedures.
• Establish and monitor quality indicators and support continuous quality improvement initiatives.
• Oversee personnel training, competency assessments, and continuing education.
• Ensure preventive maintenance, calibration, and qualification of laboratory equipment are performed and documented.
• Participate in internal audits, inspection readiness activities, and regulatory inspections.
• Collaborate with the Laboratory Director, Clinical Consultant, and laboratory staff to maintain high-quality laboratory operations.
• Provide technical consultation to laboratory personnel regarding testing procedures, troubleshooting, and result interpretation.

Minimum Qualifications

• Applicants must meet CLIA (42 CFR 493.1449) requirements for a High Complexity Technical Supervisor.
• Ph.D. or Master's degree in Chemical, Physical, Biological, or Clinical Laboratory Science (Bachelor's degree with qualifying experience may be considered where permitted under CLIA).
• Current ASCP or equivalent certification preferred.
• Minimum 3-4 years of experience supervising high-complexity laboratory testing with PCR infectious disease testing.
• Experience in one or more of the following: Molecular Diagnostics (PCR), Clinical Chemistry, Microbiology, Hematology.
• Strong knowledge of CLIA, CAP accreditation requirements, and quality management systems.
• Excellent written and verbal communication skills.
• Experience with laboratory information systems (LIS) and electronic quality management systems is preferred.