Histology Supervisor

Arbor DiagnosticsDallas, TX
36d

About The Position

Arbor-Women’s Health Elevated is the largest privately owned, exclusively focused, full-service women’s health diagnostics company in the U.S., featuring a broad and growing portfolio of products. We are elevating women's health and creating novel technology-based solutions that allow healthcare providers to devote more time to their patients. Diagnostics services include anatomic pathology, clinical pathology, cytopathology, molecular pathology, microbiology, and genetic testing. Arbor is uniquely positioned to develop services and solutions tailored to meet the needs of a women’s health practice. Every solution is created to uniquely support women’s health providers and their patients. Learn More at www.arbordiagnostics.org . Job Summary: The Histology Supervisor is responsible for the oversight of people, processes, documentation, workflow , equipment and problem solving in the histology department.

Requirements

  • Excellent organizational, communication and interpersonal skills
  • Ability to manage multiple priorities
  • Excellent attention to detail
  • Ability to work in a team environment
  • Willingness to maintain confidential information
  • Must be analyzed for color perception
  • Minimum of an associate degree in either laboratory science, chemical, physical or biological science from an accredited institution.
  • Qualify per CLIA for high complexity testing, Grossing Tissue
  • 5 years of Histology experience
  • 1 year of leadership experience

Responsibilities

  • Recruits, interviews and hire new staff.
  • Directly supervises the daily workflow of Histology
  • Provides feedback and timely performance evaluations.
  • Monitors and approves timecards
  • Manages discipline and termination of employees in accordance with company policy.
  • Serve as master trainer.
  • Writes and revises policies and procedures
  • Perform competency assessments.
  • Serves as an escalation point to resolve issues.
  • Document all corrective actions taken when test systems deviate from the laboratory’s established performance specification.
  • Participate in regulatory agency inspection readiness and onsite inspections.
  • Perform equipment validation, reagent optimization and validation following regulatory guidelines and procedures.
  • Report monthly metrics, QEB, NCE and all other compliance requirements.
  • Follow the laboratory’s procedures for specimen handling and processing.
  • Perform grossing, embedding, microtomy, and staining of patient samples.
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