Laboratory Supervisor- Point of Care

Overview

Location: Glen Ellyn. Travel Required to All Clinical Sites.

Hours: Full-Time. Monday-Friday 8am-4:30pm. Every other Weekend. Rotating Holidays.

Holistic benefits designed to help our team members flourish in all aspects of their lives, including:

• Comprehensive medical and prescription drug benefits that include medical coverage at 100% (after deductible) when utilizing a Duly provider.
• $5,250 Tuition Reimbursement per year.
• 40 hours paid volunteer time off.
• A culture committed to Diversity, Equity, and Inclusion (DEI) and Social Impact
• 12 Weeks parental leave at 100% pay and a financial benefit for adoption and surrogacy for non-physician team members.
• 401(k) Match
• Profit-sharing program
  
  

Are you ready to challenge the expected to deliver the extraordinary?

The Supervisor Laboratory is primarily responsible for the oversight of the day-to-day operations of Point of Care testing, specimen processing in the clinics and reference laboratory specimens at multiple locations. This position is responsible for training, competency, site visits and reporting of quality metrics for point of care testing.

Responsibilities

The Journeys and Adventures that Await

• Training and Competency

• Responsible for oversight of/and training of any new clinical staff that perform point of care testing.
• Responsible for oversight of/and annual competencies for clinical staff
• Site Visits
  
  

• Responsible for reviewing QC and other quality metrics at designated sites.
• Responsible for site visit follow-up with site supervisors/managers
• Responsible for preparing monthly QI reports.
• Responsible for ensuring IR dept is inspection ready.
• Troubleshooting
  
  

• Available to troubleshoot instrument issues, specimen processing and barcode/packing list issues either by phone or on site.
• Responsible for ensuring return of non-functioning instruments and meters and installing replacement instruments and meters at the sites.
• New Instrument Selection and Validation
  
  

• Involvement in evaluating new testing or instruments.
• Responsible for validation and distribution of any new testing or instruments.
• Policies and Procedures
  
  

• Responsible for writing and review of policies and procedures.
• Reference Lab
  
  

• Follow up on reference lab issues.
• On-call when manager is unavailable and every 3rd weekend
• Any other duties as assigned.
  
  

SUPERVISORY/MANAGEMENT SCOPE

2 direct reports

Local travel required 50-75% of the time for site visits, on-site training, and troubleshooting.

Qualifications

The Experiences You Bring

• American Society for Clinical Pathology (ASCP)
• Bachelor’s degree in a chemical, physical, biological or clinical lab science or medical technology.
• Eligible to become a CLIA Technical Consultant.
• Minimum of 1 year of Lead or Supervisory experience
• Plus, a minimum of 5 years of clinical laboratory experience required.
• Basic knowledge of OSHA, CLIA, HIPAA, and regulatory requirements. Proficient in laboratory information systems and Microsoft Office applications