Claims Quality Audit Supervisor supervises and coordinates daily activities of claims quality auditors. Provides assistance in developing claims audit policies and procedures. Being a Claims Quality Audit Supervisor solves day-to-day problems and monitors the results of daily staff activities, reports critical issues and problems to the management. Typically requires a bachelor's degree. Additionally, Claims Quality Audit Supervisor typically reports to a manager. The Claims Quality Audit Supervisor supervises a group of primarily para-professional level staffs. May also be a level above a supervisor within high volume administrative/ production environments. Makes day-to-day decisions within or for a group/small department. Has some authority for personnel actions. Thorough knowledge of department processes. To be a Claims Quality Audit Supervisor typically requires 3-5 years experience in the related area as an individual contributor. (Copyright 2024 Salary.com)
The ideal candidate will be responsible for reviewing and releasing Toxicology results
using the Sciex 4500 and Advia 1800 as well as overseeing and running the operation.
This includes but is not limited to the quality assurance programs, systems, processes
and procedures of the operation on a daily, weekly and monthly basis.
The ideal candidate must:
Have complete knowledge of Quantitative and Qualitative Toxicology
Have complete knowledge of QC and CS Methods including reviewing, maintenance
on LCMS and troubleshooting.
Have understanding of Levi Jennings and quality assurance programs needed to
ensure Quality resulting.
Develop positive and supportive working relationships with laboratory
management and staff in the assigned areas.
Ensure all departments maintain regulatory readiness at all times to ensure all federal,
state and local licensure and accreditations are up to date, as applicable.
Provide guidance for laboratory in implementing policies with respect to
regulatory and accreditation requirements.
Audit laboratory to identify quality issues, nonconformities and opportunities for
improvement.
Oversee proficiency testing program.
Formulate responses to accreditation and regulatory citations, nonconforming
events and complaints.
Have an in depth understanding of metabolites and testing being performed on the
LCMS. Be able to field questions from physicians and clients with regards to the
testing.
Promote and lead Quality Assurance metrics
Participate and/or lead in Quality meetings, training of employees and Regulatory
initiatives.
Other job duties as applicable.
Required Education, Experience, Skills and Qualifications:
Bachelor's degree in Chemistry, Biology, Clinical Laboratory Science or related
field or equivalent education and experience
At least 5 years of Toxicology supervisory experience
Excellent communication and interpersonal skills including written, verbal, and
listening skills
This Job Is Ideal for Someone Who Is:
Dependable -- more reliable than spontaneous
People-oriented -- enjoys interacting with people and working on group projects
Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction
Detail-oriented -- would rather focus on the details of work than the bigger picture
Achievement-oriented -- enjoys taking on challenges, even if they might fail
Able to think outside of the box with regards to problem resolution and task
completion
Plus:
Work Experience with Sciex 4500 for Quantification with both Oral and Urine methods.
Work Experience with Advis 1800 Qualitative screening and specimen validity testing.
Details:
Job Type: Full-time
Location: On site- Scotch Plains, NJ Laboratory
Shift hours must will vary between 7AM to 6pm
Pay Frequency: Bi-weekly
Job Type: Full-time
Salary: $40.00 - $60.00 per hour
Expected hours: 40 per week
Job Type: Full-time
Pay: $40.00 - $60.00 per hour
Expected hours: 40 per week
Schedule:
Ability to Relocate:
Work Location: In person
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