Technical Supervisor

BioReference Health, LLC; Elmwood Park (NJ); Presencial; USD 100 000 - 120 000; Tempo integral

Resumo da oferta

BioReference Laboratories, a leading national laboratory, seeks a Core Lab Supervisor to plan, organize, and direct the department ensuring efficiency and compliance. The role requires leadership and hands-on oversight of specimen workflow, test performance, quality and documentation while adhering to budgets and regulatory standards.

Responsibilities include scheduling, staffing, inventory management, and driving process improvements to meet turnaround times.

Qualificações

• Lead Technologist or Supervisor experience preferred.
• State licensure where applicable (CA, FL, NY often require licensing).
• 6+ years laboratory experience in a CLIA-accredited clinical lab.
• Strong mathematical, computer, reasoning, and language skills at college level.

Responsabilidades

• Plan, schedule, and direct department operations to meet turnaround time and budget.
• Ensure compliance with regulatory requirements and maintain proper documentation.
• Provide technical oversight and drive process improvements for test accuracy.

Conhecimentos

Leadership

Project planning

Communication

Computer skills

Formação académica

Bachelor's degree in Medical Technology

Ferramentas

Laboratory Information System

Descrição da oferta de emprego

This is an exciting time to join our dynamic organization! BioReference, an OPKO Health company, is the largest full service specialty laboratory in the United States that gives healthcare providers and patients the power to make confident healthcare decisions. With a focus on oncology, urology and women's health, BioReference offers comprehensive test solutions and unparalleled expertise based on a 40 year legacy of proven science and exceptional service. Join our team and become part of the journey in making our patients and customers the highest priority.

Job Description

Position Summary:

Under the directive of the Manager/Director, the Core Lab Supervisor plans, organizes, schedules, and directs the department in order to effectively utilize employees and equipment to meet established turnaround time and material utilization within budgetary constraints while adhering to quality technical standards. The Supervisor provides direct on-site analysis of the day to day operation including adjustment of specimen workflow, test performance, quality, compliance, and associated documentation to adhere to the applicable regulatory agencies, company policies and procedures. Position works some weekend and holiday rotation.

Position Responsibilities:

Duties may include but are not necessarily limited to the following:

• Performs the scheduling, planning, staffing, and monitoring of workflow based on patient load to meet established goals.
• Procures appropriate supplies and equipment to maximize department efficiency and stays within established budgetary and quality goals including accurate monthly inventory.
• Provides technical oversight of area(s) of responsibility. Serves as a technical resource for problem solving and process improvement to ensure accurate test performance and meets all quality goals. Investigates and documents non-conforming events as necessary.
• Devotes time to evaluate workflow and specimen testing to maintain adequate turnaround time and improve shift/employee productivity
• Ensures compliance with regulatory agency requirements through maintaining proper documentation, conducting audits, and corrective actions. Troubleshoots and recommends process improvements, as needed. Follows the audit calendar to ensure all quality tasks are completed.
• Supports, implements, and ensures compliance with all department and company policies and procedures.
• Monitors and ensures implementation of goals to meet established quality assurance, quality
  control, quality improvement plans and turnaround time.
• Interacts with internal and external customers to ensure proper sample handling, reporting and resolution of questions and concerns.
• Participates in the updating of departmental standard operating procedures to accurately
  reflect the current practices.
• Reviews Quality Control data as needed and at least monthly or as required.
• Maintains and updates all Standard Operating Procedures and Forms to include Safety Data Sheets.
• Review of test results prior to release when applicable.
• Responsible for validating and implementing new methods and technologies.
• Must have proven leadership, interpersonal, communication, computer and technical skills
  in the specialty area being supervised.
• Ability to express ideas and report findings in a comprehensive and thorough manner.
• Answers inquiries regarding methodology and special factors that can influence test results.
• Interacts with co-workers in a way that promotes a harmonious and cooperative working
  

Minimum Qualifications (required vs. preferred):

REQUIRED :

• Previous experience as a Lead Technologist or Supervisor
• State Licensure, where applicable (CA, FL, and NY require state licensing)
• 6 or more years laboratory experience as a Medical Technologist in a CLIA accredited clinical laboratory
• Mathematical, computer, reasoning, and language skills at the college level (2 years)

PREFERRED :

• ASCP or other national certification

BioReference Laboratories is an Equal Opportunity Employer

Pay Range

Pay Range

The estimated pay range for this job. Disclosing pay information promotes competitive and equitable pay.
The actual pay rate will depend on the person's qualifications and experience.

$100,000.00 - $120,000.00 / year

Pay Transparency

In order to support the Fair Compensation Strategy by the US Govt., HR Dept., clients are required to adhere to "Pay Transparency Law"; in the impacted states; that have mandated the employers to list the salary ranges in Job advertisements or postings for job opportunities and Job promotions.

BioReference is an Equal Opportunity Employer.