Q

Quest Diagnostics

Operates nationwide clinical laboratory testing

Medical Laboratory Scientist Group Lead

Diagnostics & Laboratory ProfessionalsConfirmed live in the last 24 hours
Full-timeClifton, NJ, USAIn-person

About the Job

Requirements

  • Six years of clinical experience as a Medical Technologist within serology is required.
  • Foreign-educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). U.S.-educated candidates must provide a detailed original transcript.
  • Candidates must have comprehensive theoretical and operational job knowledge in the designated specialty.
  • Candidates must know organizational and departmental policies and procedures.
  • Candidates must have proven leadership and problem-solving skills.
  • Candidates must be detail-oriented, able to work independently, establish work priorities for themselves and others, and handle several tasks simultaneously to maximize department efficiency.
  • Candidates must be able to schedule and manage resources to meet department goals.
  • Candidates must have interpersonal skills to deal courteously and effectively with supervisors, co-workers, and clients.
  • Candidates must have communication skills to handle telephone inquiries from clients.
  • Candidates must be able to handle client information confidentially.
  • Candidates must be proficient in Microsoft Office (Word, Excel, and Outlook) and Laboratory Information Systems.
  • A bachelor's degree in Medical Technology, Chemistry, or Biology, or prior qualification as a Technologist under 42 CFR 493.1433 published March 14, 1990, is required.
  • Candidates must demonstrate proficiency in all duties of a Medical Technologist I and II.
  • Candidates must use personal protective equipment, engineering controls, and/or work practice controls as directed by management.

Responsibilities

  • Perform moderately and highly complex test procedures requiring independent judgment and responsibility in specialties for which qualified through education, training, and experience.
  • Assist the Lab Supervisor and serve as a technical resource for the department.
  • Perform and report assigned analytical tests in accordance with applicable Standard Operating Procedures (SOPs), ensuring applicable quality control requirements are met.
  • Support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting, and maintaining patient test-result records.
  • Follow analytical schedules to maintain result turnaround times, including STAT or critical results to clients.
  • Perform, review, and document quality control analysis to ensure clinical data accuracy and proper instrument function; make quality control decisions about assay or test disposition.
  • Review requests for validity checks and recommend appropriate action, considering specimen requirement limitations and the effects of time and the quality of additional or repeat testing.
  • Investigate and resolve analytical testing problems; recommend actions when results are beyond acceptable limits; and respond to non-routine or complex inquiries and requests from clients and sales representatives as a departmental technical resource.
  • Assist the Lab Supervisor by monitoring workflow against testing schedules, distributing and reviewing work assignments, training employees in laboratory techniques, resolving staff work-related problems, and providing input for performance appraisals and disciplinary actions.
  • Expedite workflow to maximize productive capacity by evaluating production systems, recommending enhancements, and coordinating resolution of production problems involving other laboratory departments.
  • Maintain laboratory areas and equipment in a safe, functional, and sanitary condition.
  • Complete training and competency checklists as appropriate and assist with annual departmental competency testing and documentation.
  • Adhere to established CLIA, HIPAA, OSHA, and laboratory safety requirements, and review department activities for compliance.
  • Participate in government or regulatory agency inspections when needed.
  • Perform necessary supervisor functions in the absence of a Supervisor when qualified and delegated.

Desired Qualifications

  • Experience as a Medical Technologist at Quest is highly desired.
  • ASCP Certification is preferred.

About the Company

Quest Diagnostics

Operates nationwide clinical laboratory testing

Quest Diagnostics provides clinical laboratory testing and diagnostic services. It processes patient samples across a network of laboratories to run a broad menu of 3,000+ tests, including cancer diagnostics and anatomical pathology, and delivers interpretive reports through its medical staff. Tests are performed at its patient service centers, esoteric and rapid-response labs, and outpatient facilities, with results shared with clinicians via connected data systems. What sets Quest Diagnostics apart is its scale and scope: the world’s largest clinical lab network, the broadest test menu, a large team of MDs and PhDs for interpretation, and leadership in cancer diagnostics and pre-employment drug testing, plus extensive clinical trials testing. Its goal is to empower healthcare providers and patients with actionable diagnostic insights to identify, treat, and manage disease, inspire healthy behaviors, and improve health outcomes.

Company size
10,001+
Company stage
IPO
Headquarters
Secaucus, NJ
Founded
1967

Recently Posted Jobs

Explore more opportunities at Quest Diagnostics

See more jobs