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Quest Diagnostics

Operates nationwide clinical laboratory testing

Medical Laboratory Scientist Group Lead - Toxicology

Diagnostics & Laboratory ProfessionalsPosted on Nov 13
Full-timeRoyal Oak, MI, USANo salary listed

About the Job

Requirements

  • Three to five years of clinical experience as a Medical Technologist within the designated discipline.
  • Foreign-educated candidates must provide a detailed credential evaluation from the International Education Research Foundation; United States-educated candidates must provide a detailed original transcript.
  • Ability to lift and carry objects weighing 1–10 pounds frequently and 11–25 pounds occasionally; objects weighing 36–50 pounds are seldom lifted or carried, and objects over 50 pounds must not be lifted or carried without assistance.
  • Ability to stand and work at the bench for long periods, with frequent walking and/or standing.
  • Ability to use a wide variety of manual and automated pipettes and laboratory instruments and apparatus requiring significant manual dexterity.
  • Comprehensive theoretical and operational job knowledge in the designated specialty.
  • Knowledge of organizational and departmental policies and procedures.
  • Proven leadership and problem-solving skills.
  • Ability to work independently, establish work priorities for self and others, and handle multiple tasks simultaneously to maximize department efficiency.
  • Ability to schedule and manage resources to meet department goals.
  • Interpersonal skills to deal courteously and effectively with supervisors, coworkers, and clients.
  • Communication skills to handle telephone inquiries from clients.
  • Ability to handle client information confidentially.
  • Proficiency in Microsoft Office, including Word, Excel, and Outlook, and Laboratory Information Systems.
  • Bachelor’s degree in Medical Technology, Chemistry, or Biology, or qualification as a Technologist under 42 CFR 493.1433, published March 14, 1990.
  • Demonstrate proficiency in all duties of a Medical Technologist I and II.
  • Use personal protective equipment, engineering controls, and/or work-practice controls as directed by management.
  • Comply with established Clinical Laboratory Improvement Amendments, Health Insurance Portability and Accountability Act, Occupational Safety and Health Administration, and laboratory safety requirements.

Responsibilities

  • Perform moderate- and high-complexity test procedures requiring independent judgment and responsibility in specialties for which qualified by education, training, and experience.
  • Assist the Laboratory Supervisor and serve as a technical resource for the department.
  • Perform and report assigned analytical tests in accordance with applicable Standard Operating Procedures, ensuring quality control requirements are met.
  • Support laboratory policies and procedures for specimen handling and processing, test analysis, reporting, and maintaining patient test-result records.
  • Adhere to analytical schedules to maintain result turnaround times, including STAT or critical results to clients.
  • Perform, review, and document quality-control analyses 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 actions, considering specimen requirements and the effects of time and additional or repeat testing on quality.
  • Investigate and resolve analytical testing problems, recommend action when results are beyond acceptable limits, and respond to complex inquiries or requests from clients and sales representatives.
  • Assist the Laboratory 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 issues involving other laboratory departments.
  • Maintain laboratory areas and equipment in safe, functional, and sanitary condition.
  • Complete training and competency checklists as appropriate and assist with annual departmental competency testing and documentation.
  • Review department activities to ensure compliance with established laboratory requirements.
  • Participate in government or regulatory agency inspections as needed.
  • Perform necessary supervisor functions in the absence of a Supervisor when qualified and delegated.
  • Perform other duties as assigned.

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

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