Medical Laboratory Scientist Group Lead

Quest DiagnosticsIndianapolis, IN
Onsite

About The Position

This role involves performing complex medical laboratory tests, requiring independent judgment and responsibility in qualified specialties. The Medical Laboratory Scientist Group Lead will assist the Lab Supervisor and act as a technical resource for the department. The position is based in Indianapolis, IN, with a Monday to Friday schedule from 8:00 AM to 5:00 PM, including rotational weekends. The pay range is $28.94+ per hour, with salary offers dependent on skills, training, experience, education, certifications, and market/organizational factors. Successful candidates may be eligible for annual performance bonuses.

Requirements

  • Three (3) to five (5) years of clinical experience as a Medical Technologist within the designated discipline.
  • Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation).
  • United States educated candidates must provide a detailed original transcript.
  • Comprehensive theoretical and operational job knowledge in designated specialty required.
  • Knowledge of organizational/departmental policies and procedures.
  • Proven leadership and problem-solving skills.
  • Must be detail-oriented, have the ability to work independently, establish work priorities for self and others, and handle several tasks simultaneously for maximum department efficiency.
  • Ability to schedule and manage resources to meet department goals.
  • Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers, and clients.
  • Communication skills necessary to handle telephone inquiries from clients.
  • Ability to deal with client information in a confidential manner.
  • Proficiency in Microsoft Office (Word, Excel, and Outlook) and Laboratory Information Systems.
  • Bachelor’s Degree in Medical Technology, Chemistry, or Biology or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990.

Nice To Haves

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

Responsibilities

  • Demonstrate proficiency in all duties of a Medical Technologist I and II.
  • Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP), ensuring quality control requirements are met.
  • Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting, and maintaining records of patient test results.
  • Adhere to analytical schedules to maintain turnaround time of results, including STATS or critical results to clients.
  • Perform, review, and document QC analysis to ensure accuracy of clinical data and proper instrument function.
  • Make quality control decisions regarding the disposition of an assay or test.
  • Review requests for validity checks and recommend an appropriate course of action, considering specimen requirements, time effects, and the quality of additional/repeat testing.
  • Serve as a technical resource for the department by investigating and resolving analytical testing problems, recommending actions for issues beyond acceptable limits, and responding to non-routine/complex inquiries from clients and sales representatives.
  • Assist Lab Supervisor by monitoring workflow to meet 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 the flow of work to maximize productive capacity by evaluating production systems, recommending enhancements, and coordinating the resolution of production problems/issues with 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 the department’s annual competency testing process and documentation.
  • Adhere to all established CLIA, HIPAA, OSHA, and laboratory safety requirements and review department activities to ensure compliance.
  • Use personal protective equipment, engineering controls, and/or work practice controls as directed by management.
  • Participate in government or regulatory agency inspections, if needed.
  • Perform necessary supervisor functions in the absence of a Supervisor, if qualified and delegated.
  • Other duties as assigned.

Benefits

  • Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
  • Best-in-class well-being programs
  • Annual, no-cost health assessment program Blueprint for Wellness®
  • healthyMINDS mental health program
  • Vacation and Health/Flex Time
  • 6 Holidays plus 1 "MyDay" off
  • FinFit financial coaching and services
  • 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
  • Employee stock purchase plan
  • Life and disability insurance, plus buy-up option
  • Flexible Spending Accounts
  • Annual incentive plans
  • Matching gifts program
  • Education assistance through MyQuest for Education
  • Career advancement opportunities
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