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Manager, Clinical Laboratory Off Shift

Abbott


Job Location:

Madison, OH - USA

Monthly Salary: $ 86700 - 173300
Posted: 21 August 2026 (13 hours ago)
Application Deadline: 18 November 2026
Vacancies: 1 Vacancy

Job Summary

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:
Position Overview

The Manager Clinical Laboratory manages the overall daily clinical laboratory operations and develops procedures to ensure safety quality and accuracy of results. This position oversees the supervision and development of laboratory staff provides technical expertise to the laboratory and serves as the liaison to internal and external addition the Manager Clinical Laboratory oversees the quality management program within the clinical laboratory and ensures that the laboratory is in compliance with all laws and regulations required by CLIA CAP OSHA New York and any other applicable state or federal legislative organizations.

The Manager Clinical Laboratory collaborates with various departments and cross-functional teams to ensure the quality and timeliness with which patient and clinical validation study samples are processed and is accountable for the laboratory teams deliverables on designated product development and process development projects. The Manager Clinical Laboratory facilitates timely and effective communication with other departments regarding service coverage needs and resolution of issues related to commercial patient samples adjusting laboratory staffing levels as needed.

The Manager Clinical Laboratory may perform high complexity laboratory testing on patient specimens interprets and reports patient results and troubleshoots high complexity technical and non-technical problems.

Shift: Weekend PM

Essential Duties

Include but are not limited to the following:

  • Directs the daily workflow of the clinical laboratory departments; including but not limited to ensuring processing systems for patient and study samples are functioning properly monitoring quality control testing results and monitoring quality assurance performance metrics.

  • Manages designated laboratory and cross-functional projects such as process improvements quality improvements clinical validation studies and the development and launch of new products.

  • Collaborates with Exact Sciences human resources department and participates in the employee hiring and management process by interviewing candidates hiring and employee counseling.

  • Assesses scheduling needs of the departments to ensure adequate coverage to meet service needs.

  • Identifies and understands regulatory requirements to ensure that the laboratory complies with all applicable state and federal laws and regulations pertinent to the management of the laboratory; including applicable CLIA CAP and other requirements and regulations such as California and New York (CLEP) laboratory programs.

  • Manages the inspection preparation activities in the clinical laboratory such as maintaining consistent ongoing readiness for inspections and representing the clinical laboratory during inspections.

  • Provides or delegates responsibility of supervision of the clinical laboratories and is accessible to the laboratory personnel to provide on-site telephone or electronic consultation.

  • Maintains a process for staffing recruiting training evaluating competency and ongoing employee development.

  • Works strategically with department supervisors and managers to ensure testing is completed within turnaround time.

  • Partnerswith senior management in establishing strategic priorities and annual quality indicators.

  • Collaborates with the laboratory leadership to assist in developing and providing continuing education credits for the laboratory staff.

  • Ensures staff are properly trained and competent in all aspects of their job duties and departmental procedures.

  • Reviews writes and updates standard operating procedures (SOPs).

  • Reviews and writes nonconformance and deviation approval requests and other documents as appropriate.

  • Possesses effective management skills to supervise department staff and maintain departmental budgets.

  • Provides oversight to ensure prompt accurate and timely processing and delivery of all patient specimens.

  • Evaluates equipment and supply needs of the laboratory.

  • Works with the laboratory leadership to maintain operations within the budget.

  • Assures timely and appropriate ordering of supplies and equipment.

  • Partners with the laboratory supervisors to monitor supply usage and variances.

  • Reviews test volumes with laboratory leadership to develop and implement timely changes to manage workload.

  • Verifies test procedures performed and with assistance establishes the laboratorys test performance characteristics including precision and accuracy of each test and test system.

  • Ensures that the quality management program is maintained by following parameters for acceptable performance for the pre-analytical analytical and post-analytical testing processes.

  • Resolves high complexity technical problems with the aid of the technical staff and ensures that remedial action is taken whenever a test deviates from the laboratorys performance standards.

  • Ensures that all patient results are not reported until corrective actions have been taken and the systems are functioning properly.

  • Identifies training needs and ensures all training is performed as required.

  • Assists with the training of new laboratory personnel and training of new procedures with existing personnel as needed.

  • Evaluates competency of all laboratory personnel.

  • Supervises staff; including but not limited to organize and prioritize work write/conduct performance reviews train/develop and manage work performance.

  • Communicatesgoals clearly to employees to ensure understanding and success in achieving them.

  • Motivatesandinspireemployees to do their best work through coaching and mentoring.

  • Maintainsmorale and supports employee engagement initiatives.

  • Excellent customer service skills.

  • Ability to work well with all members throughout the organization.

  • Excellent verbal and written communication skills.

  • Excellent presentation skills including public speaking.

  • Excellent analytic skills.

  • Ability to organize work and meet deadlines.

  • Excellent time management skills.

  • Ability to effectively evaluate situations and work with teams to develop appropriate resolutions.

  • Ability to quickly implement and adapt to change.

  • Ability to apply project management skills to leadership of operational expansion and process improvements.

  • Ability to quickly and calmly adapt and respond to changes in priorities timelines and deliverables.

  • Ability to communicate clearly and effectively in writing and verbally to technical and non-technical audiences.

  • Ability to integrate and apply feedback in a professional manner.

  • Ability to prioritize and drive to results while maintaining a consistently high-quality standard.

  • Ability to work as part of a team.

  • Upholds company mission and values through accountability innovation integrity quality and teamwork.

  • Supports and comply with the companys Quality Management System policies and procedures.

  • Maintains regular and reliable attendance.

  • Ability to act with an inclusion mindset and model these behaviors for the organization.

  • Ability to work designated schedule.

  • Ability to work nights and/or weekends.

  • Ability to move 40 pounds for approximately 25% of a typical working day.

  • Ability to work seated for approximately 50% of a typical working day. Ability to work standing for approximately 50% of a typical working day.

  • Ability to work on a mobile device tablet or in front of a computer screen and/or perform typing for approximately 90% of a typical working day

  • Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height ability to stand bend and transfer materials

  • Ability to comply with any applicable personal protective equipment requirements

  • Ability to use various types of laboratory equipment including microscopes microtomes blades strainers pipettes for extended periods of time.

  • Ability to perform repetitious actions using lab tools.

  • Ability to use near vision to view samples at close range.

  • May be exposed to hazardous materials tissue specimens and instruments with moving parts lasers heating and freezing elements and high-speed centrifugation.

Minimum Qualifications

  • Bachelors Degree in Chemical Biological or Clinical Laboratory/Medical Technology Science or field related to the essential duties.

  • 6 years of experience working in a clinical laboratory setting.

  • 3 years of experience leading and managing teams.

  • Demonstrated ability working in a high-volume laboratory operations environment.

  • Demonstrated ability working with quality management programs.

  • Strong working knowledge in the areas of laboratory technology management principles laboratory information system (LIS) management and workflow needs and capabilities.

  • Strong knowledge of all laws and regulations that are required by CLIA CAP OSHA and other related legislative and/or state health departments and organizations.

  • Proficient in Microsoft Office.

  • Authorization to work in the United States without sponsorship.

  • Demonstrated ability to perform the Essential Duties of the position with or without accommodation.

Preferred Qualifications

  • Advanced Degree.

  • 4 years of experience with LIS requirements and workflow needs.

  • 4 years of experience working with quality management; including strong knowledge of all laws and regulations that are required by CLIA CAP OSHA New York and other related legislative and/or state health departments and organizations.

  • Experience with one or more standard molecular biology techniques such as nucleic acid isolation RNA/DNA quantification PCR and RT-PCR and DNA sequencing.

  • Experience with high-throughput robotic instruments.

  • Familiarity with FDA regulations of Laboratory Developed Tests (LDT).

  • Familiarity with ISO standards.

The base pay for this position is

$86700.00 $173300.00

In specific locations the pay range may vary from the range posted.

JOB FAMILY:
Operations Quality

DIVISION:
ONCO Cancer Diagnostics

LOCATION:
United States > Madison : 650 Forward Dr

ADDITIONAL LOCATIONS:

WORK SHIFT:
Standard

TRAVEL:
Not specified

MEDICAL SURVEILLANCE:
Not Applicable

SIGNIFICANT WORK ACTIVITIES:
Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: EEO is the Law link - Espanol: Experience:

Manager


About Company

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WHO WE ARE CREATING LIFE-CHANGING TECHNOLOGY From removing the regular pain of fingersticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s ... View more

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