Manager, Pathology Operations

InotivGaithersburg, MD
Onsite

About The Position

The Manager, Pathology Operations is responsible for the effective operations of multiple functional teams within the laboratory. This role involves planning, scheduling, and organizing resources to meet study timelines and departmental goals. The manager will oversee workflow, conduct annual performance evaluations, and collaborate with pathologists on data reports, equipment, and method validation. This position serves as the primary laboratory contact for communications with study directors and in-life technicians regarding sampling and testing issues. Additionally, the manager is responsible for the laboratory's quality control program, including the maintenance of quality control records, troubleshooting issues, and establishing new ranges for quality control materials. The role requires proficiency in operating and maintaining laboratory analyzers and equipment, directing the maintenance of associated records, and performing manual testing when necessary. The Manager, Pathology Operations will conduct testing according to GLP and internal standards, prepare and update Standard Operating Procedures (SOPs), and review/interpret data for acceptance and reporting. This role also involves collecting data using laboratory systems, proposing and implementing process improvements, and providing leadership and mentoring to junior staff. Safety precautions, including universal precautions and the use of PPE, are essential due to potential work with hazardous substances. The position also includes professional responsibilities such as attending continuing education and maintaining involvement in professional organizations.

Requirements

  • At least 10 years medical laboratory experience.
  • MT certification is required.
  • Proficiency in the operation and maintenance of the laboratory’s analyzers and equipment.
  • Conducts testing in the clinical laboratory according to GLP and internal standards, and maintains the required documentation indicating compliance.
  • Reviews and interprets data for acceptance, and reporting purposes.
  • Collects data using the laboratory data capture systems, and maintains the required documentation indicating compliance.
  • Practices universal safety precautions when working with blood samples.
  • May work with potentially hazardous substances.
  • Wears requires PPE (personal protective equipment).

Nice To Haves

  • Knowledge of Good Laboratory Practices (GLP) and regulatory agencies is desirable.

Responsibilities

  • Responsible for the effective operations of a multiple functional teams.
  • Plans, schedules and organizes necessary resources to meet study timelines and departmental goals.
  • Responsible for annual performance evaluations of supervised personnel.
  • Directs workflow within the laboratory to ensure that adequate personnel are assigned to specific tasks.
  • Works closely with the pathologist to prepare clinical pathology data reports, and to validate equipment and methods.
  • Serves as the laboratory’s point of contract for communications with study directors and in-life technicians regarding sampling and testing problems.
  • Responsible for the laboratory’s quality control program.
  • Directs the maintenance of required quality control records to ensure the accuracy and precision of the analyzers, troubleshoots quality control issues, and establishes new ranges as necessary for new lots of quality control materials.
  • Reviews study protocols to ensure that the requested tests are within the capacity of the laboratory, and ensures that the required tests are performed.
  • Directs the maintenance of analyzer operational and maintenance records.
  • Performs manual testing of samples when necessary as an effective team member, such as preparation and review of blood smears, preparation and review of reticulocyte smears, and preparation and review of urine microscopic examinations.
  • Conducts testing in the clinical laboratory according to GLP and internal standards, and maintains the required documentation indicating compliance.
  • Prepares, reviews, and updates laboratory Standard Operating Procedures (SOP).
  • Reviews and interprets data for acceptance, and reporting purposes.
  • Collects data using the laboratory data capture systems, and maintains the required documentation indicating compliance.
  • Proposes and implements process improvements to reduce costs and increase efficiencies.
  • Performs duties independently and provide leadership and mentoring to junior staff members.
  • Practices universal safety precautions when working with blood samples.
  • May work with potentially hazardous substances.
  • Wears requires PPE (personal protective equipment).
  • Perform other related duties as assigned.
  • Attends continuing education courses, as appropriate.
  • Maintains active involvement in professional medical/clinical laboratory organizations.

Benefits

  • health and dental coverage
  • short- and long-term disability
  • paid time off
  • paid parental leave
  • 401K
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service