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Labcorp Technical Director I-EC141 in Raritan, New Jersey

At Labcorp Diagnostics, you'll be a part of an innovative life sciences company that is deeply integrated with guiding patient care and providing comprehensive clinical laboratory services. With a mission to improve health and improve lives, Labcorp delivers world-class diagnostic solutions and pioneers new diagnostic technologies to improve the delivery of care. As a member of the LabCorp team, you will support a dedicated staff in resulting in over 500,000 clinical samples a day, a volume that demands the most accurate and precise analysis possible. You'll join a collegial scientific staff who appreciates that on the other side of every sample, is a person who depends on us! Labcorp is a leader in laboratory medicine and we strive to meet the rapidly evolving healthcare needs.

Do work that matters. Join Labcorp and be a part of our team bringing laboratory diagnostics to a new level.

The Northeast Division of Labcorp is seeking a Clinical Chemistry Technical Director for the core laboratory located in Raritan, NJ. The Raritan laboratory is one of the highest volume testing facilities in the country performing over 175 million tests per year. The Raritan Core Laboratory offers a broad testing menu including: Routine Chemistry, Diagnostic Immunology, Flow Cytometry, Hematology, Coagulation, Urinalysis and Clinical Toxicology. The Technical Director is responsible for providing direction and to serve as the technical advisor for clinical chemistry to the laboratory.

Responsibilities:

  • Accurately and promptly responds to client inquires that are technical in nature

  • Effectively communicates with clients, physicians, nurses, pathologists and LabCorp staff, including Science and Technology; and Laboratory teams

  • Oversees the technical component of the laboratory to ensure that patient results are reported reliably and in a timely fashion.

  • Reviews and reports patient results as needed, accurately, and with integrity

  • Ensures accuracy for all testing in the lab, including instrument performance and addressing root causes when issues arise

  • Guides implementation of new assays and instrumentation in the lab in collaboration with Science & Technology

  • Makes recommendations to improve workflow, support staffing needs as well as optimization of reagent utilization

  • Serves as last-stop to solve clients' technical problems (i.e., test rejection)

  • Assists the Quality department to ensure all required regulations are followed

  • Participates in, reviews and approves validation plans and studies, ensuring accurate and timely data are provided

  • Attends client meetings, to support business development or address customers' concerns

  • Projects credibility and builds rapport with medical providers/Labcorp clients, providing quick/accurate responses to inquires

  • Keeps up with scientific advances and other literature, offering perspectives about improvements, such as how a report reads

  • An interest in providing staff educational seminars, participation in national technical societies and publishing peer-reviewed manuscripts is encouraged

  • Sets the tone in the lab for performance and quality, ensuring techs perform duties correctly (i.e., handling specimens, pipetting)

  • Shares experiences and ideas with discipline directors, such as improvements to SOPs, reports, interfaces

  • Shall be able to work effectively and efficiently with the Medical Director of the Laboratory on the above functions and as deemed necessary.

Requirements

  • PhD in a Life Sciences in addition to Board Certification from the American Board of Clinical Chemistry or equivalent clinical board program.

  • 3-7 years of post-graduate experience

  • Leadership skills to work with lab staff, developing their capabilities and enrolling them in problem-solving/urgent matters

  • Deductive reasoning/analytical skills to reach a resolution to customer inquiries or lab opportunities/issues

  • Depth and breadth of experience within a clinical lab, understanding validation, quality control and quality management; proficiency testing; and regulatory requirements

  • Ability to respond to stressful and urgent situations in a timely manner.

  • Knowledge of quality standards and accountable for providing accurate results

  • Candidates with operational experience strongly preferred

Requirements

License/Certification/ Education: Ph.D. or MD Board Certified in Anatomic and Clinical Path or Clinical Chemistry preferred w/6 years of experience in related field. Must meet CLIA requirements.

Shift

1

Schedule

Schedule Shift: 1 Schedule: Monday - Friday 8am-5pm

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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