Genetics Dir - Lewisville, TX req40625 in Lewisville, TX at Quest Diagnostics

Date Posted: 5/13/2020

Job Snapshot

  • Employee Type:
  • Location:
    2501 South State Highway 121
    Lewisville, TX
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

Genetics Director - Lewisville, Texas - Mon-Friday

Look for more than answers.  Patients and Physicians rely on our diagnostic testing, information and services to help them make better healthcare decisions. These are often serious decisions with far reaching consequences, and require sensitivity, tact and a clear dedication to service. It’s about providing clarity and hope.

As a R&D Professional you will work for the world leader in the industry, with a career where you can expand your skills and knowledge. You’ll have a role where you can act with professionalism, you can inspire colleagues, and you can care about the work we do and the people we serve.

At Quest, our R&D Professionals play an essential role in our success and in the services we provide. As a career, we offer a unique opportunity to develop your career with the #1 Diagnostic Lab in the US. We are research and development driven, and we’re creating the lab of the future – an environment where you can deliver cutting edge diagnostics and help us drive new discoveries and breakthroughs.


 The Director, Genetics, reports to the licensed Medical or Scientific Director or Chief Director and is responsible for providing technical interpretation of results and signing reports in the specialty of Molecular Oncology; implementing new assays, assay troubleshooting, acting as a technical consultant to operations staff and participation in QA & QM activities, and reviewing SOPs.  Assumes Technical Supervisor responsibilities as assigned by the Medical Director.




•         Assist in assay trouble-shooting and implementation of new assays

•         Monitor compliance in regards to a safe working environment.

•         Assist, as needed, in the training of technologists.

•         Observe compliance with regulatory agencies, including inspections.

•         Monitor of quality assurance at all levels of practice.

•         Participate in working groups of related or associated professionals.

•         Represent Quest Diagnostics at professional meetings and sales events

•         Actively reads and disseminates current and relevant medical publications, guidelines and approvals

Assume Clinical Consultant or Technical Supervisor responsibilities in Specialty as delegated by the “Laboratory Director Responsibilities” Policy:

•         Approve of the test method selection and validation.

•         Ensure that the proficiency testing program is conducted in a timely manner, reviewed by appropriate staff, and approve of corrective action when a proficiency testing result is found to be unsatisfactory.

•         Establish and monitor quality control to ensure that acceptable levels of analytical performance are maintained for each test system.  Ensure that patient test results are reported only when the system is functioning properly. 

•         Approve all corrective action and preventative action plans and procedure.

•         Approve Job Assignments and Authorization Matrix (JAAM) and annual Performance and Development Review (PDR) to ensure that all personnel have the appropriate training and demonstrated performance for the type of testing offered.

•         Annually review Standard Operating Procedures for test systems.





  •         Ph.D. degree, or equivalent

•         Fellowship Trained and Board certified in the appropriate genetic subspeciality by the American Board of Medical Genetics or equivalent

•         Preferably hold NY-CQ in Oncology

 Work Experience:

•         0-3 years related experience

•         Highly developed verbal and written communications skills.

•         Demonstrated good decision-making and organizational skills.


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