Scientist, Flow Cytometry

Quest DiagnosticsLewisville, TX
Onsite

About The Position

We are seeking a highly motivated scientist to support flow cytometry MRD assay development. As a member of the Oncology R&D team, this role will collaborate with other scientists and staff from cross-functional team to develop, validate and transfer flow cytometry assay to laboratory operations. Activities may be focused on individual projects or assignments as a member of a project team which may include project leadership duties.

Requirements

  • Requires minimum of 3 (three) years of experience in a clinical laboratory setting, with one (1) year full-time clinical experience in Flow Cytometry.
  • Bachelor’s degree in medical technology, biology, chemistry or relevant fields with at least 3 (three) years of clinical experience.
  • Knowledgeable in the use of common laboratory equipment and safe chemical handling.
  • Requires a thorough knowledge of related products and technologies gained through developmental experience in an academic or industrial setting.
  • Ability to read and interpret documents such as professional journals, operating instructions, and procedure manuals.
  • Ability to write complete reports and correspondence.
  • Ability to speak effectively in one-on-one and small group situations.
  • Ability to apply mathematical concepts to problem-solving situations.
  • Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance and correlation techniques.
  • Ability to apply commonsense understanding to carry out instructions furnished in written, oral, or diagram form.
  • Ability to deal with problems involving several variables in a variety of situations.

Nice To Haves

  • Comprehensive theoretical expertise and hands-on operational proficiency in Flow Cytometry.
  • Strong analytical skills with the ability to interpret and communicate experimental results
  • Familiarity with regulatory and quality standards for diagnostic assay development (e.g., CAP/CLIA) is a plus.
  • Ability to work collaboratively in a fast-paced, cross-functional environment.

Responsibilities

  • Perform laboratory experiments following defined protocols and company procedures, including specimen handling, processing, and test analysis.
  • Under the direction of the Scientific Director/Lab Manager, report status of assigned projects through the preparation of detailed reports and documentation that summarize experiment results.
  • Ensures quality control and compliance procedures are documented and followed for assay development, validation, and transfer.
  • Work within established parameters on individual assignments, on project teams for longer-term projects and as a technical leader to Assistant Scientists or Associate Scientists.
  • Identify problems, investigate alternatives and recommend possible courses of action.
  • Maintain knowledge of technological developments that may assist in the completion of an assignment or lead to new products, processes or procedures by reading current literature.
  • Effectively utilize and apply advanced methods or technologies.
  • Contribute ideas for new product development typically within existing markets.
  • Responsibilities include supporting and complying with the company hazard waste handling practices and other safety procedures and protocols.
  • Other duties as assigned.
  • This is not an exhaustive list of all duties and responsibilities, but rather a general description of work performed by the position.
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