Director Quality Systems

GeneDx, Inc

• $110K — $130K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in medical technology, chemistry, biology, or a related science.
  • Minimum of four years in clinical laboratory or quality compliance roles.
  • At least one year in management and leadership positions.
  • Experience in a clinical diagnostic laboratory with CAP accreditation.

Responsibilities

  • Develop and implement quality control and monitoring programs adhering to ACMG and CAP standards.
  • Define and oversee objectives and processes for quality control programs.
  • Establish and manage documentation procedures related to quality control.
  • Coordinate document control processes vital to maintaining quality standards.
  • Conduct regular internal quality audits across laboratories and follow up on corrective actions.
  • Ensure laboratory personnel qualifications meet CLIA, CAP, and NYS standards.
  • Oversee maintenance and calibration of laboratory equipment.

Benefits

  • Comprehensive paid time off including vacation, sick leave, and holidays.
  • Health, dental, vision, and life insurance options available.
  • Flexible Spending Account (FSA) and Health Savings Account (HSA) participation.
  • 401K retirement savings plan with a 4% company match and immediate vesting.
  • Tuition Assistance for professional development.
  • Employee Discounts on services and amenities.
  • Regular performance reviews to support career growth.
  • Opportunities for promotion from within the organization.
Full Job Description
Job Description

GeneDx is seeking a Director, Quality Systems (FT, 40 hours) to work at our Gaithersburg, MD location, Monday through Friday, 8:30 a.m. to 5:00 p.m.

Role: The Quality Systems Director is responsible for planning, coordinating and overseeing all of the functions within the scope of Quality Systems, including the Quality Control Program, Quality audits, standard operating procedures, regulatory standards, and obtaining and maintaining all accreditation to ensure that services are of the highest quality.

Essential Duties:
  • Develop, implement, communicate, and maintain quality control (QC) and quality monitoring programs according to standards of ACMG and CAP.
  • Define and maintain QC/QMP objectives, targets, processes and review new targets, plans, and protocols for maintenance of the QCP as needed.
  • Establish and maintain QC/QMP documentation procedures as needed.
  • Maintain, develop, and coordinate document control processes.
  • Perform regular internal quality audits in all laboratories; follow up with recommendations, corrective, and preventive actions as needed.
  • Assure proper qualification of laboratory personnel according to CLIA, CAP, and NYS standards.
  • Assure proper maintenance and calibration of laboratory equipment.
  • Assist in the maintenance of accreditation, permits and licenses in regard to inspections and communication.


Qualifications

REQUIRED :
  • Experience in a clinical diagnostic laboratory, in a facility holding CAP accreditation. Bachelor's degree in medical technology, chemistry, biology, or related science.
  • Four years clinical laboratory or quality compliance experience.
  • 1 year of management and leadership experience.


Benefits include:
  • Paid Time Off (vacation, sick, personal, holiday, jury duty, bereavement leave)
  • Health, dental, vision, life insurance, LT/ST disability plans
  • Flexible Spending Account (FSA)
  • Health Savings Account (HSA)
  • 401K retirement savings plan with a 4% company match and immediate vesting
  • Tuition Assistance
  • Employee Discounts (cell phone service, movie tickets, etc.)
  • Regular performance appraisals
  • Many promotions from within

Business casual, dog-friendly work environment

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