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General Supervisor- Pathology Lab

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Onsite

General Supervisor- Pathology Lab

Curalta Foot and Ankle

General Supervisor- Pathology Lab

Skills

Testing & QACompliance

2 months ago

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Important information


Contract type:

Permanent, Freelance / Contract

Salary:

$90,000 – $100,000 / year

Location:

Ridgewood, NJ 07450, USA

Work mode:

Onsite

Published on:

9 September 2026

What they need


Curalta Foot + Ankle is the largest and foremost network of podiatrists in the Northeast, focused on delivering high-quality, complete foot and ankle care. Curalta’s providers combine decades of experience with a forward thinking, innovative approach to treatment in order to maximize patient outcomes and experiences across all lower extremity conditions.

This opportunity is for a Full Time General Supervisor for our established molecular lab in Ridgewood, NJ.

The General Supervisor shall perform the professional and administrative services as may be necessary for oversight of the Pathology Lab, without limitation, as deemed necessary by the organization.

Essential Functions, Job Duties & Responsibilities:

  • Oversee compliance with all applicable laws, rules, regulations, and accepted professional and ethical standards and guidelines
  • Oversee compliance under contracts identified by Employer from time to time (including contracts with third party payors)
  • Collect, process, and analyze samples in accordance with Employer policies and applicable law;
  • Maintain equipment and assist in ordering laboratory supplies, and advise Employer as to suitability of equipment
  • Coordinate services, staff, and policies of the Lab
  • Train, supervise and evaluate all testing and/or support personnel
  • Review, revise, and implement policies and procedures of the Lab
  • Organize and store chemicals substances, and fluids according to safety instructions
  • Oversee Lab quality control and quality assurance programs
  • Supervise and monitor the quality of test results
  • Without limiting the generality of the foregoing:
    • Assist in the development and implementation of such quality systems appropriate for all Laboratory Developed Polymerase Chain Reaction tests ("LDTs")
    • Monitor and report on the analytic performance of LDTs being performed by Employer
    • Establish performance criteria, including accuracy and precision of each LDT test and system

Education & Experience:

  • Bachelor's degree or higher in Medical Technology or related field required
  • Must be certified by ASCP or AMT
  • 2-4 years Laboratory experience

Skills and Abilities:

  • Aspect Technique
  • Clinical Laboratory testing
  • Laboratory Equipment Operation
  • Laboratory Practice Quality Assurance (LPQA)
  • Laboratory Results Reporting
  • Microscopy
  • Medical Specialty: Pathology
  • Laboratory Information Management System (LMIS) Software
  • Must demonstrate proficiency in the English language (TOEL) or (IELTS)

Physical Requirements:

  • Prolonged standing
  • Clinical laboratory work environment
  • Ability to lift up to 25 pounds maximum

This job description may not be inclusive of all assigned duties, responsibilities or aspects of the job described, and may be amended at any time at the sole discretion of the employer.

The employee must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodation will be made to enable the employee with disabilities to perform the essential functions of the position, absent undue hardship.

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