QA/QC Manager

Accurate Diagnostic Labs

South Plainfield, NJ

ID: 7070830
Posted: October 9, 2020
Application Deadline: Open Until Filled

Job Description

Accurate Diagnostic Labs is a dynamic, fast-paced and growing full service clinical diagnostic testing facility offering blood testing for various branches of medicine. We specialize in physician office based services and have conveniently located patient service centers throughout NJ-NY metro areas. Established in 1999, Accurate Diagnostic Labs prides itself in providing the highest level of customer service and quality assurance. Currently, Accurate Diagnostic Labs is looking for a QA/QC Manager.

The QA/QC Manager, plays a critical role in the development, maintenance and continuous improvement of Laboratory Quality Management Systems. He/She also serves as the head of quality assurance for Accurate laboratories and provides guidance and support to ensure that laboratory quality systems support compliance in an effective and efficient manner. Responsible for performing duties so as to operate the lab with the highest quality, safety and integrity, and in an efficient, economical and businesslike manner.

Duties and Responsibilities:

1. Provide support and backup of the laboratory day manager in all areas of the laboratory including IA, Chem, Special Chem, Hem, Slide Review, UA, and Coagulation. Hands On Bench work as needed from time to time for Backup and Training.

2. Provides oversight of the QA/QC program, SOP process, assures monitoring Maintenance Schedules are followed, QC and QA are within specified SOP guidelines. Assists director’s is writing SOP’s.

3. Reviews test performance, PT, drives process and project management, and prepares and submits required reports to meet established deadlines as assigned.

4. Monitor and Improve Quality Indicators to constantly improve Overall Laboratory Quality. Monitor and Trend shifts between PT. Seek out to eliminate Analytical Errors.

5. Experience and Knowledge of EP Evaluator, Unity, Westgard, Rule Setting, Establish Auto-verification Rules, monitors and updates reference ranges.

6. Oversee and Schedule activities related to Validating Laboratory Instruments and Reagents.

7. Document Deviations, errors, and provides ongoing Training Programs.


Bachelor's of Science degree in Medical Technology required with (ASCP) . Masters degree and or PhD preferred.


Must have experience in Quality Assurance and Quality Control, with knowledge of departments including Hematology, Serology, Immunology Departments, including Specialty sections.

Experienced in Reporting PT to NY CLEP and CAP Proficiency Testing Programs

Minimum 6 years Clinical laboratory experience,

Should have a general understanding of Microsoft Office Word, Email other office programs.


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