Sign upLog in

Spec, Quality Assurance

Lancesoft

Clifton, NJ

Apply
JOB DETAILS
SALARY
$31.20
SKILLS
Accreditation Standards, Analysis Skills, Best Practices, Business Processes, CAP - Certification Authorization Professional, Change Management, Clinical Laboratory, Communication Skills, Corrective Action, Federal Laws and Regulations, Interpersonal Skills, Laboratory Operations, Licensing, Maintain Compliance, Matrix Management, Multitasking, Organizational Skills, Pathology, Physical Chemistry, Problem Solving Skills, Project/Program Management, Quality Assurance, Quality Management, Quality Monitoring, Regulations, Regulatory Compliance, Specimen Collection, Specimens/Samples, Standard Operating Procedures (SOP), State Laws and Regulations, Surveillance, Technical Leadership, Testing, University/School Regulations
LOCATION
Clifton, NJ
POSTED
6 days ago
Title: Quality Assurance Spec
Location: Clifton NJ 07012
Duration: 5/26/2026 - 11/25/2026

Shift/Time Zone: First Shift (8 AM - 4: 30 PM)/EST

Job Description:
Support and coordinate efforts that foster quality and ensure that all pre-analytical, analytical and post-analytical processes are consistent with our company values and mission.

Duties and Responsibilities
Licensing and Accreditation
Support the internal inspection process of the business unit, associated laboratories and specimen collection sites to ensure compliance with applicable federal, state, and local regulations, College of American Pathologists (CAP) accreditation requirements and Client standards.
Serve as a resource regarding Clinical Laboratory Improvement Amendments of 1988 (CLIA '88) regulations and CAP accreditation standards.
Proficiency Testing
Assist and ensure enrollment and participation in proficiency testing for each test to include Corrective Action when necessary.
Coordinate the Validity Check program and Blind Samples resubmission program, if applicable.
Assist in maintaining a defined instrument-to-instrument, method-to-method, and laboratory-to-laboratory comparison process.
Quality Assurance/Quality
Improvement Support and assist on monthly Quality Assurance (QA) meetings. Support each department's comprehensive Quality Improvement (QI) plan. Assist in maintaining and monitoring Quality Assurance specific quality indicators.
Facilitate the preparation, distribution and review of the QA Manual.
Support the Corporate Quality Surveillance Program, Patient Results Distribution Program, Best Practice Team Initiative/Database Changes Verification Program and other monitoring programs specifically assigned by National Quality Assurance. Quality Assurance Initiatives
Assist in the prompt and complete reporting of Reportable Quality Issues in compliance with the Standard Operating Procedure (SOP).
Assist in the complete tracking of revised reports in compliance with the SOP.
Assist in any other duties as assigned by the Technical Manager.

Job Qualifications (Work Experience, Physical & Mental Requirements, Knowledge, Skills)
Required Work Experience:
Qualification as General Laboratory Supervisor as defined by CLIA '88required
At least three years employment in a laboratory setting required
Experience with Quality Assurance, statistical Quality Control, and laboratory regulations/accreditation requirements required.

Preferred Work Experience:
N/A
Physical and Mental Requirements:
N/A
Knowledge:
N/A

Skills:
Strong interpersonal communication skills required
Demonstrated strong writing and composition skills required
Understands clinical laboratory operations required
Able to effect Quality Improvement through problem solving skills and knowledge of quality tools required
Able to manage change required Organization skills required Project management skills required
Analytical skills required
Technical skills required
Computer skills required
Able to function in a matrix organization desirable
Multi-tasking skills desirable
Demonstrated success in motivating team members to reach objectives desirable

Works in a biohazard environment

Bachelor's Degree - Chemical, physical, biological or clinical laboratory science or medical technology - REQUIRED

Certifications Qualification as General Laboratory Supervisor as defined by CLIA '88 is REQUIRED

About the Company

L

Lancesoft

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc). 

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

COMPANY SIZE
2,000 to 2,499 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
2000
WEBSITE
http://www.lancesoft.com/

Resume Resources

Free Resume TemplatesFree Resume Builder