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Job Requirements of Spec, Quality Assurance:
-
Employment Type:
Contractor
-
Location:
Clifton, NJ (Onsite)
Do you meet the requirements for this job?
Spec, Quality Assurance
Careers Integrated Resources Inc
Clifton, NJ (Onsite)
Contractor
Job Title: Quality Assurance Specialist
Jo Location: Clifton, NJ
Job Duration: 6+ Months
Shift: 08:00 AM to 4:30 PM
Pay Range: $31.20 - $ 56.12/hr. on W2.
Job Summary:
The Quality Assurance Specialist supports and coordinates initiatives that uphold quality standards throughout all phases of laboratory testing — pre-analytical, analytical, and post-analytical. This role ensures processes align with company values, regulatory requirements, and industry best practices.
Education: Bachelor’s degree in chemical, physical, biological, or clinical laboratory science, or medical technology – Required
Certifications: Qualification as a General Laboratory Supervisor as defined by CLIA '88 – Required
Experience: Minimum of 3 years in a laboratory setting – Required
Licensing & Accreditation:
Proficiency Testing:
Quality Assurance & Quality Improvement
Support key programs such as:
Quality Reporting & Compliance
Demonstrated experience in:
Work Environment:
Jo Location: Clifton, NJ
Job Duration: 6+ Months
Shift: 08:00 AM to 4:30 PM
Pay Range: $31.20 - $ 56.12/hr. on W2.
Job Summary:
The Quality Assurance Specialist supports and coordinates initiatives that uphold quality standards throughout all phases of laboratory testing — pre-analytical, analytical, and post-analytical. This role ensures processes align with company values, regulatory requirements, and industry best practices.
Education: Bachelor’s degree in chemical, physical, biological, or clinical laboratory science, or medical technology – Required
Certifications: Qualification as a General Laboratory Supervisor as defined by CLIA '88 – Required
Experience: Minimum of 3 years in a laboratory setting – Required
Licensing & Accreditation:
- Assist in internal inspections of laboratories and collection sites to ensure compliance with federal, state, and local regulations, CAP accreditation standards, and company protocols.
- Serve as a knowledgeable resource on CLIA '88 regulations and CAP accreditation guidelines.
Proficiency Testing:
- Ensure participation in proficiency testing for each laboratory test and coordinate necessary corrective actions.
- Oversee the Validity Check Program and Blind Sample Resubmission Program (as applicable).
- Support method comparisons across instruments, methods, and laboratory sites.
Quality Assurance & Quality Improvement
- Assist in monthly Quality Assurance (QA) meetings and support department-specific Quality Improvement (QI) plans.
- Monitor and help maintain quality indicators relevant to QA activities.
- Prepare, distribute, and review the QA Manual.
Support key programs such as:
- Corporate Quality Surveillance Program
- Patient Results Distribution Program
- Best Practice Team Initiative
- Database Changes Verification Program
Quality Reporting & Compliance
- Promptly report all Reportable Quality Issues according to Standard Operating Procedures (SOP).
- Track and document all revised reports in accordance with SOPs.
- Perform other duties as assigned by the Technical Manager.
Demonstrated experience in:
- Quality Assurance (QA)
- Statistical Quality Control (SQC)
- Regulatory/Accreditation Compliance (e.g., CLIA, CAP)
Work Environment:
- Biohazard Environment — must follow safety and handling protocols.
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