Quality assurance specialist jobs in Wayne, New JerseyCreate job alerts

Job Title: Quality Assurance Specialist Jo Location: Clifton, NJ Job Duration: 6+ Months Shift: M-F, 08:00 AM to 4:30 PM EST. Pay Rate: $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.

Job Description Job Title: Quality Assurance Specialist (Clinical Lab) Duration: 6 months Location: Clifton NJ 07012 Hours: First Shift (8 AM - 4:30 PM)/EST Payrate: $48.50/hr. - $56.00/hr. (W2) depending on exp. 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 Quest Diagnostics 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. 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 Additional information: • 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

Job Description Responsibilities Join Our Team: $7,500 Sign-On Bonus Computed Tomography Technologist Trainee Reports to: Chief Technologist and/or Site Manager and/or CT Modality Specialist FLSA Status: Non-Exempt *This position does not meet the criteria for exemption from the provisions of the Fair Labor Standards Act; thus you will be eligible to receive overtime compensation, as appropriate. Overtime requires prior approval from your supervisor. Job Summary The CT Technologist Trainee is an entry-level position designed for individuals who are actively pursuing a career in Computed Tomography. Under direct supervision, the trainee participates in patient care activities and assists with CT technical procedures. The individual in this role must successfully complete all required training and obtain ARRT (CT) certification and/or State licensure (as applicable by state regulations) within the designated timeframe in order to transition into a CT Technologist position. Essential Duties and Responsibilities • Assists with preparing patients for CT exams and explains procedures in a courteous and professional manner., • Learns proper positioning techniques, immobilization methods, and safety procedures for CT imaging under supervision., • Observes and assists with administering contrast media (only after obtaining venipuncture certification and under direct supervision, if applicable)., • Supports technologists with image processing, PACS transmission, and quality assurance checks., • Maintains patient confidentiality and adheres to HIPAA guidelines., • Participates in educational activities, in-service training, and on-the-job instruction to gain competency in CT imaging., • Ensures exam rooms are clean, stocked, and prepared for patient procedures., • Provides professional and compassionate care to patients throughout the imaging process., • Completes administrative tasks, paperwork, and data entry as assigned., • Performs other related duties as assigned while learning the full scope of the CT Technologist role.Minimum Qualifications, Education, and Experience, • Must have current ARRT(R) and State License in Diagnostic Radiologic Technology (CRT)., • Must obtain ARRT (CT) certification and/or applicable State CT license within the timeframe required by RadNet policy or state regulations. Continued employment in the trainee role is contingent upon meeting this requirement., • Completion of an accredited Radiology program required., • BLS (Basic Life Support) certification required., • Venipuncture certification preferred; if not held, must obtain within required timeframe., • Ability to learn and apply specialized CT equipment operation., • Strong interpersonal and communication skills with ability to relate to patients, physicians, and team members., • Must be detail-oriented, highly organized, and committed to professional development.Quality Standards, • Participates fully in RadNet training, policies, and protocols., • Practices universal safety and radiation protection precautions., • Demonstrates commitment to professional growth through coursework, continuing education, and licensure preparation., • Provides excellent patient service and upholds RadNet’s values and compliance standards.Physical Demands This position often requires sitting, standing, walking, bending, twisting, reaching, handling or palpating, speaking, and listening. Must be able to lift over 50 pounds occasionally. Assists and participates as part of the lift team for patient transfers. Working Environment Work is performed in an outpatient medical office setting with low to moderate noise levels. Accommodations Reasonable accommodations may be made to enable individuals with disabilities to perform essential job functions. I have read and understand the responsibilities and requirements of the position. Pay Range: $39.00 - $45.00 per hour #CTNJ

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Conduct thorough investigations for quality events. Analyze quality data to identify trends and areas for improvement. Create and maintain essential quality documentation.

This role focuses on maintaining compliance within a regulated environment by ensuring adherence to quality standards and procedures. You will be instrumental in investigating quality issues, analyzing data, and implementing effective corrective actions. Ensure adherence to GMP and ISO quality stand

Job Description Join Our Dynamic Laboratory Support Team as a Clerical - Administrative Specialist Are you passionate about ensuring quality and compliance in a clinical laboratory environment? Do you thrive in roles that combine administrative precision with a deep understanding of laboratory operations? If so, this is your chance to contribute to a respected healthcare setting dedicated to excellence in patient care and laboratory standards. We are seeking a highly organized and detail-oriented Clerical - Administrative professional to support laboratory quality assurance, accreditation, and compliance initiatives in a fast-paced, collaborative environment. What You’ll Do: Support Accreditation and Compliance Efforts: Assist with internal inspections of laboratory facilities and specimen collection sites ensuring adherence to federal, state, and local regulations. Serve as a resource on CLIA '88 regulations and CAP accreditation standards to maintain laboratory certification and quality. Coordinate Proficiency Testing: Manage enrollment, participation, and corrective actions related to proficiency testing programs. Ensure the timely resubmission of blind samples and validity checks, maintaining rigorous instrument-to-instrument, method-to-method, and laboratory-to-laboratory comparison processes. Enhance Quality Assurance Programs: Support monthly QA meetings, maintain quality indicators, and assist in the distribution and review of QA Manuals. Contribute to monitoring corporate quality surveillance, patient results distribution, and best practice initiatives. Facilitate Quality Improvement Initiatives: Track and report reportable quality issues in compliance with SOPs, ensuring complete documentation and resolution. Support the implementation of quality improvements and process enhancements across laboratory departments. Administrative and Organizational Support: Maintain accurate documentation, coordinate schedules, and ensure compliance with SOPs and accreditation standards. Handle multiple tasks efficiently within a matrix organizational structure. Required Skills and Qualifications: Professional Experience: Minimum of three years working in a laboratory setting with a strong understanding of laboratory operations, quality assurance, and accreditation requirements. Certifications: Qualification as a General Laboratory Supervisor as defined by CLIA '88 is mandatory. Technical Proficiency: Proficient in laboratory quality tools, statistical quality control, and relevant computer applications. Communication: Exceptional interpersonal, written, and verbal communication skills to effectively collaborate with team members and regulatory agencies. Problem-Solving and Organization: Demonstrated ability to manage change, multi-task, and lead quality improvement projects. Strong analytical skills and attention to detail are essential. Additional Qualifications: Ability to motivate teams, function effectively in a biohazard environment, and operate within a matrix organization are highly desirable. Nice-to-Have Skills: Experience with project management tools and methodologies. Familiarity with laboratory information systems. Previous involvement in biohazard or infectious disease laboratory environments. Multilingual abilities are a plus for diverse team coordination. Preferred Education and Experience: Bachelor’s degree in chemical, physical, biological, clinical laboratory science, or medical technology. Proven track record supporting laboratory compliance and quality assurance programs. Other Requirements: Must be able to work in a biohazard environment adhering to safety protocols. Flexibility to handle varied administrative responsibilities. Commitment to continuous improvement and professional development. This is a fantastic opportunity to leverage your laboratory knowledge and administrative skills in a role that directly impacts quality outcomes and patient safety. If you thrive in detail-oriented, compliance-focused roles with a collaborative team environment, we want to hear from you! Apply now to become an integral part of a leading medical support team committed to excellence. Please reference Job number: 292868

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Formalize and maintain the Quality Policy and Quality Objectives in alignment with business goals. Ensure proper calibra

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Strong knowledge of quality assurance principles, audits, CAPA, and continuous improvement methodologies. Ensure proper

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Formalize and maintain the Quality Policy and Quality Objectives in alignment with business goals. Ensure proper calibra

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Formalize and maintain the Quality Policy and Quality Objectives in alignment with business goals. Ensure proper calibra

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Formalize and maintain the Quality Policy and Quality Objectives in alignment with business goals. Ensure proper calibra

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Ensure proper calibration, verification, and frequency of all measuring and testing equipment used for quality assurance

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Ensure proper calibration, verification, and frequency of all measuring and testing equipment used for quality assurance

Insight Global is seeking an experienced and detail-oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). Formalize and maintain the Quality Policy and Quality Objectives in alignment with business goals. Ensure proper calibra

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Partnership for Children of Essex (PCE) is currently seeking a Quality Assurance Specialist. Computer literate a must with proficient skills in MS Office (Word, Excel, and PowerPoint) and an ability to learn new software that may be utilized in the agency's quality assurance program. Preparation of

The Quality Systems Specialist I (Material Review Coordinator), is responsible for managing the review, documentation, and control of nonconforming material in accordance with prescribed dispositions. Participate in other Quality Systems activities, including but not limited to internal audits and r

The Quality Management Specialist utilizes broad experience in Quality System Management to ensure that ConnectiveRx's Quality Management System conforms to internal policies, applicable regulations, and customer expectations. Additionally, the Quality Management Specialist leverages knowledge in Qu

The Quality Management Specialist utilizes broad experience in Quality System Management to ensure that ConnectiveRx's Quality Management System conforms to internal policies, applicable regulations, and customer expectations. Additionally, the Quality Management Specialist leverages knowledge in Qu

Eligibilities & Qualifications.Eligibilities & Qualifications.

The manager will lead efforts to improve quality outcomes and clinic operations in a way that contributes to an enhanced experience for staff and patients; these quality improvements include (but are not limited to) Practice, Health & Safety Assessments, and accreditation surveys. Responsible for on

Partner with key stakeholders to drive quality improvements across the organization. Support advanced product quality planning in high‑reliability product development and NPI programs. At least 5 years of experience in a people‑management or quality leadership role.

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