Quality Coordinator Nesco Resource, LLCQuality CoordinatorMonroe, NCSelects inspection and test equipment needed to support product inspection activities Communicates and documents significant issues or developments identified during quality analysis activities. Ability to read and interpret documents such as department work instructions, blue prints, process code documents, computer software manuals, safety rules, employee handbook and procedure manuals.
Warehouse Quality Coordinator Ryder System IncWarehouse Quality CoordinatorBurlington, NCImportant Note: Some positions require additional screening that may include employment and education verification; motor vehicle records check and a road test; and/or badging or background requirements of the customer to which you are assigned. Assist in effectively inspecting product for quality issues and remove defects/contaminants such as stones, wood, glass, plastic, etc., prior to packaging in accordance to specifications.
NewQuality Improvement and Infection Control Coordinator Sampson Regional Medical CenterQuality Improvement and Infection Control CoordinatorClinton, NCThe Quality Improvement and Infection Control Coordinator is responsible for supporting Sampson Regional Medical Center's (SRMC) mission of excellence in patient care delivery and outcomes. The coordinator in collaboration with the Quality Service Department will utilize a data driven, and best practices approach to measurably improve process and patient outcomes.
Onsite Quality Control Coordinator EASOnsite Quality Control CoordinatorHigh Point, North CarolinaWitness EAS welding quality assurance procedure is being implemented including current weld documentation. Conducts various quality control activities and assists with the application and monitoring of established inspection procedures and methods.
Quality & Regulatory Program Coordinator Carolinas HealthCare System Blue RidgeQuality & Regulatory Program CoordinatorMorganton, NCYoull love working with us because: We are a teaching hospital We work together to ensure our patients receive outstanding, holistic care Your expertise and ideas are valued Your health and well-being matter And much more I love working atUNCHealth Blue Ridge because I know I am seen and valued. Working closely with the Director of Quality, this role serves as a central point of coordination across departments, supporting regulatory compliance efforts, facilitating survey readiness activities, and enabling the efficient execution of quality program operations.
Quality Coordinator Cummins IncQuality CoordinatorForest City, NCChampion Quality Leadership and Systems Management by applying COS and TQM principles, effectively utilizing quality tools, and continuously improving the QMS-while embracing diverse perspectives to strengthen decision-making and overall organizational performance. Strengthen quality capability across teams by supporting implementation, auditing, and training on AIAG Core Tools (FMEA, APQP, MSA, SPC, PPAP), building organization-wide competency.
Quality Associate Materials Evaluation Coordinator Grifols SAQuality Associate Materials Evaluation CoordinatorClayton, NCSummary: The Quality Operations (QO) Assistant/Associate Materials Evaluation Coordinator evaluates critical quality attributes (visual, dimensional, functioncoordinates required chemical and/or biological testing, and executes approved usage decisions on all quality managed material used at the facility These evaluations are performed on a wide variety of materials including, but not limited to, chemicals, labeling components, primary drug containcomponents, process hoses, sterilizing filters, and other critical raw materials. This is done by verifying compliance to specifications and testingrequirements and ensuring required documentation is complete and accurate thus minimizing the possibility that the safety and efficacy of finalproducts manufactured and tested using these quality managed materials is compromised or adulterated.
Warehouse Quality Coordinator RyderWarehouse Quality CoordinatorBurlington, North CarolinaImportant Note: Some positions require additional screening that may include employment and education verification; motor vehicle records check and a road test; and/or badging or background requirements of the customer to which you are assigned. At Ryder, you will be part of a team-first culture built on respect when joining a community of proud women and men in Supply Chain, including many Military Reservists and Veterans.
NewHybrid Billing Quality Control Coordinator (Burlington / Durham NC) LabCorpHybrid Billing Quality Control Coordinator (Burlington / Durham NC)Burlington, NC$42,000–$65,000 / yearAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Revenue Cycle Leadership: Actively manage high-risk accounts and systemic billing challenges, implementing strategic solutions to prevent revenue leakage and improve collection rates.
HYBRID Billing Quality Control Coordinator (Burlington / Durham NC) LabcorpHYBRID Billing Quality Control Coordinator (Burlington / Durham NC)North CarolinaAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
HYBRID Billing Quality Control Coordinator (Burlington / Durham NC) Labcorp Holdings IncHYBRID Billing Quality Control Coordinator (Burlington / Durham NC)Burlington, NC$42,000–$65,000 / yearAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Revenue Cycle Leadership: Actively manage high-risk accounts and systemic billing challenges, implementing strategic solutions to prevent revenue leakage and improve collection rates.
Program Director, Quality Assurance/Quality Improvement/Risk Manager East Carolina UniversityProgram Director, Quality Assurance/Quality Improvement/Risk ManagerGreenville, NC$54,249–$71,716 / yearThe Administrative units include the Offices of the Dean, Vice Dean, Associate Dean for Student Affairs, Associate Dean for Research, Associate Dean for Clinical Affairs, Associate Dean for Extramural Clinical Practices, Assistant Dean for Dental Education and Informatics, Assistant Dean for Educational Support and Faculty Development, Assistant Dean for Academic Success and the Assistant Dean for Business Operations and Financial Affairs. The Quality Assurance/Quality Improvement/Risk Management Program Director, under the direction of the Vice Dean, will be responsible for design, implementation, and continued support of the Quality Assurance/Quality Improvement/Risk Management programs to ensure the highest quality, patient-centered care is provided in a safe and compassionate environment.
Quality Associate II/III, QA (Packaging) Grifols SAQuality Associate II/III, QA (Packaging)Clayton, NCIn addition to the duties described above the Quality Associate Ill, Quality Assurance may also perform the following duties based upon the business unit to which he/she is assigned: Responsibilities may include roles (such as author, reviewer, administrator or coordinator) in all quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, and Annual Product Reviews as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. The Quality Associate II, Quality Assurance for QA Packaging provides routine technical support for various tasks (i.e. documentation, training, compliance, product release, scheduling, etc.), assignments, projects, etc.
Quality Associate II/III, QA Grifols SAQuality Associate II/III, QAClayton, NCAdditional Responsibilities: In addition to the duties described above the Quality Associate III, Quality Assurance may also perform the following duties based upon the business unit to which he/she is assigned: Responsibilities may include roles (such as author, reviewer, administrator or coordinator) in all quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, and Annual Product Reviews as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Additional Responsibilities: In addition to the duties described above in the Quality Associate II, Quality Assurance may also perform the following duties based upon the business unit to which he/she is assigned: Responsibilities may include roles (such as author, reviewer) in quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, as well as provide Quality input for Validation projects, capital engineering.
Senior Quality Associate I/II, QA General Computer Systems Grifols SASenior Quality Associate I/II, QA General Computer SystemsClayton, NCProvide independent Quality Assurance oversight of computer system administration activities, including user access management, role and permission assignment, periodic access reviews, system configuration activities, and verification that administrative controls are executed in accordance with approved procedures, data integrity requirements, and applicable regulatory expectations. The Senior Quality Associate provides Quality Assurance oversight for GxP computerized systems throughout the system lifecycle, including validation, data integrity governance, regulatory compliance, computerized system administration oversight, and ongoing lifecycle management activities.
Quality Associate II/III, QA, Final Container Release Grifols SAQuality Associate II/III, QA, Final Container ReleaseClayton, NCAdditional Responsibilities: In addition to the duties described above the Quality Associate III, Quality Assurance may also perform the following duties based upon the business unit to which he/she is assigned: Responsibilities may include roles (such as author, reviewer, administrator or coordinator) in all quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, and Annual Product Reviews as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Additional Responsibilities: In addition to the duties described above in the Quality Associate II, Quality Assurance may also perform the following duties based upon the business unit to which he/she is assigned: Responsibilities may include roles (such as author, reviewer) in quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, as well as provide Quality input for Validation projects, capital engineering.
Principal Quality Associate, QA, General Computer Systems Grifols SAPrincipal Quality Associate, QA, General Computer SystemsClayton, NCAdditional Responsibilities: In addition to the duties described above, the Principal Quality Associate may also perform the following duties based upon the business unit to which he/she is assigned: Responsibilities may include advanced roles (such as author, reviewer, approver, administrator or coordinator) in all quality systems as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. The person in this role will primarily support site Data Integrity Initiatives for GXP computer systems used in Manufacturing and QC Laboratories and provide Quality Assurance oversight and document review for computer system validation for the QC Laboratories.
QRM Support Manager - National Tax Quality Assurance (Ntqa), Quality Risk DeloitteQRM Support Manager - National Tax Quality Assurance (Ntqa), Quality RiskRaleigh, NC$93,000–$191,000 / yearOur team supports client-facing teams in how they approach the marketplace, develop service offerings, evaluate and onboard prospective clients, contract for services, deliver quality client service, and fulfill post-engagement and other recurring obligations. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.
Sr. Quality Associate II / Principal Quality Associate - Filling Business Unit Grifols SASr. Quality Associate II / Principal Quality Associate - Filling Business UnitClayton, NCIn addition to the duties described above, the incumbant may also perform the following duties: Responsibilities may include advanced roles (such as author, reviewer, approver, administrator or coordinator) in all quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, and Annual Product Reviews as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Specific duties will depend on the assignment and may include; review of manufacturing or testing records, preparation or review of failure investigations, product/raw material sampling and/or testing, sampling/testing/data analysis of environmental monitoring samples and data, auditing, data analysis for stability, etc.
Quality Engineer II-III, Quality Assurance MedPharm LtdQuality Engineer II-III, Quality AssuranceDurham, NCThis position is responsible for monitoring and control the quality processes supporting incoming, in-process and final disposition including batch record review and release for GMP, clinical, and commercial programs through broad knowledge of GLP/GMP manufacturing theories and principles. Collaborate with cross-functional teams, including production, engineering, supply chain, and customer service, to address quality issues and drive continuous improvement initiatives.