Process Improvement Coordinator Salary in Los Angeles, California

Join our dynamic team in Irvine, CA (onsite position) as we pioneer the future of industrial control systems. We're seeking an experienced Project Manager to drive our engineering projects to success. If you have a background in industrial controls or control engineering, this is your opportunity to make an impact in a rapidly growing field. Responsibilities: Lead project teams, ensuring adherence to best practices. Cultivate client relationships and manage project scope. Develop and maintain project budgets and schedules. Advocate for risk management and process improvement. Coordinate project activities and support team development. Ensure safety throughout all project phases. Your Profile: Experience in industrial controls or control engineering. Proven project management skills, PMP preferred. Ability to manage billable staff and handle multiple projects. Bachelors degree in engineering or related field. Proficiency in MS Project, Excel, Word, and OneNote. Willingness to travel to

The mission of the USC Suzanne Dworak-Peck School of Social Work is to improve the well-being of vulnerable individuals and communities, advance social and economic justice, and eradicate pressing societal problems in complex and culturally diverse urban environments throughout Southern California, the nation, and the world. Our mission is achieved by providing students with experiential, practice, and competency-based learning, and culturally responsive training that is informed by evidence and best practices. The USC Suzanne Dworak-Peck School of Social Work, Office of Academic Affairs is seeking an Online Programs Administrator. The Online Programs Administrator executes operations for multiple online/hybrid programs that offer the Master of Social Work (MSW), Master of Science in Nursing-Family Nurse Practitioner (MSN-FNP), Doctor of Social Work (DSW) and graduate certificate courses. The Administrator fulfills operational and administrative functions including scheduling, evaluati

Job Description Job Description SUMMARY: Under the leadership of the Chief Medical Officer, the QI Coordinator helps to facilitate quality improvement efforts throughout the organization. Monitors and helps develop quality improvement projects to meet LACHC’s evidence-based goals related to preventative and chronic care for all patients. Collaborates with other staff to execute the Quality Assurance/ Quality Improvement (QAQI) Plan and related projects. Manages data collection, monitoring, and reporting of clinical performance data and other quality-related data. Provides accurate, timely information to committees and staff involved with Quality Improvement. Supports LACHC’s mission “to follow Christ by loving and serving our neighbors through comprehensive, quality healthcare” in all job duties and responsibilities and demonstrate Christ-like behavior and attitude. ESSENTIAL DUTIES AND RESPONSIBILITIES: Includes but are not limited to the following: (Other duties may be assigned.) Qua

Job Description Job Description Job Title: Quality Improvement Coordinator Target Compensation Range: $20.00-$25.00/hour, depending on relevant qualifications and experience About Us: Astiva Health, Inc., located in Orange, CA is a premier healthcare provider specializing in Medicare and HMO services. With a focus on delivering comprehensive care tailored to the needs of our diverse community, we prioritize accessibility, affordability, and quality in all aspects of our services. Join us in our mission to transform healthcare delivery and make a meaningful difference in the lives of our members. Summary: The Quality Improvement Coordinator will be responsible for coordinating and implementing quality improvement initiatives related to HEDIS measures and risk adjustments/HCC. This individual will work with internal and external stakeholders to ensure compliance with HEDIS specifications, data collection, reporting, and improvement strategies. ESSENTIAL DUTIES AND RESPONSIBILITIES: inclu

The quality engineer position will ensure product and process producibility is optimized through: Reduced Costs, Improved Quality, Effective Corrective action, Reduced Cycle Times, and Process Capability. Job Summary Perform Engineering and Quality tasks requiring knowledge and experience of engineering principles, theories, and concepts as applied to manufacturing and tooling throughout the product cycle. Develops solutions to a wide range of technical problems related to the product being manufactured. Develops, monitors, and analyzes product/process trend data and or tooling/manufacturing & inspection techniques in order to optimize performance and minimize product and process variability and associated production costs. Provides support for the MRR system including submitting non-conforming parts to the customer, and working with other departments to develop root cause and corrective action plans necessary to reduce: Scrap, Rework and Repair costs. Evaluates initial/existing progra

Job Description The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities Independent st