Director of Clinical Quality
Responsible for the day-to-day operations of the Quality Services departments. Oversees the areas of Performance Improvement, , Peer Review, Patient Relations, Regulatory Compliance. Responsible for identifying cost reduction opportunities through review of physician practice patterns. Demographic information, limited Patient Health Information related to job function.
Required: Bachelor’s Degree in business, management or health related field 10 years experience in ...
QA Assistant Manager needed ASAP!
Crown Technical Systems, a leading manufacturer of Protective Relay Panels, Medium Voltage Switchgear and Metal Control Buildings for the Utility Power Industry, has an immediate opening for a QA Assistant Manager in our Fontana, CA facility.
We are seeking a QA Assistant Manager to join our growing QA Department.
•Minimum of (2) years experience working in Quality Assurance with an ISO 9001 system.
•Electrical or ...
We have a facility seeking an experienced Clinical Director of Quality. They require 1-2 years of recent clinical director experience working in Quality. Must be a graduate of an accredited RN program, BSN required. Must be licensed in this state or eligible. Excellent compensation. Possible sign-on and relocation bonus. Not the right job for you? Still contact us and let us know your select specialty or geographic area of interest. We have access to hundreds of jobs across the country, many of which ...
Consult with Manufacturing, Information Management, Research Development & Engineering, Quality Assurance Operations and Product Performance Analysis teams to ensure compliance to LifeScan software development procedures and industry regulations.
Review and approve deliverables of the software development lifecycle.
Lead teams in performing Hazard Analysis.
Occasionally assist teams in developing Standard Operating Procedures and Work Instructions for software development activities that meet ...
Job Responsibilities and Requirements: Responsibilities The Quality Engineer III will act as the Quality interface and provide expertise between the organization and it's customer's to proactively assure that their quality needs and expectations are understood and satisfied. Provide support to the Supply Chain Management organization relative to the collection and analysis of supplier quality data. Provide expertise in Quality Assurance and process improvement tools and methods. Execute the ...
~~R & D Fasteners is currently interviewing qualified candidates for the position of Quality Inspector. Through his/her daily activities, this Quality Inspector is expected to support advanced production output, improve product integrity, and initiate required employee training. R & D Fasteners has established aggressive goals for advanced production output supported by dimensionally correct product, and this Quality Inspector is essential in meeting these goals through proactive and reliable ...
Growing Specialty Food Company in the Inland Empire is seeking a QC Manager.
The Quality Control Manager is responsible for enforcing the food safety programs and policies to ensure the continuous production of quality products consistent with established standards. This position will be responsible for the assessment, design, and implementation of all Operations training programs, to include Manufacturing and Support functions such as Safety and Quality.
Duties and Responsibilities
Engineer needed to develop and ensure the proper execution of quality activities in a cGMP regulated medical device manufacturing environment.
*** Prepare, review and or approve validation documents for new and existing products
*** Create and execute development testing, field acceptance testing, and site acceptance testing protocols.
*** Maintain IQ, OQ, PQ protocols and revise when necessary.
*** Troubleshoot process issues, process characterization and root cause investigations. ...
Seeking at least 5 years Quality Process Engineering experience in a manufacturing environment focused on injection molded plastic products to support the development and manufacturing of novel medical devices.
*** Managed CAPA system, reported root causes, and developed corrective actions.
*** Validated new and modified manufacturing equipment, laboratory instruments, and manufacturing processes.
*** Designed and implemented qualification and test protocols.
*** Provided Quality ...
QM Coordinator needed to ensure that clinical documentation is performed accurately and timely.
Review Start of Care, Resumption and Recertification packets to ensure accuracy and completeness.
Work with clinicians to select and prioritize appropriate patient diagnoses and accurately assign ICD-9 codes to each diagnosis.
Review 485's for completeness and accuracy.
Prepare, coordinate and participate in quarterly clinical record review.
Meet agency timelines for completion of work.
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