Your primary job responsibilities are to manage our Portal user access, enter data in our Account Management system, and provide customer service with third-party secure file transfer platform access. Entry of data in our Account Management system for our new Clinical and Commercial sites while supp...
The Document Control and Records Management Specialist II is responsible for a variety of tasks within the Records Management organization. Title: Document Control and Records Management Specialist II - Imaging Operations. Provide document control and record management support to requesting organiza...
The Document Control and Records Management Specialist III is responsible for a variety of tasks within the Records Management organization. Title: Document Control & Records Management Specialist III. Provide document control and record management support to requesting organizations. Ability to eva...
The Document Control Specialist is a full-time exempt position that reports to the Records Management and Document Control (RMDC) Manager. TITLE: Document Control Specialist. Understand and support nuclear regulatory and quality assurance document management practices and TerraPower Records M...
A company is looking for an AML Quality Assurance Sr. ...
Key Responsibilities:Manage multiple large- and small-scale complexity projects that have a direct impact on the companyCreate power point slides and provide project updates for programsDrive projects based on defined priorities; ensure scope of deliverables, timelines and budget are met; identify r...
A company is looking for a RN-Clinical Documentation Specialist, Level 2 Reviewer. ...
A company is looking for a Receptionist/Administrative Assistant. ...
A company is looking for a CDI Specialist to implement processes related to clinical documentation improvement in an inpatient setting. ...
A company is looking for a Repatriation Administrative Assistant to facilitate efficient operations of the Repatriation Program through administrative support. ...
A company is looking for a Quality Assurance Specialist to monitor and improve customer service interactions in their Ambulatory Contact Center. ...
A company is looking for a Federal Project Manager to oversee and mentor technical staff while managing projects related to geospatial services. ...
A company is looking for a Document Control Specialist II to support quality and regulatory activities. ...
A company is looking for a Senior Analyst, GTM Data and Analytics. ...
A company is looking for a Coding Quality Assurance Specialist to execute the quality assurance program related to CODER+ services. ...
A company is looking for a Product Data Analyst to support their mission in health and technology. ...
A company is looking for a Data and Reporting Professional II to generate reports and analyze data for process improvements. ...
A company is looking for a Project Manager with Genesys Cloud experience for a 100% remote role. ...
A company is looking for a Senior Quality Assurance Specialist to support VA Quality Compliance by ensuring high standards of quality assurance in processes and products. ...
A company is looking for a Data Entry Clerk II to join their Accounting, Revenue Recognition team. ...
A company is looking for a Total Quality Management (TQM) Specialist to ensure quality standards in call handling and operational processes. ...
A company is looking for a Quality Improvement Specialist II to assist with daily operations and support within the Quality Improvement department. ...
In this role, you will be responsible for handling general administrative needs and contribute to maintaining a positive and active environment for residents. ...
The Document Control Specialist is responsible for controlling all documentation in the ERP system. This opening is for a Document Control Specialist that embraces new opportunities. Maintenance, control, and input of all client & Volex documentation, including:. Previous Document Control Experience...
Education: Associate degree or equivalent in Biology, Chemistry, or related field.Work Experience: 2+ years’ experience in a regulated manufacturing industry or equivalent combination of education and experience.Working knowledge of device/drug/biotech manufacturing processes.Detail oriented and abl...