Optime Care
Specialty Pharmacy
QualityCoordinator
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Coordinator at Optime Care. Skills: Quality Initiatives, Documentation Management, CAPA. Coordinate Quality Initiatives. Investigate complaints”
Industry & Context.
Problem solving
First 120 days in office, 4 days in-office required (hybrid)
What You'll Do.
Coordinate Quality Initiatives
Investigate complaints
Assign quality management training
Document corrective action events
Conduct internal audits
Conduct external audits
Administer patient satisfaction surveys
Communicate with Corporate Management
Communicate with Division Management
Communicate with Operations/QA Management
Communicate with site QA Project Leader
Communicate with Site Management
Maintain controlled documentation
Change controlled documentation
Create controlled documentation
Communicate documentation updates
Support CAPA initiations
Support correction plans
Document events in Document control system
Understand complex issues
Coordinate with other professionals
Make decisions to solve problems
Gather necessary information
Maintain Quality initiative tracking boards
Maintain Quality initiative programs
Collect patient satisfaction information
Analyze patient satisfaction information
Perform other related duties
Remain flexible in work schedules
Remain adaptable in assignments
How You'll Work.
Team & Collaboration
Work as part of a team
Communication Scope
Oral communication; Written communication
Full Job Description
What we are looking for Optime Care is seeking a Quality Systems Coordinator at our Earth City, MO, location. We are looking for someone passionate about supporting an organization. The Quality Systems Coordinator will coordinate Quality Initiatives, including complaint and incident investigation/management; quality management meetings; training assignments for all levels of staff; performance improvement; and corrective action events, including time studies, internal and external audits, and patient/client satisfaction surveys. This position will be required to be in the office for the first 120 days for training purposes. It can then be a hybrid role with 4 days in-office required, depending on business needs. What the position will be doing Effectively communicate with Corporate, Division, Operations/QA Management, site QA Project Leader, and Site Management Maintain, change, and create controlled documentation within the Optime Care Management System (OCMS) Effectively communicate updates of controlled documentation to all levels of the corporation to ensure compliance with requirements Prepare and coordinate the delivery of correspondence with patients and clients as required Supporting the implementation of Corrective and Preventive Actions (CAPA) initiations, correction plans, and action plans A strong focus on technical writing is necessary as the employee will be writing instructions as well as documenting events in the Document control system. These documents will be reviewed by clients, regulators, certifying bodies, and staff at all levels Requires the ability to plan and understand often complex issues, coordinate with other professionals, and make appropriate decisions to solve problems and gather necessary information Maintain Quality initiative tracking boards and programs Collect and analyze patient satisfaction information Perform other related duties as assigned or necessary; remain flexible and adaptable in work schedules and assignments as defin
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